首页> 外文期刊>Clinical breast cancer >A Phase II Randomized Study of Lapatinib Combined With Capecitabine, Vinorelbine, or Gemcitabine in Patients With HER2-Positive Metastatic Breast Cancer With Progression After a Taxane (Latin American Cooperative Oncology Group 0801 Study)
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A Phase II Randomized Study of Lapatinib Combined With Capecitabine, Vinorelbine, or Gemcitabine in Patients With HER2-Positive Metastatic Breast Cancer With Progression After a Taxane (Latin American Cooperative Oncology Group 0801 Study)

机译:拉帕替尼联合卡培他滨,长春瑞滨或吉西他滨治疗紫杉烷后HER2阳性转移性乳腺癌患者的II期随机研究(拉丁美洲合作肿瘤学组0801研究)

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In LACOG 0801 phase II study 142 patients with HER2+ MBC with progression after taxane were randomized between Lapatinib (L) combined with Capecitabine (C), Vinorelbine (V) or Gemcitabine (G). ORR was 49% in LC, 56% in LV and 41% in LG group. The overall toxicity was manageable in all regimens. Background: Novel targeted agents and combinations have become available in multiple lines of treatment for human epidermal growth factor receptor 2-positive (HER2+) metastatic breast cancer (MBC). In this context, alternatives to the lapatinib (L) and capecitabine (C) regimen, evaluating L combined with other cytotoxic drugs, are warranted. Patients and Methods: In the present phase II, multicenter study, patients with HER2+ MBC with progression after taxane were randomized between L, 1250 mg, combined with C, 2000 mg/m(2) on days 1 to 14 (LC), vinorelbine (V), 25 mg/m(2) on days 1 and 8 (LV), or gemcitabine (G), 1000 mg/m(2) on days 1 and 8 (LG), every 21 days. The primary endpoint was the overall response rate. Results: A total of 142 patients were included from 2009 to 2012. No differences were found in the patient baseline characteristics. The median age was 51 years, 69% were postmenopausal, 32% had liver metastasis, 57% were hormone receptor negative, and 48% had been previously treated with trastuzumab. The overall response rate was 49% (95% confidence interval [CI], 34.8%-63.4%), 56% (95% CI, 40%-70.4%), and 41% (95% CI, 27%-56.8%) in the LC, LV, and LG groups, respectively. The median progression-free survival was 9 months in the LC arm and 7 months in the other 2 arms (P = .28). The most common grade 3 and 4 adverse events were hand-foot syndrome (18%), diarrhea (6%), and increased alanine anninotransferase/aspartate aminotransferase (4%) in the LC arm; neutropenia (36%), diarrhea (9%), and febrile neutropenia (6%) in the LV arm; and neutropenia (47%), alanine aminotransferase/aspartate aminotransferase (13%), and rash (4%) in the LG arm. Conclusion: LV and LG seem to be active combinations in patients with HER2+ MBC after taxane failure. The overall toxicity was manageable in all regimens. (C) 2016 The Authors. Published by Elsevier Inc.
机译:在LACOG 0801 II期研究中,将142例紫杉烷后进展的HER2 + MBC患者随机分为拉帕替尼(L)联合卡培他滨(C),长春瑞滨(V)或吉西他滨(G)。 LC组的ORR为49%,LV组为56%,LG组为41%。在所有方案中,总毒性都是可以控制的。背景:新型靶向药物及其组合已在多种治疗人类表皮生长因子受体2阳性(HER2 +)转移性乳腺癌(MBC)的治疗中获得。在这种情况下,有必要选择拉帕替尼(L)和卡培他滨(C)方案,与其他细胞毒性药物联合评估L。患者和方法:在当前的II期多中心研究中,在紫杉烷后进展的HER2 + MBC患者中,在第1天至第14天(LC)将长春瑞滨随机分为L组1250 mg,C组2000 mg / m(2) (V),第1天和第8天(LV)为25 mg / m(2),或吉西他滨(G),第21天和第1和8天(LG)为1000 mg / m(2)。主要终点是总体缓解率。结果:2009年至2012年共纳入142例患者。患者基线特征无差异。中位年龄为51岁,绝经后为69%,肝转移为32%,激素受体阴性为57%,曲妥珠单抗以前曾治疗过48%。总体回应率为49%(95%置信区间[CI],34.8%-63.4%),56%(95%CI,40%-70.4%)和41%(95%CI,27%-56.8%) )分别位于LC,LV和LG组中。 LC组的中位无进展生存期为9个月,其他2组为7个月(P = 0.28)。最常见的3级和4级不良反应是手足综合征(18%),腹泻(6%)和LC臂中丙氨酸氨基转移酶/天冬氨酸转氨酶升高(4%); LV组中性粒细胞减少症(36%),腹泻(9%)和发热性中性粒细胞减少症(6%); LG臂中的中性粒细胞减少症(47%),丙氨酸氨基转移酶/天冬氨酸氨基转移酶(13%)和皮疹(4%)。结论:紫杉烷失败后,HER2 + MBC患者中的LV和LG似乎是有效的组合。在所有方案中,总毒性都是可以控制的。 (C)2016作者。由Elsevier Inc.发布

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