Mahmoud Shereen Fathy, Holah Nanis Shawky, Alhanafy Alshimaa Mahmoud, Serag El-Edien Marwa Mohammed
Department of Pathology, Faculty of Medicine, Menoufia University, Minufiyah, Egypt.
Department of Clinical Oncology and Nuclear Medicine, Faculty of Medicine, Menoufia University, Minufiyah, Egypt.
Iran J Pathol. 2024 Winter;19(1):81-88. doi: 10.30699/IJP.2024.2012115.3180. Epub 2024 Mar 29.
BACKGROUND & OBJECTIVE: Bladder carcinoma ranks second in prevalence among males in Egypt. As a family of tyrosine kinases, fibroblast growth factor receptor (FGFR) dysregulation has been linked to some malignancies in humans. The aim of this study is to analyze the clinicopathological data of patients while investigating FGFR2 and FGFR3 immunohistochemical expression in invasive urothelial bladder carcinoma.
This retrospective cross-sectional study included 60 invasive urothelial carcinoma (UC) cases in the Pathology department, Faculty of Medicine, Menoufia University, from 2009 to 2020. All biopsies were stained for FGFR2 and FGFR3 antibodies. Complete clinical data were available for 44 patients treated and followed in clinical oncology and nuclear medicine departments.
Advanced stage and high grade are significantly correlated with FGFR2 positivity (=0.048 and 0.044, respectively). Cases presented with Perineural invasion showed a higher percentage of FGFR2 (=0.023). There is a significant indirect linear correlation between FGFR3 expression and lymph node positivity (r= -0.265, =0.041).
A high FGFR2 expression could be associated with poor prognostic parameters, while high FGFR3 expression would be associated with good prognostic parameters. These findings might highlight the importance of FGFR-targeted therapy as a FGFR2 antagonist and FGFR3 agonist for the treatment of urothelial carcinoma patients.
膀胱癌在埃及男性中的患病率位居第二。作为酪氨酸激酶家族,成纤维细胞生长因子受体(FGFR)失调与人类的某些恶性肿瘤有关。本研究旨在分析浸润性尿路上皮膀胱癌患者的临床病理数据,同时研究FGFR2和FGFR3的免疫组化表达。
这项回顾性横断面研究纳入了2009年至2020年在曼苏拉大学医学院病理科的60例浸润性尿路上皮癌(UC)病例。所有活检标本均用FGFR2和FGFR3抗体染色。44例在临床肿瘤学和核医学科接受治疗及随访的患者可获得完整的临床数据。
晚期和高级别与FGFR2阳性显著相关(分别为=0.048和0.044)。出现神经周围侵犯的病例FGFR2阳性率更高(=0.023)。FGFR3表达与淋巴结阳性之间存在显著的间接线性相关性(r = -0.265,=0.041)。
高FGFR2表达可能与不良预后参数相关,而高FGFR3表达可能与良好预后参数相关。这些发现可能突出了FGFR靶向治疗作为FGFR2拮抗剂和FGFR3激动剂治疗尿路上皮癌患者的重要性。