Pietrantonio F, Caporale M, Morano F, Scartozzi M, Gloghini A, De Vita F, Giommoni E, Fornaro L, Aprile G, Melisi D, Berenato R, Mennitto A, Volpi C C, Laterza M M, Pusceddu V, Antonuzzo L, Vasile E, Ongaro E, Simionato F, de Braud F, Torri V, Di Bartolomeo M
Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Medical Oncology Department, Azienda Ospedaliera Universitaria Cagliari, Presidio Policlinico Universitario "Duilio Casula", Cagliari, Italy.
Int J Cancer. 2016 Dec 15;139(12):2859-2864. doi: 10.1002/ijc.30408. Epub 2016 Sep 16.
Mechanisms of acquired resistance to trastuzumab-based treatment in gastric cancer are largely unknown. In this study, we analyzed 22 pairs of tumor samples taken at baseline and post-progression in patients receiving chemotherapy and trastuzumab for advanced HER2-positive [immunohistochemistry (IHC) 3+ or 2+ with in-situ hybridization (ISH) amplification] gastric or gastroesophageal cancers. Strict clinical criteria for defining acquired trastuzumab resistance were adopted. Loss of HER2 positivity and loss of HER2 over-expression were defined as post-trastuzumab IHC score <3+ and absence of ISH amplification, and IHC "downscoring" from 2+/3+ to 0/1+, respectively. HER2 IHC was always performed, while ISH was missing in 3 post-progression samples. Patients with initial HER2 IHC score 3+ and 2+ were 14 (64%) and 8 (36%), respectively. Loss of HER2 positivity and HER2 over-expression was observed in 32 and 32% samples, respectively. The chance of HER2 loss was not associated with any of the baseline clinicopathological variables. The only exception was in patients with initial IHC score 2+ versus 3+, for both endpoints of HER2 positivity (80 vs. 14%; p = 0.008) and HER2 over-expression (63 vs. 14%; p = 0.025). As already shown in breast cancer, loss of HER2 may be observed also in gastric cancers patients treated with trastuzumab-based chemotherapy in the clinical practice. This phenomenon may be one of the biological reasons explaining the failure of anti-HER2 second-line strategies in initially HER2-positive disease.
胃癌中对基于曲妥珠单抗治疗获得性耐药的机制在很大程度上尚不清楚。在本研究中,我们分析了22对肿瘤样本,这些样本取自接受化疗和曲妥珠单抗治疗的晚期HER2阳性[免疫组织化学(IHC)3+或2+且原位杂交(ISH)扩增]胃癌或胃食管癌患者的基线期和疾病进展后。采用了严格的临床标准来定义获得性曲妥珠单抗耐药。HER2阳性丧失和HER2过表达丧失分别定义为曲妥珠单抗治疗后IHC评分<3+且ISH无扩增,以及IHC从2+/3+“降分”至0/1+。总是进行HER2 IHC检测,而在3个疾病进展后的样本中未进行ISH检测。初始HER2 IHC评分为3+和2+的患者分别为14例(64%)和8例(36%)。分别在32%和32%的样本中观察到HER2阳性丧失和HER2过表达丧失。HER2丧失的可能性与任何基线临床病理变量均无关联。唯一的例外是初始IHC评分为2+与3+的患者,对于HER2阳性(80%对14%;p = 0.008)和HER2过表达(63%对14%;p = 0.025)这两个终点均如此。正如在乳腺癌中已经显示的那样,在临床实践中接受基于曲妥珠单抗化疗的胃癌患者中也可能观察到HER2丧失。这种现象可能是解释抗HER2二线策略在初始HER2阳性疾病中失败的生物学原因之一。