Litcius/Paper detail

Chemotherapy efficacy after first-line immunotherapy in 18 advanced melanoma patients

M. Saint‐Jean, Clémentine Fronteau, L. Peuvrel, Amir Khammari, Émilie Varey, G. Quéreux, Brigitte Dréno

2020Medicine22 citationsDOIOpen Access PDF

Abstract

In BRAF wild type advanced melanoma, immune checkpoint blockers such as anti-PD1 (anti-programmed cell death 1) are usually continued beyond progression for a hypothetical rare further response. Chemotherapy as a second-line option is considered ineffective by many practitioners based on historical data. Continuing anti-PD1 beyond progression has a high health-economic impact and is not recommended by the FDA. This study aimed to describe the efficacy and survival of advanced melanoma patients who received second-line (or more) chemotherapy after immunotherapy failure.This was a retrospective single center study conducted in a French University Hospital during an 11-month period. All advanced melanoma patients treated with chemotherapy after immunotherapy failure were included.Eighteen patients were analyzed. Therapeutic response to chemotherapy was evaluable in 16 patients: partial response was achieved in 3/16 (19%), stable disease in 1/16 (6%) and progressive disease in 12/16 (75%). Median overall survival from chemotherapy start was 12 months. Median progression-free survival was 5.4 months. The 6-month overall survival rate was 81% and the 6-month progression-free survival rate was 40%.Although the disease control rate with chemotherapy was low (25%), survival data in our study are far superior to those previously published. This could be linked to a high proportion of patients treated with anti-PD1 just prior to chemotherapy, which may suggest a potential synergy between immunotherapy and chemotherapy.

Topics & Concepts

MedicineChemotherapyImmunotherapyMelanomaInternal medicineOncologyProgressive diseaseRetrospective cohort studySurvival rateSurvival analysisSurgeryCancerCancer researchMelanoma and MAPK PathwaysCutaneous Melanoma Detection and ManagementCAR-T cell therapy research