Efficacy and safety of second-line camrelizumab combined with apatinib and chemotherapy in patients with advanced lung adenocarcinoma: A prospective, open-label, multicentric study

被引:0
|
作者
Yao, Yiwei [1 ]
Wang, Yong [1 ]
Du, Yingying [2 ]
Jiang, Fengshou [1 ]
Liang, Hui [3 ]
Bi, Minghong [4 ]
Xie, Hua [5 ]
Peng, Wanren [2 ]
Pan, Yueyin [1 ,6 ]
机构
[1] USTC, Affiliated Hosp 1, Dept Oncol Chemotherapy, Hefei 230001, Anhui, Peoples R China
[2] Anhui Med Univ, Affiliated Hosp 1, Dept Oncol, Hefei 230001, Anhui, Peoples R China
[3] Tradit Chinese Hosp Luan, Dept Radiol, Luan 237006, Anhui, Peoples R China
[4] First Affiliated Hosp, Bengbu Med Coll, Dept Oncol, Bengbu 233004, Anhui, Peoples R China
[5] Xuancheng Peoples Hosp, Dept Oncol, Xuancheng 242000, Anhui, Peoples R China
[6] USTC, Affiliated Hosp 1, Dept Oncol Chemotherapy, 17 Lujiang Rd, Hefei 230001, Anhui, Peoples R China
关键词
Camrelizumab; Apatinib; Second-line; Advanced lung adenocarcinoma; Efficacy and safety; CANCER; DOCETAXEL;
D O I
10.1016/j.intimp.2023.111147
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objectives: Camrelizumab (a programmed cell death protein 1 inhibitor) and apatinib (an angiogenesis inhibitor) are considered as potential treatments for advanced lung adenocarcinoma (LUAD). This study aimed to evaluate the efficacy and safety of second-line camrelizumab combined with apatinib and chemotherapy (albumin-bound paclitaxel, docetaxel, or pemetrexed) in patients with advanced LUAD.Methods: Twenty-nine patients with advanced LUAD underwent second-line camrelizumab combined with apatinib and chemotherapy were enrolled in this prospective, open-label, multicentric study. Follow-up with a median duration of 18.0 months was conducted.Results: There were 0 (0.0 %), 11 (37.9 %), 14 (48.4 %), and 3 (10.3 %) patients achieving complete response, partial response, stable disease, and progressive disease, respectively. Meanwhile, treatment response was not evaluated in 1 (3.4 %) patient. The objective response and disease control rates were 37.9 % and 86.3 %, respectively. In terms of survival, the median (95 % confidence interval) progression-free survival (PFS) was 11.1 (5.2-17.0) months, with 1-year and 2-year PFS rates of 40.4 % and 20.5 %, respectively. The median overall survival (OS) was not reached; the 1-year and 2-year OS rates were 72.0 % and 64.8 %, respectively. Current treatment cycles >= 8 were associated with better PFS and OS (both P < 0.001). In addition, 21 (72.4 %) patients experienced at least one treatment-emergent adverse event (TEAE), which was mostly of grade I and II. The most commonly occurring TEAE was leukopenia (17.2 %), liver dysfunction (17.2 %), hypothyroidism (13.8 %), hand-foot syndrome (13.8 %), and thrombocytopenia (13.8 %).Conclusion: Second-line camrelizumab combined apatinib and chemotherapy might serve as a potential treatment with acceptable safety in patients with advanced LUAD.
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页数:7
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