Skip to main navigation Skip to search Skip to main content

Rechallenge patients with immune checkpoint inhibitors following severe immune-related adverse events: Review of the literature and suggested prophylactic strategy

  • John Haanen
  • , Marc Ernstoff
  • , Yinghong Wang
  • , Alexander Menzies
  • , Igor Puzanov
  • , Petros Grivas
  • , James Larkin
  • , Solange Peters
  • , John Thompson
  • , Michel Obeid
  • , Michel Obeid
  • Netherlands Cancer Institute
  • Roswell Park Cancer Institute
  • University of Texas MD Anderson Cancer Center
  • Melanoma Institute Australia
  • Royal North Shore and Mater Hospitals
  • University of Washington
  • Royal Marsden NHS Foundation Trust
  • University of Lausanne

Research output: Contribution to journalReview articlepeer-review

158 Scopus citations

Abstract

Patients with cancer who developed severe, grade 3 or 4 immune-related adverse events (irAEs) during therapy with immune checkpoint inhibitors are at risk for developing severe toxicities again on rechallenge with checkpoint inhibitors. Consequently, medical oncologists and multidisciplinary teams are hesitant to retreat in this scenario, despite the fact that a number of patients may derive clinical benefit from this approach. Balancing such clinical benefit and treatment-related toxicities for each patient is becoming increasingly challenging as more and more patients with cancer are being treated with checkpoint inhibitors. In this manuscript, we provide an extensive overview of the relevant literature on retreatment after toxicity, and suggest prophylactic approaches to minimize the risk of severe irAE following rechallenge with immune checkpoint blockade, since treatment may be lifesaving in a number of occasions.

Original languageEnglish
Article numberjitc-2020-000604
JournalJournal for ImmunoTherapy of Cancer
Volume8
Issue number1
DOIs
StatePublished - Jun 12 2020

Keywords

  • autoimmunity

Fingerprint

Dive into the research topics of 'Rechallenge patients with immune checkpoint inhibitors following severe immune-related adverse events: Review of the literature and suggested prophylactic strategy'. Together they form a unique fingerprint.

Cite this