Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/34931
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    CNU IR > Offices > 456 >  Item 310902800/34931
    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/34931


    Title: HER2 amplification in colorectal cancer with brain metastasis: A propensity score matching study
    Authors: Chen, Po-Chuan
    Yeh, Yu-Min
    Chu, Chun-Ting
    Su, Pei-Fang
    Chiu, Pin-Hsuan
    Lin, Bo-Wen
    Chen, Shang-Hung
    Lin, Peng-Chan
    Lee, Chung-Ta
    Chen, Helen H. W.
    Chen, Chien-Chin
    Contributors: Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Dept Surg,Div Colorectal Surg
    Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Dept Oncol
    Chia Yi Christian Hosp, Ditmanson Med Fdn, Dept Surg, Div Colorectal Surg
    Natl Cheng Kung Univ, Dept Stat
    Natl Cheng Kung Univ Hosp, Ctr Quantitat Sci, Clin Med Res Ctr
    Natl Hlth Res Inst, Natl Inst Canc Res
    Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Dept Genom Med
    Natl Cheng Kung Univ, Coll Elect Engn & Comp Sci, Dept Comp Sci & Informat Engn
    Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Dept Pathol
    Chia Yi Christian Hosp, Ditmanson Med Fdn, Dept Pathol
    Chia Nan Univ Pharm & Sci, Dept Cosmet Sci
    Natl Cheng Kung Univ, Coll Biosci & Biotechnol, Dept Biotechnol & Bioind Sci
    Natl Chung Hsing Univ, Rong Hsing Res Ctr Translat Med, PhD Program Translat Med
    Keywords: HER2 amplification
    Colorectal cancer
    Brain metastasis
    Heterogeneity
    Propensity score matching
    Date: 2023
    Issue Date: 2024-12-25 11:05:50 (UTC+8)
    Publisher: ELSEVIER SCI LTD
    Abstract: Background: The association between human epidermal growth factor receptor -2 (HER2) amplification and brain metastasis (BM) in patients having colorectal cancer (CRC) has been suggested but not yet established. This study investigated the expression pat-terns of HER2, its association with BM, and its prognostic value in patients having CRC.Methods: We retrospectively identified 99 patients having metastatic CRC (mCRC) and BM (the BM cohort) and compared them with a cohort of 249 patients having mCRC and without BM (the stage IV cohort) by propensity score matching. Immunohistochemical studies of HER2 on all available paraffin-embedded tumour samples, either from the primary tumour, the metastasis (brain and/or extracranial sites) or both, were performed and analysed. HER2 fluorescent in situ hybridisation was applied when necessary. The expression of HER2 was compared and correlated with survival.Results: HER2 amplifications were detected in 16 (18.4%) of 87 and 9 (3.6%) of 249 patients who had specimens available in the BM and stage IV cohorts, respectively (P < .001). After propensity score matching, HER2 amplification was significantly associated with BM (odds ratio: 5.38, P = .003). HER2 heterogeneity was frequently observed not only at the single tumour level but also in paired tumour samples. A marginally significant longer survival since BM was found in patients having HER2-amplified mCRC than in those without (P = .07).Conclusions: HER2 amplification was significantly associated with BM in patients having mCRC and might have prognostic value for survival since BM. Given the heterogeneity of HER2 expression, the testing of HER2 status on available tissues from both primary and met-astatic tumours should be encouraged.(c) 2022 Elsevier Ltd. All rights reserved.
    Relation: European Journal of Cancer, v.181
    Appears in Collections:[Offices] 456

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