Molecular determinants of clinical outcomes with pembrolizumab versus paclitaxel in a randomized, open-label, phase III trial in patients with gastroesophageal adenocarcinoma ☆
Annals of Oncology, ISSN: 0923-7534, Vol: 32, Issue: 9, Page: 1127-1136
2021
- 48Citations
- 63Captures
- 1Mentions
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Metrics Details
- Citations48
- Citation Indexes48
- 48
- CrossRef17
- Captures63
- Readers63
- 63
- Mentions1
- News Mentions1
- 1
Most Recent News
Study Identifies Molecular Determinants of Gastric/Gastroesophageal Junction Cancer
An exploratory analysis from the randomized KEYNOTE-061 trial showed a strong association between tissue tumor mutational burden (tTMB) and clinical efficacy with second-line pembrolizumab but
Article Description
In the phase III KEYNOTE-061 trial (NCT02370498), pembrolizumab did not significantly improve overall survival versus paclitaxel as second-line therapy for gastric/gastroesophageal junction (GEJ) adenocarcinoma with programmed death-ligand 1 (PD-L1) combined positive score (CPS) ≥1 tumors. The association of tissue tumor mutational burden (tTMB) status and clinical outcomes was determined, including the relationship with CPS and microsatellite instability-high (MSI-H) status. In patients with whole exome sequencing (WES) data [420/592 (71%); pembrolizumab, 218; paclitaxel, 202], the association of tTMB with objective response rate (ORR; logistic regression), progression-free survival (PFS; Cox proportional hazards regression), and overall survival (OS; Cox proportional hazards regression) were measured using one-sided (pembrolizumab) and two-sided [paclitaxel] P values. tTMB was also evaluated using FoundationOne®CDx [205/592 (35%)]. Prespecified equivalent cut-offs of 175 mut/exome for WES and 10 mut/Mb for FoundationOne®CDx were used. WES-tTMB was significantly associated with ORR, PFS, and OS in pembrolizumab-treated (all P < 0.001) but not paclitaxel-treated patients (all P > 0.6) in univariate analysis. The area under the receiver operating characteristics curve for WES-tTMB and response was 0.68 [95% confidence interval (CI) 0.56-0.81] for pembrolizumab and 0.51 (95% CI 0.39-0.63) for paclitaxel in univariate analysis. There was low correlation between WES-tTMB and CPS in both treatment groups ( r ≤ 0.16). WES-tTMB remained significantly associated with all clinical endpoints with pembrolizumab after adjusting for CPS and with PFS and OS after excluding known MSI-H tumors ( n = 26). FoundationOne®CDx-tTMB demonstrated a positive association with ORR, PFS, and OS in pembrolizumab-treated patients (all P ≤ 0.003) but not PFS or OS in paclitaxel-treated patients ( P > 0.1). This exploratory analysis from KEYNOTE-061 is the first to demonstrate a strong association between tTMB and efficacy with pembrolizumab but not paclitaxel in patients with gastric/GEJ adenocarcinoma in a randomized setting. Data further suggest tTMB is a significant and independent predictor beyond PD-L1 status.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0923753421020287; http://dx.doi.org/10.1016/j.annonc.2021.05.803; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85109047875&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/34082019; https://linkinghub.elsevier.com/retrieve/pii/S0923753421020287; https://dx.doi.org/10.1016/j.annonc.2021.05.803
Elsevier BV
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