Department of Oncology, Gastroenterology, Hepatology, Pulmonology and Infectious Disease, Leipzig University Medical Center, University Cancer Center Leipzig (UCCL), Leipzig, Germany.
Institute of Pathology, Heilbronn SLK-Kliniken GmbH, Heilbronn, Germany.
J Cancer Res Clin Oncol. 2023 Mar;149(3):1319-1329. doi: 10.1007/s00432-022-04208-6. Epub 2022 Aug 27.
The prospective multicenter VARIANZ study aimed to identify resistance biomarkers for HER2-targeted treatment in advanced gastric and esophago-gastric junction cancer (GC, EGJC). HER2 test deviations were found in 90 (22.3%) of 404 cases (central versus local testing) and were associated with negative impact on survival for trastuzumab-treated patients. Here, we investigated methodological and biological variables that may promote deviating HER2 test results.
We analyzed HER2 testing procedures and participation in quality assurance programs of 105 participating local pathology laboratories. Furthermore, tumor localization and histological subtypes were compared between patients with centrally confirmed (central HER2 + /local HER2 + , n = 68) and unconfirmed HER2 status (central HER2 -/local HER2 + , n = 68).
For central HER2 testing, concordance between in situ hybridization (ISH) and immunohistochemistry (IHC) was 98.3%, with IHC sensitivity of 93.3% (84 IHC + of 90 ISH +), specificity of 99.5% (389 IHC- of 391 ISH-), and a positive diagnosis rate of 97.7%. Central confirmation of the local HER2 IHC scores were seen for the majority of locally HER2- IHC 0/1 (172/178; 96.6%), but less frequently for locally IHC3 + (57/124; 46.0%) cases. Deviation rate was not associated with IHC antibody platform used in the local pathology institute neither with participation in quality-assuring tests. Regarding tumor characteristics, deviating test results were more frequently found in GC vs. EGJC (69.1% vs. 39.7%; p = 0.001) and in Laurén diffuse vs. intestinal subtype (23.5% vs. 5.9%, p = 0.004).
Tumor localization and histological subtype have an impact on HER2 test deviation rates. Assessment of HER2 remains challenging for GC and EGJC.
前瞻性多中心 VARIANZ 研究旨在确定晚期胃癌和胃食管交界处癌(GC,EGJC)中 HER2 靶向治疗的耐药生物标志物。在 404 例病例中(中心检测与本地检测相比)发现了 90 例(22.3%)HER2 检测偏差,并且与曲妥珠单抗治疗患者的生存负面影响相关。在这里,我们研究了可能导致 HER2 检测结果偏差的方法学和生物学变量。
我们分析了 105 个参与的本地病理学实验室的 HER2 检测程序和参与质量保证计划的情况。此外,还比较了经中心确认(中心 HER2 + /本地 HER2 + ,n = 68)和未确认 HER2 状态(中心 HER2-/本地 HER2 + ,n = 68)患者的肿瘤定位和组织学亚型。
对于中心 HER2 检测,原位杂交(ISH)和免疫组织化学(IHC)之间的一致性为 98.3%,IHC 的敏感性为 93.3%(84 个 ISH + / 90 个 ISH + ),特异性为 99.5%(389 个 IHC-/391 个 ISH-),阳性诊断率为 97.7%。大多数本地 HER2- IHC 0/1(172/178;96.6%)的本地 HER2 IHC 评分得到了中心确认,但本地 IHC3+(57/124;46.0%)病例的确认频率较低。偏差率与本地病理学研究所使用的 IHC 抗体平台无关,也与参与质量保证测试无关。关于肿瘤特征,在 GC 与 EGJC(69.1%比 39.7%;p = 0.001)和 Lauren 弥漫型与肠型(23.5%比 5.9%;p = 0.004)中,更频繁地发现了 HER2 检测结果偏差。
肿瘤定位和组织学亚型对 HER2 检测偏差率有影响。对 GC 和 EGJC 评估 HER2 仍然具有挑战性。