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每日口服长春瑞滨节拍化疗作为内分泌耐药的 HR+/HER2-晚期/转移性乳腺癌一线治疗的 II 期研究:VinoMetro-AGO-B-046。

Phase II study of metronomic treatment with daily oral vinorelbine as first-line chemotherapy in patients with advanced/metastatic HR+/HER2- breast cancer resistant to endocrine therapy: VinoMetro-AGO-B-046.

机构信息

Department of Gynaecology and Obstetrics, University Medical Centre, Mainz, Germany.

Haematology and Oncology Outpatient Clinic, Ravensburg, Germany.

出版信息

J Cancer Res Clin Oncol. 2021 Nov;147(11):3391-3400. doi: 10.1007/s00432-021-03599-2. Epub 2021 Mar 20.

Abstract

PURPOSE

Metronomic chemotherapy (MCT) is an increasingly used treatment option in hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2-) advanced/metastatic breast cancer (MBC) after failure of endocrine-based therapies.

METHODS

VinoMetro was a multicentre, open-label, single-arm, phase II study of metronomic oral vinorelbine (VRL; 30 mg/day) as a first-line chemotherapy (CT) in patients with HR+/HER2- MBC after endocrine failure. The primary endpoint was the clinical benefit rate (CBR) at 24 weeks.

RESULTS

Between January 2017 and April 2019, nine patients were enrolled. The CBR was 22.2% (90% confidence interval [CI] 4.1-55.0), p = 0.211. The median progression-free survival (PFS) was 12.0 weeks (95% CI 11.3-12.7). Grade 3-4 adverse events (AEs) occurred in 22.2% of patients. One patient died of febrile neutropenia.

CONCLUSION

VinoMetro (AGO-B-046) was closed early after nine patients and occurrence of one grade 5 toxicity in agreement with the lead institutional review board (IRB). Metronomic dosing of oral VRL in HR+/HER2- MBC as first-line CT after failure of endocrine therapies showed only limited benefit in this population.

TRIAL REGISTRATION NUMBER AND DATE OF REGISTRATION

ClinicalTrials.gov Identifier: NCT03007992; December 15, 2016.

摘要

目的

节拍化疗(MCT)是一种越来越多被应用于激素受体阳性(HR+)/人表皮生长因子受体 2 阴性(HER2-)晚期/转移性乳腺癌(MBC)的治疗选择,用于内分泌治疗失败后的患者。

方法

VinoMetro 是一项多中心、开放标签、单臂、Ⅱ期研究,评估了米托蒽醌节拍口服(VRL;30mg/天)作为 HR+/HER2-MBC 患者内分泌治疗失败后的一线化疗(CT)。主要终点是 24 周的临床获益率(CBR)。

结果

2017 年 1 月至 2019 年 4 月期间,共纳入 9 例患者。CBR 为 22.2%(90%置信区间[CI]:4.1-55.0),p=0.211。中位无进展生存期(PFS)为 12.0 周(95%CI:11.3-12.7)。3-4 级不良事件(AE)发生率为 22.2%。1 例患者死于发热性中性粒细胞减少症。

结论

VinoMetro(AGO-B-046)在纳入 9 例患者后提前关闭,1 例患者发生 5 级毒性,与主要机构审查委员会(IRB)一致。HR+/HER2-MBC 患者在失败的内分泌治疗后,作为一线 CT 接受米托蒽醌节拍口服治疗,仅在该人群中显示出有限的获益。

临床试验注册号和注册日期

ClinicalTrials.gov 标识符:NCT03007992;2016 年 12 月 15 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27dc/11801923/3e33373d402b/432_2021_3599_Fig1_HTML.jpg

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