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IMpassion132 三期临床试验:阿替利珠单抗联合化疗治疗早期复发转移性三阴性乳腺癌。

IMpassion132 Phase III trial: atezolizumab and chemotherapy in early relapsing metastatic triple-negative breast cancer.

机构信息

IOB Institute of Oncology, Quironsalud Group, Madrid & Barcelona, & Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.

Institut Gustave Roussy, Université Paris Sud, 114, rue Edouard Vaillant, 94800 Villejuif, France.

出版信息

Future Oncol. 2019 Jun;15(17):1951-1961. doi: 10.2217/fon-2019-0059. Epub 2019 Apr 12.

Abstract

The PD-L1 inhibitor atezolizumab received US FDA accelerated approval as treatment for PD-L1-positive metastatic triple-negative breast cancer (TNBC). In IMpassion130, combining atezolizumab with first-line nab-paclitaxel for metastatic TNBC significantly improved progression-free survival and showed a clinically meaningful effect on overall survival in patients with PD-L1-positive tumors. The placebo-controlled randomized Phase III IMpassion132 (NCT03371017) trial is evaluating atezolizumab with first-line chemotherapy (capecitabine [mandatory in platinum-pretreated patients] or gemcitabine/carboplatin) for inoperable locally advanced/metastatic TNBC recurring ≤12 months after completing standard (neo)adjuvant anthracycline and taxane chemotherapy. Stratification factors are: visceral metastases, tumor immune cell PD-L1 status and selected chemotherapy. Patients are randomized to atezolizumab 1200 mg or placebo every 3 weeks with the chosen chemotherapy, continued until progression, unacceptable toxicity or withdrawal. The primary end point is overall survival.

摘要

PD-L1 抑制剂阿替利珠单抗获美国 FDA 加速批准,用于治疗 PD-L1 阳性转移性三阴性乳腺癌(TNBC)。在 IMpassion130 研究中,阿替利珠单抗联合一线 nab-紫杉醇治疗转移性 TNBC 可显著改善无进展生存期,并在 PD-L1 阳性肿瘤患者的总生存期方面显示出具有临床意义的疗效。安慰剂对照、随机 III 期 IMpassion132 (NCT03371017)试验正在评估阿替利珠单抗联合一线化疗(卡培他滨[铂类预处理患者必需]或吉西他滨/卡铂)用于不可切除的局部晚期/转移性 TNBC,这些患者在完成标准(新)辅助蒽环类和紫杉烷化疗后 12 个月内复发。分层因素为:内脏转移、肿瘤免疫细胞 PD-L1 状态和选定的化疗。患者按 1:1 的比例随机分配至阿替利珠单抗 1200mg 或安慰剂,每 3 周一次,联合所选化疗,持续至疾病进展、无法耐受的毒性或退出。主要终点为总生存期。

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