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帕妥珠单抗治疗人表皮生长因子受体 2 阳性晚期乳腺癌的随机、开放标签 III 期研究(PRECIOUS)。

Pertuzumab retreatment for HER2-positive advanced breast cancer: A randomized, open-label phase III study (PRECIOUS).

机构信息

Department of Breast and Endocrine Surgery, Kumamoto University Hospital, Kumamoto, Japan.

Department of Breast Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.

出版信息

Cancer Sci. 2022 Sep;113(9):3169-3179. doi: 10.1111/cas.15474. Epub 2022 Jul 23.

DOI:10.1111/cas.15474
PMID:35754298
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9459345/
Abstract

No standard options existed for human epidermal growth factor receptor 2 (HER2)-positive advanced breast cancer that progresses after second-line trastuzumab emtansine therapy before 2020. The purpose of this study was to examine the efficacy of pertuzumab retreatment after disease progression following pertuzumab-containing therapy for HER2-positive locally advanced or metastatic breast cancer for the first time. This randomized, open-label, multicenter phase III trial was undertaken in 93 sites in Japan. Eligible patients with HER2-positive breast cancer who had received pertuzumab, trastuzumab, and chemotherapy as first- and/or second-line therapy were randomly assigned (1:1) to: (i) pertuzumab, trastuzumab, and physician's choice chemotherapy (PTC), or (ii) trastuzumab and physician's choice chemotherapy (TC). The primary end-point was investigator-assessed progression-free survival (PFS). Between August 1, 2015 and December 31, 2018, 219 patients were randomized to PTC (n = 110) or TC (n = 109). Median follow-up was 14.2 months (interquartile range, 9.0-22.2), and median PFS was 5.3 months (95% confidence interval [CI], 4.0-6.6) with PTC and 4.2 months (95% CI, 3.2-4.8) with TC (stratified hazard ratio 0.76 [95% CI upper limit 0.967]; p = 0.022). Progression-free survival was improved by adding pertuzumab in all prespecified subgroups. The PTC arm showed a trend towards better overall survival and duration of response, but similar objective response and health-related quality of life. The incidence of treatment-related adverse events was similar between groups except for diarrhea. Pertuzumab retreatment contributes to disease control for HER2-positive locally advanced or metastatic breast cancer previously treated with pertuzumab-containing regimens.

摘要

在 2020 年之前,对于曲妥珠单抗-恩美曲妥珠单抗治疗二线进展后的人表皮生长因子受体 2(HER2)阳性晚期乳腺癌,尚无标准治疗选择。本研究的目的是首次评估曲妥珠单抗治疗后进展的 HER2 阳性局部晚期或转移性乳腺癌患者再次使用帕妥珠单抗治疗的疗效。这是一项在日本 93 个地点开展的、随机、开放标签、多中心 III 期临床试验。纳入标准为:接受过曲妥珠单抗、帕妥珠单抗和化疗作为一线和/或二线治疗的 HER2 阳性乳腺癌患者,随机(1:1)分配至:(i)帕妥珠单抗、曲妥珠单抗和医生选择的化疗(PTC)组,或(ii)曲妥珠单抗和医生选择的化疗(TC)组。主要终点为研究者评估的无进展生存期(PFS)。2015 年 8 月 1 日至 2018 年 12 月 31 日,219 例患者被随机分配至 PTC 组(n=110)或 TC 组(n=109)。中位随访时间为 14.2 个月(四分位距,9.0-22.2),PTC 组和 TC 组的中位 PFS 分别为 5.3 个月(95%置信区间 [CI],4.0-6.6)和 4.2 个月(95% CI,3.2-4.8)(分层风险比 0.76 [95% CI 上限 0.967];p=0.022)。在所有预设亚组中,添加帕妥珠单抗均改善了无进展生存期。PTC 组的总生存期和缓解持续时间有改善趋势,但客观缓解率和健康相关生活质量相似。两组间治疗相关不良事件发生率除腹泻外相似。对于先前接受过曲妥珠单抗为基础治疗方案的 HER2 阳性局部晚期或转移性乳腺癌,再次使用帕妥珠单抗治疗有助于控制疾病。

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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6cc/9459345/eaf41a8d3242/CAS-113-3169-g003.jpg
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