Defining unique clinical hallmarks for immune checkpoint inhibitor-based therapies.

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Version: Final published version
License: CC BY-NC 4.0
Serval ID
serval:BIB_8EB4E8449258
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Institution
Title
Defining unique clinical hallmarks for immune checkpoint inhibitor-based therapies.
Journal
Journal for immunotherapy of cancer
Author(s)
Michielin O., Lalani A.K., Robert C., Sharma P., Peters S.
ISSN
2051-1426 (Electronic)
ISSN-L
2051-1426
Publication state
Published
Issued date
01/2022
Peer-reviewed
Oui
Volume
10
Number
1
Pages
e003024
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't ; Review
Publication Status: ppublish
Abstract
IntroductionImmuno-oncology therapies, including immune checkpoint inhibitors (ICIs), have transformed cancer care and have brought into question whether classic oncology efficacy assessments adequately describe the distinctive responses observed with these agents. With more ICI-based therapies being approved across multiple tumor types, it is essential to define unique clinical hallmarks of these agents and their associated assessments to better reflect the therapeutic impact for both patients and physicians. Long-term survival and objective responses, such as depth and durability of responses, treatment-free survival, efficacy in brain metastases, improved health-related quality of life, and unique safety profiles, are among the hallmarks that have emerged for ICI therapies. An established clinical hallmark is a sustained long-term survival, as evidenced by a delayed separation of Kaplan-Meier survival curves, and a plateau at ~3 years. Combination ICI therapies provide the opportunity to raise this plateau, thereby affording durable survival benefits to more patients. Deepening of responses over time is a unique clinical ICI hallmark, with patients responding long term and with more durable complete responses. Depth of response has demonstrated prognostic value for long-term survival in some cancers, and several ICI studies have shown sustained responses even after discontinuing ICI therapy, offering the potential for treatment-free intervals. Although clinical evidence supporting efficacy in brain metastases is limited, favorable ICI intracranial responses have been seen that are largely concordant with extracranial responses. While patient outcomes can be significantly improved with ICIs, they are associated with unique immune-mediated adverse reactions (IMARs), including delayed ICI toxicities, and may require multidisciplinary management for optimal care. Interestingly, patients discontinuing ICIs for IMARs may maintain responses similar to patients who did not discontinue for an IMAR, whether they restarted ICI therapy or not.ConclusionHerein, we comprehensively review and refine the clinical hallmarks uniquely associated with ICI therapies, which not only will rejuvenate our assessment of ICI therapeutic outcomes but also will lead to a greater appreciation of the effectiveness of ICI therapies.
Keywords
Brain Neoplasms/drug therapy, Humans, Immune Checkpoint Inhibitors/adverse effects, Immune Checkpoint Inhibitors/therapeutic use, Ipilimumab/therapeutic use, Neoplasms/drug therapy, Neoplasms/immunology, Neoplasms/mortality, Neoplasms/psychology, Quality of Life, CTLA-4 antigen, combination, drug therapy, immunotherapy, programmed cell death 1 receptor, review
Pubmed
Web of science
Open Access
Yes
Create date
31/01/2022 10:01
Last modification date
25/01/2024 7:40
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