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Pembrolizumab in patients from China with microsatellite instability-high/mismatch repair deficient tumors: KEYNOTE-158.
Xu, Jianming; Mao, Yimin; Xu, Nong; Bai, Yuxian; Wang, Dong; Chen, Xiaojun; Yin, Xianli; Deng, Yanhong; Yang, Jianwei; Zhang, Jieqing; Tang, Jie; Huang, Yi; Li, Jiayi; Luo, Suxia; Zheng, Hong; Zhao, Weidong; Xu, Miaomiao; Li, Nan; Mao, Yixiang; Gozman, Alexander; Wu, Xiaohua.
Affiliation
  • Xu J; Fifth Medical Center of CPLA General Hospital, Beijing, China.
  • Mao Y; Renji Hospital Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Xu N; The First Affiliated Hospital Zhejiang University, Hangzhou, China.
  • Bai Y; Harbin Medical University Cancer Hospital, Harbin, China.
  • Wang D; Chongqing University Cancer Hospital, Chongqing, China.
  • Chen X; Obstetrics & Gynecology Hospital of Fudan University, Shanghai, China.
  • Yin X; Hunan Cancer Hospital, Changsha, China.
  • Deng Y; The Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
  • Yang J; Fujian Provincial Cancer Hospital, Fuzhou, China.
  • Zhang J; Affiliated Cancer Hospital of Guangxi Medical University, Nanning, China.
  • Tang J; Hunan Cancer Hospital, Changsha, China.
  • Huang Y; Hubei Cancer Hospital, Wuhan, China.
  • Li J; The First Affiliated Hospital of Xiamen University-Oncology, Xiamen, China.
  • Luo S; Henan Cancer Hospital, Zhengzhou, China.
  • Zheng H; Beijing Cancer Hospital, Beijing, China.
  • Zhao W; Anhui Provincial Hospital-Obstetrics & Gynecology, Hefei, China.
  • Xu M; MSD (China) Co., Ltd, Beijing, China.
  • Li N; MSD (China) Co., Ltd, Beijing, China.
  • Mao Y; MSD (China) Co., Ltd, Shanghai, China.
  • Gozman A; Merck & Co., Inc., Rahway, NJ, USA.
  • Wu X; Fudan University Shanghai Cancer Center, Shanghai, China.
Immunotherapy ; 2024 Mar 20.
Article in En | MEDLINE | ID: mdl-38506258
ABSTRACT

Aim:

To evaluate pembrolizumab in patients of Chinese descent with microsatellite instability-high (MSI-H)/deficient mismatch repair (dMMR) tumors enrolled in KEYNOTE-158 (Cohort L).

Methods:

Patients with MSI-H/dMMR advanced tumors received pembrolizumab 200 mg IV Q3W. Primary end point was overall response rate (ORR). Secondary end points were duration of response (DOR), progression-free survival (PFS) and overall survival (OS).

Results:

24 patients were enrolled (20 were evaluable for efficacy). With median follow-up of 12.4 months, the ORR was 70%. DOR, PFS and OS were all not reached. A total of 19 (79%) patients had a treatment-related adverse event (AE; grade ≥3 in 4 [17%]), and 8 (33%) had an immune-mediated AE (grade ≥3 in (4 [17%]).

Conclusion:

Pembrolizumab provided meaningful and durable responses with manageable safety. These results are consistent with those reported for the global trial.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Immunotherapy Journal subject: ALERGIA E IMUNOLOGIA / TERAPEUTICA Year: 2024 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Immunotherapy Journal subject: ALERGIA E IMUNOLOGIA / TERAPEUTICA Year: 2024 Type: Article Affiliation country: China