Retreatment of Patients With Metastatic Cutaneous Melanoma Who Relapse After Elective Checkpoint Inhibitor Discontinuation After a Complete Remission

Oncologist. 2023 May 8;28(5):e270-e275. doi: 10.1093/oncolo/oyad016.

Abstract

Introduction: Checkpoint blockade has improved the response rate and survival in metastatic melanoma. Elective treatment discontinuation appears to be reasonable in most patients who have achieved a confirmed complete remission. It seems crucial to understand whether restarting immune checkpoint inhibitor therapy can induce additional responses or remissions in rare patients who relapse.

Methods: A retrospective analysis identified only 10 patients who relapsed after elective treatment discontinuation after a radiologically confirmed remission. These patients were retreated with single-agent PD-1 or combined CTLA-4 plus PD-1-directed monoclonal antibodies.

Results: We found an initial complete response rate of 20% (2 patients) following retreatment. With a median follow-up of 26 months, the addition of individualized salvage therapies converted an additional 4 patients to a 2nd remission. All 6 of these patients have again discontinued therapy. Three patients have died of metastatic melanoma, while another is receiving salvage therapy. Six of our 10 patients experienced grades 2-3 retreatment-related toxicity. There were no hospitalizations or fatalities.

Discussion: Retreatment of relapsing patients resulted in 20% complete responses with checkpoint inhibitors. The planned addition of other treatment modalities converted another 4 patients (40%) to a durable 2nd remission. This sequential approach merits further exploration in prospective clinical trials.

Keywords: ipilimumab; nivolumab; pembrolizumab; stereotactic ablative radiotherapy; targeted therapy.

MeSH terms

  • Humans
  • Ipilimumab / therapeutic use
  • Melanoma* / pathology
  • Melanoma, Cutaneous Malignant
  • Neoplasm Recurrence, Local / drug therapy
  • Programmed Cell Death 1 Receptor / therapeutic use
  • Prospective Studies
  • Retreatment
  • Retrospective Studies
  • Skin Neoplasms* / pathology

Substances

  • Programmed Cell Death 1 Receptor
  • Ipilimumab