Prostate Cancer News - Prostate Cancer Foundation of Australia
Transcription
Prostate Cancer News - Prostate Cancer Foundation of Australia
Queensland Prostate Cancer News The magazine is a publication of the Queensland Chapter, Prostate Cancer Foundation of Australia. June 2012 In this issue Letter from the Editor, Medicine and science are always evolving. It is not that long ago that the only test available for detection of prostate disease was by estimating levels of an enzyme called acid phosphatase in the blood. The problem Editor - Judith with this test was that an elevated acid O’Malley-Ford. phosphatase level carried with it the MBBS (Qld), inherent knowledge that prostate cancer MPH, JP(Q), had already metastasised to the bones. FRACGP Then came prostate specific antigen or PSA, which looked promising for detecting disease earlier, but it is not a highly specific test. In addition, levels of PSA may vary depending on a number of factors, such as recent sexual activity, strenuous exercise, and the presence of urinary tract infections and thus may vary accordingly. It is important to take these factors into consideration when looking at PSA results. Age related levels of PSA are commonly quoted, but in the very early stages of prostate disease, it is difficult to know if changing levels of PSA represent cause for serious concern. Refinement of PSA levels has led to the estimation of the PROSTATE HEALTH INDEX, which is now being offered as an improvement and refinement in diagnostic ability for prostate cancer. Other forms of prostate assessment are available with the advent of radiological and surgical investigation techniques for prostate cancer detection apart from the oldest method of examination, the DRE or digital rectal examination. Ultrasound examination and prostate biopsy add to the diagnostic paradigm of prostate cancer. 2 Resources: Web Links, Associated and Affiliated Groups. Whilst ultrasound investigation is a relatively noninvasive technique of assessment, prostate biopsy on the other hand is a much more invasive procedure and carries with it more inherent risk, particularly that of post-procedure infection. In addition, prostate biopsy often requires that multiple biopsies be taken at the time of the procedure which adds to the potential risk of infection. 3 Peer Support Volunteers Wanted. Contributing Guest Editor: The Plight of Men with Prostate Cancer in Country Queensland. 4 Pizza Could Cure Cancer, Study Says. Making an early diagnosis of prostate cancer is essential for achieving the best surgical results, minimising the risk of spread of the disease, reducing the likelihood of post-operative side effects and most significantly ensuring long term disease-free survival. Improving the yield of information from the PSA estimation has been a positive step in the direction of better diagnostic procedures for prostate disease and for the wellbeing of men, especially those with prostate cancer. This milestone is another positive step towards better outcomes. There will always be new ways of doing things as long as there is continuing medical research and development, and curious minds to challenge the status quo and to ask the important and relevant questions. Editor Calendar of Events 2012 Prostate Cancer Foundation of Australia www.prostate.org.au Cancer Council Queensland www.cancerqld.org.au T 1800 22 00 99 T 1300 65 65 85 June 3-9 Bowel Cancer Week www.bowelcanceraustralia.org June 10-17 Men’s Health Week www.menshealthweek.org.au July 22-29 National Pain Week www.nationalpainweek.org.au Anytime BBQ for Prostate Cancer www.pcfa.org.au Anytime C-vivor (free sessions) www.cancerqld.org.au Nov 19 International Men’s Health Day. Keep the day free for a celebration event. www.pcfa.org.au 5 Spotlight on Central Queensland (Rockhampton). 6 Public System Delays Diagnosis and Treatment of Prostate Cancer. 7 Abbott Licenses Biomarkers for use in differentiating Aggressive From Nonaggressive Prostate Cancer. 8 Radical Prostatectomy Versus Watchful Waiting in Early Prostate Cancer. 10 Does Smoking History Predict PDA Levels in a Clinically Significant Manner? 11 Conference Report ‘The Oncology Nurse Community’. New Prostate Heath Test - Prostate Health Index. 12 Men’s Health Daily Dose Newsletter - True Story. Problems with the PSA Test. 13 News Round Up. 14 Vale Garry Franklin. A Urine Test to Detect Prostate Cancer. 15 ‘The Inbox’, Tell Your Story to Readers of QPCN, Bonus for Subscribers. 16 Letters to the Editor; Forward a Copy; Thought for the Day. Brisbane Program; Contact Us; Disclaimer; Privacy. [email protected] The Queensland Chapter of the Prostate Cancer Foundation of Australia is grateful for the generous support of Cancer Council Queensland in the printing of this magazine. The content of this magazine is selected by the Queensland Chapter of the PCFA. Cancer Council Queensland does not necessarily endorse, or otherwise, any content contained within this publication. Resources Andrology Australia www.andrologyaustralia.org Ph 1300 303 878 Andrology Australia is the Australian Centre of Excellence in Male Reproductive Health. APCC Bio-Resource www.apccbioresource.org.au The national tissue resource underpinning continuing research into prostate cancer. Australian Prostate Research Centre – Queensland www.australianprostatecentre.org Research, collaborative opportunities, clinical trials, industry news. Cancer Council Helpline Ph 13 11 20 8am-6pm Monday to Friday. www.cancerqld.org.au/cancerHelpline Mater Prostate Cancer Research Centre www.mmri.mater.org.au Comprehensive information for those affected by prostate cancer, including the latest research news. Cancer Council Queensland www.cancerqld.org.au Research to beat cancer and comprehensive community support services. Cochrane Library www.cochrane.org Australians now have free access to the best available evidence to aid decision-making. Prostate Cancer Foundation of Australia www.prostate.org.au Phone 1800 22 00 99 Assistance with the experience of diagnosis and treatment for prostate cancer. HealthInsite www.healthinsite.gov.au Your gateway to a range of reliable, up-to-date information on important health topics. Queensland Chapter www.prostate.org.au Information, patient support materials, and contacts for advice on living with prostate cancer in Queensland. Lions Australian Prostate Cancer www.prostatehealth.org.au The first stop for newly diagnosed men seeking information on the disease. Prostate Cancer Support Groups in the Queensland Chapter There are 23 PCSGs in the Chapter with a total membership of approximately 3,300 men. Peer Support Group Contact Phone Peer Support Group Contact Phone Advanced (all areas) Jim Marshall 07 3878 4567 Hervey Bay Ros Male 07 4197 7244 Beenleigh Peter Keech 0407 070 194 Ipswich Terry Carter 07 3281 2894 Brisbane Peter Dornan 07 3371 9155 Mackay Philip Lane 07 4957 2518 Bundaberg Rob McCulloch 07 4159 9419 Maryborough Leoll Barron 07 4123 1190 Capricorn Coast (Yeppoon) Jack Dallachy 07 4933 6466 North Burnett Russell Tyler 07 4161 1306 Central Queensland (Rockhampton) Lloyd Younger 07 4928 6655 North Queensland (Townsville) Clarke Berglin 07 4773 3303 Far North Queensland (Cairns) Jim Hope 07 4039 0335 Northern Rivers (Evening) Craig Thurgate 0412 661 942 Far North Queensland Partners Margaret Rolfe 07 4045 1031 Northern Rivers (Day) David Hughes 02 6687 0008 Gladstone Geoff Lester 07 4979 2725 Northern Tablelands Peter Martin 07 4096 6315 Glass House Country Bob McLean 07 5496 9601 North West Qld (Mt Isa) Yvonne McCoy 07 4743 2054 Gold Coast Central Peter Jamieson 07 5570 1903 Sunshine Coast Rob Tonge 07 5446 1318 Gold Coast North John Caldwell 07 5594 7317 Toowoomba David Abrahams 07 4613 6974 Gold Coast Partners Maggie Angus 07 5577 5507 Twin Towns and Tweed Coast Ross Davis 07 5599 7576 Gympie Robert Griffin 07 5482 4659 Whitsunday Dave Roberts 07 4945 4886 Associated Support Groups 2 Group Contact Phone Group Contact Phone Brisbane Partners Wendy Marshall 07 3878 4567 Innisfail Desleigh Barrow 07 4061 9177 Kingaroy Robert Horn 07 4690 5800 PEER SUPPORT VOLUNTEERS WANTED Are you interested in making a difference for other men facing prostate cancer diagnosis and treatment? If so, we need your help! We are looking for men interested in becoming Peer Support Volunteers for the Living with Prostate Cancer project, part of the prostate cancer research program at Cancer Council Queensland. The Living with Prostate Cancer program delivers telephone-based support and information to men recently diagnosed with localised prostate cancer. It combines self-management and group peer support to improve unmet supportive care needs about cancer and physical activity for men with early prostate cancer. In this project, peer support is provided through monthly telephone support group meetings for six months that are led by two specially trained peer support volunteers. Each group will have two peer support volunteers as leaders to help manage the group effectively, and the peers will be supported by a Nurse Counsellor who will also be present during the calls. The Living with Prostate Cancer team includes psychologists, nurses and research staff and we will provide you with all the necessary training to take on this important role. The training will be held at the Cancer Council Queensland Brisbane office If it is more than 12 months since your treatment and you would like to find out more about the Peer Support Volunteer role, please contact the Project Manager, Anna Stiller, on (07) 3634 5356 or email [email protected]. CONTRIBUTING GUEST EDITOR: THE PLIGHT OF MEN WITH PROSTATE CANCER IN COUNTRY QUEENSLAND Many of us in the support group network of the Prostate Cancer Foundation of Australia [PCFA], as volunteers are concerned for the public patients who live outside the city. Men in Country Qld confront shortages of services and in some locations medical skills to deal with prostate cancer are simply not good enough. This factor is compounded by having to travel long distances to access doctors and this in turn results in men tending to delay seeking help until their symptoms or discomfort become serious. Prostate cancer is a very difficult disease to diagnose in its early stage. The most urgent need today, as emphasised by researchers, is the need to find a better and more accurate method of diagnosis. Men who are self employed, or are employed for example by a mining company or a local council, in fact any man who lives and works well away from health services is impacted by the time and distance factors to access doctors and hospitals where skill shortages for dealing with this disease are often a factor. Some time ago, I received a phone call from a gentleman who was a drag line operator working at a major mine. He drove to his local doctor some 100 kilometres distance asking for a check up and blood test to determine his PSA level. Some 12 months later he developed specific prostate symptoms. The end result was the man had to fly to Brisbane for treatment which included eight weeks of radiotherapy plus a long duration of other drugs with long term side effects. As he said, with some sense of humour, ”The new kitchen will have to wait,” as he had to enter into a short term rent agreement to be near the medical treatment. Think about what could have been if the doctor had been more aware of the facts of this terrible disease. Many men seek help in the city, which means not only time away from the family but big costs of travel and short term rent agreements, both compromising disincentives to care for their health. Cancer Council Queensland is doing a fantastic job providing advice and accommodation for some cancer patients, but the demand for assistance far exceeds the supply of resources. Another gentleman rang me from a hospital in North Qld where he was about to have a prostate biopsy and the anaesthetist did not arrive. He eventually came to Brisbane, found that he had early prostate cancer, had the prostate removed and after a month had no side effects. Being a public patient he borrowed the money on his family house to pay for immediate private surgery. Not infrequently, men in country Australia receive a delayed diagnosis of prostate cancer for a variety of reasons which include difficulty of access to medical services, reluctance to raise the topic of urinary symptoms and the fear of the diagnosis itself. Often the delayed diagnosis arises from lack of awareness regarding the possibility of the disease, and the fear of what it might entail. Prostate cancer diagnosis is difficult for many men in the country as it can be just luck that they find out early or late. It is logical that many men want to come to the city for medical help for prostate cancer treatment because they hear a long list of problems from others, information which is often exaggerated by country folklore. Men hear of the good doctors in the city and about those doctors who do nothing else except treat prostate cancer. The problem in the city is the ever increasing load on hospital urology departments caused by the ever increasing incidence of this terrible disease, terrible because it can cause a state of terror in a man when told of the diagnosis. I will remember for the rest of my life where I was standing when the phone call came from the urologist. Men suffer a multitude of thoughts at that instant. I remember a phone call from a man who had just been diagnosed with prostate cancer. He wanted to know how to achieve the best outcome, so he came to the city and found he had advanced cancer. He cried while he told me he had 400 people employed and would have to sell the business because he was going to die as he had ignored the early warning symptoms, or did not understand the significance of the signs. He received the best treatment, finally accepted he had side effects for Continued... 3 The Plight of Men with Prostate Cancer in Country Queensland Continued... life, sold the business and went to Italy to see all the relations. His wife said to him, “So you can see there can be a benefit in being a victim. It has saved our marriage.” Whilst access to health information is taken for granted in the city it should not be taken for granted that the same ease of access exists for country people, especially people in remote places in this vast country of ours. The Prostate Cancer Foundation of Australia has received an ongoing grant to assist to open new support groups. I am often asked what the benefits of a support group are. My answer is there are many answers to that question but probably the biggest advantage is to be able to talk to other men who have experienced the curse of prostate cancer. This, for many men, is the first opportunity to listen and talk to other men openly about their issues and problems. The most moving experience for me was when a stranger came to the Brisbane Support Group and stood up in front of the meeting and told us with tears on his cheek that he had been told he had about five months to live. Those present were moved and some set out to help. At the end of the night everyone knew him and he was laughing at jokes and comments as he found himself around friends who really cared as some had similar problems. Support groups are not for everyone but they do provide an experience and an opportunity to understand the disease from a different perspective to that discussion they have with their GP and/or urologist. Not all GPs are aware of the existence of prostate cancer support groups, and not all men are made aware of the groups by their urologist. There is a role here for the Prostate Cancer Foundation to increase awareness amongst the professionals, and to encourage a partnership in treatment and support for men with prostate cancer. A support group is a very different place to be when compared to the office of the GP, or indeed that of the specialist urologist or hospital outpatient department. Each has a distinctive role and the functions compliment each other to the benefit of the patient and his family and, most of all, allow dialogue in the decision making process regarding appropriate treatment. In 1984 the Federal Government handed the responsibility for a range of costs to the States as part of a rearrangement of the so-called Grants Commission. This included an agreement to fund the Patient Travel Subsidy Scheme [PTSS] and including an undertaking to maintain the level of service with adjustments based on the inflation rate or some similar method. Since that date there have been many efforts by many organisations and individuals in Queensland to gain an increase, and today it remains the same rate except for a 10 cent increase per kilometre in the travel rate and GST on accommodation [$30.00 plus GST]. The LNP Government has announced it will increase the contribution by 100%. Past years have been grossly unfair to many country patients and their families and have contributed to the fact that many men with prostate cancer find out they have this disease when it has reached a more advanced stage. There is no doubt that more urologists are being trained in the speciality and some are more than willing to go to the country where new cancer centres are being opened, Cairns being a good example. The travel and accommodation problems remain for many - a recent example was it is cheaper to fly to Brisbane from Mt Isa than to go to Townsville. My suggestion is to make sure all new politicians are reminded on a regular basis that $60 per day does not “buy” a bed in almost all motels and hotels, and that patients and their families still have to travel long distances and find accommodation to access health services in many parts of Queensland. Why should those men who live in the country be at such a disadvantage when compared to those in the city? Ian Smith Brisbane Support Group, Deputy Chair Queensland Chapter Council Member Queensland Board Prostate Cancer Foundation of Australia PIZZA COULD CURE CANCER, STUDY SAYS By Clarissa Wei, 1 May 2012, Categories: Health, Pizza Can pizza be the cure to cancer? According to a new study by researchers at Long Island University the herb oregano, a key ingredient in most pizza sauces, can potentially be used to treat prostate cancer. “We know that oregano possesses antibacterial as well as antiinflammatory properties, but its effects on cancer cells really elevate the spice to the level of a super-spice like turmeric,” said Dr Supriya Bavadekar, Assistant Professor of Pharmacology. Dr Bavadekar’s research shows that carvacrol, a component of oregano, induces apoptosis or “cell suicide”. Dr Bavadekar and her team are currently trying to pinpoint exactly how the compound causes this cancer cell suicide. 4 This isn’t the first time the Italian dish has been associated with cancercuring properties. “Some researchers have previously shown that eating pizza may cut down cancer risk,” Dr Bavadekar said. “This effect has been mostly attributed to lycopene, a substance found in tomato sauce, but we now feel that even the oregano seasoning may play a role.” Though the study is at its preliminary stage, Dr Bavadekar believes the compound in oregano has a huge potential in being used as an anti-cancer agent. “If the study continues to yield positive results, this super-spice may represent a very promising therapy for patients with prostate cancer,” she said. SPOTLIGHT on Central Queensland (Rockhampton) ‘Welcome’ is the first sign you see as you travel from town to town throughout Central Queensland (CQ) and this is especially so when arriving in Rockhampton, the hub of CQ. Rocky, as it’s affectionately known, is famous not only for its welcome but also for the Bulls that accompany it! There is at least one on every main road and many of the local businesses have been able to incorporate them into their facades and logos. The Great Western Hotel (a local watering hole) has got an arena that regularly hosts rodeos and bull riding competitions and, of course, has great steaks! The city, situated on the Tropic of Capricorn (look for the Spire at the Information Centre), sits on the Fitzroy River which has the second largest catchment area in Australia. No wonder it has been flood prone in the last few years! A stroll along the river bank will take you past many beautiful old buildings such as the Criterion Hotel (said to have its own ghost), the Customs House and Walter Reid Buildings. For another trip back in time head out to the Heritage Village. There are several old houses, a school, hospital, church, fire station and various workshops. This was the venue for a stop-over for the Rumble Riders in past years who raised large amounts of money for the Prostate Cancer Foundation of Australia (PCFA). following: Blackwater Mine Workers Club Charity Golf Day $16,200, Rocky Crocs Masters Swimming Club $2,000, Rockhampton Correctional Centre $963, Rockhampton Chapter Order Eastern Star $100, North Rockhampton Bowls Club $2,023 (donated to prostate cancer research), Gracemere Croquet Club $300, Fishing Competition held in Moura with the John Milne on the Hustings Creating Awarenes proceeds of $8,200 donated to PCFA and Ergon Energy $3,000, also donated to PCFA. Carol Hobson and her merry band of helpers ran two very successful charity golf days raising $7,091. From Rocky there are many and varied sights to be seen in our area, the beautiful coastline around Yeppoon and Emu Park, a day trip to Great Keppel Island, the rugged hills of Mount Morgan (known for its old gold and silver mines) and the township of Emerald with its cotton, beef and gemstone attractions. The Central Queensland Prostate Support and Awareness Group has been part of the local scene for many years. It was established in October 1999 under the guidance of Dr Kenny P’ng. The meetings were originally held at Hillcrest Hospital but since then we have had a couple of moves with our current location being the Community Health Centre. Nowadays we have a membership of over 120 with regular meeting attendances of 35 to 40. The Group is steered by Lloyd Younger (Chairman), John Milne (Vice-Chair), Rita Milne (Secretary) and Graeme Dougan (Treasurer). Until recently, John Milne and Bill Forday were representatives on PCFA’s Queensland Chapter Council. For several years now Lloyd has been actively promoting men’s health issues and prostate cancer awareness. He has visited Rotary Clubs, Stanwell Power Station and the Railway Electrical Workshops talking, presenting and encouraging his listeners to become more aware of male health matters, particularly prostate problems, and to spread the message whenever and wherever appropriate. Lloyd and John are often called upon as representatives to accept donations. We have been very fortunate to receive help from the Gordon Campbell, Fran Campbell, Kevin Hinchcliffe, Jenny Leyland with fellow members John Milne, Don Neaton in background Our members all look forward to reading Rita’s regular newsletters each month. She does a great job of keeping us up to date about various members’ health, up and coming guest speakers and reminders of meeting dates. The guest speakers are from a variety of backgrounds, and willingly share their knowledge and expertise with us. We have been particularly privileged to have hosted Professor Colleen Nelson and Dr Bruce Kynaston, with local presenters being Sherree Schnieder (Physiotherapist), Joe Keoch (Organ Donation), Alana Richardson (Rockhampton Cancer Council Accommodation), Peter Aylwood (Public Trustee) and Dr Peter Reaburn (Exercise). A regular event on the Group’s calendar is the Bunnings Sausage Sizzle in September, International Prostate Cancer Awareness Month. This is always well supported by the members and is a Continued... 5 SPOTLIGHT on Central Queensland (Rockhampton) Continued... major fundraiser for the Group. It’s a very busy day with lots of laughter and camaraderie. Last year we raised $1,055. collaboration and innovation. This was an excellent opportunity for us to reach out to the “Man on the Land.” We had a booth as usual and many busy support group members donated their time to talk and hand out information pamphlets. A great time to fly the flag! Every group enjoys a social outing and ours is no exception. We usually have a couple of luncheons during the year and run a very popular Multi-Draw. With over 40 prizes (wine, chocolates, scratchits, novelty items) it is always well supported and many people leave with something tucked under their arm! Lloyd Younger, Betty Hinchcliffe, Kevin Hincliff, Bill Forday, Len Mahon, Fran Campbell and, Marie Mahonenjoying at the mid-year luncheon at Suzies CQU Rocky is known as the Beef Capital of Australia and hosted BEEF AUSTRALIA in May 2012. The BEEF Expositions are one of the world’s great cattle events and are held triennially in Rockhampton. The organisers expected over 75,000 international, interstate and local visitors to attend the latest in beef cattle production, During the winter months Central Queensland is a destination for the “Grey Nomads”, with caravans, recreational vehicles, boats and bikes in tow. We have great weather and lots to see and do! The Central Queensland Prostate Support and Awareness Group meets on the third Thursday of the month and like the sign says “VISITORS WELCOME!” So if you are holidaying in the area please join us. Lloyd Younger 07- 4928 6655 John Milne 07- 4936 3434 PUBLIC SYSTEM DELAYS DIAGNOSIS AND TREATMENT OF PROSTATE CANCER Press release CCQ, 14 March 2012. Gemma Ward, Media Manager, Cancer Council Qld (07) 3634 5372. Research has found differences in waiting times for diagnosis and treatment of prostate cancer between the public and private health systems, with public health patients likely to wait longer than private patients. The study by Cancer Council Queensland is the first of its kind to demonstrate the link between delayed diagnosis and treatment for prostate cancer and the Queensland health service system. Lead researcher, Associate Professor Peter Baade, said targeted strategies were needed to address the inequity. “The results of our study show that there are systematic differences in men’s prostate cancer management, both for diagnosis and treatment,” he said. “These differences are predominately related to access to private hospital care, suggesting that there are inequities in health-care service provision that are system based. “Without acknowledgment and targeted strategies, these inequities are likely to persist and widen as health-care budgets tighten and prostate cancer incidence increases, and indeed there is ecological evidence that this is occurring. 6 “It is hoped that the results of this study will increase the motivation of Government and health care planners to act.” The study found men without private health insurance were twice as likely to wait more than 70 days for a definitive diagnosis and nearly three times as likely to wait more than 70 days between diagnosis and treatment. “While the clinical implications of delay to diagnosis and treatment for prostate cancer are unclear, longer time intervals before and after diagnosis mean greater uncertainty and accompanying anxiety,” A/Prof Baade said. “With its high and increasing incidence and substantial treatment burden, the management of prostate cancer is a critical issue.” Prostate cancer is the most common cancer diagnosed in Queensland men. “Importantly, the findings suggest that greater funding and resources is urgently required to improve clinical care for men with prostate cancer by ensuring men receive better education and decision support about diagnosis and treatment at the primary care level.” ABBOTT LICENSES BIOMARKERS FOR USE IN DIFFERENTIATING AGGRESSIVE FROM NONAGGRESSIVE PROSTATE CANCER Reference. BIORESEARCH ONLINE - Company’s website at http://www.abbott.com/, 17 April 2012 Detection of Gene Abnormalities May Help Men Determine the Best Approach to Treatment Abbott Park, Ill/PRNewswire/ - Abbott announced today it has acquired an exclusive license for several novel biomarkers from Stanford University for use in developing a molecular diagnostic test that could satisfy a longstanding unmet medical need: differentiating aggressive from nonaggressive prostate cancer. Recent data point to certain genetic biomarkers that may identify which patients have fast-growing malignancies and should be treated aggressively versus those who can be directed to “active surveillance” or close monitoring. The National Comprehensive Cancer Network prostate cancer treatment guidelines were also recently updated to include recommendations for patients who fall into these categories. “Developing a clinically validated prostate cancer prognostic assay with actionable data represents the ‘holy grail’ in improving disease management,” said James Brooks MD, Associate Professor and Acting Chair, Department of Urology, Stanford University Medical Center. “It clearly would fulfill an unmet medical need to help men with prostate cancer know which treatment options will yield the best outcomes for their long-term survival and best quality of life. Certain men found to have slow-growing cancers could safely opt for no treatment and avoid life-altering side effects.” Prostate cancer, the second most common cancer in men, with an estimated US prevalence of 2.3 million, is usually diagnosed with a biopsy of prostate tissue. If cancer is found, the patient and physician must decide on treatment options, ranging from no treatment to aggressive management with radiation and chemotherapy or surgical removal of the prostate. Because prostate cancer treatments may have side effects like erectile dysfunction and urinary incontinence, treatment decisions may focus on balancing therapeutic goals with a patient’s age and other factors such as diet, exercise and lifestyle. In most cases, decisions rest on health-adjusted life expectancies. In certain men, prostate tumors may grow so slowly that no treatment is required. However, there is no test or procedure available at this time that can optimally discriminate benign from aggressive disease. Fearing the worst outcomes, many men opt for aggressive treatment even though it might not be needed. Abbott will develop a molecular assay based on its proprietary FISH (fluorescence in situ hybridization) technology to detect rearrangements of the ERG and ETV1 genes and measure loss of the PTEN gene. A study published in the British Journal of Cancer evaluated 308 men diagnosed with prostate cancer who were treated conservatively. Those who did not show ERG/ETV1 genetic aberrations with no PTEN gene loss had excellent prognosis, evidenced by an 85 percent survival rate after 11 years. Men who showed PTEN gene loss in the absence of the gene rearrangements had a poor survival rate of 13.7 percent. The study showed the promise of the new biomarkers to identify patients who would benefit most from intensive therapies. Abbott’s FISH probes to detect the ERG/ETV1 gene and measure PTEN gene loss will be evaluated as part of scientific research starting some time later this year. “This is a meaningful breakthrough for men who have to make the agonizing decision regarding treatments for prostate cancer,” said Stafford O’Kelly, head of Abbott’s molecular diagnostics business. “Without knowing if the cancer is life threatening, men have no way to know if prostate surgery or chemotherapy is the right option. This newest advance in personalised medicine will provide individualised genetic evidence for informed clinical decision making in choosing the right approach to prostate cancer treatment.” Abbott is a leader in personalised medicine through its ongoing development of molecular diagnostic tests for use in new drug research and targeted cancer therapies and treatments. About Abbott Molecular Abbott Molecular is a leader in molecular diagnostics the analysis of DNA and RNA at the molecular level. Abbott Molecular’s tests can also detect subtle but key changes in patients’ genes and chromosomes and have the potential for earlier detection or diagnosis, provide information relevant to the selection of appropriate therapies, and may improve monitoring of disease progression. 7 RADICAL PROSTATECTOMY VERSUS WATCHFUL WAITING IN EARLY PROSTATE CANCER Anna Bill-Axelson MD PhD, Lars Holmberg, et al N Engl J Med 2011; 364:1708-1717 5 May, 2011. The randomised Scandinavian Prostate Cancer Group Study Number 4 (SPCG-4) showed that radical prostatectomy decreased the risk of metastases, the rate of death from prostate cancer, and the rate of death from any cause. Although the participants in SPCG-4 were predominantly men whose cancers were detected on the basis of symptoms, rather than by elevated prostate-specific antigen (PSA) levels, prostate-cancer events have also accumulated during an extended follow-up period in a subgroup of men with low-risk disease. Determining whether there is a survival benefit for men with low-risk disease is relevant in light of the risk of over diagnosis resulting from PSA testing and the adverse events associated with therapy. Whether the previously observed lack of benefit in men older than 65 years of age and the absence of increased benefit after 9 years of follow-up persist is also of interest. We now present estimates of 15-year results, with a median follow-up period of 12.8 years. Methods Subjects Between October 1989 and December 1999, at 14 centers in Sweden, Finland, and Iceland, we randomly assigned 695 men with newly diagnosed, localised prostate cancer to radical prostatectomy or watchful waiting, as described in detail in a previous report and in the study protocol (available with the full text of this article at NEJM.org). Men were eligible for inclusion in the study if they were younger than 75 years of age and had a life expectancy of more than 10 years, had no other known cancers, and had a localised tumor of stage T0d (later named T1b), T1, or T2, as assessed according to the 1978 criteria of the International Union against Cancer. After revision of the staging criteria in 1987, T1c tumors were also included starting in 1994. On the basis of the results of a core biopsy or fine-needle aspiration, the tumor had to be well differentiated to moderately well differentiated according to the World Health Organization (WHO) classification. All patients included in the study were required to have a serum PSA level of less than 50ng per milliliter and a negative bone scan. Results A total of 347 men were assigned to the radical-prostatectomy group, and 348 to the watchful-waiting group. The baseline characteristics of the two groups were similar; the mean age of the men in both groups was 65 years. Only 12% of the patients had nonpalpable T1c tumors at the time of enrollment in the study. The mean PSA level was approximately 13ng per milliliter. By 31 December 2009, a total of 294 men in the radical-prostatectomy group had undergone a radical prostatectomy, and 302 men in the watchfulwaiting group had not undergone curative treatment. The median follow-up time was 12.8 years (range 3 weeks to 20.2 years). Histopathological Characteristics in the RadicalProstatectomy Group Positive surgical margins, which were present in 99 of the 283 prostatectomy specimens that could be evaluated, were associated with a poor prognosis in a model that adjusted only for age. However in a multivariate analysis that included extra-capsular tumour growth, PSA level at randomisation, and Gleason score, the relative risk associated with positive surgical margins was not significantly increased (data not shown). Extra-capsular tumour growth was found in 132 of the 284 radicalprostatectomy specimens (46%); tumours with extra-capsular growth, as compared with those without extra-capsular growth, were associated with a risk of death from prostate cancer that was increased by a factor of 7 (relative risk, 6.92; 95% CI, 2.6 to 18.4). Gleason score was also highly predictive of the risk of death from prostate cancer; among 129 men who had tumours with Gleason scores of 2 to 6, only 5 died from prostate cancer (data not shown). Discussion As of the current follow-up analysis, there continues to be a significant reduction in the rate of death from any cause, the rate of death from prostate cancer, and the risk of metastases in the radical-prostatectomy group as compared with the watchfulwaiting group. The benefit is obvious among men younger than 65 years of age, but it is still unclear whether the benefit extends to older men. The risk of death from prostate cancer after radical prostatectomy among men who had tumours with extra-capsular growth, as compared with men who had tumours without extracapsular growth, was increased by a factor of 7. We also observed a benefit of radical prostatectomy among men with low-risk tumours. The data on mortality are in accordance with our previous follow-up reports. However, in the current analysis, the number needed to treat to avert one death was 15, as compared with 19 in a previous analysis, in the case of the whole cohort, and the number was 7 in the case of men younger than 65 years of age. A previous analysis Continued... 8 indicated that the difference between the two groups remained constant after 9 years. In the current analysis, a continuing benefit with radical prostatectomy was observed also after 9 years of follow-up. The finding that the effect of radical prostatectomy is modified by age has not been confirmed in other studies of radical prostatectomy or external-beam radiation. The SPCG-4 data show that men younger than 65 years of age in whom the tumor is left in situ have a worse outcome than do all other subgroups. The apparent lack of effect in men older than 65 years of age should be interpreted with caution because, owing to a lack of power, the subgroup analyses may falsely dismiss differences. At 15 years, there was a trend toward a difference between the two groups in the development of metastases, and more men in the watchfulwaiting group than in the radical-prostatectomy group died from causes other than prostate cancer, but with metastases present. Current hormonal treatments might induce remissions long enough for older patients to die from other diseases. Therefore, competing risks of death may blur the long-term effects of treatment, and different classification rules of disease-free survival will influence survival estimates. The cumulative incidence in our study of death from prostate cancer among men treated with radical prostatectomy was high as compared with the incidence in other studies; nearly 80% of the men enrolled in our study had palpable tumors, with extra-capsular tumor growth in 46% of the radical-prostatectomy specimens. All but five men who died of prostate cancer in the radicalprostatectomy group had extra-capsular tumor growth. Although extra-capsular growth is not a perfect predictor of lethal disease, our findings indicate that these men could be a group for which adjuvant local or systemic therapy would be beneficial. In studies of active surveillance, a high proportion of patients with extracapsular growth among those who were switched to radical prostatectomy could be an indication that the trigger point for active treatment is too late. In men with low-risk disease, the absolute benefit of surgery with respect to death from prostate cancer and the risk of metastases was similar to that in the whole cohort. We caution that our low-risk group cannot be compared directly with men who are currently included in active-surveillance protocols because few of the men in our low-risk group had a tumor that was detected by means of a screening test. Furthermore, the biopsy protocol in this study entails a lower sensitivity for diagnosing high-risk disease than the extensive protocol in a more recent study; the lower sensitivity in our study is highlighted by the reclassification of the diagnostic Gleason score in the radical-prostatectomy specimens. However, our findings show that some tumors that are considered to be lowrisk at diagnosis do pose a threat to life, especially if they are not surgically removed. The cumulative incidence of side effects of surgery reflects a situation in which, historically, the need for radical excision of the tumor dictated extensive surgery more often than is the case today. Furthermore, the surgical techniques were not as well developed, and the number of surgeries performed was far from today’s levels. The data in the current analysis are based on information from medical records. We have previously shown that a complete understanding of the complex balance in effects between surgery and watchful waiting also requires obtaining patient-reported data on the severity of symptoms and on how much the patient is bothered by them. The strengths of our study include the randomised design, the completeness of follow-up, and the independent and blinded evaluation of the cause of death. Adherence to the assigned treatment was high despite the diversity of the two interventions. Our interpretation relies on stable long-term quantitative estimates, as illustrated in the cumulative-incidence curves and the consistency of the results over an extended follow-up period. The subgroup analyses were not pre-specified in the protocol and lack the power to rule out a treatment difference. We emphasise that these results should be interpreted with caution and should be viewed as hypothesis-generating for other studies. The current analysis adds to our knowledge in several areas. The benefit of radical prostatectomy continued to be seen beyond 9 years, which contradicts the notion that there is only a distinct subpopulation that responds to radical surgery with an early reduction in risk. The accruing numbers of events for the older age group indicate that in our study, a reduction in disease-specific mortality is unlikely ever to become apparent in this age group, owing to competing causes of death. The finding that some lowrisk tumours will progress and become lethal emphasises the importance of protocols with well-defined end points at which men in active surveillance switch to curative treatment. With continued follow-up, data from the SPCG-4 study may allow us to identify prognostic markers in men assigned to watchful waiting that can serve as trigger points for active treatment; the prognostic value of these markers can then be validated in cohorts that are under active surveillance. 9 DOES SMOKING HISTORY PREDICT PSA LEVELS IN A CLINICALLY SIGNIFICANT MANNER? Reference. The New Prostate Cancer Infolink, 21 Feb 2012 A new paper published online in the Journal of Urology suggests that the PSA and %free PSA levels of current smokers and former smokers may be statistically significantly impacted compared to those of men who have very rarely or never smoked. Li et al. were able to examine data from 3,820 men, all aged 40 years or older, who had previously participated in the National Health and Nutrition Examination Survey (NHANES) between 2001 and 2006. The men were divided into three groups: • Men with serum cotinine levels >10ng/ml or who had smoked at least 100 cigarettes during their lifetime and, at the time of interview, reported smoking every day or some days (“current smokers”) • Men with serum cotidine levels <10ng/ml who had smoked at least 100 cigarettes during their lifetime and who responded “not at all” to the question about whether they smoked now, at the time of their interview, were classified as (“former smokers”) • Men with a serum cotidine level <10ng/ml who stated that they had smoked fewer than 100 cigarettes in their lifetime (“never smokers”) *Note that a serum cotidine level of >10ng/ml is associated with active smoking within the immediately preceding few days. The core findings of this study were that: • For all ages and all patients combined o The average (median) total PSA level was 0.90ng/ml (range, 0.81–0.90ng/ml). o The median free PSA level was 0.26ng/ml (range, 0.25–0.28ng/ml). • For all “current smokers” (n= 1,188) o The median total PSA level was 0.80ng/ml (range, 0.80–0.90ng/ml). o The median free PSA level was 0.24ng/ml (range, 0.23–0.25ng/ml) 10 • For all “former smokers” (n= 1,359) o The median total PSA level was 0.95ng/ml (range, 0.83–1.01ng/ml). o The median free PSA level was 0.28ng/ml (range, 0.27–0.30ng/ml). • For all ”never smokers” (n= 1,270) o The median total PSA level was 0.9ng/ml (range, 0.80–0.94ng/ml). o The median free PSA level was 0.27ng/ml (range, 0.25–0.29ng/ml). • Multivariate linear regression analysis showed that, compared to “never smokers,” o The median total PSA level was 7.9 percent lower among “current smokers” o The median total PSA level was 12.2 percent lower among “former smokers.” • 34.2 percent of all participants had a %free PSA level of <25 percent. • “Current smokers” had a significantly lower %free PSA level than former smokers. • High body mass index and a diagnosis of diabetes were also significantly associated with a lower total PSA level. Exactly what impact such data may have on the interpretation of PSA levels and the need for a man to have a biopsy cannot be determined on the basis of a single study like this. It would be interesting to know if a larger, prospective study could give greater insight into any association between smoking, PSA level and risk for diagnosis with relatively indolent or clinically significant forms of prostate cancer. It should be noted that an 8 to 10 percent drop in PSA level is small (say from 4.0ng/ml to 3.6ng/ml). It is hard to believe that the clinical significance of such a change in value could be accurately determined in a specific individual on the basis of a single PSA test result - or that it would be likely to make much difference to whether a primary care physician did or did not refer the patient to a urologist for further work-up. CONFERENCE REPORT ‘THE ONCOLOGY NURSE COMMUNITY’ The data, part of the AFFIRM study, was presented by Dr Howard I Scher, chief of the genitourinary oncology service at Memorial Sloan-Kettering Cancer Center, a late-breaking presentation at the 2012 American Society of Clinical Oncology Genitourinary Cancers Symposium. Novel Drug, MDV3100, Will Likely Have a Major Role in Prostate Cancer Treatment By Anna Azvolinsky, PhD | 15 February 2012 The new drug, MDV3100, extended overall survival by 4.8 months (P < .001) in men with castration-resistant prostate cancer who had progressed after treatment with docetaxel (Drug information on docetaxel). It also reduced the risk for death by 37% as compared to placebo. This is an impressive feat. Currently, there is no standard of care for this group of patients. MDV3100 is an oral, androgen receptor signaling inhibitor that competitively inhibits the binding of androgens to the androgen receptor, and uniquely inhibits the receptor from translocating to the nucleus and binding DNA. MDV3100 was chosen for development based on robust prostate cancer model systems and activity in early stage trials in both chemotherapy-treated and chemotherapy-naive prostate cancer patients. It is the first in a new class of agents and different from the mechanism of action of currently available treatments. In total, 1199 patients were randomised over a 1-year time period starting in 2009. Patients had advanced disease, about 90% with bone metastases and 70% with soft tissue metastases. The estimated median overall survival was 18.4 months for the MDV3100-treated patients compared to 13.6 months for patients treated with placebo. MDV3100 treatment was also associated with a 50% reduction in prostate-specific antigen (PSA) levels in 54% of MDV3100-treated patients compared with 1.5% of placebo patients. The median time to PSA progression was 8.3 months in the experimental group compared to 3 months in the untreated group. Safety was also favorable, with mild adverse events, mostly fatigue, diarrhea and hot flashes, which were reported in about 2% of patients in both the experimental and placebo arms. One potential concern is a rare incidence of seizure seen in 5 patients in the MDV3100 arm. According to the trial authors, these cases were studied carefully and could be due to confounding events including brain metastases. The drug is made by Medivation in collaboration with Astellas. There is an ongoing clinical trial testing the efficacy of MDV3100 in prostate cancer patients who have not yet received docetaxel. Abiraterone (Zytiga) and cabazitaxel (Jevtana) have also recently showed a benefit in survival in phase III trials among prostate cancer patients after a docetaxel regime. Cabazitaxel, a microtubule inhibitor, was approved by the Food and Drug Administration in 2010. The trial that led to the approval showed a 30% reduced risk of death and improved overall survival by 2.4 months for cabazitaxel combined with prednisone. Abiraterone, a steroidal compound with antiandrogen activity, was approved this April, in combination with prednisone, demonstrating a survival benefit of 3.9 months. NEW PROSTATE HEALTH TEST - PROSTATE HEALTH INDEX Reference source. Dr David Kanoski. Sullivan Nicolaides Pathology Sullivan Nicolaides Pathology has introduced the next generation in prostate health assessment – Prostate Health Index (phi) combines the results of three blood tests into one index that estimates the likelihood of histologically confirmed cancer diagnosis on biopsy. diagnostic accuracy of phi (~75%) over total PSA (~55%) and free/ total PSA ratio (~65%) may provide patients and doctors with better information to assist in the decision about proceeding with a biopsy. It is important to note that a Medicare rebate is not available for phi. The fee for phi is $95 and the patient will be unable to claim a Medicare rebate towards the cost of the test. The composite score involves the measurement of 3 proteins; total PSA, free PSA and p2PSA, an isoform of PSA. The improved 11 MEN’S HEALTH DAILY DOSE NEWSLETTER - TRUE STORY (Men's Health Daily Dose Newsletter Editor's note: Men's Health Daily Dose Newsletter was awarded a 2011 American Society of Magazine Editor's award for personal service, honoring the superior and consistent use of print to serve readers' needs and aspirations, for this article.) It's June 20th, the first day of summer in 2008. I'm knocked out on an operating table and a robot is removing my prostate gland. In April I learned I had stage II prostate cancer, and after questioning experts and survivors, I've decided surgery is the way to go. Let's git 'er done. My mom died of cancer, but not me. No way. Now, almost 2 years later, I'm not going to say, "thank god they caught it in time...I'm so blessed, each new morning is a miracle...Blah blah blah blah." No, what I'm thinking is more along the lines of: I want my prostate back. Your prostate gland labors in obscurity. The size of a golf ball, it's tucked away under your bladder, biding its time until you and your reproductive system decide to emit the sacred seed. Then the semen assembly line kicks in: The sperm swim up from your testicles to the seminal vesicles, and there they are mixed in a happy bath of fructose, vitamin C, and prostaglandins. This brew then proceeds to your prostate, which tops it off with enzymes, citric acid, and zinc before your man milk is propelled out of your body and into hers with rather pleasant smooth-muscle contractions. This long bomb triumphantly delivers your DNA into the end zone. Ah, glory days. But around the time in your life when you start to think more about your 401(k) than foreplay, your prostate starts to misfire. It swells in size, and the swelling clamps your urethra in a vice grip. If the cause of the swelling is benign, you're lucky. That's what those running-to-themen's-room commercials for Flomax are all about. But some of the very same symptoms can also be caused by a prostate-cancer tumor. Prostate cancer is the second most common cancer among men; only some skin cancers are more rampant. In 2009, it caused an estimated 27,360 deaths - long, slow, embattled deaths, as the cancer spread beyond men's prostates to nearby bones, notably their spines. Once the cancer advances past your prostate, you have only a 30 percent chance of surviving 5 years. But catch it early, before the cancer cells escape, and your chance of surviving 5 years is 100 percent. Here's the good news about prostate cancer: Deaths are down because it is being diagnosed much earlier. In fact, 94 percent of all diagnoses these days peg the malignancy at stage I or stage II, before it metastasises beyond the prostate. (Stage III cancers have begun to break out of the prostate; stage IV cancers have invaded nearby tissue and bone.) That has resulted in a steadily declining death rate of 4 percent a year since 1994. The declining mortality has generally been attributed to the widespread use - starting in the 1990s - of a simple test for the prostate-specific antigen, or PSA. THESE DAYS, THE PSA TEST IS SO ROUTINE for middle-aged men that your doctor might order one for you without even asking. My internist did that for me in the summer of 2007, as part of a regular physical. Mostly he was worried about my cholesterol levels. The results showed mildly troubling cholesterol - but a very troubling PSA number. Standards in place at the time held that it should be less than 4; some evidence has suggested that it should be less than 2.5 if you're younger than 50. Mine was 12.6. Read more at Men's Health: http://www.menshealth.com/health/ coping-prostate-cancer#ixzz1oQWWYUVb PROBLEMS WITH THE PSA TEST - “PSA screening for early detection of prostate cancer has more harms than benefits,” USPSTF co-vice chair Michael LeFevre MD, a professor of family and community medicine at the University of Missouri, told menshealth.com. The risk for false-positives looms large: PSA levels can increase due to an enlarged or inflamed prostate—both benign conditions. According to the American Cancer Society, only 25 to 35 percent of men who have a biopsy due to an elevated PSA level actually have prostate cancer. And unnecessary biopsies are needlessly invasive, expensive, and carry an acute risk of prostate infection in about 1 percent of patients. There is also the risk of temporary problems using the bathroom. 12 More Testing Leads to Unnecessary Treatment “Most prostate cancers are not fast growing and many men are being treated for cancers that would never cause them harm,” Dr LeFevre says. Otis W Brawley MD, Chief Medical Officer of the ACS, noted earlier this year, “Many prostate cancers are cured, but do not need to be cured.” Then there are the undesirable treatment side effects: Dr LeFevre says that for every 1000 men surgically treated for prostate cancer, 200 to 300 will suffer urinary incontinence, impotence or both; 10 to 70 will experience serious post-operative complications and five will die within 30 days from complications. One man’s experience tells how, ‘I want my prostate back.’ NEWS ROUND UP 7 Steps To Prevent Prostate Cancer - It’s one of those weird anatomical-arboreal coincidences: The human prostate is about the size and shape of a walnut. But what if it really were a walnut? For one thing, you’d never get prostate cancer. Which sounds great, until you realize that you could get “walnut curculio” or “walnut-husk maggot” instead. Better to deal with the devil you know. And what a devil it is. Last year, 221,000 men (one of them Robert De Niro) were diagnosed with prostate cancer; that’s more than lung, colon, and brain cancers combined. And nearly 29,000 men died of it last year. These are grim statistics, but there’s reason to be optimistic. Make that seven reasons. Here is the latest, hot-out-of-the-lab research on how you can prevent, detect, and treat the disease. Putting this science into action (read: more sex, more wine) won’t confer absolute immunity, but it will make your prostate one tough nut to crack. TAKE CHARGE OF YOUR HEALTH, BODY, AND LIFE! 1. Love Thyself - As if masturbation didn’t already provide enough of a payoff, a recent Australian study found that DIY sex may also help prevent prostate cancer. The study of 2,338 men showed that the guys who masturbated five or more times a week were 34 percent less likely to develop prostate cancer by age 70 than those who handled matters less often. “Seminal fluid contains substances that are carcinogenic,” says Graham Giles, PhD, the lead study author. “Regular ejaculation may help flush them out.” And in case you’re wondering, no, masturbating more than once a day won’t offer more protection, and yes, straight-up sex works, too. But before you have unprotected nookie with your partner, be sure she’s been tested for cytomegalovirus, a type of herpes recently found in cancerous prostate tissue. 2. Be Happy You’re Going Bald - Turns out the hair-loss drug Propecia has one impressive side effect. In a National Cancer Institute (NCI) study of 18,882 men, researchers found that the men who took 5 milligrams (mg) of Propecia, aka finasteride, daily for 7 years had a 25 percent lower risk of prostate cancer than those taking a placebo. Finasteride blocks production of dihydrotestosterone, a hormone that triggers hair loss and prostate growth. “It’s the first study to prove that prostate cancer is preventable,” says Peter Greenwald MD, the NCI’s director of cancer prevention - and one of those 18,882 men. “My prostate’s normal,” he adds. One caution: Men on finasteride had a slightly greater chance of being diagnosed with a more aggressive form of the disease than did the placebo takers. More research on the drug is needed, but if you’re concerned about prostate cancer, discuss these findings with your doctor. 3. Wine and Dine - There’s a good reason Western European men have lower prostate-cancer rates than we do. And it has nothing to do with Speedo thongs. New research suggests that certain staples of the Mediterranean diet have prostate-cancer-fighting properties. For starters, a recent study published in the Journal of the National Cancer Institute shows that men who eat more than 10grams (g) of garlic or scallions (about three cloves of garlic or 2 tablespoons of scallions) daily have a 50 percent lower risk of prostate cancer than those who eat less than 2g. (Give credit to organosulfur compounds, which are common to both vegetables.) Then there’s red wine; red grapes are flush with resveratrol, an antioxidant found in some plants that may help inhibit the growth of prostate cancer, according to a report from the MD Anderson Cancer Center at the University of Texas. A glass or two of red wine daily should suffice. “If you drink too much,” says Catherine O’Brian PhD, the lead study author, “you can neutralize the beneficial effects.” 4. Lower the Bar - Here’s a PSA (public-service announcement) regarding your PSA (prostate-specific antigen): Using a score of 4.1 or greater as the alarm for prostate cancer could prove fatal. A recent study of 6,691 men, published in the New England Journal of Medicine (NEJM), showed that this traditional threshold for ordering a follow-up biopsy may be missing 82 percent of prostate-cancer diagnoses in men under 60. “The threshold of 4.1 that’s being used has never been rigorously studied,” says Karen M Kuntz, ScD, one of the study’s authors. And while critics say a lower threshold will lead to unnecessary biopsies, Rinaa Punglia, MD, another of the study authors, believes that the broader standard could be worth it. “It’s a trade-off,” she admits. “But it could save lives.” So how low should you go? Dr Punglia recommends that when you have your PSA level checked (annually beginning at age 50 - or 45 if you have a family history or are African-American), you observe a threshold of 2.6, especially if you’re under age 60; according to the NEJM study, following this guideline doubled the cancer-detection rate, from 18 percent to 36 percent. 5. Calculate Your Risk - Let’s say your PSA is 2.6. You still may not need a biopsy. Instead, ask your doctor to use a nomogram. This needle-free analysis turns a patient’s age, PSA density (PSA divided by the volume of the prostate), digital-rectal-exam result, and transrectal-ultrasound result into a score that helps determine whether a biopsy is really warranted. “We can say whether or not, for your prostate, that’s a high PSA,” says Mark Garzotto, MD, Director of Urologic Oncology at the Portland VA Medical Center. In a study of 1200 men, Dr Garzotto found that if a nomogram had been used in every case, it would have spared 24 percent of the men from unnecessary biopsies. If your doctor can’t crunch the numbers, ask for copies of your test results; you can find and print out the same nomogram here, and do the math yourself. 6. Hit the Spice Rack - Researchers at the Center for Holistic Urology at Columbia-Presbyterian Medical Center in New York City recently found that a blend of herbs including ginger, oregano, rosemary, and green tea reduced prostate-cancer cell growth by 78 percent in the lab. Sold as Zyflamend, it’s thought to inhibit the activity of COX-2, a protein linked to the progression of the disease. “We’re using it with promising results in some of our patients,” says Aaron Katz, MD, the center director. Another herbal option is FBL 101. When researchers at the National Cancer Institute gave FBL 101 to mice with prostate cancer, they found that it decreased a tumor blood-vessel growth factor called VEGF to undetectable levels. Crimp the blood supply and cancer can’t survive, says William Figg PharmD, the principal investigator. “Men who want to delay the time before they begin traditional treatment should check this out,” he says. 7. Use a Computer-Assisted Doctor - The radical prostatectomy recently became a lot less radical, thanks to a new robotic version of the procedure. With the da Vinci system, doctors use three-dimensional imaging to direct two nimble robotic hands through a few small slits in the patient’s abdomen to remove the cancerous prostate. According to data from the Vattikuti Urology Institute at the Henry Ford Health System in Detroit, 90 percent fewer men became incontinent and 50 percent fewer became impotent with the da Vinci system than with manual gland removal. “It’s like playing golf with a titanium driver versus a wooden driver,” says chief of urology Mani Menon, MD Another plus: Patients spent an average of 1.5 days in the hospital, compared with 2.3 days for open surgery. Above Information Sourced from Cancer Daily News 13 VALE GARY FRANKLIN by PCFA-Q Manager Graeme Higgs Much of what is good in life is the people you share it with. In the Rumble Rides completed so far, it was PCFA’s very great pleasure to know Gary Franklin. Gary was also instrumental in leading the fundraising in the country towns the riders visited. So much so that at the end of the last ride he was awarded the inaugural Spirit of Rumble Down Under 2010. Sadly, on Friday 17 February 2012 Gary passed as a result of an accident on his Gold Wing. Gary was a quiet gentleman who will be sorely missed. His funeral was by invitation only. However a memorial ride was held on Saturday 25 February. Assembling at the Kalbar Hotel participating mourners travelled to Gary’s Boonah property to pass their condolences to his family. Rumblers’ gather in the Royal Albert Hotel at Kalbar on a rainy Saturday afternoon in February, to remember Gary Franklin Gary Franklin is third from the left in this photo, standing slightly in front of and to the right of PCFAs Queensland manager, Graeme Higgs. The occasion was the cheque presentation ceremony for monies raised in the 2010 Rumble Ride. A URINE TEST TO DETECT PROSTATE CANCER Source. Reference. Men’s Health News, March 2012 Catching prostate cancer before it progresses could soon be as easy as a trip to the urinal. Scientists at the University of Parma in Italy have developed a chip that’s able to detect a suspected marker of aggressive prostate cancer, called sarcosine, in urine. Previous research has linked elevated levels of sarcosine - an amino acid produced by the metabolism of creatinine in muscles - to more aggressive forms of the disease. “If true, the detection of sarcosine in urine opens the door to the early stage detection of prostate cancer using a non-invasive method,” says Enrico Dalcanale, a researcher 14 at the University of Parma involved with developing the chip. The chip is a special receptor grafted onto a silicone-based wafer. Testing revealed that it was able to detect sarcosine in urine while ignoring other compounds not linked to cancer. How does this compare to the hotly debated prostate-specific antigen (PSA) blood test typically used to screen for prostate cancer? The researchers can’t say yet. Dalcanale says he and his colleagues are working on an updated version that will allow testing for sensitivity and ease of use. You might also be able to combine these results with your PSA levels for a better estimate of your risk. Down the road, the same science could be used to detect other biologically similar compounds found in drugs, neurotransmitters, painkillers, and antidepressants. And, Dalcanale says, the cost of the chip would be comparable to a PSA screening. For decades, men have dutifully shown up at their doctor’s office sometime around their 50th birthday for a baseline PSA (prostatespecific antigen test). As PSA levels rise, the theory went, so do your odds of having prostate cancer. “THE INBOX” Once again, you have put out a marvelous newsletter – congratulations. Between you and John (and others), you’ve maintained the high tradition and standard which the men (and their partners) need. It’s healthy for us to see the changes But now, the US Preventive Services Task Force - the same group of medical experts who made 2009 headlines by proposing that women under age 50 forego mammograms - has drafted a recommendation that men no longer receive the PSA test. The new recommendation applies to men both with and without risk factors, such as being of African-American heritage or having a family history of prostate cancer. The prostate cancer death rate has dropped since PSAs became common in the early 90s, but it’s unclear whether this drop is a direct result of screening or due to improvements in treatment. over the years in the support group and the contribution they make, and to hope for improvements in years to come. Full name and address provided TELL YOUR STORY TO READERS OF QPCN (Anonymity preserved if requested) The Queensland Writers’ Group (QWG) is located in the Queensland State Library and offers seminars and advice to budding writers and authors. If you need assistance with telling and expressing your story, contact the experts at the Queensland Writers’ Group [email protected]. The QWG offers regular advice to wouldbe authors. Some tips from Imogen Smith’s recent article in the QWG March edition of the magazine include: • Listen to your inner self • Read the work aloud • Find your writing voice • Bring your characters and story to life • Don’t be shy in telling your story BONUS FOR SUBSCRIBERS Special bonus for e-mail subscribers to the newsletter. Copy the following details into your search engine: http://www.brl.ntt.co.jp/people/hara/fly.swf See if you can put this puzzle together. Say goodbye to Alzheimer’s! 15 FORWARD A COPY THOUGHT FOR THE DAY Forward a copy of QPCN to a friend, a neighbour or relative. The key to conquering prostate cancer is prevention, greater awareness and early diagnosis. The journey of a thousand miles starts with a single step. Chinese proverb. Contact details: Queensland Prostate Cancer Foundation News (QPCN) Mail: PO Box 201, Spring Hill Qld 4004 E-mail: [email protected] Phone: via Cancer Council helpline 13 11 20 LETTERS TO THE EDITOR May be forwarded to the QPCN at the above address or e-mail. As the editor of your newsletter I encourage your feedback, and will attempt to address areas of your concern. Brisbane PCSG - 2012 meeting program - Cancer Council Queensland, 553 Gregory Terrace, Fortitude Valley. Evenings at 7.00pm (Even months). Mornings at 9.30am (Odd months) June 13 July 11 TBA Troy Gianduzzo, urologist, “Where does the bar sit - in relation to brachy therapy”? Partners of Men with Prostate Cancer meet on the 4th Wednesday of each month between 6pm and 8pm at Cancer Council Queensland’s Gregory Terrace building. Members come together to share, learn and support each other in a warm open environment. Light refreshments are provided and there is parking underneath the building. For more information phone Karen Ward on (07) 3356 8106. Contact Details Queensland Prostate Cancer News Mail: PO Box 201, Spring Hill Qld 4004 Email: [email protected] Phone: via Cancer Council Helpline 13 11 20 Prostate Cancer Foundation of Australia and Queensland Chapter Council Mail: (PO Box 10444) Adelaide Street, Brisbane, QLD 4000 Email: [email protected] Phone: 07 3166 2140. Disclaimer Council (ie. the Council of the Queensland Chapter) accepts no responsibility for information contained in this magazine. Whilst the information is presented in good faith, it may contain information beyond the knowledge of Council and therefore cannot be taken to be the opinion of Council. Important privacy information You have received this magazine because you have provided your contact details to Cancer Council Queensland or to a Prostate Cancer Support Group (PCSG). The primary purpose of collecting your contact details was to enable support, resources and information to be offered to you as a person affected by or interested in prostate cancer. Your contact details are held in the local office of Cancer Council Queensland. Cancer Council Queensland ensures compliance with the Privacy Act, and does not use or disclose your details except as you might reasonably expect. You may access your details and you may request that we correct or amend (ie. update) or delete your details. 16 The information in this magazine is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read here. If you are a member of an affiliated PCSG you will initially receive by post or email your local group’s news-sheet, the monthly Queensland Prostate Cancer News (QPCN), and the national quarterly Prostate News. You may also receive other communications from time to time such as advice on upcoming symposia, news or surveys from research establishments, details of open clinical trials, and guidelines being reviewed. You may ‘opt-out’ of any of these services at any time, ie. you will no longer receive any material of that type, by letting us know your wishes. QPCN is available online at http://www.pcfa.org. au/qld/newsletter.htm. Should you receive multiple copies, please let us know which address(es) to remove from which mailing list(s).