University Cancer Center Leipzig (UCCL), Leipzig University Medical Center, Leipzig, Germany.
Institute of Pathology, Leipzig University Medical Center, Leipzig, Germany.
J Clin Oncol. 2021 May 1;39(13):1468-1478. doi: 10.1200/JCO.20.02761. Epub 2021 Mar 25.
Trastuzumab is the only approved targeted drug for first-line treatment of human epidermal growth factor receptor 2-positive (HER2+) metastatic gastric cancer (mGC). However, not all patients respond and most eventually progress. The multicenter VARIANZ study aimed to investigate the background of response and resistance to trastuzumab in mGC.
Patients receiving medical treatment for mGC were prospectively recruited in 35 German sites and followed for up to 48 months. HER2 status was assessed centrally by immunohistochemistry and chromogenic in situ hybridization. In addition, gene expression was assessed using qPCR.
Five hundred forty-eight patients were enrolled, and 77 had HER2+ mGC by central assessment (14.1%). A high deviation rate of 22.7% between central and local test results was seen. Patients who received trastuzumab for centrally confirmed HER2+ mGC (central HER2+/local HER2+) lived significantly longer as compared with patients who received trastuzumab for local HER2+ but central HER2- mGC (20.5 months, n = 60 10.9 months, n = 65; hazard ratio, 0.42; 95% CI, 8.2 to 14.4; < .001). In the centrally confirmed cohort, significantly more tumor cells stained HER2+ than in the unconfirmed cohort, and the amplification ratio was significantly higher. A minimum of 40% HER2+ tumor cells and a amplification ratio of ≥ 3.0 were calculated as optimized thresholds for predicting benefit from trastuzumab.
Significant discrepancies in HER2 assessment of mGC were found in tumor specimens with intermediate HER2 expression. Borderline HER2 positivity and heterogeneity of HER2 expression should be considered as resistance factors for HER2-targeting treatment of mGC. HER2 thresholds should be reconsidered. Detailed reports with quantification of expression and amplification levels may improve selection of patients for HER2-directed treatment.
曲妥珠单抗是唯一被批准用于治疗人表皮生长因子受体 2 阳性(HER2+)转移性胃癌(mGC)的靶向药物。然而,并非所有患者均对此药有反应,且大多数患者最终会出现疾病进展。多中心 VARIANZ 研究旨在探究 mGC 患者对曲妥珠单抗的反应和耐药的背景。
在 35 个德国研究中心前瞻性招募接受 mGC 治疗的患者,并随访长达 48 个月。HER2 状态通过免疫组化和显色原位杂交法进行中心评估。此外,还使用 qPCR 评估基因表达。
共纳入 548 例患者,77 例患者经中心评估为 HER2+ mGC(14.1%)。中心和局部检测结果之间存在 22.7%的高偏差率。与接受曲妥珠单抗治疗但经中心评估为 HER2- mGC(局部 HER2+/中心 HER2-)的患者相比,经中心评估为 HER2+ mGC(中心 HER2+/局部 HER2+)并接受曲妥珠单抗治疗的患者生存时间显著延长(20.5 个月,n=60 vs. 10.9 个月,n=65;风险比,0.42;95%CI,8.2 至 14.4;<0.001)。在经中心确认的队列中,与未经确认的队列相比,更多的肿瘤细胞染色呈 HER2+,且扩增比显著更高。计算出的预测曲妥珠单抗获益的最佳阈值为:肿瘤细胞中至少有 40%的 HER2+和≥3.0 的扩增比。
在肿瘤标本中存在 HER2 表达水平为中间值的 mGC 患者中,HER2 评估存在显著差异。边界性 HER2 阳性和 HER2 表达异质性应被视为 mGC 接受 HER2 靶向治疗的耐药因素。HER2 阈值应重新考虑。详细报告 表达和扩增水平的定量可能会改善 HER2 定向治疗患者的选择。