Targos Molecular Pathology GmbH und Pathologie Nordhessen, 34119 Kassel, Germany.
Virchows Arch. 2010 Sep;457(3):299-307. doi: 10.1007/s00428-010-0952-2. Epub 2010 Jul 28.
Trastuzumab-based therapy has been shown to confer overall survival benefit in HER2-positive patients with advanced gastric cancer in a large multicentric trial (ToGA study). Subgroup analysis identified adenocarcinomas of the stomach and gastroesophageal (GE) junction with overexpression of HER2 according to immunohistochemistry (IHC) as potential responders. Due to recent approval of trastuzumab for HER2 positive metastatic gastric and GE-junction cancer in Europe (EMEA) HER2 diagnostics is now mandatory with IHC being the primary test followed by fluorescence in situ hybridization (FISH) in IHC2+ cases. However, in order to not miss patients potentially responding to targeted therapy determination of a HER2-positive status for gastric cancer required modification of scoring as had been proposed in a pre-ToGA study. To validate this new HER2 status testing procedure in terms of inter-laboratory and inter-observer consensus for IHC scoring a series of 547 gastric cancer tissue samples on a tissue microarray (TMA) was used. In the first step, 30 representative cores were used to identify specific IHC HER2 scoring issues among eight French and German laboratories, while in the second step the full set of 547 cores was used to determine IHC HER2 intensity and area score concordance between six German pathologists. Specific issues relating to discordance were identified and recommendations formulated which proved to be effective to reliably determine HER2 status in a prospective test series of 447 diagnostic gastric cancer specimens.
曲妥珠单抗为基础的治疗已被证明在一个大型多中心试验(ToGA 研究)中为 HER2 阳性的晚期胃癌患者带来了总生存获益。亚组分析确定了根据免疫组织化学(IHC)过表达 HER2 的胃腺癌和胃食管(GE)交界处腺癌为潜在的应答者。由于曲妥珠单抗最近在欧洲(EMEA)被批准用于治疗 HER2 阳性转移性胃癌和 GE 交界处癌,因此现在 HER2 诊断是强制性的,IHC 是主要检测方法,在 IHC2+病例中随后进行荧光原位杂交(FISH)。然而,为了不遗漏可能对靶向治疗有反应的患者,需要对胃癌的 HER2 阳性状态进行评分修改,这是在 ToGA 研究之前提出的。为了验证这种新的 HER2 状态测试程序在 IHC 评分的实验室间和观察者间一致性方面的有效性,使用了一系列 547 个胃癌组织样本的组织微阵列(TMA)。在第一步中,使用 30 个代表性核心来确定八个法国和德国实验室之间特定的 IHC HER2 评分问题,而在第二步中,使用全部 547 个核心来确定六个德国病理学家之间的 IHC HER2 强度和面积评分一致性。确定了与不一致相关的具体问题,并提出了建议,这些建议被证明在 447 个诊断性胃癌标本的前瞻性测试系列中能够可靠地确定 HER2 状态。