Article

Original Article

Korean J Lab Med 2008; 28(5): 392-399

Published online October 1, 2008 https://doi.org/10.3343/kjlm.2008.28.5.392

Copyright © Korean Society for Laboratory Medicine.

Availability of Fine Needle Aspirates for the Assessment of HER2 Gene Amplification in Invasive Breast Cancer Patients

Ji Won Lee, M.D.1, Woo Chul Noh, M.D.2, Min Suk Kim, M.D.3, Hyun-Ah Kim, M.D.2, Yoon Hwan Chang, M.D.1, Young Joon Hong, M.D.1, Seok Il Hong, M.D.1, and Jin Kyung Lee, M.D.1

Departments of Laboratory Medicine1, Surgery2, and Pathology3, Korea Cancer Center Hospital, Seoul, Korea

Correspondence to: 이 진 경
우 139-706 서울시 노원구 노원길 75 원자력병원 진단검사의학과
전화: 02-970-1287, Fax : 02-973-7143
E-mail: jklee@kcch.re.kr
*본 연구는 원자력의학원 방사선조직유전자은행 운영사업비 지원에 의하여 수행된 것임.

Received: July 7, 2008; Revised: August 18, 2008; Accepted: August 18, 2008

Abstract

Background : FISH and immunohistochemistry (IHC) on formalin-fixed paraffin embedded (FFPE) tissue are currently used in the clinical laboratory to determine HER2 status in invasive breast cancer patients. Since tissue-based methods are relatively time-consuming and have a limitation for standardization of procedure, we evaluated the availability of fine needle aspirates (FNA) for the assessment of HER2 status in invasive breast cancer patients.
Methods : FNA were obtained from 51 invasive breast cancer patients and were submitted for the evaluation of HER2 status. After invasive breast cancer components were ascertained by morphological evaluation, HER2 gene amplification was evaluated by FISH. The results of HER2 FISH on FNA cells were compared with those of both FISH and IHC on corresponding FFPE tissues. FISH results were interpreted by American Society of Clinical Oncology (ASCO)/College of American Pathologists (CAP) guidelines issued in 2007.
Results : Of 51 FNA specimens, one was excluded due to an insufficient number of cancer cells for tests. Excluding the cases that showed ‘equivocal’ results, 47 (98%) out of 48 cases were concordant between the results of FISH on FNA and FISH on corresponding FFPE tissue (kappa, 0.969), and 43 (93%) out of 46 cases were concordant between the results of FISH on FNA and IHC on corresponding FFPE tissue (kappa, 0.912).
Conclusions : An excellent correlation was found between FISH on FNA cells and corresponding FFPE sections. We recommend FNA specimens for more rapid determination of HER2 status by FISH, which will be helpful for patient selection for individualized therapy.

Keywords: HER2, Fine needle aspirates, FISH