| Literature DB >> 29313813 |
Katsuyuki Hotta1, Keisuke Aoe2, Toshiyuki Kozuki3, Kadoaki Ohashi4, Kiichiro Ninomiya4, Eiki Ichihara4, Toshio Kubo4, Takashi Ninomiya4, Kenichi Chikamori2, Daijiro Harada3, Naoyuki Nogami3, Taizo Hirata4, Shiro Hinotsu5, Shinichi Toyooka6, Katsuyuki Kiura4.
Abstract
Trastuzumab emtansine (T-DM1), an anti-erb-b2 receptor tyrosine kinase 2 (HER2) antibody-drug conjugate, has been shown to significantly improve survival in HER2-positive breast cancer. We report a phase II trial of T-DM1 monotherapy in relapsed NSCLC with documented HER2 positivity (an immunohistochemistry [IHC] score of 3+, both an IHC score of 2+ and fluorescence in situ hybridization positivity, or exon 20 mutation). This study was terminated early because of limited efficacy. The demographic characteristics in the 15 assessable patients were as follows: median age, 67 years; male sex, 47%; performance status of 0 to 1, 80%; HER2 status IHC 3+, 33%; HER status IHC 2+/fluorescence in situ hybridization-positive, 20%; and exon 20 mutation, 47%. The median number of delivered cycles was 3 (range 1-11). One patient achieved a partial response with an objective response rate of 6.7% (90% confidence interval: 0.2-32.0). With a median follow-up time of 9.2 months, the median progression-free survival time and median survival time were 2.0 and 10.9 months, respectively. Grade 3 or 4 adverse events included thrombocytopenia (40%) and hepatotoxicity (20%) without any treatment-related deaths. T-DM1 had a limited efficacy for HER2-positive NSCLC in our cohort. Applying the concept of precision medicine to tumors appears challenging; thus, additional molecular approaches are warranted.Entities:
Keywords: HER2; Non–small cell lung cancer; precision medicine; trastuzumab emtansine
Mesh:
Substances:
Year: 2017 PMID: 29313813 DOI: 10.1016/j.jtho.2017.10.032
Source DB: PubMed Journal: J Thorac Oncol ISSN: 1556-0864 Impact factor: 15.609