Albumin bound-paclitaxel combined with anlotinib and immunotherapy in the second-line treatment of ES-SCLC: a retrospective cohort study.

IF 2 4区 医学 Q3 ONCOLOGY Neoplasma Pub Date : 2024-10-01 DOI:10.4149/neo_2024_240716N299
Xiaobing Li, De Wu, Jing Tang, Yuebing Wu
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Abstract

Effective treatment strategies for second-line therapy in extensive-stage small cell lung cancer (ES-SCLC) are currently lacking. For this reason, we collected and recorded efficacy and safety data from patients with ES-SCLC who had disease progression after first-line treatment and received albumin-bound paclitaxel, anlotinib, and immunotherapy. Preliminary data showed an objective response rate of 37.78%. Median progression-free survival and overall survival were 5 months and 10 months, respectively. Treatment-related adverse events were mostly tolerable. Subgroup analysis indicated that efficacy correlated with the interval from last chemotherapy to treatment initiation and specific drug-related adverse events. Further analysis of immune cell subtypes suggested that the mechanism may involve depletion of immune suppression to activate immune responses synergistically against tumors. With its promising efficacy and manageable adverse effects, this regimen holds potential as a significant option for second-line therapy in ES-SCLC. However, due to the limited sample size, further clinical validation is needed to ascertain its true clinical value.

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白蛋白结合型紫杉醇联合安罗替尼和免疫疗法在ES-SCLC二线治疗中的应用:一项回顾性队列研究。
目前,广泛期小细胞肺癌(ES-SCLC)的二线治疗缺乏有效的治疗策略。为此,我们收集并记录了接受白蛋白结合紫杉醇、安罗替尼和免疫疗法治疗后病情进展的 ES-SCLC 患者的疗效和安全性数据。初步数据显示,客观反应率为37.78%。中位无进展生存期和总生存期分别为5个月和10个月。治疗相关的不良反应大多可以耐受。亚组分析表明,疗效与最后一次化疗到开始治疗的间隔时间和特定药物相关不良事件有关。对免疫细胞亚型的进一步分析表明,其机制可能是消耗免疫抑制,从而激活协同抗肿瘤的免疫反应。该方案具有良好的疗效和可控的不良反应,有望成为ES-SCLC二线治疗的重要选择。然而,由于样本量有限,还需要进一步的临床验证才能确定其真正的临床价值。
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来源期刊
Neoplasma
Neoplasma 医学-肿瘤学
CiteScore
5.40
自引率
0.00%
发文量
238
审稿时长
3 months
期刊介绍: The journal Neoplasma publishes articles on experimental and clinical oncology and cancer epidemiology.
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