Camrelizumab combined with anlotinib as second-line therapy for metastatic or recurrent small cell lung cancer: a retrospective cohort study

被引:0
|
作者
Shen, Shujing [1 ]
Li, Xingya [2 ]
Guo, Sanxing [2 ]
Xu, Liang [3 ]
Yan, Ningning [2 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Radiat Oncol, Zhengzhou, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Dept Med Oncol, Zhengzhou, Peoples R China
[3] Third Hosp Nanchang City, Prevent & Cure Ctr Breast Dis, Nanchang, Jiangxi, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2024年 / 14卷
基金
中国国家自然科学基金;
关键词
camrelizumab; anlotinib; small-cell lung cancer; extensive stage; second-line setting; SINTILIMAB PLUS ANLOTINIB; PHASE-III TRIAL; SINGLE-ARM; OPEN-LABEL; TOPOTECAN; MULTICENTER; IPILIMUMAB; CARCINOMA; PEMBROLIZUMAB; NIVOLUMAB;
D O I
10.3389/fonc.2024.1391828
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: This retrospective study evaluates the efficacy of camrelizumab combined with anlotinib versus chemotherapy in patients with extensive-stage small-cell lung cancer (ES-SCLC) undergoing second-line treatment. Methods: Data were sourced from medical records at a Chinese medical facility, involving 34 patients diagnosed with ES-SCLC after failing first-line treatment. Patients were divided into two groups: one received camrelizumab (200 mg every 3 weeks) with anlotinib (12 mg daily for 14 days followed by a 7-day rest), while the other group received physician-chosen chemotherapy administered every 3 weeks. The primary endpoint was progression-free survival (PFS), with secondary endpoints including overall survival (OS), objective response rate (ORR), and disease control rate (DCR). Results: The combination therapy group showed a significant improvement in PFS compared to the chemotherapy group (median PFS: 7 months vs. 3 months; hazard ratio (HR): 0.34; 95% confidence interval (CI): 0.15-0.77; p<0.001). However, there was no statistically significant difference in OS between the groups (16.3 months vs. 17.3 months; p=0.82). The ORR was 52.9% in the combination therapy group versus 23.5% in the chemotherapy group (p=0.08), and the DCR was 82.4% compared to 58.8% (p=0.26). Grade 3 or higher adverse events were observed in 17.6% of the combination therapy group and 29.4% of the chemotherapy group. Conclusions: The findings suggest that the combination of camrelizumab and anlotinib offers a superior anti-tumor response with a manageable safety profile in a second-line setting for ES-SCLC patients. This combination regimen may be a viable option for second-line ES-SCLC treatment.
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页数:8
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