Tislelizumab in previously treated, locally advanced unresectable/metastatic microsatellite instability-high/ mismatch repair-deficient solid tumors

被引:3
|
作者
Li, Jian [1 ]
Xu, Ye [2 ]
Zang, Aimin [3 ]
Gao, Yunong [4 ]
Gao, Quanli [5 ]
Zhang, Yanqiao [6 ]
Wang, Dong [7 ]
Xu, Jianming [8 ]
Yuan, Ying [9 ]
Jiang, Haiping [10 ]
Ying, Jieer [11 ]
Shi, Chunmei [12 ]
Deng, Yanhong [13 ]
Wang, Jing [14 ]
Liu, Tianshu [15 ]
Huang, Yi [16 ]
Qian, Xiaoping [17 ]
Pan, Yueyin [18 ]
Cheng, Ying [19 ]
Hu, Sheng [20 ]
Wang, Jin [21 ]
Shi, Mengyue [21 ]
Wang, Ke [22 ]
Hu, Han [22 ]
Shen, Lin [1 ]
机构
[1] Peking Univ Canc Hosp & Inst, Dept Gastrointestinal Oncol, State Key Lab Holist Integrat Management Gastroint, Beijing Key Lab Carcinogenesis & Translat Res, 52 Fucheng Rd, Beijing 100142, Peoples R China
[2] Fudan Univ, Shanghai Canc Ctr, Dept Oncol, Shanghai 200032, Peoples R China
[3] Hebei Univ, Affiliated Hosp, Dept Med Oncol, Baoding 071000, Peoples R China
[4] Peking Univ Canc Hosp & Inst, Dept Gynecol, Key Lab Carcinogenesis & Translat Res, Minist Educ Beijing, Beijing 100142, Peoples R China
[5] Henan Canc Hosp, Dept Immunotherapy, Zhengzhou 450008, Peoples R China
[6] Harbin Med Univ, Affiliated Canc Hosp, Dept Gastrointestinal Oncol, Harbin 150086, Peoples R China
[7] Chongqing Univ Canc Hosp, Dept Gastrointestinal Oncol, Chongqing 400030, Peoples R China
[8] Peoples Liberat Army Gen Hosp, Med Ctr 5, Dept Gastrointestinal Oncol, Beijing 100048, Peoples R China
[9] Zhejiang Univ, Affiliated Hosp 2, Sch Med, Dept Med Oncol, Hangzhou 310009, Peoples R China
[10] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Dept Med Oncol, Hangzhou 310003, Zhejiang, Peoples R China
[11] Univ Chinese Acad Sci, Canc Hosp, Dept Med Oncol, Hangzhou 310022, Peoples R China
[12] Fujian Med Univ, Union Hosp, Dept Med Oncol, Fuzhou 350001, Peoples R China
[13] Sun Yat Sen Univ, Affiliated Hosp 6, Dept Oncol, Guangzhou 510655, Peoples R China
[14] Hunan Canc Hosp, Dept Med Oncol, Changsha 410013, Peoples R China
[15] Fudan Univ, Zhongshan Hosp, Dept Med Oncol, Shanghai 200032, Peoples R China
[16] Hubei Canc Hosp, Dept Immunotherapy, Wuhan 430079, Peoples R China
[17] Nanjing Univ, Affiliated Hosp, Dept Med Oncol, Med Sch, Nanjing 210008, Peoples R China
[18] Anhui Prov Hosp, Dept Med Oncol, Hefei 230001, Peoples R China
[19] Jilin Canc Hosp, Dept Med Oncol, Changchun 130012, Peoples R China
[20] Hubei Canc Hosp, Dept Med Oncol, Wuhan 430079, Peoples R China
[21] BeiGene Shanghai Co Ltd, Clin Dev, Shanghai 200001, Peoples R China
[22] BeiGene Beijing Co Ltd, Biostat, Beijing 102206, Peoples R China
关键词
Biomarkers; DNA mismatch repair; immune checkpoint inhibitors; microsatellite instability; phase II clinical trials; programmed cell death 1 receptor; COLORECTAL-CANCER; PLACEBO; TRIAL;
D O I
10.21147/j.issn.1000-9604.2024.03.03
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The open-label, phase II RATIONALE-209 study evaluated tislelizumab (anti-programmed cell death protein 1 antibody) as a tissue-agnostic monotherapy for microsatellite instability-high (MSI-H)/mismatch repair-deficient (dMMR) tumors. Methods: Adults with previously treated, locally advanced unresectable or metastatic MSI-H/dMMR solid tumors were enrolled. Patients received tislelizumab 200 mg intravenously every 3 weeks. Objective response rate (ORR; primary endpoint), duration of response (DoR), and progression-free survival (PFS) were assessed by independent review committee (Response Evaluation Criteria in Solid Tumors v1.1). Results: Eighty patients were enrolled and treated; 75 (93.8%) patients had measurable disease at baseline. Most had metastatic disease and received at least one prior therapy for advanced/metastatic disease (n=79; 98.8%). At primary analysis (data cutoff July 8, 2021; median follow-up 15.2 months), overall ORR [46.7%; 95% confidence interval (95% CI), 35.1 -58.6; one-sided P<0.0001] and ORR across tumor-specific subgroups [colorectal (n=46): 39.1% (95% CI, 25.1-54.6); gastric/gastroesophageal junction (n=9): 55.6% (95% CI, 21.2 -86.3); others (n=20): 60.0% (95% CI, 36.1 -80.9)] were significantly greater with tislelizumab vs. a prespecified historical control ORR of 10%; five (6.7%) patients had complete responses. Median DoR, PFS, and overall survival were not reached with long-term follow-up (data cutoff December 5, 2022; median follow-up 28.9 months). Tislelizumab was well tolerated with no unexpected safety signals. Treatment-related adverse events (TRAEs) of grade >= 3 occurred in 53.8% of patients; 7.5% of patients discontinued treatment due to TRAEs. Conclusions: Tislelizumab demonstrated a significant ORR improvement in patients with previously treated, locally advanced unresectable or metastatic MSI-H/dMMR tumors and was generally well tolerated.
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页数:22
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