Efficacy of immune checkpoint inhibitors in patients with KRAS-mutant advanced non-small cell lung cancer: A retrospective analysis

被引:3
|
作者
Gu, Xiaodong [1 ,3 ]
Si, Jinfei [2 ,3 ]
Guan, Yelan [1 ]
Xu, Yibing [1 ]
Shao, Lan [1 ]
Zhang, Yiping [1 ]
Xu, Chunwei [4 ]
Pan, Weiwei [5 ]
Lu, Yuanzhi [6 ]
Song, Zhengbo [2 ]
Wang, Wenxian [1 ]
机构
[1] Chinese Acad Sci Univ, Zhejiang Canc Hosp, Canc Hosp, Dept Thorac Med Oncol, 1 Banshan East St, Hangzhou 310022, Zhejiang, Peoples R China
[2] Univ Chinese Acad Sci, Zhejiang Canc Hosp, Dept Clin Trial, Canc Hosp, 1 Banshan East St, Hangzhou 310002, Zhejiang, Peoples R China
[3] Zhejiang Chinese Med Univ, Clin Med Coll 2, Hangzhou 310053, Zhejiang, Peoples R China
[4] Nanjing Univ, Jinling Hosp, Dept Resp Med, Sch Med, Nanjing 210002, Jiangsu, Peoples R China
[5] Jiaxing Univ, Coll Med, Dept Cell Biol, Jiaxing 314001, Zhejiang, Peoples R China
[6] Jinan Univ, Affiliated Hosp 1, Dept Clin Pathol, Guangzhou 510630, Guangdong, Peoples R China
来源
OPEN MEDICINE | 2023年 / 18卷 / 01期
关键词
KRAS; NSCLC; ICIs; chemotherapy; KRAS G12C; 1ST-LINE THERAPY; PEMBROLIZUMAB; MUTATIONS; SURVIVAL;
D O I
10.1515/med-2023-0653
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The efficacy of immune checkpoint inhibitors (ICIs) on KRAS-mutant advanced non-small cell lung cancer (NSCLC) remains controversial. This retrospective study compared the effects of ICIs treatment and chemotherapy on the prognosis of patients with KRAS-mutant advanced NSCLC and different mutant subtypes in the real world. The study included 95 patients with KRAS-mutant advanced NSCLC. Patients treated with first-line ICIs plus platinum-containing chemotherapy had better progression-free survival (PFS) (7.4 vs 4.5 months, P = 0.035) and overall survival (OS) (24.1 vs 13.2 months, P = 0.007) than those receiving platinum-containing chemotherapy alone, and second-line ICI monotherapy was associated with better PFS (4.8 vs 3.0 months, P = 0.043) and OS (18.0 vs 13.8 months, P = 0.013) than chemotherapy monotherapy. There was no significant difference in PFS (5.267 vs 6.734 months, P = 0.969) and OS (19.933 vs 20.933 months, P = 0.808) between patients with KRAS-mutant and KRAS-wild-type NSCLC treated with ICIs or between KRAS G12C and KRAS non-G12C patients (PFS: 8.1 vs 4.8 months, P = 0.307; OS: 21.3 vs 21.8 months, P = 0.434). In summary, patients with advanced NSCLC with KRAS mutations can benefit from ICIs, but no difference between KRAS mutant subtypes was observed.
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页数:8
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