Article Text

Download PDFPDF
CASE REPORT
Risk of cumulative toxicity after complete melanoma response with pembrolizumab
  1. Amy Hsin-Chieh Hsieh1,
  2. Sarah Faithfull2,
  3. Michael P Brown1
  1. 1Department of Medical Oncology, Royal Adelaide Hospital, Adelaide, South Australia, Australia
  2. 2Radiology Department, Royal Adelaide Hospital, Adelaide, South Australia, Australia
  1. Correspondence to Dr Amy Hsin-Chieh Hsieh, hsinchiehamy.hsieh{at}sa.gov.au

Summary

Pembrolizumab is an approved first-line systemic therapy for unresectable metastatic melanoma. Despite the achievement of complete and durable responses in a small subgroup of patients, it is standard practice that pembrolizumab therapy continues beyond complete response. Nevertheless, the incidence of immune-related toxicities gradually increases with continuing pembrolizumab therapy. We report a case highlighting the occurrence of serious induced immune-related adverse events, which were attributed to pembrolizumab in a patient with metastatic melanoma who obtained a complete response (CR) after receiving pembrolizumab for a total of 6.5 months. Although mild pembrolizumab-related toxicity persists, the patient remains disease-free 5.5 months after discontinuation of pembrolizumab. Accordingly, we believe that cessation of pembrolizumab should be considered in patients who achieve a CR because of the ongoing risk of toxicity with extended pembrolizumab administration.

Statistics from Altmetric.com

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Footnotes

  • Contributors AH-CH contributed by writing, proof reading and finalising of manuscript SF was involved in image processing, proof reading and finalising of manuscript. MPB participated in writing, proof reading and finalising of manuscript.

  • Competing interests None declared.

  • Patient consent Obtained.

  • Provenance and peer review Not commissioned; externally peer reviewed.