The Association Between Baseline Hepatic or Renal Function and Clinical Outcomes for Patients With Non‐Small Cell Lung Cancer Treated With a PD‐1/PD‐L1 Blocking Antibody Using Real‐World and Trial Data

Author:

Liu Qi1ORCID,Mathur Raina2,Xu Yuan1,Torres Aracelis Z.2ORCID,Miksad Rebecca A.2ORCID,Liu Chao3,Smithson Haixia1,Wang Yaning4,Zhu Hao1,Booth Brian1,Huang Shiew‐Mei1ORCID,Zhi Jizu1,Sridhara Rajeshwari1,Blumenthal Gideon Michael5,Larkins Erin1,Mishra‐Kalyani Pallavi S.1,Rivera Donna R.1,Kluetz Paul G.1,Sharon Elad6

Affiliation:

1. US Food and Drug Administration Silver Spring Maryland USA

2. Flatiron Health, Inc New York New York USA

3. BeiGene USA, Inc Fulton Maryland USA

4. Greaterna Science and Technology Shanghai China

5. Merck Rahway New Jersey USA

6. National Cancer Institute Bethesda Maryland USA

Abstract

Clinical trials have demonstrated the benefit of PD‐1/PD‐L1 blocking antibodies for the treatment of patients with advanced non‐small cell lung cancer (NSCLC) in defined patient populations that often exclude patients with moderate or severe hepatic or renal impairment. We assessed the association between overall survival (OS) and baseline organ function in patients with advanced NSCLC treated with PD‐1/PD‐L1 blocking antibodies in real‐world data (RWD; patient‐level data from electronic health records) and pooled clinical trial data submitted to the US Food and Drug Administration (FDA). The Kaplan–Meier estimator was used to estimate OS in different subgroups based on organ function. Unadjusted and adjusted Cox proportional hazards models were used to estimate the association between OS and organ function. In this hypothesis‐generating study, baseline renal impairment did not appear to be associated with OS, while patients with baseline liver impairment had shorter OS. RWD provided information on a broader range of renal and hepatic function than was evaluated in clinical trials and hold promise to complement trial data in better understanding populations not represented in clinical trials.

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

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