Department of Pathology, National Taiwan University Hospital, Taipei, Taiwan.
Graduate Institute of Pathology, National Taiwan University, Taipei, Taiwan.
Histopathology. 2018 Apr;72(5):795-803. doi: 10.1111/his.13441. Epub 2018 Jan 4.
Mutations in FGFR3 and the promoter region of the telomerase reverse transcriptase (TERT) gene have been found frequently in urothelial carcinoma of the urinary bladder. However, related data for papillary urothelial neoplasm of low malignant potential (PUNLMP) are limited. In this study, we investigated the mutation status of the TERT promoter, FGFR3 and HRAS in low-grade papillary urothelial neoplasms and evaluated their prognostic significance.
The cases included in this study comprised 21 inverted papillomas, 30 PUNLMPs and 34 low-grade non-invasive papillary urothelial carcinomas (NIPUCs). TERT promoter mutations were observed in 10 (33%) PUNLMPs and 17 (50%) low-grade NIPUCs, but not in any inverted papilloma. FGFR3 mutations were observed more frequently in PUNLMP and low-grade NIPUC than in inverted papillomas (P = 0.009), whereas the opposite trend was noted for HRAS mutations (P < 0.001). Regarding the clinical outcome, TERT promoter mutation was associated with a higher recurrence rate in PUNLMP (P = 0.024) but not in low-grade NIPUC (P = 0.530). Notably, PUNLMP cases with TERT promoter mutations had a similar recurrence rate to that in low-grade NIPUC cases (P = 0.487).
Our results suggest that the status of the TERT promoter mutation may serve as a biomarker of prognostic stratification in patients with PUNLMP.
FGFR3 基因突变和端粒酶逆转录酶(TERT)基因启动子区域的突变已在膀胱癌的尿路上皮癌中频繁发现。然而,相关数据对于低级别尿路上皮乳头状肿瘤(PUNLMP)有限。在这项研究中,我们调查了低级别尿路上皮乳头状肿瘤中 TERT 启动子、FGFR3 和 HRAS 的突变状态,并评估了它们的预后意义。
本研究包括 21 例 inverted papillomas、30 例 PUNLMPs 和 34 例低级别非浸润性乳头状尿路上皮癌(NIPUCs)。TERT 启动子突变在 10 例 PUNLMPs 和 17 例低级别 NIPUCs 中观察到,但在任何 inverted papilloma 中均未观察到。与 inverted papillomas 相比,PUNLMP 和低级别 NIPUC 中 FGFR3 突变更为常见(P=0.009),而 HRAS 突变则呈现相反的趋势(P<0.001)。就临床结局而言,TERT 启动子突变与 PUNLMP 的复发率升高相关(P=0.024),但与低级别 NIPUC 无关(P=0.530)。值得注意的是,PUNLMP 病例中 TERT 启动子突变的复发率与低级别 NIPUC 病例相似(P=0.487)。
我们的结果表明,TERT 启动子突变状态可能成为 PUNLMP 患者预后分层的生物标志物。