Effect of Ischemic Time, Fixation Time, and Fixative Type on HER2/neu Immunohistochemical and Fluorescence In Situ Hybridization Results in Breast Cancer

固定剂 免疫组织化学 乳腺癌 HER2/东北 活检 荧光原位杂交 病理 乳腺癌 医学 内科学 癌症 生物 染色 生物化学 染色体 基因
作者
Neda A. Moatamed,Gouri J. Nanjangud,Richard Pucci,Alarice Lowe,I. Peter Shintaku,Saeedeh Shapourifar-Tehrani,Nagesh Rao,David Lu,Sophia K. Apple
出处
期刊:American Journal of Clinical Pathology [Oxford University Press]
卷期号:136 (5): 754-761 被引量:77
标识
DOI:10.1309/ajcp99wzgbpkcxoq
摘要

Accurate determination of HER2/neu status in breast carcinoma is essential. Alteration of preanalytic variables is known to affect HER2/neu results. American Society of Clinical Oncology (ASCO) and the College of American Pathologists (CAP) issued guidelines to standardize fixation for increased HER2/neu accuracy. We studied the effects of changing preanalytic variables on HER2/neu immunohistochemical and fluorescence in situ hybridization (FISH) results in a known HER2/neu+ invasive carcinoma. The clinical specimen was processed according to ASCO/CAP guidelines, with remaining tumor stored fresh without any fixatives for 4 days at 4°C and cut into core biopsy-sized pieces. Each was fixed in 10% formalin, 15% formalin, Pen-Fix (Richard-Allan Scientific, Kalamazoo, MI), Bouin solution, Sakura molecular fixative (Sakura Tissue-Tek Xpress, Torrance, CA), or zinc formalin for 0 to 168 hours. Immunohistochemical studies and FISH were performed. Compared with the clinical specimen, the samples showed no tumor degradation or marked difference by immunohistochemical studies, except the 1-hour 10% formalin and Bouin samples, or FISH, except the Bouin-fixed samples. Our study demonstrates that HER2/neu results remain accurate beyond ASCO/CAP-recommended preanalytic variables, with the exception of Bouin solution for FISH analysis.

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