首页> 外文期刊>The lancet oncology >Neoadjuvant bevacizumab, trastuzumab, and chemotherapy for primary inflammatory HER2-positive breast cancer (BEVERLY-2): An open-label, single-arm phase 2 study
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Neoadjuvant bevacizumab, trastuzumab, and chemotherapy for primary inflammatory HER2-positive breast cancer (BEVERLY-2): An open-label, single-arm phase 2 study

机译:新辅助贝伐单抗,曲妥珠单抗和化学疗法治疗原发性HER2阳性炎性乳腺癌(BEVERLY-2):一项开放性单臂2期研究

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Background: Bevacizumab and trastuzumab are efficacious for treatment of advanced or HER2-positive metastatic breast cancer; however, few data exist for this regimen in inflammatory breast cancer. In our phase 2 trial, we aimed to assess efficacy and safety of neoadjuvant bevacizumab combined with trastuzumab and chemotherapy in patients with primary HER2-positive inflammatory breast cancer. Methods: In our phase 2, multicentre, open-label, single-arm, non-comparative trial, we enrolled women (aged ≥18 years) with histologically confirmed HER2-positive non-metastatic inflammatory breast cancer at private or public oncology centres in France. Before surgery, patients were treated with fluorouracil, epirubicin, cyclophosphamide, and bevacizumab (cycles 1-4) and docetaxel, bevacizumab, and trastuzumab (cycles 5-8) in 3-week cycles. After surgery, patients received adjuvant radiotherapy, trastuzumab, and bevacizumab. For the primary endpoint, we assessed the proportion of patients who achieved a pathological complete response (defined by central review of surgical specimens according to Sataloff classification, counting missing data as failure) and adverse events in all enrolled patients. This study is registered with . ClinicalTrials.gov, number . NCT00717405. Findings: Between Oct 23, 2008, and Oct 28, 2009, we enrolled 52 patients at 21 centres. 42 (81%) of 52 patients received all eight cycles of neoadjuvant therapy and 49 (94%) underwent surgery. After neoadjuvant therapy, 33 of 52 patients had a pathological complete response according to central review (63·5%, 95% CI 49·4-77·5). The most common adverse events were asthenia and nausea (both occurred in 36 [69%] of 52 patients). 25 (48%) patients had grade 3-4 neutropenia, which was the most common grade 3-4 adverse event. Only one grade 3 or worse adverse event regarded as related to bevacizumab was reported (hypertension, one patient). Four patients (8%) had cardiac failure. Interpretation: Neoadjuvant treatment with bevacizumab, trastuzumab, and chemotherapy was efficacious and well tolerated in patients with previously untreated primary inflammatory breast cancer. Further confirmation of use of bevacizumab in inflammatory breast cancer is needed. Funding: Roche (France).
机译:背景:贝伐单抗和曲妥珠单抗对晚期或HER2阳性转移性乳腺癌有效。然而,在炎症性乳腺癌中,该方案的数据很少。在我们的2期试验中,我们旨在评估新辅助贝伐单抗联合曲妥珠单抗和化疗对原发性HER2阳性炎性乳腺癌患者的疗效和安全性。方法:在我们的第二阶段,多中心,开放标签,单组,非对照试验中,我们在美国私人或公共肿瘤学中心招募了经组织学证实为HER2阳性的非转移性炎性乳腺癌的女性(≥18岁)。法国。手术前,患者在3周的周期内接受了氟尿嘧啶,表柔比星,环磷酰胺和贝伐单抗(1-4周期)和多西他赛,贝伐单抗和曲妥珠单抗(5-8周期)的治疗。手术后,患者接受了辅助放疗,曲妥珠单抗和贝伐单抗。对于主要终点,我们评估了所有入组患者中达到病理完全缓解(通过根据Sataloff分类对手术标本进行集中检查,将缺失数据计数为失败)和不良事件的患者比例。该研究已在进行注册。 ClinicalTrials.gov,编号。 NCT00717405。结果:在2008年10月23日至2009年10月28日之间,我们在21个中心招募了52位患者。 52例患者中有42例(81%)接受了所有八个周期的新辅助治疗,其中49例(94%)接受了手术。新辅助治疗后,根据中央评价,52例患者中有33例具有病理完全缓解(63·5%,95%CI 49·4-77·5)。最常见的不良事件是乏力和恶心(52位患者中有36位[69%]都发生了)。 25(48%)患者患有3-4级中性粒细胞减少,这是最常见的3-4级不良事件。仅报道了一种与贝伐单抗有关的3级或更严重的不良事件(高血压,一名患者)。四名患者(8%)患有心力衰竭。解释:贝伐单抗,曲妥珠单抗和化学疗法的新辅助治疗在先前未治疗的原发性炎性乳腺癌患者中有效且耐受性良好。需要进一步确认贝伐单抗在炎性乳腺癌中的应用。资金来源:罗氏(法国)。

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