F. Gessoni1, F. Matrone1, G. Pirrone2, J. Polesel3, L. Vinante1, A. Caroli1, A. A. M. Donofrio1, F. Bertini1, G. Fanetti1, F. Navarria1, G. Malfatti1, L. Barresi2, A. Drigo2, M. Mascarin1, and A. Revelant1; 1Department of Radiation Oncology, Centro di Riferimento Oncologico of Aviano, Aviano, Italy, 2Division of Medical Physics, Centro di Riferimento Oncologico Aviano IRCCS, Aviano, Italy, 3Department Cancer Epidemiology, Centro di Riferimento Oncologico of Aviano, Aviano, Italy
Purpose/Objective(s):Limited second-line therapeutic options are available in Malignant Pleural Mesothelioma (MPM). In this patients Stereotactic Ablative Body Radiotherapy (SABR) could postpone the begin of a second-line systemic therapy in those with radiological findings of oligorecurrent disease. Primary aim of our study was to determine the time to second-line systemic therapy (TTST) in this setting. In this population we also evaluated Progression-Free Survival (PFS) and Overall Survival (OS). Materials/
Methods: All patients with MPM enrolled in this analysis were previously treated with platinum-based chemotherapy, surgery (thoracoscopic biopsy, pleural decortication or pleurectomy plus decortication), Radical Hemithoracic Radiotherapy (RHR). An additional inclusion criteria was a minimum follow-up of 6 months. During the first radiotherapy course, all the patients received a total dose of 50 Gy in 25 fractions with a concomitant boost of 60 Gy to PET/TC positive macroscopic residual disease. Patients showing an oligorecurrent ipsilateral pleural disease (defined as radiological evidence of lesion numbers = 3) underwent SABR re-irradiation following a fractionation scheme of 25-30 Gy in 3-5 daily fractions. TTST was defined as the time between the first day of SABR retreatment and the first day of second-line systemic treatment. PFS was defined as the time between SABR re-irradiation and the first radiological finding of disease progression, while OS was defined as the time between SABR retreatment and the patient death. All considered outcomes were calculated with Kaplan-Meier method. Toxicities of RHR and SABR re-irradiation were assessed with Common Terminology Criteria for Adverse Events (CTCAE) Vers. 5.0. Results: Twenty-two patients were treated between January 2011 and December 2022, with a median follow-up of 11.4 months (6-36 months). At the time of analysis, only 5 patients were alive, including 2 patients with no evidence of disease. After SABR re-irradiation, only 9 patients developed a plurimetastatic disease (3 patients with extensive local progression and 6 patients with distant progression) and started a second-line systemic treatment. Median TTST was 10.2 months [Q1-Q3: 4.8-17.1]. PFS rates at 6,12, 36 months were 71.8% [47.6%-86.2%], 33.5% [15.0%-53.3%] and 14% [3.6%-32.2%], respectively. OS rates at 6,12, 36 months were 95.2% [70.7%-99.3%], 56.4% [32.8%-74.5%], 27.4% [9.5%-48%], respectively. Only one patient developed acute G2 gastrointestinal toxicity while no other acute or late toxicities were reported. Conclusion: Results of a very homogeneous population were reported in this study. SABR re-irradiation in patients with oligorecurrent MPM appears to be safe and useful to postpone second-line systemic treatment. Further prospective studies and randomized trials are needed to support our findings.