il tumore della prostata. ii. stadiazione
Transcription
il tumore della prostata. ii. stadiazione
Università degli Studi di Pavia AA 2010 - 2011 Corso Integrato di Clinica Medica Insegnamento di Oncologia Medica IL TUMORE DELLA PROSTATA. II. STADIAZIONE Prof. Alberto Riccardi STAGING METHODS PROSTATIC CANCER Clinical staging. I. * TNM staging system includes categories for cancers palpable on DRE, those identified solely on basis of abnormal PSA (T1c), those palpable but clinically confined to gland (T2) and those extended outside gland (T3 and T4) PROSTATIC CANCER Clinical staging. II. * DRE alone inaccurate in assessing extent of disease within gland, capsular invasion, involvement of seminal vescicles and spread to nodal or more distant sites; * assessment refined by imaging studies [ultrasound, computed tomoghraphy (CT), magnetic resonance imaging (MRI) and bone scan]; - however, no single test accurately predicts pathologic stage (organ - confined disease? seminal vesical involvement? lymph node spread?) PROSTATIC CANCER Clinical staging. III. Transrectal ultrasound * transrectal ultrasound (TRUS) most frequently used → no consistent finding predicts PC with certainty → primarly used to direct prostate biopsy PROSTATIC CANCER Clinical staging. IV. CT scan * CT scans lack sensitivity and specificity for extraprostatic extension and inferior to MRI in visualization of lymph nodes * CT scan can show abnormal lymph nodes in pelvis and abdomen, but not sensitive enough to identify microscopic cancer cells in lymph nodes = CT scans do not provide reliable enough information about condition of prostate or stage of prostate cancer PROSTATIC CANCER Clinical staging. V. MRI * MRI (still lacking sensitivity and specificity) ↑ lymph node detection, especially of endorectal coil; [- T1 - weighted images: periprostatic fat and venous plexus, perivesicular tissues, lymph nodes, and bone marrow; - T2 - weighted images: internal architecture of prostate and seminal vesicles (low signal in most cancers, high signal in normal peripheral zone)]; - MRI also useful for planning of surgery and radiation therapy = neither TC nor MRI accurately predicts pathologic stage at surgery PROSTATIC CANCER Clinical staging. VI. Radionuclide bone scanning * to evaluate spread to osseous sites; - sensitive but relatively non specific (areas of ↑uptake from osteoblastic activity secondary to metastases or other condition, including healing fractures, arthritis and Paget's disease); * true+ bone scan rare if PSA < 8 and uncommon if PSA < 10 ng / mL (unless high grade tumor) = when PSA < 10 ng / mL, false+ scan common → additional low yield testing, including CT and MRI PROSTATIC CANCER Clinical staging. VII. Molecular diagnostic (experimental) * seeks to identify presence of circulating PC cells using an assay for PSA based on reverse transcriptase - polymerase chain reaction (RT - PCR) in leukocyte fraction of peripheral blood or bone marrow; - test+ in large % of pts with tumors seemingly confined to organ (unclear significance) STAGING STAGING * two schemes commonly used to stage PC; - TNM stage system: most common (by American Joint Committee on Cancer, AJCC), evaluating size of tumor, extent of involved lymph nodes, metastasis and cancer grade; - Whitmore - Jewett stage: now used less commonly for research, but often still used by clinicians TNM STAGING PROSTATIC CANCER TNM clinical staging * T categories: * clinically inapparent, not palpable tumor (T1a - T1b) or detected from ↑ serum PSA (T1c); * palpable but clinically confined to gland (T2), and: * extended outside gland (T3 and T4); * N categories: presence or absence of nodal metastases; * M categories: presence or absence of distant metastases PROSTATIC CANCER TNM clinical staging PROSTATIC CANCER Clinical staging TNM definitions: T1 * TX: primary tumor cannot be assessed; * T0: no evidence of primary tumor; * T1: clinically inapparent tumor not palpable nor visible by imaging: T1a: incidental histologic finding in ≤ 5% of tissue resected; T1b: incidental histologic finding in > 5% of tissue resected; T1c: identified by needle biopsy due to elevated PSA PROSTATIC CANCER Clinical staging TNM definitions: T2 * T2: confined within prostate: - T2a: involving 1 lobe; - T2b: involving both lobes; [- note: tumor found in 1 or both lobes by needle biopsy, but not palpable or visible by imaging, classified as T1c] PROSTATIC CANCER Clinical staging TNM definitions: T3 - T4 * T3: tumor extends through prostatic capsule: T3a: extracapsular extension (uni- or bilateral); T3b: tumor invades seminal vesicle(s); [- note: invasion into prostatic apex or into (but not beyond) prostatic capsule is not classified as T3, but as T2]; * T4: tumor fixed to or invading adjacent structures other than seminal vesicles (bladder neck, external sphincter, rectum, levator muscles and / or pelvic wall) LOCAL STAGING OF PROSTATE CANCER PROSTATIC CANCER Clinical staging. TNM definitions: Regional nodes (N) * = nodes of true pelvis (= nodes below bifurcation of common iliac arteries, including pelvic, hypogastric, obturator, iliac, periprostatic, and sacral); * distant lymph nodes = outside confines of true pelvis (aortic, common iliac, inguinal, superficial inguinal, supraclavicular, cervical, scalene, and retroperitoneal nodes) and their involvement = distant metastases; * NX: regional lymph nodes cannot be assessed; * N0: no regional lymph node metastasis; * N1: metastasis in regional lymph node(s) [- note: laterality does not affect N classification] PROSTATIC CANCER Clinical staging. TNM definitions Distant metastasis (M) * MX: distant metastasis cannot be assessed; * M0: no distant metastasis; * M1: distant metastasis; M1a: nonregional lymph node(s); M1b: bone(s); M1c: other site(s) PROSTATIC CANCER Clinical staging: limits. I. * limit of TNM system = most PC are now diagnosed as T1c (by needle biopsy, often because ↑ PSA) or T2 (still confined within prostate) disease, leading to attempts at refining prediction of local disease extent: - multiplex staging models (based on a combination of findings of digital examination, biopsy, Gleason score and baseline PSA); - models based on no. of cores and % of each core involved by tumor; * unproven efficacy at predicting node involvement PROSTATIC CANCER Variables in multiplex staging models PROSTATIC CANCER Clinical staging. Differentiation (G) PROSTATIC CANCER AJCC stage groupings Stage I T1a, N0, M0, G1 Stage III T3, N0, M0, any G Stage II T1a, N0, M0, G 2, 3 - 4 T1b, N0, M0, any G T1c, N0, M0, any G T2, N0, M0, any G Stage IV T4, N0, M0, any G any T, N1, M0, any G any T, any N, M1, any G PROSTATIC CANCER AJCC stage groupings STAGING WHITEMORE - JEWETT STAGING PROSTATIC CANCER Whitemore - Jewett Staging System. Stage A * stage A = clinically undetectable tumor confined to prostate gland, as incidental finding at prostatic surgery; - substage A1: G1 with focal involvement, usually left untreated; - substage A2: G2 - G3 or involving multiple foci in gland Multicentricity of prostate cancer whole mount section of prostate showing two distinct foci of adenocarcinoma illustrating the frequent finding of multicentricity PROSTATIC CANCER Whitemore - Jewett Staging System. Stages B - C * stage B = confined to prostate gland: substage B0: nonpalpable, PSA - detected; substage B1: single nodule in 1 lobe; substage B2: more extensive involvement of 1 lobe or involvement of both lobes * stage C = clinically localized to periprostatic area but extending through prostatic capsule, with seminal vesicles possibly involved: substage C1: clinical extracapsular extension; substage C2: extracapsular tumor producing bladder outlet or ureteral obstruction PROSTATIC CANCER Whitemore - Jewett Staging System. Stage D * Stage D = metastatic disease: substage D0: clinically localized disease (prostate only) but persistently elevated enzymatic serum acid phosphatase titers; substage D1: regional lymph nodes only; substage D2: metastases to distant lymph nodes, bone or visceral organs; substage D3: D2 prostate cancer pts who relapsed after adequate endocrine therapy STAGING COMPARISON BETWEEN TNM AND WHITEMORE - JEWETT STAGING CLINICAL STAGES BY TNM CLASSIFICATION AND WHITMORE - JEWETT STAGING SYSTEM