Monteiro Camila Ribeiro de Arruda, Korkes Fernando, Krutman-Zveibil Deborah, Glina Sidney
Centro Universitário FMABC, Santo André, SP, Brazil.
Einstein (Sao Paulo). 2022 Apr 1;20:eAO6450. doi: 10.31744/einstein_journal/2022AO6450. eCollection 2022.
To understand the feasibility of FGFR3 tests in the Brazilian public health context, and to sample the mutational burden of this receptor in high-grade muscle invasive bladder cancer.
A total of 31 patients with high-grade muscle-invasive bladder cancer were included in the present study. Either transurethral resection of bladder tumor or radical cystectomy specimens were analyzed. Formalin-fixed paraffin-embedded tissue blocks were sectioned, hematoxylin and eosin stained, and histologic sections were reviewed. Total RNA was extracted using the RNeasy DSP formalin-fixed paraffin-embedded kit. Qualitative results were displayed in Rotor-Gene AssayManager software.
Six patients were excluded. From the samples analyzed, four (16.7%) were considered inadequate and could not have their RNA extracted. Two patients presented FGFR3 mutations, accounting for 9.5% of material available for adequate analysis. The two mutations detected included a Y373C mutation in a male patient and a S249C mutation in a female patient.
FGFR3 mutations could be analyzed in 84% of our cohort and occurred in 9.5% of patients with high-grade muscle invasive bladder cancer in this Brazilian population. FGFR3 gene mutations are targets for therapeutic drugs in muscle-invasive bladder cancer. For this reason, know the frequency of these mutations can have a significant impact on public health policies and costs provisioning.
了解在巴西公共卫生背景下进行FGFR3检测的可行性,并对高级别肌层浸润性膀胱癌中该受体的突变负担进行抽样调查。
本研究共纳入31例高级别肌层浸润性膀胱癌患者。对膀胱肿瘤经尿道切除术或根治性膀胱切除术标本进行分析。将福尔马林固定石蜡包埋组织块切片,进行苏木精和伊红染色,并对组织学切片进行复查。使用RNeasy DSP福尔马林固定石蜡包埋试剂盒提取总RNA。定性结果在Rotor-Gene AssayManager软件中显示。
6例患者被排除。在分析的样本中,4例(16.7%)被认为不合格,无法提取RNA。2例患者出现FGFR3突变,占可进行充分分析材料的9.5%。检测到的两个突变包括一名男性患者的Y373C突变和一名女性患者的S249C突变。
在我们的队列中,84%的患者能够分析FGFR3突变,在该巴西人群的高级别肌层浸润性膀胱癌患者中,FGFR3突变发生率为9.5%。FGFR3基因突变是肌层浸润性膀胱癌治疗药物的靶点。因此,了解这些突变的频率会对公共卫生政策和成本供应产生重大影响。