Shak S
Department of BioOncology, Medical Affairs, Genentech, Inc., South San Francisco, CA 94080-4990, USA.
Semin Oncol. 1999 Aug;26(4 Suppl 12):71-7.
The recombinant humanized anti-HER2 monoclonal antibody trastuzumab (Herceptin; Genentech, San Francisco, CA) was evaluated in human clinical trials for treatment of women with metastatic breast cancer who have tumors that overexpress HER2. The trastuzumab clinical program consisted of a series of phase I, phase II, and phase III clinical trials. Clinical experience with this novel biologic has been obtained in more than 1,000 women with HER2-overexpressing metastatic breast cancer. Two pivotal trials were performed to evaluate trastuzumab efficacy and safety: (1) trastuzumab in combination with chemotherapy as first-line therapy and (2) trastuzumab as a single agent in second- and third-line chemotherapy. Preliminary results of the pivotal clinical trials that have been presented at national meetings are summarized below. The data suggest that trastuzumab will be an important new treatment option for women with HER2-overexpressing metastatic breast cancer.
重组人源化抗HER2单克隆抗体曲妥珠单抗(赫赛汀;基因泰克公司,加利福尼亚州旧金山)在针对患有HER2过表达肿瘤的转移性乳腺癌女性患者的人体临床试验中进行了评估。曲妥珠单抗临床项目包括一系列I期、II期和III期临床试验。超过1000名HER2过表达转移性乳腺癌女性患者积累了使用这种新型生物制剂的临床经验。进行了两项关键试验以评估曲妥珠单抗的疗效和安全性:(1)曲妥珠单抗联合化疗作为一线治疗;(2)曲妥珠单抗单药用于二线和三线化疗。在全国会议上公布的关键临床试验初步结果总结如下。数据表明,曲妥珠单抗将成为HER2过表达转移性乳腺癌女性患者的一种重要新治疗选择。