Department of Medical Thoracic Oncology, Zhejiang Cancer Hospital, No. 1 Banshan East Road, Hangzhou, China.
Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Br J Cancer. 2019 Oct;121(8):640-646. doi: 10.1038/s41416-019-0583-6. Epub 2019 Sep 16.
Small-cell lung cancer (SCLC) remains an aggressive cancer with short-term survival due to limited therapeutic options. Apatinib is a small-molecule tyrosine kinase inhibitor that selectively inhibits vascular endothelial growth factor receptor-2. This study aimed to investigate the efficacy and safety of apatinib in patients with extensive-stage (EC) SCLC who had progressed after two or three previous therapies.
Eligible patients were histologically confirmed ES-SCLC after two or three previous treatments, including a platinum-based regimen. Patients received apatinib at an initial dose of 500 mg once daily. The primary endpoint was the objective response rate.
Forty patients were enrolled. At the data cut-off time (November 15, 2018), the median follow-up was 7.4 months; no patients remained on treatment, and five were still in follow-up. An objective response was achieved in 7 of 40 patients (17.5%) in the intention-to-treat population, and 7 of 38 patients (18.4%) in the per-protocol population. The median progression-free survival and overall survival were 3.0 months and 5·8 months, respectively. The most commonly observed grade 3 or greater treatment-related adverse events were hypertension, hand-foot syndrome, increased L-gamma-glutamyltransferase.
Apatinib exhibited efficacy and an acceptable safety profile in previously heavily-treated ES-SCLC patients. Further exploration of apatinib in phase III trials is warranted.
NCT02945852.
由于治疗选择有限,小细胞肺癌(SCLC)仍然是一种具有短期生存的侵袭性癌症。阿帕替尼是一种小分子酪氨酸激酶抑制剂,选择性地抑制血管内皮生长因子受体-2。本研究旨在探讨阿帕替尼在经过两次或三次先前治疗(包括铂类方案)后进展的广泛期(ES)SCLC 患者中的疗效和安全性。
符合条件的患者为经组织学确认的 ES-SCLC,在两次或三次先前治疗(包括铂类方案)后进展。患者接受初始剂量为 500mg 的阿帕替尼,每日一次。主要终点是客观缓解率。
共纳入 40 例患者。在数据截止时间(2018 年 11 月 15 日),中位随访时间为 7.4 个月;没有患者仍在接受治疗,有 5 例仍在随访中。在意向治疗人群中,40 例患者中有 7 例(17.5%)达到客观缓解,在符合方案人群中,38 例患者中有 7 例(18.4%)达到客观缓解。中位无进展生存期和总生存期分别为 3.0 个月和 5.8 个月。最常见的 3 级或更高级别的治疗相关不良事件是高血压、手足综合征、L-γ-谷氨酰转移酶升高。
阿帕替尼在先前接受过大量治疗的 ES-SCLC 患者中显示出疗效和可接受的安全性特征。进一步在 III 期试验中探索阿帕替尼是合理的。
NCT02945852。