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Apatinib in patients with extensive-stage small-cell lung cancer after second-line or third-line chemotherapy: a phase II, single-arm, multicentre, prospective study

机译:Apatinib患者在二线或第三线化疗后广泛的小细胞肺癌:II期,单臂,多环境,前瞻性研究

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Background 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. Methods 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. Results 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. Conclusions 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. Trial registration NCT02945852.
机译:背景技术小细胞肺癌(SCLC)仍然是由于有限的治疗选择而存在短期存活的侵略性癌症。 Apatinib是一种小分子酪氨酸激酶抑制剂,其选择性地抑制血管内皮生长因子受体-2。本研究旨在探讨Apatinib在两次以前疗法后进展的广泛阶段(EC)SCLC患者的疗效和安全性。方法后,符合条件的患者在两次或三次以前治疗后是组织学证实的ES-SCLC,包括基于铂类的方案。患者每天一次以500μmg的初始剂量接受磷钛。主要终点是客观响应率。结果450名患者注册。在数据截止时间(2018年11月15日),中位后续时间为7.4个月;没有患者治疗,五个仍在随访中。在40名患者(17.5%)中,在意向治疗人群中的7名患者和38名患者中的7名(18.4%),达到客观反应。中位进展的生存和整体生存率分别为3.0个月和5·8个月。最常见的3级或更高的治疗相关的不良事件是高血压,手足综合征,增加的L-Gamma-谷氨酰胺转移酶。结论Apatinib在预先治疗的ES-SCLC患者中表现出疗效和可接受的安全性曲线。有必要进一步探索Apatinib阶段试验。试验登记NCT02945852。

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