1. Dosimetric and NTCP advantages of robust proton therapy over robust VMAT for Stage III NSCLC in the immunotherapy era.
- Author
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Dionisi, F., Landoni, V., Widesott, L., Nardangeli, A., Fracchiolla, F., Siniscalchi, B., Soriani, A., Turkaj, A., Righetto, R., Amelio, D., Farace, P., Goanta, L., Trianni, A., Lorentini, S., Cianchetti, M., and Sanguineti, G.
- Abstract
• Robust proton vs x-ray planning on free-breathing (FB) STAGE III NSCLC was tested. • A reduction of NTCP risk of pulmonary and cardiac toxicity was scored with protons. • A reduction in the dose to the immune system was observed with protons. • Robust optimization is an interesting and novel solution also for x-ray therapy. • Robust FB proton therapy could be an effective option for selected STAGE III NSCLC. To assess the robustness and to define the dosimetric and NTCP advantages of pencil-beam-scanning proton therapy (PBSPT) compared with VMAT for unresectable Stage III non-small lung cancer (NSCLC) in the immunotherapy era. 10 patients were re-planned with VMAT and PBSPT using: 1) ITV-based robust optimization with 0.5 cm setup uncertainties and (for PBSPT) 3.5 % range uncertainties on free-breathing CT 2) CTV-based RO including all 4DCTs anatomies. Target coverage (TC), organs at risk dose and TC robustness (TCR), set at V95%, were compared. The NTCP risk for radiation pneumonitis (RP), 24-month mortality (24MM), G2 + acute esophageal toxicity (ET), the dose to the immune system (EDIC) and the left anterior descending (LAD) coronary artery V15 < 10 % were registered. Wilcoxon test was used. Both PBSPT methods improved TC and TCR (p < 0.01). The mean lung dose and lung V20 were lower with PBSPT (p < 0.01). Median mean heart dose reduction with PBSPT was 8 Gy (p < 0.001). PT lowered median LAD V15 (p = 0.004). ΔNTCP > 5 % with PBSPT was observed for two patients for RP and for five patients for 24 MM. ΔNTCP for ≥ G2 ET was not in favor of PBSPT for all patients. PBSPT halved median EDIC (4.9/5.1 Gy for ITV/CTV-based VMAT vs 2.3 Gy for both ITV/CTV-based PBSPT, p < 0.01). PBSPT is a robust approach with significant dosimetric and NTCP advantages over VMAT; the EDIC reduction could allow for a better integration with immunotherapy. A clinical benefit for a subset of NSCLC patients is expected. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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