Abscopal Response in Metastatic Melanoma: Real-World Data of a Retrospective, Multicenter Study

Author:

Ollivier LucORCID,Orione Charles,Bore PaulORCID,Misery LaurentORCID,Legoupil DelphineORCID,Leclere Jean-ChristopheORCID,Coste AnneORCID,Girault Gilles,Sicard-Cras Iona,Kacperek Clemence,Lucia Francois,Stefan Dinu,Thillays FrançoisORCID,Rio Emmanuel,Lesueur Paul,Berthou Christian,Heymann DominiqueORCID,Champiat StéphaneORCID,Supiot StéphaneORCID,Vaugier LoigORCID,Kao William

Abstract

Objective: To evaluate the incidence of the abscopal response (AR) in patients with metastatic melanoma requiring palliative radiotherapy (RT). Patients and methods: Patients treated for metastatic melanoma between January 1998 and February 2020 in four oncology departments were screened. Patients with progression under immune checkpoint inhibitors or without ongoing systemic treatment, and requiring palliative RT were considered. The AR was defined as an objective response according to RECIST and/or iRECIST for at least one non-irradiated metastasis at distance (≥10 cm) from the irradiated lesion. Primary endpoint was the rate of AR. Secondary endpoints were overall survival (OS), progression-free survival (PFS), local control (LC) of the irradiated lesion, and toxicity as assessed by CTCAE v5. Results: Over the period considered, 118 patients were included and analyzed. Fifteen patients (12.7%) had an AR. With a median follow-up of 7.7 months (range, 0.2–242.2), median OS and PFS after RT were significantly longer in patients with an AR compared to those without: 28 vs. 6.6 months (p < 0.01) and not reached vs. 3.2 months, respectively. No grade ≥2 toxicity was reported. Patients who developed an AR were more likely to be treated with immunotherapy (93.3% vs. 55.9%, p = 0.02). In multivariate analysis, they had a higher number of irradiated metastases treated concomitantly (HR = 16.9, p < 0.01) and a higher rate of mild infections during RT (HR = 403.5, p < 0.01). Conclusions: AR in metastatic melanoma seems to be highly prognostic of overall survival, although it is a rare phenomenon. It may be promoted by multiple concomitant treatments with RT and immunotherapy and by acute inflammatory events such as infection.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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