ERBB2 (HER2) protein expression in uterine sarcomas

被引:0
|
作者
Zafrakas, M. [1 ]
Zepiridis, L. [1 ]
Theodoridis, T. D. [1 ]
Venizelos, I. D. [2 ]
Papanicolaou, A. [1 ]
Agorastos, T. [1 ]
Bontis, J. N. [1 ]
机构
[1] Aristotle Univ Thessaloniki, Dept Obstet & Gynecol 1, Papageorgiou Gen Hosp, Thessaloniki 56403, Greece
[2] Hippokrateio Gen Hosp, Dept Pathol, Thessaloniki, Greece
关键词
Uterine sarcoma; ERBB2; HER2; Targeted therapy; Trastuzumab; Herceptin (R); Lapatinib; Tykerb (R); METASTATIC BREAST-CANCER; RECEPTOR TYROSINE KINASES; GROWTH-FACTOR RECEPTOR; OF-THE-LITERATURE; ADJUVANT CHEMOTHERAPY; GENE AMPLIFICATION; TRASTUZUMAB; CARCINOSARCOMA; HER-2/NEU; THERAPY;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Multiple clinical trials in recent years have shown that breast cancer patients with primary tumors overexpressing ERBB2 can be effectively treated with specific forms of modern anti-ERBB2-targeted therapy. The aim of the present study was to analyze the expression of the ERBB2 (HER2) protein in uterine sarcomas, in order to investigate the possibility of applying this treatment modality in uterine sarcomas. Methods: The expression of ERBB2 has been analyzed immunohistochemical in formalin-fixed paraffin-embedded primary uterine sarcomas (n = 11). Results: Using a semi-quantitative immunohistochemical score, we found that ERBB2 expression was very weak in the majority of tumors, with only three sarcomas showing moderate ERBB2 expression. Published studies evaluating the same issue in small numbers of uterine sarcomas reached similar findings. Conclusion: Overall, ERBB2 expression appears to be weak in uterine sarcomas. However, targeted treatment might still be feasible in a subgroup of patients with uterine sarcomas overexpressing ERBB2.
引用
收藏
页码:292 / 294
页数:3
相关论文
共 50 条
  • [31] Single Domain Monoclonal Antibody Specific for Her2 or ERBB2
    Omidfar, Kobra
    HYBRIDOMA, 2011, 30 (01): : 105 - 105
  • [32] Treatment options in ErbB2 (HER2)-overexpressing breast cancer
    Jackisch, Christian
    BREAST CARE, 2008, 3 : 1 - 1
  • [33] ERBB2/HER2 mutations are transforming and therapeutically targetable in leukemia
    Sunil K. Joshi
    Jamie M. Keck
    Christopher A. Eide
    Daniel Bottomly
    Elie Traer
    Jeffrey W. Tyner
    Shannon K. McWeeney
    Cristina E. Tognon
    Brian J. Druker
    Leukemia, 2020, 34 : 2798 - 2804
  • [34] Challenges in the treatment of ErbB2 (HER2)-positiive breast cancer
    Jackisch, Christian
    EJC SUPPLEMENTS, 2008, 6 (05): : 7 - 14
  • [35] PRACTICE ADVANCES ERBB2 (HER2) Alterations in Colorectal Cancer
    Roy-Chowdhuri, Sinchita
    Davies, Kurtis D.
    Ritterhouse, Lauren L.
    Snow, Anthony N.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2022, 24 (10): : 1064 - 1066
  • [36] HER2 therapy - HER2 (ERBB2): functional diversity from structurally conserved building blocks
    Landgraf, Ralf
    BREAST CANCER RESEARCH, 2007, 9 (01)
  • [37] ERBB2 (HER2/NEU) ONCOGENE IS FREQUENTLY AMPLIFIED IN SQUAMOUS-CELL CARCINOMA OF THE UTERINE CERVIX
    MITRA, AB
    MURTY, VVVS
    PRATAP, M
    SODHANI, P
    CHAGANTI, RSK
    CANCER RESEARCH, 1994, 54 (03) : 637 - 639
  • [38] Dual inhibition of ErbB1 (EGFR/HER1) and ErbB2 (HER2/neu)
    Reid, Alison
    Vidal, Laura
    Shaw, Heather
    de Bono, Johann
    EUROPEAN JOURNAL OF CANCER, 2007, 43 (03) : 481 - 489
  • [39] ErbB2 (HER2)-positives MammakarzinomResistenzmechanismenErbB2 (HER2) positive breast cancer Mechanisms of resistance
    K. Kast
    W. Distler
    Der Gynäkologe, 2010, 43 (7): : 574 - 578
  • [40] Detection of ERBB2 Amplification by Next Generation Sequencing Predicts HER2 Expression in Colorectal Carcinoma
    Cenaj, Odise
    Hornick, Jason L.
    Sholl, Lynette
    LABORATORY INVESTIGATION, 2018, 98 : 250 - 250