Department of Pulmonary Medicine, Shanghai Chest Hospital, Shanghai Jiaotong University, Shanghai, China.
Cancer Med. 2023 Mar;12(5):5372-5383. doi: 10.1002/cam4.5360. Epub 2022 Oct 17.
Treatments for advanced small-cell lung cancer (SCLC) patients who are resistant to first-line chemotherapy are limited. Given that antiangiogenic agents and immune-checkpoint inhibitors (ICIs) can confer synergistic therapeutic benefits, combination therapy should be considered. We explored the efficacy and safety of combination therapy with anlotinib and programmed cell death protein 1 (PD-1)/programmed cell death-ligand 1 (PD-L1) inhibitors as second-line and subsequent therapy for advanced SCLC.
We reviewed advanced SCLC patients at Shanghai Chest Hospital who had received anlotinib in combination with ICIs from November 2016 to November 2020 as second- and subsequent-line treatment. Patients with advanced SCLC who had received paclitaxel monotherapy as second-line treatment were included as the control group.
A total of 141 patients were included in the final analysis (40 in the combination therapy group and 101 in the paclitaxel monotherapy group). The median progression-free survival (PFS) times for the combination therapy and paclitaxel monotherapy groups were 3.40 and 2.83 months (p = 0.022), respectively, while the median overall survival (OS) times for the combination therapy and paclitaxel monotherapy groups were 8.20 and 5.87 months (p = 0.048), respectively. Hypertension and hepatic dysfunction were the most pronounced adverse events of combination therapy and two patients changed regimens due to severe fatigue and anorexia.
The combination of anlotinib and PD-1/PD-L1 blockade has promising efficacy and safety as a second-line or subsequent therapy for SCLC.
对于一线化疗耐药的晚期小细胞肺癌(SCLC)患者,治疗方法有限。鉴于抗血管生成药物和免疫检查点抑制剂(ICI)可带来协同治疗益处,应考虑联合治疗。我们探讨了安罗替尼联合程序性细胞死亡蛋白 1(PD-1)/程序性细胞死亡配体 1(PD-L1)抑制剂作为二线及后线治疗晚期 SCLC 的疗效和安全性。
我们回顾了 2016 年 11 月至 2020 年 11 月期间在上海胸科医院接受安罗替尼联合 ICI 二线及后线治疗的晚期 SCLC 患者。将接受紫杉醇单药二线治疗的晚期 SCLC 患者作为对照组。
最终分析纳入了 141 例患者(联合治疗组 40 例,紫杉醇单药治疗组 101 例)。联合治疗组和紫杉醇单药治疗组的中位无进展生存期(PFS)分别为 3.40 个月和 2.83 个月(p=0.022),中位总生存期(OS)分别为 8.20 个月和 5.87 个月(p=0.048)。联合治疗最显著的不良反应是高血压和肝功能异常,有 2 例患者因严重乏力和厌食而改变治疗方案。
安罗替尼联合 PD-1/PD-L1 阻断剂作为 SCLC 的二线或后线治疗具有良好的疗效和安全性。