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Abscopal Response in Metastatic Melanoma: Real-World Data of a Retrospective, Multicenter Study.
Ollivier, Luc; Orione, Charles; Bore, Paul; Misery, Laurent; Legoupil, Delphine; Leclere, Jean-Christophe; Coste, Anne; Girault, Gilles; Sicard-Cras, Iona; Kacperek, Clemence; Lucia, Francois; Stefan, Dinu; Thillays, François; Rio, Emmanuel; Lesueur, Paul; Berthou, Christian; Heymann, Dominique; Champiat, Stéphane; Supiot, Stéphane; Vaugier, Loig; Kao, William.
Afiliación
  • Ollivier L; Department of Radiation Oncology, Institut de Cancérologie de l'Ouest (ICO), 44800 Saint-Herblain, France.
  • Orione C; Département de Médecine Interne et Pneumologie, Centre Hospitalo-Universitaire de Brest, Université de Bretagne Occidentale, 29609 Brest, France.
  • Bore P; Oncology Department, Institut de Cancérologie de l'Ouest (ICO), 44800 Saint-Herblain, France.
  • Misery L; Service de Dermatologie, CHU, 2, Avenue Foch, 29200 Brest, France.
  • Legoupil D; Laboratoire sur les Interactions Épithéliums-Neurones (LIEN-EA4685), Université de Bretagne Occidentale, 29200 Brest, France.
  • Leclere JC; Service de Dermatologie, CHU, 2, Avenue Foch, 29200 Brest, France.
  • Coste A; Laboratoire sur les Interactions Épithéliums-Neurones (LIEN-EA4685), Université de Bretagne Occidentale, 29200 Brest, France.
  • Girault G; Service d'ORL et de Chirurgie Cervico-Faciale, Hôpital Morvan, Centre Hospitalo-Universitaire de Brest, Université de Bretagne Occidentale, 5, Avenue Foch, 29200 Brest, France.
  • Sicard-Cras I; Département de Maladie Infectieuses, Centre Hospitalo-Universitaire de Brest, Université de Bretagne Occidentale, 29609 Brest, France.
  • Kacperek C; Unicancer, Comprehensive Cancer Center F. Baclesse, Medical Library, F-14000 Caen, France.
  • Lucia F; Service de Pédiatrie, Hôpital Morvan, Centre Hospitalo-Universitaire de Brest, Université de Bretagne Occidentale, 5, Avenue Foch, 29200 Brest, France.
  • Stefan D; Département of Radiation Oncology, Centre Hospitalier de Cornouaille, 14 Avenue Yves Thepot, 29000 Quimper, France.
  • Thillays F; Radiation Oncology Department, Centre Hospitalo-Universitaire de Brest, Université de Bretagne Occidentale-Hôpital Morvan-2 Avenue Foch, 29200 Brest, France.
  • Rio E; Service de Pédiatrie, Hôpital Morvan, Centre Hospitalo-Universitaire de Brest, Université de Bretagne Occidentale, 5, Avenue Foch, 29200 Brest, France.
  • Lesueur P; Department of Radiation Oncology, Institut de Cancérologie de l'Ouest (ICO), 44800 Saint-Herblain, France.
  • Berthou C; Department of Radiation Oncology, Institut de Cancérologie de l'Ouest (ICO), 44800 Saint-Herblain, France.
  • Heymann D; Unicancer, Comprehensive Cancer Center F. Baclesse, Medical Library, F-14000 Caen, France.
  • Champiat S; Centre Guillaume le Conquérant, Radiation Oncology Department, 76600 Le Havre, France.
  • Supiot S; U1227 B Lymphocytes & Autoimmunity, University of Brest, INSERM, IBSAM, 29200 Brest, France.
  • Vaugier L; Nantes Université, CNRS, UMR6286, US2B, 44300 Nantes, France.
  • Kao W; Department of Oncology and Metabolism, University of Sheffield, Sheffield S10 2RX, UK.
Cancers (Basel) ; 14(17)2022 Aug 30.
Article en En | MEDLINE | ID: mdl-36077747
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.
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Risk_factors_studies Idioma: En Revista: Cancers (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Risk_factors_studies Idioma: En Revista: Cancers (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Francia