Combining Immunotherapy with Anlotinib in Extensive-Stage Small Cell Lung Cancer: A Multicenter Analysis of Efficacy and Safety.

IF 2.7 4区 医学 Q3 ONCOLOGY
Technology in Cancer Research & Treatment Pub Date : 2025-01-01 Epub Date: 2025-03-20 DOI:10.1177/15330338251329248
Guogang Gao, Meiling Sun, Zhongfei Yang, Jingyi Li, Huaijun Ji, Ge Yu
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Abstract

BackgroundExtensive-stage small cell lung cancer (ES-SCLC) is a highly aggressive malignancy with poor prognosis. This study aimed to assess the efficacy of combining immunotherapy (IT) with Anlotinib in ES-SCLC patients.MethodsThis study was a multicenter retrospective cohort analysis. Survival outcomes were evaluated using Kaplan-Meier curves and Cox proportional hazards regression models.ResultsA total of 147 patients were included in the analysis. The median overall survival (mOS) for the cohort was 15.5 months (95% CI: 13.9-17.1). Patients in the chemotherapy(CT) plus IT group had an mOS of 17.8 months, compared to 12.6 months in the CT-alone group (p = 0.055). When stratified into CT + IT + Anlotinib, CT + IT, and CT-alone groups, the mOS were 18.5, 16.3, and 12.6 months, respectively, with the CT + IT + Anlotinib group demonstrating significantly improved OS compared to CT-alone (p = 0.044). The ORR and DCR for the entire cohort were 71.4% and 85.7%, respectively. Subgroup analysis revealed ORRs of 74.1% (CT + IT + Anlotinib), 73.9% (CT + IT), and 70.1% (CT-alone), with corresponding DCRs of 92.6%, 91.3%, and 82.5%. Multivariate analysis revealed that radiotherapy (RT, p = 0.003) and IT (p = 0.021) were independent prognostic factors for OS, while liver metastasis (p = 0.023) and RT (p = 0.018) were associated with PFS. Patients receiving RT in combination with CT showed markedly improved OS (17.5 vs 12.5 months; p = 0.002) and PFS (7.3 vs 6.3 months; p = 0.004). The incidence of adverse events was comparable across all groups (p = 0.721).ConclusionThe combined application of Anlotinib with IT and the combination of CT with RT both significantly improved survival outcomes in patients with ES-SCLC while maintaining a favorable safety profile. These findings warrant further investigation in future studies.

联合免疫疗法与安洛替尼治疗广泛期小细胞肺癌:疗效和安全性的多中心分析。
广泛期小细胞肺癌(ES-SCLC)是一种高度侵袭性的恶性肿瘤,预后较差。本研究旨在评估免疫治疗(IT)联合安洛替尼治疗ES-SCLC患者的疗效。方法采用多中心回顾性队列分析。使用Kaplan-Meier曲线和Cox比例风险回归模型评估生存结果。结果共纳入147例患者。队列的中位总生存期(mOS)为15.5个月(95% CI: 13.9-17.1)。化疗(CT)加IT组患者的生存期为17.8个月,而单独CT组为12.6个月(p = 0.055)。CT + IT +安洛替尼组、CT + IT组和单独使用CT组的生存期分别为18.5个月、16.3个月和12.6个月,CT + IT +安洛替尼组的生存期较单独使用CT组有显著改善(p = 0.044)。整个队列的ORR和DCR分别为71.4%和85.7%。亚组分析显示,orr分别为74.1% (CT + IT + Anlotinib)、73.9% (CT + IT)和70.1%(单独使用CT),相应的dcr分别为92.6%、91.3%和82.5%。多因素分析显示放疗(RT, p = 0.003)和IT (p = 0.021)是OS的独立预后因素,而肝转移(p = 0.023)和RT (p = 0.018)与PFS相关。接受RT联合CT治疗的患者OS明显改善(17.5个月vs 12.5个月;p = 0.002)和PFS (7.3 vs 6.3个月;p = 0.004)。各组不良事件发生率具有可比性(p = 0.721)。结论安洛替尼与IT联合应用、CT与RT联合应用均可显著改善ES-SCLC患者的生存结局,同时保持良好的安全性。这些发现值得在未来的研究中进一步调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
202
审稿时长
2 months
期刊介绍: Technology in Cancer Research & Treatment (TCRT) is a JCR-ranked, broad-spectrum, open access, peer-reviewed publication whose aim is to provide researchers and clinicians with a platform to share and discuss developments in the prevention, diagnosis, treatment, and monitoring of cancer.
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