Dose Accumulation
Transcription
Dose Accumulation
Deformable Registration and Dose Accumulation for Liver StereotacticBody Radiotherapy Michael Velec Liver SBRT • Planning: – Individualized, highly conformal – Rx based on liver NTCP – Goal: ↑tumor dose, ↓normal tissue dose • Image-guided RT (IGRT): – – – – Planning CT 3D soft-tissue targeting 3D motion quantification Rigid liver registration Goal: Planned = Delivered dose Treatment CBCT 9/21/2011 Rationale • Deformable image registration (DIR) – Morfeus: biomechanical DIR – Accuracy < 2 mm in the liver – Allows tissue tracking • 4D CT Dose accumulation – ∆ in min tumor up to 15% – ∆ in max normal tissue up to 25% – Planned Dose ≠ Predicted Dose How well do the Planned and Predicted doses compare to what is actually delivered? 9/21/2011 17 mm 12 mm 8 mm 4D CT Breathing Map Rationale • Deformable image registration (DIR) – Morfeus: biomechanical DIR – Accuracy < 2 mm in the liver – Allows tissue tracking • 4D CT Dose accumulation – ∆ in min tumor up to 15% – ∆ in max normal tissue up to 25% – Planned Dose ≠ Predicted Dose How well do the Planned and Predicted doses compare to what is actually delivered? 9/21/2011 Predicted – Planned Dose Methods I – Clinical Data • N=30 previous SBRT patients – Primary 50%, Mets 50%, # GTVs 1 – 5 – Free-breathing 36%, Compression plate 64% • Rx: 27 – 60 Gy in 6 fractions over 2 weeks – Planned on Exhale 4D CT – Clinical-IGRT: 2D Fluoroscopy + 3D CBCT – IGRT tolerance: 3 mm • Full dose accumulation with MORFEUS – Daily 4D CBCT in the treatment position – External, Liver and Spleen contoured on 4D CBCT 9/21/2011 Methods I – Dose Accumulation Part A Predicted Accumulated Dose, Dacc Dose, Dpred Planned, Dplan ╳ 6 fractions Exhale 4D CT Exhale 4D CBCT Inhale 4D CT Inhale 4D CBCT 9/21/2011 Methods I – Dose Accumulation Part A Predicted Accumulated Dose, Dacc Dose, Dpred Planned, Dplan Exhale 4D CT ╳ 6 fractions Exhale 4D CBCT Part B • Extract impact of interfraction geometric uncertainties on dose: – Residual Setup Errors • Rigid liver-liver error • Exh CT vs Exh CBCT – Abdominal Deformation Inhale 4D CT Inhale 4D CBCT • Rigid registration vs. DIR • Exh CT vs Exh CBCT – Breathing Variations • DIR of 4D CT vs 4D CBCT 9/21/2011 Results I – Geometric Uncertainties DIR of 4D CBCT revealed geometric uncertainties for the tumor that exceeded the clinical IGRT tolerance (3 mm): • Exhale CT to Exhale CBCT – 30% of patients (n=9) had residual systematic errors >3 mm (maximum systematic error: 11 mm) • Exhale CBCT to Inhale CBCT (vs. 4D CT) – 53% of patients (n=16) had mean ∆ in breathing motion >3 mm (∆ amplitude motion of -11 to 8 mm) 9/21/2011 Results I – Dose Accumulation ∆ Dose (% of Rx) *p < 0.05 Dacc - Dplan Mean (SD) Dacc - Dpred Range Mean (SD) Range Tumor min -0.8 (3.3) -14.6 4.5 0.2 (4.0) -14.2 13.4 Liver mean -0.6 (1.6) -5.8 2.5 -0.1 (1.6) -5.1 2.6 Bowel max -3.2 (4.0) -15.0 2.7 -0.8 (3.8) -6.6 9.9 * Duodenum max -4.6 (8.6) -41.9 2.6 -0.9 (7.6) -38.4 9.1 * • Proportion of patients with Dacc |∆| > 5% to any tissue: – 70% (n=21) relative to the Planned Dose (Dplan) – 53% (n=16) relative to the Predicted Dose (Dpred) 9/21/2011 Results I – Dose Accumulation ∆ Dose (% of Rx) *p < 0.05 Dacc - Dplan Mean (SD) Dacc - Dpred Range Mean (SD) Range Tumor min -0.8 (3.3) -14.6 4.5 0.2 (4.0) -14.2 13.4 Liver mean -0.6 (1.6) -5.8 2.5 -0.1 (1.6) -5.1 2.6 Bowel max -3.2 (4.0) -15.0 2.7 -0.8 (3.8) -6.6 9.9 * Duodenum max -4.6 (8.6) -41.9 2.6 -0.9 (7.6) -38.4 9.1 * • Proportion of patients with Dacc |∆| > 5% to any tissue: – 70% (n=21) relative to the Planned Dose (Dplan) – 53% (n=16) relative to the Predicted Dose (Dpred) 9/21/2011 Results I – Dose Accumulation % Δ Max Bowel (0.5 cc) 15 10 5 0 -5 -10 -15 9/21/2011 Accumulated – Predicted Results I – Dose Accumulation % Δ Max Bowel (0.5 cc) 15 Accumulated – Predicted 10 5 0 -5 -10 -15 9/21/2011 Residual Setup Errors Deformation Breathing Variations Methods II – DIR-IGRT 1. DIR between exhale CT and exhale CBCT • GTVs Liver 2. Translate patient model to correct tumor (‘DIRIGRT’) • Tumor displacement on exhale CBCT, modeled with biomechanical DIR 9/21/2011 Calculate centre-of-mass (COM) tumor motion AVG COM ∆ for multiple tumors 3. Compare Dacc with DIRIGRT to Clinical-IGRT, relative to Dpred Results II – Dose Accumulation Clinical-IGRT Dacc Vs. Predicted Dose DIR-IGRT Dacc Vs. Predicted Dose Pts with Max Min Pts with Max Min |∆| ≥ 5% %∆of Rx |∆| ≥ 5% %∆of Rx Min Tumor 10 % -14 13 7% -6 4 Mean Liver 3% -5 3 0% -4 3 Max Bowel 20 % -7 10 17 % -6 8 7% -38 9 17 % -21 7 Max Duodenum DIR-IGRT Dacc Vs. Predicted dose: 50% overall of patients overall have still |∆| > 5% 9/21/2011 Conclusions • Direct tumor targeting (e.g. DIR-IGRT) for IGRT, reduces dose deviations relative to the Predicted Dose • Deformable dose accumulation over the course of SBRT is warranted to reduce the uncertainties in the dose record 9/21/2011 Future Directions • Optimize the Predicted 4D dose distributions’ treatment margins and dose gradients • Investigate the potential for margin reduction and dose escalation with DIR-IGRT • Adaptive re-planning may be warranted to correct for deformation and breathing changes • Correlate accumulated doses with clinical outcomes 9/21/2011 9/21/2011