Xiong Jin, Xia Lei
Department of Cancer Center, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Tianjin Key Laboratory of Radiation Medicine and Molecular Nuclear Medicine, Institute of Radiation Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
Front Oncol. 2025 Jan 14;14:1462581. doi: 10.3389/fonc.2024.1462581. eCollection 2024.
Patients with extensive-stage small cell lung cancer (ES-SCLC) have a poor Q6 prognosis and there is no standard protocol for maintenance treatment. Anlotinib as a third-line or beyond therapy for ES-SCLC was proved to be effective.
We retrospectively screened of patients with ES-SCLC who started receiving anlotinib as first-line or second-line therapy at the Second Affiliated Hospital of Chongqing Medical University from November 2018 to December 2022. 30 patients treated with anlotinib based combination therapy and subsequent maintenance therapy were included. The primary study endpoint was progression-free survival (PFS) and the secondary study endpoints were overall survival (OS), clinical response and adverse events (AEs).
In 30 ES-SCLC patients, the median PFS and OS were 7.2 months and 17.6 months respectively. The ORR and DCR were 50.0% (15/30) and 86.7% (26/30) respectively. The median PFS was 8.2 months and 5.6 months for patients who received synchronized immunotherapy or chemotherapy. The median OS was 20.1 months and 15.1 months for patients who received synchronized immunotherapy or chemotherapy. The median time to intracranial progression (TTP) was 7.2 months for patients who were without brain metastases before receiving anlotinib. No unexpected AEs were reported. Grade 3-4 adverse events were reported in 10 patients (33.3%). No treatment-related deaths occurred during this study. Our study has indicated the good efficacy and safety about the application of anlotinib in the maintenance therapy in the first-line or second-line treatment of ES-SCLC and it can also achieve good intracranial control.
广泛期小细胞肺癌(ES-SCLC)患者预后较差,且尚无标准的维持治疗方案。安罗替尼作为ES-SCLC的三线或更后线治疗被证明是有效的。
我们回顾性筛选了2018年11月至2022年12月在重庆医科大学附属第二医院开始接受安罗替尼作为一线或二线治疗的ES-SCLC患者。纳入30例接受基于安罗替尼的联合治疗及后续维持治疗的患者。主要研究终点为无进展生存期(PFS),次要研究终点为总生存期(OS)、临床反应和不良事件(AE)。
30例ES-SCLC患者的中位PFS和OS分别为7.2个月和17.6个月。客观缓解率(ORR)和疾病控制率(DCR)分别为50.0%(15/30)和86.7%(26/30)。接受同步免疫治疗或化疗的患者中位PFS分别为8.2个月和5.6个月。接受同步免疫治疗或化疗的患者中位OS分别为20.1个月和15.1个月。接受安罗替尼治疗前无脑转移的患者颅内进展中位时间(TTP)为7.2个月。未报告意外不良事件。10例患者(33.3%)报告了3-4级不良事件。本研究期间未发生与治疗相关的死亡。我们的研究表明,安罗替尼在ES-SCLC一线或二线治疗的维持治疗中的应用具有良好的疗效和安全性,并且还可以实现良好的颅内控制。