Phase 1b Study of Sintilimab Plus Anlotinib as First-line Therapy in Patients With Advanced NSCLC

被引:191
|
作者
Chu, Tianqing [1 ]
Zhong, Runbo [1 ]
Zhong, Hua [1 ]
Zhang, Bo [1 ]
Zhang, Wei [1 ]
Shi, Chunlei [1 ]
Qian, Jialin [1 ]
Zhang, Yanwei [1 ]
Chang, Qing [1 ]
Zhang, Xueyan [1 ]
Dong, Yu [1 ]
Teng, Jiajun [1 ]
Gao, Zhiqiang [1 ]
Qiang, Huiping [1 ]
Nie, Wei [1 ]
Zhao, Yiming [1 ]
Han, Yuchen [2 ]
Chen, Ya [1 ]
Han, Baohui [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Resp Dept, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Pathol Dept, Shanghai, Peoples R China
关键词
Non?small cell lung cancer; First-line; Anti?PD-1; Antiangiogenic TKIs; Chemotherapy-free; CELL LUNG-CANCER; EARLY TUMOR SHRINKAGE; PEMBROLIZUMAB; TRIAL; CHEMOTHERAPY; INHIBITOR; DEPTH;
D O I
10.1016/j.jtho.2020.11.026
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Although the interaction between tumor immune microenvironment and angiogenesis has been well established, evidence supporting the chemo-free combination of immune checkpoint inhibitors plus antiangiogenic tyrosine kinase inhibitors in treatment-naive patients with advanced NSCLC is insufficient. This report provides the efficacy and safety of sintilimab combined with anlotinib as first-line therapy for advanced NSCLC from a phase 1b trial (NCT03628521). Methods: Eligible patients who were treatment-naive and had unresectable stage IIIB/C or IV NSCLC without EGFR/ ALK/ROS1 mutations received sintilimab (200 mg, day 1) and anlotinib (12 mg, day 1-14) every 3 weeks till disease progression or unacceptable toxicity. Baseline programmed death-ligand 1 expression and tumor mutation burden status was assessed in all patients. The primary end points were objective response rate and safety. Results: A total of 22 patients received sintilimab and anlotinib. Median follow-up was 15.8 months (range: 8.3- 19.3). Sixteen patients achieved confirmed partial response with an objective response rate of 72.7% (95% confidence interval [CI]: 49.8%-89.3%) and disease control rate of 100% (95% CI: 84.6%-100%). Median progression-free survival was 15 months (95% CI: 8.3 m, not reached), and the 12-month progression-free survival rate was 71.4% (95% CI: 47.2%-86.0%). The incidence rate of grade 3 or higher treatment-related adverse events was 54.5%, and grade 3 hypertension was predominant (two of 22, 9.1%). No grade 4 treatment-related adverse events were observed, and one case of grade 5 immune-related pneumonitis occurred. Conclusions: To the best of our knowledge, this is the first study that assessed an anti-programmed cell death protein 1 antibody combined with a multitarget antiangiogenic tyrosine kinase inhibitor in the frontline setting for patients with NSCLC. In view of its encouraging efficacy, durability, and safety profile, sintilimab plus anlotinib represents a novel chemotherapy-free regimen in this patient population. (c) 2020 Published by Elsevier Inc. on behalf of International Association for the Study of Lung Cancer.
引用
收藏
页码:643 / 652
页数:10
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