Overall Survival With Second-Line Pembrolizumab in Patients With Non-Small-Cell Lung Cancer: Randomized Phase III Clinical Trial Versus Propensity-Adjusted Real-World Data.


Journal

JCO clinical cancer informatics
ISSN: 2473-4276
Titre abrégé: JCO Clin Cancer Inform
Pays: United States
ID NLM: 101708809

Informations de publication

Date de publication:
01 2021
Historique:
entrez: 13 1 2021
pubmed: 14 1 2021
medline: 24 8 2021
Statut: ppublish

Résumé

To compare and characterize overall survival (OS) differences between clinical trial data from the KEYNOTE-010 trial and real-world data (RWD) from the Flatiron Health database in patients with programmed death ligand 1 (PD-L1)-expressing advanced non-small-cell lung cancer (NSCLC) who received second-line pembrolizumab monotherapy. Clinical trial data were from the randomized phase II/III KEYNOTE-010 trial that enrolled patients from August 28, 2013, to February 27, 2015. At data cutoff for KEYNOTE-010, the median survival follow-up time for pembrolizumab patients was 11.2 months. RWD were from Flatiron Health advanced NSCLC database and included patients who initiated second-line pembrolizumab from January 26, 2015, to February 28, 2019. At data cutoff for Flatiron, the median survival follow-up time for pembrolizumab-treated patients was 6.1 months. Clinical trial data from KEYNOTE-010 and RWD from Flatiron were analyzed without adjustment, with propensity adjustment, and filtered per the main KEYNOTE-010 eligibility criteria (EC) of histologically/cytologically confirmed PD-L1-positive NSCLC, Eastern Cooperative Oncology Group performance status of 0/1, no prior therapy with docetaxel for NSCLC, and laboratory values indicative of adequate organ function in addition to prior line of therapy requirements. Among 243 patients from KEYNOTE-010 and 782 from Flatiron, median age was 63 Without any adjustment, as well as after applying similar EC and appropriate statistical methods, RWD demonstrated similar effectiveness for pembrolizumab in second-line NSCLC as observed in randomized clinical trials.

Identifiants

pubmed: 33439727
doi: 10.1200/CCI.20.00099
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Docetaxel 15H5577CQD
pembrolizumab DPT0O3T46P

Banques de données

ClinicalTrials.gov
['NCT01905657']

Types de publication

Clinical Trial, Phase II Clinical Trial, Phase III Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

56-65

Auteurs

Thomas Jemielita (T)

Biostatistics and Research Decision Sciences (BARDS), Merck & Co, Inc, Kenilworth, NJ.

Xiaoyun Nicole Li (XN)

Biostatistics and Research Decision Sciences (BARDS), Merck & Co, Inc, Kenilworth, NJ.

Bilal Piperdi (B)

Oncology Clinical Development, Merck & Co, Inc, Kenilworth, NJ.

Wei Zhou (W)

Center for Observational and Real World Evidence (CORE), Merck & Co, Inc, Kenilworth, NJ.

Thomas Burke (T)

Center for Observational and Real World Evidence (CORE), Merck & Co, Inc, Kenilworth, NJ.

Cong Chen (C)

Biostatistics and Research Decision Sciences (BARDS), Merck & Co, Inc, Kenilworth, NJ.

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Classifications MeSH