首页> 外文期刊>The Lancet >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.
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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.

机译:对于HER2阳性的局部晚期乳腺癌患者,使用曲妥珠单抗的新辅助化疗联合曲妥珠单抗辅助与单独的新辅助化疗相比(NOAH试验):一项平行HER2阴性队列的随机对照优势试验。

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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.
机译:背景:单克隆抗体曲妥珠单抗对患有HER2(也称为ERBB2)过表达或扩增的早期,可手术和转移性乳腺癌的患者进行化疗时具有生存获益。我们的目的是评估接受或不接受曲妥珠单抗1年的新辅助化疗的HER2阳性局部晚期或炎症性乳腺癌患者的无事件生存率。方法:我们比较了接受曲妥珠单抗治疗1年(作为新辅助和辅助治疗; n = 117)和不接受曲妥珠单抗治疗[118]的女性在HER2阳性局部晚期或炎症性乳腺癌中接受了由阿霉素组成的新辅助化疗方案的妇女,紫杉醇,环磷酰胺,氨甲蝶呤和氟尿嘧啶。考虑到地理区域,疾病阶段和激素受体状态,使用计算机程序和最小化技术进行了随机分组。研究者被告知治疗分配。纳入了99例HER2阴性患者的平行队列,并采用相同的化疗方案进行治疗。主要终点是无事件生存。分析是按意向进行的。该研究已注册,编号ISRCTN86043495。结果:曲妥珠单抗显着改善了HER2阳性乳腺癌患者的无事件生存率(曲妥珠单抗3年无事件生存率,71%[95%CI 61-78; n = 36事件],而56%[46- 65; n = 51事件]无;危险比0.59 [95%CI 0.38-0.90]; p = 0.013)。曲妥珠单抗耐受性良好,尽管与阿霉素同时给药,但只有两名患者(2%)出现症状性心力衰竭。两者都对心脏药物有反应。 HER2阳性的局部晚期或炎症性乳腺癌女性应考虑在新辅助化疗中加入新辅助和曲妥珠单抗辅助治疗,以提高无事件生存率,生存率以及临床和病理性肿瘤反应。资金来源:霍夫曼·拉罗什(F Hoffmann-La Roche)。

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