Gong Yun, Sweet William, Duh Yi-Jing, Greenfield Larry, Fang Yuan, Zhao Jianxin, Tarco Emily, Symmans W Fraser, Isola Jorma, Sneige Nour
Department of Pathology, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX 77030, USA.
Am J Clin Pathol. 2009 Apr;131(4):490-7. doi: 10.1309/AJCPI00TVGIGYXAA.
Chromogenic in situ hybridization (CISH) has shown the potential to replace fluorescence in situ hybridization (FISH) to determine HER2 gene status. To validate the reliability of CISH, we used 226 consecutive breast carcinomas from 2 institutions and tested CISH and FISH on the same tumor set simultaneously at different test sites. Besides manufacturers' scoring criteria, the new American Society of Clinical Oncology/College of American Pathologists (ASCO/CAP) guidelines were used to interpret HER2 status. The concordance between CISH and FISH for positive and negative results was 98.5% at site A and 98.6% at site B using the manufacturers' criteria, and 99.0% at site A and 99.1% at site B using the ASCO/CAP criteria. Reproducibility of CISH results was more than 98.0% among 3 sites using the manufacturers' criteria and 100.0% between 2 sites using the ASCO/CAP criteria. Our results confirm that CISH is reliable for HER2 testing per ASCO/CAP guidelines.
显色原位杂交(CISH)已显示出取代荧光原位杂交(FISH)来确定HER2基因状态的潜力。为验证CISH的可靠性,我们使用了来自2家机构的226例连续性乳腺癌病例,并在不同检测地点同时对同一组肿瘤进行CISH和FISH检测。除了制造商的评分标准外,还采用了美国临床肿瘤学会/美国病理学家学会(ASCO/CAP)的新指南来解读HER2状态。使用制造商的标准时,A检测点CISH与FISH阳性和阴性结果的一致性为98.5%,B检测点为98.6%;使用ASCO/CAP标准时,A检测点为99.0%,B检测点为99.1%。使用制造商的标准时,CISH结果在3个检测点之间的可重复性超过98.0%,使用ASCO/CAP标准时在2个检测点之间为100.0%。我们的结果证实,根据ASCO/CAP指南,CISH用于HER2检测是可靠的。