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甲磺酸艾日布林治疗既往接受蒽环类、紫杉类和卡培他滨治疗的局部晚期或转移性乳腺癌的Ⅱ期临床研究。

Phase II study of the halichondrin B analog eribulin mesylate in patients with locally advanced or metastatic breast cancer previously treated with an anthracycline, a taxane, and capecitabine.

机构信息

Vall d'Hebron University Hospital, Barcelona, Spain.

出版信息

J Clin Oncol. 2010 Sep 1;28(25):3922-8. doi: 10.1200/JCO.2009.25.8467. Epub 2010 Aug 2.

Abstract

PURPOSE

The activity and safety of eribulin mesylate (E7389), a nontaxane microtubule dynamics inhibitor with a novel mechanism of action, were evaluated in patients with locally advanced or metastatic breast cancer previously treated with an anthracycline, taxane, and capecitabine.

PATIENTS AND METHODS

Eligible patients in this single-arm, open-label phase II study received eribulin mesylate (1.4 mg/m(2)) administered as a 2- to 5-minute intravenous infusion on days 1 and 8 of a 21-day cycle. The primary end point was objective response rate (ORR) assessed by independent review.

RESULTS

Of 299 enrolled patients who had received a median of four prior chemotherapy regimens, 291 received eribulin (for a median of four cycles). Of these, 269 patients met key inclusion criteria for the primary efficacy analysis. The primary end point of ORR by independent review was 9.3% (95% CI, 6.1% to 13.4%; all partial responses [PRs]), the stable disease (SD) rate was 46.5%, and clinical benefit rate (complete response + PR + SD > or = 6 months) was 17.1%. The investigator-reported ORR was 14.1% (95% CI, 10.2% to 18.9%). Median duration of response was 4.1 months, and progression-free survival was 2.6 months. Median overall survival was 10.4 months. The most common treatment-related grade 3 or 4 toxicities were neutropenia (54%; febrile neutropenia, 5.5%), leukopenia (14%), and asthenia/fatigue (10%; no grade 4); grade 3 neuropathy occurred in 6.9% of patients (no grade 4).

CONCLUSION

Eribulin demonstrated antitumor activity in extensively pretreated patients who had previously received an anthracycline, taxane, and capecitabine, with a manageable tolerability profile.

摘要

目的

甲磺酸艾瑞布林(E7389)是一种非紫杉烷微管动力学抑制剂,作用机制新颖。本研究评估了其在既往接受过蒽环类、紫杉烷类和卡培他滨化疗的局部晚期或转移性乳腺癌患者中的活性和安全性。

方法

这项单臂、开放标签的 II 期研究中,符合条件的患者接受甲磺酸艾瑞布林(1.4mg/m2)治疗,每 21 天周期的第 1 天和第 8 天静脉输注 2 至 5 分钟。主要终点是独立评估的客观缓解率(ORR)。

结果

299 例入组患者既往中位接受过 4 种化疗方案,其中 291 例接受了甲磺酸艾瑞布林治疗(中位 4 个周期)。其中,269 例患者符合主要疗效分析的关键纳入标准。独立评估的主要终点是客观缓解率为 9.3%(95%CI,6.1%至 13.4%;所有部分缓解[PR]),疾病稳定(SD)率为 46.5%,临床获益率(完全缓解+PR+SD≥6 个月)为 17.1%。研究者报告的客观缓解率为 14.1%(95%CI,10.2%至 18.9%)。中位缓解持续时间为 4.1 个月,无进展生存期为 2.6 个月,总生存期为 10.4 个月。最常见的治疗相关 3 级或 4 级毒性为中性粒细胞减少症(54%;发热性中性粒细胞减少症,5.5%)、白细胞减少症(14%)和乏力/疲劳(10%;无 4 级);3 级神经病变发生率为 6.9%(无 4 级)。

结论

甲磺酸艾瑞布林在既往接受过蒽环类、紫杉烷类和卡培他滨化疗的广泛预处理患者中显示出抗肿瘤活性,且耐受性良好。

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