Moelans Cathy B, Kibbelaar Robby E, van den Heuvel Marius C, Castigliego Domenico, de Weger Roel A, van Diest Paul J
Department of Pathology, University Medical Centre Utrecht, Utrecht, The Netherlands.
Cell Oncol. 2010;32(1-2):149-55. doi: 10.3233/CLO-2010-0514.
Testing for HER2 amplification and/or overexpression is currently routine practice to guide Herceptin therapy in invasive breast cancer. At present, HER2 status is most commonly assessed by immunohistochemistry (IHC). Standardization of HER2 IHC assays is of utmost clinical and economical importance. At present, HER2 IHC is most commonly performed with the HercepTest which contains a polyclonal antibody and applies a manual staining procedure. Analytical variability in HER2 IHC testing could be diminished by a fully automatic staining system with a monoclonal antibody.
219 invasive breast cancers were fully automatically stained with the monoclonal antibody-based Oracle HER2 Bond IHC kit and manually with the HercepTest. All cases were tested for amplification with chromogenic in situ hybridization (CISH).
HercepTest yielded an overall sharper membrane staining, with less cytoplasmic and stromal background than Oracle in 17% of cases. Overall concordance between both IHC techniques was 89% (195/219) with a kappa value of 0.776 (95% CI 0.698-0.854), indicating a substantial agreement. Most (22/24) discrepancies between HercepTest and Oracle showed a weaker staining for Oracle. Thirteen of the 24 discrepant cases were high-level HER2 amplified by CISH, and in 12 of these HercepTest IHC better reflected gene amplification status. All the 13 HER2 amplified discrepant cases were at least 2+ by HercepTest, while 10/13 of these were at least 2+ for Oracle. Considering CISH as gold standard, sensitivity of HercepTest and Oracle was 91% and 83%, and specificity was 94% and 98%, respectively. Positive and negative predictive values for HercepTest and Oracle were 90% and 95% for HercepTest and 96% and 91% for Oracle, respectively.
Fully-automated HER2 staining with the monoclonal antibody in the Oracle kit shows a high level of agreement with manual staining by the polyclonal antibody in the HercepTest. Although Oracle shows in general some more cytoplasmic staining and may be slightly less sensitive in picking up HER2 amplified cases, it shows a higher specificity and may be considered as an alternative method to evaluate the HER2 expression in breast cancer with potentially less analytical variability.
检测HER2扩增和/或过表达目前是指导浸润性乳腺癌赫赛汀治疗的常规做法。目前,HER2状态最常通过免疫组织化学(IHC)进行评估。HER2 IHC检测的标准化具有至关重要的临床和经济意义。目前,HER2 IHC最常使用包含多克隆抗体并采用手工染色程序的赫赛汀检测法进行。使用单克隆抗体的全自动染色系统可减少HER2 IHC检测中的分析变异性。
219例浸润性乳腺癌使用基于单克隆抗体的Oracle HER2 Bond IHC试剂盒进行全自动染色,并使用赫赛汀检测法进行手工染色。所有病例均采用显色原位杂交(CISH)检测扩增情况。
在17%的病例中,赫赛汀检测法产生的膜染色总体上更清晰,细胞质和基质背景比Oracle检测法少。两种IHC技术的总体一致性为89%(195/219),kappa值为0.776(95% CI 0.698 - 0.854),表明一致性较高。赫赛汀检测法与Oracle检测法之间的大多数(22/24)差异显示Oracle检测法的染色较弱。24例差异病例中有13例通过CISH检测为HER2高水平扩增,其中12例中赫赛汀检测法的IHC能更好地反映基因扩增状态。所有13例HER2扩增差异病例赫赛汀检测法至少为2+,而其中10/13例Oracle检测法至少为2+。以CISH为金标准,赫赛汀检测法和Oracle检测法的敏感性分别为91%和83%,特异性分别为94%和98%。赫赛汀检测法和Oracle检测法的阳性和阴性预测值分别为90%和95%以及96%和91%。
使用Oracle试剂盒中的单克隆抗体进行全自动HER2染色与使用赫赛汀检测法中的多克隆抗体进行手工染色显示出高度一致性。尽管Oracle检测法总体上显示出更多的细胞质染色,并且在检测HER2扩增病例时可能略不敏感,但它显示出更高的特异性,可被视为评估乳腺癌中HER2表达的替代方法,其分析变异性可能更小。