Is Immunotherapy Beneficial in Patients with Oncogene-Addicted Non-Small Cell Lung Cancers? A Narrative Review

Author:

McMahon David John1ORCID,McLaughlin Ronan2,Naidoo Jarushka3456

Affiliation:

1. Trinity St James’s Cancer Institute, St. James’s Hospital, James’s Street, D08 NHY1 Dublin, Ireland

2. St. Vincent’s University Hospital, D04 T6F4 Dublin, Ireland

3. Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD 21287, USA

4. Beaumont RCSI Cancer Centre, D09 V2NO Dublin, Ireland

5. RCSI University of Health Sciences, D02 YN77 Dublin, Ireland

6. Beaumont Hospital, D09 Y177 Dublin, Ireland

Abstract

Over the past 20 years, there has been a paradigm shift in the care of patients with non-small cell lung cancer (NSCLC), who now have a range of systemic treatment options including targeted therapy, chemotherapy, immunotherapy (ICI), and antibody–drug conjugates (ADCs). A proportion of these cancers have single identifiable alterations in oncogenes that drive their proliferation and cancer progression, known as “oncogene-addiction”. These “driver alterations” are identified in approximately two thirds of patients with lung adenocarcinomas, via next generation sequencing or other orthogonal tests. It was noted in the early clinical development of ICIs that patients with oncogene-addicted NSCLC may have differential responses to ICI. The toxicity signal for patients with oncogene-addicted NSCLC when treated with ICIs also seemed to differ depending on the alteration present and the specific targeted agent used. Developing a greater understanding of the underlying reasons for these clinical observations has become an important area of research in NSCLC. In this review, we analyze the efficacy and safety of ICI according to specific mutations, and consider possible future directions to mitigate safety concerns and improve the outcomes for patients with oncogene-addicted NSCLC.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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