| Literature DB >> 27497829 |
Kadoaki Ohashi1, Katsuyuki Hotta2, Taizo Hirata2, Keisuke Aoe3, Toshiyuki Kozuki4, Kiichiro Ninomiya5, Hiroe Kayatani5, Hiroyuki Yanai6, Shinichi Toyooka7, Shiro Hinotsu2, Minoru Takata8, Katsuyuki Kiura9.
Abstract
The treatment outcome has been unsatisfactory for patients with non-small-cell lung cancer (NSCLC) refractory to standard first-line chemotherapy. Trastuzumab emtansine (T-DM1), an anti-HER2 antibody conjugated with a vinca alkaloid, has been approved for clinical use in HER2+ breast cancer in many countries. Approximately 5% of NSCLC tumors possess HER2 alterations, and T-DM1 has shown excellent antitumor effects against HER2+ lung cancer cell lines in preclinical models. Therefore, we hypothesized that T-DM1 could significantly inhibit the growth of HER2+ lung cancers. We have launched a nonrandomized phase II trial of T-DM1 monotherapy for patients with HER2+ lung cancers. The major eligibility criteria are as follows: age ≥ 20 years, pathologically diagnosed NSCLC with documented HER2 positivity (immunohistochemistry 3+, both immunohistochemistry 2+ and fluorescence in situ hybridization positive, or exon 20 insertion mutation), and previous chemotherapy. Thirty patients will receive T-DM1 3.6 mg/kg every 3 weeks. The primary endpoint is the overall response rate. This trial will provide information on whether T-DM1 monotherapy is effective against HER2+ lung cancer.Entities:
Keywords: HER2 amplification; HER2 mutations; HER2 over-expression; NSCLC; Trastuzumab emtansine
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Year: 2016 PMID: 27497829 DOI: 10.1016/j.cllc.2016.06.014
Source DB: PubMed Journal: Clin Lung Cancer ISSN: 1525-7304 Impact factor: 4.785