Literature DB >> 29382669

Treatment-Related Adverse Events Predict Improved Clinical Outcome in NSCLC Patients on KEYNOTE-001 at a Single Center.

Aaron Lisberg1, D Andrew Tucker1, Jonathan W Goldman1, Brian Wolf1, James Carroll1, Ariana Hardy1, Karolyn Morris1, Paulina Linares1, Carlos Adame1, Marshall L Spiegel1, Courtney Wells1, Jordan McKenzie1, Blanca Ledezma1, Melody Mendenhall1, Phillip Abarca1, Krikor Bornazyan1, Jaime Hunt1, Nima Moghadam1, Natalie Chong1, Danielle Nameth1, Caitlin Marx1, John Madrigal1, Sitaram Vangala1, Narek Shaverdian1, David Elashoff1, Edward B Garon2.   

Abstract

We retrospectively analyzed non-small cell lung cancer (NSCLC) patients from a single center treated with pembrolizumab on the KEYNOTE-001 trial and evaluated the association between treatment-related adverse events (trAEs) and clinical outcomes. Investigators reported AEs on trial and graded them according to Common Terminology Criteria for Adverse Events v4.0, labeling them as unlikely, possibly, or probably treatment-related. AEs labeled as possibly/probably related were considered trAEs for this analysis. The relationship between the incidence of a trAE and clinical outcomes was evaluated. Ninety-seven NSCLC patients treated on KEYNOTE-001 at the University of California, Los Angeles were evaluated. Ten percent (85/826) of AEs were trAEs, occurring in 40% (39/97) of patients. The most frequent trAEs were rash (21% patients), fatigue (6% patients), and hypothyroidism (6% patients). The 39 patients that experienced a trAE had increased objective response rate (ORR, 38.5%), progression-free survival (PFS: median, 248 days), and overall survival (OS: median, 493 days), compared with the 58 patients that did not (ORR: 8.9%, PFS: median 60 days, OS: median 144.5 days). The observed association between trAEs and improved clinical outcome persisted when using Cox proportional hazards regression models to assess the confounding effect of covariates and mitigate guarantee-time bias. The association also remained when data were substratified by grade, degree of association, and treatment-related select AE designation. This single-center analysis revealed that trAEs predicted for improved clinical outcome with pembrolizumab, and when controlling for guarantee-time bias and plausible confounders, this association remained. This observed relationship adds to our understanding of anti-PD-1 therapy and could aid clinicians in identifying patients most likely to benefit from therapy. Cancer Immunol Res; 6(3); 288-94. ©2018 AACR. ©2018 American Association for Cancer Research.

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Year:  2018        PMID: 29382669      PMCID: PMC6066474          DOI: 10.1158/2326-6066.CIR-17-0063

Source DB:  PubMed          Journal:  Cancer Immunol Res        ISSN: 2326-6066            Impact factor:   11.151


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