| Literature DB >> 33653801 |
Thomas U Marron1, Aideen E Ryan2, Sangeetha M Reddy3, Sabina Kaczanowska4, Rania H Younis5,6, Dipti Thakkar7, Jiajia Zhang8, Todd Bartkowiak9, Rachel Howard10, Kristin G Anderson11,12, Daniel Olson13, Abdul Rafeh Naqash14, Ravi B Patel15, Esha Sachdev16, Maria E Rodriguez-Ruiz17, Michal Sheffer18, Sarah Church19, Christopher Fuhrman19, Abigail Overacre-Delgoffe20, Rosa Nguyen21, Vaia Florou22, Jessica E Thaxton23,24,25, David H Aggen26, Jennifer L Guerriero27,28.
Abstract
Immune checkpoint inhibitors (ICIs) have improved overall survival for cancer patients, however, optimal duration of ICI therapy has yet to be defined. Given ICIs were first used to treat patients with metastatic melanoma, a condition that at the time was incurable, little attention was initially paid to how much therapy would be needed for a durable response. As the early immunotherapy trials have matured past 10 years, a significant per cent of patients have demonstrated durable responses; it is now time to determine whether patients have been overtreated, and if durable remissions can still be achieved with less therapy, limiting the physical and financial toxicity associated with years of treatment. Well-designed trials are needed to identify optimal duration of therapy, and to define biomarkers to predict who would benefit from shorter courses of immunotherapy. Here, we outline key questions related to health, financial and societal toxicities of over treating with ICI and present four unique clinical trials aimed at exposing criteria for early cessation of ICI. Taken together, there is a serious liability to overtreating patients with ICI and future work is warranted to determine when it is safe to stop ICI. © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ.Entities:
Keywords: Costimulatory and Inhibitory T-Cell Receptors; Immunotherapy; Melanoma; Review
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Year: 2021 PMID: 33653801 PMCID: PMC7929825 DOI: 10.1136/jitc-2020-001901
Source DB: PubMed Journal: J Immunother Cancer ISSN: 2051-1426 Impact factor: 13.751