Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Department of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Clin Cancer Res. 2018 Mar 1;24(5):1082-1089. doi: 10.1158/1078-0432.CCR-17-2781. Epub 2017 Dec 5.
Refining the selection of HER2-positive metastatic gastric cancer patient candidates for trastuzumab is a challenge of precision oncology. Preclinical studies have suggested several genomic mechanisms of primary resistance, leading to activation of tyrosine kinase receptors other than HER2 or downstream signaling pathways. We carried out this multicenter, prospective, case-control study to demonstrate the negative predictive impact of a panel of candidate genomic alterations (AMNESIA panel), including mutations and amplifications. Hypothesizing a prevalence of candidate alterations of 30% and 0% in resistant and sensitive HER2-positive patients, respectively, 20 patients per group were needed. AMNESIA panel alterations were significantly more frequent in resistant (11 of 20, 55%) as compared with sensitive (0% of 17) patients ( < 0.001), and in HER2 IHC 2 (7 of 13, 53.8%) than 3 (4 of 24, 16.7%) tumors ( = 0.028). Patients with tumors bearing no candidate alterations had a significantly longer median progression-free [5.2 vs. 2.6 months; HR, 0.34; 95% confidence interval (CI), 0.07-0.48; = 0.001] and overall survival (16.1 vs. 7.6 months; HR, 0.38; 95% CI, 0.09-0.75; = 0.015). The predictive accuracy of the AMNESIA panel and HER2 IHC was 76% and 65%, respectively. The predictive accuracy of the combined evaluation of the AMNESIA panel and HER2 IHC was 84%. Our panel of candidate genomic alterations may be clinically useful to predict primary resistance to trastuzumab in patients with HER2-positive metastatic gastric cancer and should be further validated with the aim of molecularly stratifying HER2-addicted cancers for the development of novel treatment strategies. .
筛选曲妥珠单抗治疗的 HER2 阳性转移性胃癌患者候选人群是精准肿瘤学的一个挑战。临床前研究提示了几种原发性耐药的基因组机制,导致除 HER2 以外的酪氨酸激酶受体或下游信号通路的激活。我们进行了这项多中心、前瞻性、病例对照研究,以证明候选基因组改变(AMNESIA 组)的阴性预测影响,包括 突变和 扩增。假设耐药和敏感的 HER2 阳性患者中候选改变的患病率分别为 30%和 0%,每组需要 20 例患者。与敏感(17 例中 0%)患者相比,耐药(20 例中有 11 例,55%)患者的 AMNESIA 组改变明显更频繁(<0.001),与 HER2 IHC 2(13 例中有 7 例,53.8%)相比,HER2 IHC 3(24 例中有 4 例,16.7%)肿瘤(=0.028)更为频繁。未发生候选改变的肿瘤患者的中位无进展生存期[5.2 个月比 2.6 个月;风险比,0.34;95%置信区间(CI),0.07-0.48;=0.001]和总生存期[16.1 个月比 7.6 个月;风险比,0.38;95%CI,0.09-0.75;=0.015]明显更长。AMNESIA 组和 HER2 IHC 的预测准确性分别为 76%和 65%。AMNESIA 组和 HER2 IHC 联合评估的预测准确性为 84%。我们的候选基因组改变组可能对预测曲妥珠单抗治疗 HER2 阳性转移性胃癌患者的原发性耐药具有临床意义,应进一步验证,旨在对 HER2 依赖性癌症进行分子分层,以制定新的治疗策略。