Abstract | BACKGROUND: METHODS: This phase Ib study included six cohorts. Cohort A-C were sintilimab monotherapy settings, and enrolled pretreated patients (2/3 L cohorts). Cohort D-F were treatment-naïve patients (1 L cohorts), and received sintilimab plus different chemotherapies. The primary endpoints were safety and objective response rate (ORR). Exploratory endpoints were potential biomarkers for the prognosis after treatment, such as tumor mutation burden scores (TMB), PD-L1 and lymphocyte-to-monocyte ratio (LMR). RESULTS: The ORR was 14.6% in the 2/3 L cohorts (n=146), and 73.2% in the 1 L cohorts (n=61). The incidence of grade 3-4 adverse events occurred in 55 patients (37.7%) in 2/3 L cohorts, and in 38 (62.3%) in 1 L cohorts. 157 patients had available TMB scores, and in 2/3 L cohorts, patients in the high TMB groups (TMB≥10) showed a longer progression-free survival (PFS) and overall survival (OS) than those in the low TMB groups (TMB<10). No significant differences in PFS and OS were observed across different PD-L1 groups in both 1 L and 2/3 L cohorts. A high LMR was significantly associated with an improved PFS in 1 L cohorts (P=0.022). CONCLUSION: TRIAL REGISTRATION: ClinicalTrials.gov, number NCT02937116. Registered 18 October 2016.
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Authors | Haiping Jiang, Ning Li, Huan Wang, Zhenguang Chen, Yulong Zheng, Jiong Qian, Chenyu Mao, Xin Xu, Cheng Xiao, Xiaochen Zhang, Hui Zhou, Shuyan Wang, Weisheng Chen, Xia Yin, Jiya Sun, Bo Peng, Lisong Teng, Nong Xu |
Journal | American journal of cancer research
(Am J Cancer Res)
Vol. 11
Issue 9
Pg. 4259-4276
( 2021)
ISSN: 2156-6976 [Print] United States |
PMID | 34659886
(Publication Type: Journal Article)
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Copyright | AJCR Copyright © 2021. |