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安罗替尼单药治疗难治性转移性结直肠癌的随机、双盲、安慰剂对照 III 期临床试验(ALTER0703)。

Anlotinib Monotherapy for Refractory Metastatic Colorectal Cancer: A Double-Blinded, Placebo-Controlled, Randomized Phase III Trial (ALTER0703).

机构信息

Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.

Department of Medical Oncology, Jiangsu Province Hospital, Nanjing, People's Republic of China.

出版信息

Oncologist. 2021 Oct;26(10):e1693-e1703. doi: 10.1002/onco.13857. Epub 2021 Jun 25.

Abstract

BACKGROUND

Treatment options for refractory metastatic colorectal cancer (mCRC) were limited. Anlotinib is a novel multitarget tyrosine kinase inhibitor. ALTER0703 study was conducted to assess efficacy and safety of anlotinib for patients with refractory mCRC.

MATERIALS AND METHODS

This was a multicenter, double-blinded, placebo-controlled, randomized phase III trial involving 33 hospitals in China. Patients had taken at least two lines of therapies were 2:1 randomized to receive oral anlotinib (12 mg/day; days 1-14; 21 days per cycle) or placebo, plus best supportive care. Randomization was stratified by previous VEGF-targeting treatments and time from diagnosis to metastases. The primary endpoint was overall survival (OS). The secondary endpoints were progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), quality of life (QoL), and safety.

RESULTS

A total of 419 patients (anlotinib: 282; placebo: 137) were treated from December 2014 to August 2016. The median PFS was improved in anlotinib group (4.1 months; 95% confidence interval [CI], 3.4-4.5) over placebo group (1.5 months; 95% CI, 1.4-1.5), with a hazard ratio (HR) of 0.34 (95% CI, 0.27-0.43; p < .0001). However, median OS was similar between two groups (8.6 months; 95% CI, 7.8-9.7 vs. 7.2 months; 95% CI, 6.2-8.8; HR, 1.02; p = .870). Improvements of ORR and DCR were observed in anlotinib over placebo. The most common grade ≥ 3 anlotinib related adverse events were hypertension (20.92%), increased γ-GT (7.09%), and hand-foot skin reaction (6.38%).

CONCLUSION

Anlotinib was tolerated in Chinese patients with refractory mCRC. Although OS did not reach significant difference, anlotinib still provided clinical benefits by substantially prolonged PFS in these patients.

IMPLICATIONS FOR PRACTICE

In this randomized clinical trial that included 419 patients with refractory metastatic colorectal cancer, substantial prolonged in progression-free survival was noted in patients who received anlotinib compared with those given placebo. Improvements on objective response rate and disease control rate was also observed in anlotinib group. However, overall survival was similar between the two groups. In a word, in third-line or above treatment of Chinese patients with refractory metastatic colorectal cancer, anlotinib provided clinical benefit by significantly prolonged progression-free survival.

摘要

背景

难治性转移性结直肠癌(mCRC)的治疗选择有限。安罗替尼是一种新型的多靶点酪氨酸激酶抑制剂。ALTER0703 研究旨在评估安罗替尼治疗难治性 mCRC 患者的疗效和安全性。

材料和方法

这是一项在中国 33 家医院进行的多中心、双盲、安慰剂对照、随机 III 期试验。患者接受了至少两线治疗,按 2:1 随机接受口服安罗替尼(12mg/天;第 1-14 天;每 21 天为一个周期)或安慰剂,联合最佳支持治疗。随机分组按既往 VEGF 靶向治疗和诊断至转移时间进行分层。主要终点是总生存期(OS)。次要终点是无进展生存期(PFS)、客观缓解率(ORR)、疾病控制率(DCR)、生活质量(QoL)和安全性。

结果

共有 419 例患者(安罗替尼:282 例;安慰剂:137 例)于 2014 年 12 月至 2016 年 8 月接受治疗。与安慰剂组(1.5 个月;95%置信区间,1.4-1.5)相比,安罗替尼组的中位 PFS 得到改善(4.1 个月;95%置信区间,3.4-4.5),风险比(HR)为 0.34(95%置信区间,0.27-0.43;p<0.0001)。然而,两组的中位 OS 相似(8.6 个月;95%置信区间,7.8-9.7 vs. 7.2 个月;95%置信区间,6.2-8.8;HR,1.02;p=0.870)。与安慰剂相比,安罗替尼组的 ORR 和 DCR 均有改善。安罗替尼最常见的≥3 级不良反应为高血压(20.92%)、γ-GT 升高(7.09%)和手足皮肤反应(6.38%)。

结论

安罗替尼在难治性 mCRC 中国患者中可耐受。尽管 OS 未达到显著差异,但安罗替尼仍通过显著延长这些患者的无进展生存期为患者带来了临床获益。

启示

在这项包括 419 例难治性转移性结直肠癌患者的随机临床试验中,与安慰剂相比,接受安罗替尼治疗的患者无进展生存期显著延长。在安罗替尼组中,客观缓解率和疾病控制率也有所提高。然而,两组的总生存期相似。总之,在中国难治性转移性结直肠癌患者的三线或以上治疗中,安罗替尼通过显著延长无进展生存期为患者带来了临床获益。

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