Prospective Clinical Trials to Advance the Study of Immune Checkpoint Inhibitor Toxicity

Immune checkpoint inhibitors (ICIs) are a class of drug that produces durable and sustained anti-tumour responses in a wide variety of malignancies. The exponential rise in their use has been mirrored by a rise in immune-related adverse events (IrAEs). Knowledge of such toxicities, as well as effect...

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Bibliographic Details
Main Authors: Christopher Cluxton, Jarushka Naidoo
Format: Article
Language:English
Published: MDPI AG 2023-07-01
Series:Current Oncology
Subjects:
Online Access:https://www.mdpi.com/1718-7729/30/7/502
Description
Summary:Immune checkpoint inhibitors (ICIs) are a class of drug that produces durable and sustained anti-tumour responses in a wide variety of malignancies. The exponential rise in their use has been mirrored by a rise in immune-related adverse events (IrAEs). Knowledge of such toxicities, as well as effective management algorithms for these toxicities, is essential to optimize clinical efficacy and safety. Currently, the guidelines for management of the IrAEs are based largely on retrospective studies and case series. In this article, we review the current landscape of clinical trials investigating the management of IrAEs with an aim to develop standardised, randomised controlled trial-based management algorithms for ICI-related toxicities.
ISSN:1198-0052
1718-7729