Department of Respiratory Medicine, Okayama University Hospital, Okayama, Japan; Center of Innovative Clinical Medicine, Okayama University Hospital, Okayama, Japan.
Department of Medical Oncology, National Hospital Organization Yamaguchi-Ube Medical Center, Ube, Japan.
J Thorac Oncol. 2018 Feb;13(2):273-279. doi: 10.1016/j.jtho.2017.10.032. Epub 2017 Dec 5.
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.
曲妥珠单抗-美坦新偶联物(T-DM1)是一种抗 erb-b2 受体酪氨酸激酶 2(HER2)的抗体药物偶联物,已被证明可显著改善 HER2 阳性乳腺癌患者的生存。我们报告了一项 T-DM1 单药治疗 HER2 阳性(免疫组化[IHC]评分 3+,IHC 评分 2+且荧光原位杂交阳性,或外显子 20 突变)复发性非小细胞肺癌(NSCLC)的 II 期试验。由于疗效有限,该研究提前终止。15 例可评估患者的人口统计学特征如下:中位年龄 67 岁;男性 47%;体力状况 0-1 分,占 80%;HER2 状态 IHC 3+,占 33%;HER2 状态 IHC 2+/荧光原位杂交阳性,占 20%;外显子 20 突变,占 47%。中位给药周期数为 3 个(范围 1-11)。1 例患者获得部分缓解,客观缓解率为 6.7%(90%置信区间:0.2-32.0)。中位随访时间为 9.2 个月时,中位无进展生存期和中位总生存期分别为 2.0 和 10.9 个月。3 级或 4 级不良事件包括血小板减少症(40%)和肝毒性(20%),但无治疗相关死亡。在我们的队列中,T-DM1 对 HER2 阳性 NSCLC 的疗效有限。将精准医学的概念应用于肿瘤似乎具有挑战性;因此,需要额外的分子方法。