Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/34704
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    CNU IR > Offices > 123 >  Item 310902800/34704
    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/34704


    Title: High Expression of Folate Receptor Alpha (FOLR1) is Associated With Aggressive Tumor Behavior, Poor Response to Chemoradiotherapy, and Worse Survival in Rectal Cancer
    Authors: Chen, Chih-, I
    Li, Wan-Shan
    Chen, Hsin-Pao
    Liu, Kuang-Wen
    Tsai, Chia-Jen
    Hung, Wei-Ju
    Yang, Ching-Chieh
    Contributors: E-Da Hospital
    E-Da Hospital
    I Shou University
    I Shou University
    I Shou University
    National Sun Yat Sen University
    Chi Mei Hospital
    Chung Hua University
    Chi Mei Hospital
    Chia Nan University of Pharmacy & Science
    Keywords: preoperative chemoradiotherapy
    mirvetuximab soravtansine
    epithelial ovarian
    binding-protein
    chemotherapy
    carcinoma
    carcinogenesis
    antibody
    target
    Date: 2022
    Issue Date: 2023-12-11 14:06:07 (UTC+8)
    Publisher: SAGE PUBLICATIONS INC
    Abstract: Objectives: Recently, molecular medicine targeting Folate Receptor Alpha (FOLR1), which mediates intracellular folate uptake and tumor cell proliferation, has been identified in several malignancies. However, the association between FOLR1 expression and rectal cancer remains unclear. Methods: Immunostaining of FOLR1 was performed on biopsy specimens from 172 rectal cancer patients undergoing preoperative chemoradiotherapy (CRT). FOLR1 expression was measured and divided into low (0+-2+) or high (3+-4+) level. Correlations between FOLR1 status and clinicopathologic features, tumor regression grade, disease-specific survival (DSS), local recurrence-free survival, and metastasis-free survival (MeFS) were analyzed, retrospectively. Results: High FOLR1 expression was significantly associated with advanced post-treatment tumor and nodal status (T3-4; N1-2, P = .001), vascular invasion (P = .042), perineural invasion (P = .012), and poor regression change after CRT (P = .001). In uni- and multi-variable survival analysis, FOLR1 overexpression remained a significant predictor of lower DSS (hazard ratio [HR], 2.328; 95% confidence interval [CI], 1.014-5.344; P = .046) and MeFS (HR, 2.177; 95% CI, 1.000-1.1286; P = .050). Conclusion: These results indicate that high FOLR1 status is associated with aggressive tumor behavior, poor response to CRT, and worse survival. Therefore, FOLR1 expression at initial biopsy may be useful in predicting outcomes and also be a target for the exploration of FOLR1-based therapeutic agents.
    Relation: TECHNOLOGY IN CANCER RESEARCH & TREATMENT, v.21, n.CB2, pp.CC2, pp.-1183,
    Appears in Collections:[Offices] 123

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