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曲妥珠单抗新辅助化疗联合辅助曲妥珠单抗与单纯新辅助化疗治疗人表皮生长因子受体 2 阳性局部晚期乳腺癌患者(NOAH 试验):一项具有平行人表皮生长因子受体 2 阴性队列的随机对照优效性试验。

Neoadjuvant chemotherapy with trastuzumab followed by adjuvant trastuzumab versus neoadjuvant chemotherapy alone, in patients with HER2-positive locally advanced breast cancer (the NOAH trial): a randomised controlled superiority trial with a parallel HER2-negative cohort.

机构信息

Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.

出版信息

Lancet. 2010 Jan 30;375(9712):377-84. doi: 10.1016/S0140-6736(09)61964-4.

Abstract

BACKGROUND

The monoclonal antibody trastuzumab has survival benefit when given with chemotherapy to patients with early, operable, and metastatic breast cancer that has HER2 (also known as ERBB2) overexpression or amplification. We aimed to assess event-free survival in patients with HER2-positive locally advanced or inflammatory breast cancer receiving neoadjuvant chemotherapy with or without 1 year of trastuzumab.

METHODS

We compared 1 year of treatment with trastuzumab (given as neoadjuvant and adjuvant treatment; n=117) with no trastuzumab (118), in women with HER2-positive locally advanced or inflammatory breast cancer treated with a neoadjuvant chemotherapy regimen consisting of doxorubicin, paclitaxel, cyclophosphamide, methotrexate, and fluorouracil. Randomisation was done with a computer program and minimisation technique, taking account of geographical area, disease stage, and hormone receptor status. Investigators were informed of treatment allocation. A parallel cohort of 99 patients with HER2-negative disease was included and treated with the same chemotherapy regimen. Primary endpoint was event-free survival. Analysis was by intention to treat. This study is registered, number ISRCTN86043495.

FINDINGS

Trastuzumab significantly improved event-free survival in patients with HER2-positive breast cancer (3-year event-free survival, 71% [95% CI 61-78; n=36 events] with trastuzumab, vs 56% [46-65; n=51 events] without; hazard ratio 0.59 [95% CI 0.38-0.90]; p=0.013). Trastuzumab was well tolerated and, despite concurrent administration with doxorubicin, only two patients (2%) developed symptomatic cardiac failure. Both responded to cardiac drugs.

INTERPRETATION

The addition of neoadjuvant and adjuvant trastuzumab to neoadjuvant chemotherapy should be considered for women with HER2-positive locally advanced or inflammatory breast cancer to improve event-free survival, survival, and clinical and pathological tumour responses.

FUNDING

F Hoffmann-La Roche.

摘要

背景

曲妥珠单抗是一种单克隆抗体,当与化疗联合用于治疗早期可手术和转移性乳腺癌时,具有生存获益,这些乳腺癌存在人表皮生长因子受体 2(HER2)过表达或扩增。我们旨在评估曲妥珠单抗辅助治疗与无曲妥珠单抗辅助治疗对接受新辅助化疗的 HER2 阳性局部晚期或炎性乳腺癌患者的无事件生存情况。

方法

我们比较了曲妥珠单抗(新辅助和辅助治疗)治疗组(n=117)与无曲妥珠单抗治疗组(n=118)的 1 年治疗情况,入组患者为接受多柔比星、紫杉醇、环磷酰胺、甲氨蝶呤和氟尿嘧啶新辅助化疗方案治疗的 HER2 阳性局部晚期或炎性乳腺癌患者。通过计算机程序和最小化技术进行随机分组,考虑了地理区域、疾病分期和激素受体状态。研究者了解治疗分组情况。纳入了 99 例 HER2 阴性疾病的平行队列患者,他们接受了相同的化疗方案治疗。主要终点为无事件生存。分析为意向治疗。本研究注册于 ISRCTN86043495。

发现

曲妥珠单抗显著改善了 HER2 阳性乳腺癌患者的无事件生存(3 年无事件生存率,曲妥珠单抗组为 71%[95%CI 61-78;n=36 例事件],无曲妥珠单抗组为 56%[46-65;n=51 例事件];风险比 0.59[95%CI 0.38-0.90];p=0.013)。曲妥珠单抗耐受性良好,尽管与多柔比星同时给药,仅有 2 例(2%)患者发生症状性心力衰竭。两者均对心脏药物有反应。

结论

对于 HER2 阳性局部晚期或炎性乳腺癌患者,新辅助化疗联合曲妥珠单抗的辅助治疗应考虑用于改善无事件生存、生存以及临床和病理肿瘤反应。

资助

罗氏制药。

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