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一项 Mirvetuximab Soravtansine 在三阴性乳腺癌中的 II 期研究。

A phase II study of Mirvetuximab Soravtansine in triple-negative breast cancer.

机构信息

Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Dan L. Duncan Building CPB5.3542, 1515 Holcombe Blvd. Unit 1354, Houston, TX, 77030, USA.

Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

出版信息

Invest New Drugs. 2021 Apr;39(2):509-515. doi: 10.1007/s10637-020-00995-2. Epub 2020 Sep 28.

Abstract

Folate receptor alpha (FRα) has been reported to be expressed in up to 80% of triple-negative breast cancers (TNBC) with limited expression in normal tissues, making it a promising therapeutic target. Mirvetuximab soravtansine (mirvetuximab-s) is an antibody drug conjugate which has shown promise in the treatment of FRα-positive solid tumors in early phase clinical trials. Herein, are the results of the first prospective phase II trial evaluating mirvetuximab-s in metastatic TNBC. Patients with advanced, FRα-positive TNBC were enrolled on this study. Mirvetuximab-s was administered at a dose of 6.0 mg/kg every 3 weeks. 96 patients with advanced TNBC consented for screening. FRα staining was performed on tumor tissue obtained from 80 patients. The rate of FRα positivity by immunohistochemistry was 10.0% (8/80). Two patients were treated on study, with best overall responses of stable disease in one and progressive disease in the other. Adverse events were consistent with earlier studies. The study was terminated early due to the low rate of FRα positivity in the screened patient population and lack of disease response in the two patients treated. The observed rate of FRα positivity was considerably lower than previously reported and none of the patients had a partial or complete response. Treatment with mirvetuximab-s should only be further explored in TNBC if an alternate biomarker strategy is developed for patient selection on the basis of additional preclinical data.

摘要

叶酸受体 alpha(FRα)已被报道在高达 80%的三阴性乳腺癌(TNBC)中表达,而在正常组织中表达有限,使其成为有前途的治疗靶点。Mirvetuximab soravtansine(mirvetuximab-s)是一种抗体药物偶联物,在早期临床试验中已显示出对 FRα 阳性实体瘤的治疗潜力。本文介绍了首个评估 mirvetuximab-s 在转移性 TNBC 中的前瞻性 II 期临床试验结果。该研究纳入了晚期 FRα 阳性 TNBC 患者。mirvetuximab-s 以 6.0mg/kg 的剂量每 3 周给药一次。共有 96 名晚期 TNBC 患者同意接受筛选。对 80 名患者的肿瘤组织进行了 FRα 染色。免疫组织化学检测 FRα 阳性率为 10.0%(8/80)。两名患者接受了研究治疗,其中一名患者的最佳总体反应为疾病稳定,另一名患者的最佳总体反应为疾病进展。不良事件与早期研究一致。由于筛选患者人群中 FRα 阳性率较低且两名接受治疗的患者均无疾病反应,该研究提前终止。观察到的 FRα 阳性率明显低于先前报道,且没有患者出现部分或完全缓解。如果在基于额外的临床前数据的基础上开发出替代生物标志物策略来选择患者,那么只有在这种情况下才能进一步探索 TNBC 中使用 mirvetuximab-s 的治疗方法。

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