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阿帕替尼治疗二线或三线化疗后广泛期小细胞肺癌患者的疗效:一项 II 期、单臂、多中心、前瞻性研究。

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.

机构信息

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.

出版信息

Br J Cancer. 2019 Oct;121(8):640-646. doi: 10.1038/s41416-019-0583-6. Epub 2019 Sep 16.

Abstract

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.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

试验注册

NCT02945852。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/794b/6889407/f72b3c7850c5/41416_2019_583_Fig1_HTML.jpg

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