Abstract

To date, there have been only few studies investigating rechallenge with checkpoint inhibitors in melanoma patients. Herein, we present the first review of all internationally published, English-language articles. A total of 570 patients were included in our analysis, divided into four groups: 1) rechallenge with anti-PD1 following disease progression on anti-PD1 therapy; 2) rechallenge with anti-PD1 and anti-CTLA4 following disease progression on anti-PD1 therapy; 3) rechallenge with anti-CLTA-4 following disease progression on anti-CTLA-4 therapy; and 4) rechallenge following toxicity-related treatment discontinuation. In the first group (85 patients), the mean disease control rate (DCR) was 45.8%, with a mean overall response rate (ORR) of 15.5%. The second group (114 patients) showed a mean DCR of 40.6% and an ORR of 20%. In the third group (182 patients), the mean DCR was 50.9%, with an ORR of 20.4%. Thus, even patients with a history of disease progression on initial checkpoint inhibitor therapy may benefit from rechallenge. Patients in the fourth group (189 patients) showed a mean DCR of 89.5% and an ORR of 70.2%. Of these individuals, 18% saw recurrence of the same toxicity; 23% were affected by adverse events different from the ones previously experienced.

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