Salvage radiotherapy for oligo-progressive malignant pleural mesothelioma
Menée à partir de données portant sur 37 patients atteints d'un mésothéliome pleural malin non résécable avec progression observable radiologiquement et ayant reçu au moins 1 ligne de chimiothérapie, cette étude analyse l'efficacité, du point de vue du délai nécessaire avant reprise du traitement systémique et du contrôle local, d'un traitement par radiothérapie focalisée
Objectives: No standard treatment option is available for patients with unresectable malignant pleural mesothelioma (MPM) progressing after upfront chemotherapy. We aimed to explore the role of focal radiotherapy (FRT) as a treatment modality for oligo-progressive MPM. Materials and Methods: In this retrospective study, consecutive patients pretreated with ≥1 lines of chemotherapy were included. Oligo-progressive MPM was defined as an unresectable disease with radiological progression at ≤3 sites according to a chest-abdominal contrast-enhanced computed tomography. Patients were treated with either stereotactic body radiotherapy (SBRT, ≥5 Gy per fraction) or hypo-fractionated radiotherapy (hypoRT, <5 Gy per fraction). Time to further systemic therapy (TFST) and local control (LC) after FRT were the primary endpoints. Biologically effective dose (BED) was calculated using three different alpha/beta models (1.5 Gy, 3 Gy and 10 Gy). Results: From April 2006 to March 2019, 37 patients were treated on 43 pleural lesions; 16/37 (43%) had undergone upfront multimodality treatment (MMT) including surgery. FRT was given in 22/37 (59.5%) after one line of chemotherapy. SBRT was delivered for 26/43 lesions (60.5%), hypoRT for 17/43 (39.5%). Median TFST was 6 months (95% CI 4.9-7.1). LC at 6 months and 1 year was 84% and 76%, respectively. Median TFST was longer in patients treated after 1 vs >1 line of chemotherapy (9 vs 4 months, p = 0.001) and in patients pretreated with MMT (6 vs 3 months, p = 0.021). Six-month LC was better in patients treated with a BED > 100 using alpha/beta 1.5 and 3. No ≥ G3 acute or late toxicities were reported. Conclusion: FRT was feasible in selected patients with oligo-progressive MPM, allowing delay of further systemic therapies, with no severe toxicity. FRT was more effective when performed at progression after one line of systemic therapy. Our results suggest a radio-resistant behavior of MPM.