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TERT 启动子突变和循环肿瘤细胞对肌层浸润性膀胱癌的预后意义。

Prognostic implication of TERT promoter mutation and circulating tumor cells in muscle-invasive bladder cancer.

机构信息

Laboratori i Servei d Urologia, Hospital Clínic de Barcelona, Barcelona, Spain.

Institut d'Investigacions Biomèdiques August Pi i Sunyer, IDIBAPS, Barcelona, Spain.

出版信息

World J Urol. 2022 Aug;40(8):2033-2039. doi: 10.1007/s00345-022-04061-9. Epub 2022 Jun 17.

DOI:10.1007/s00345-022-04061-9
PMID:35713686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9203260/
Abstract

PURPOSE

Current clinical prognostic factors are not accurate enough to identify and monitor those muscle-invasive bladder cancer (MIBC) patients at high risk of progression after radical cystectomy (RC). Here, we determined genetic alterations in the tumor and circulating tumor cell (CTC) enumeration to find biomarkers useful for the management of MIBC after RC.

METHODS

Thirty-nine MIBC patients undergoing RC were included. Tumoral tissue DNA was analyzed by next generation sequencing. CTCs were isolated from blood collected before RC and one, four and 12 months later.

RESULTS

Sixteen (41%) patients progressed in a median time of 8.5 months and 11 (69%) of these patients harbored the TERT c.-124C > T mutation. All progressive patients harboring the TERT c.-124C > T mutation presented a significant increase in CTC number 12 months after RC compared to those without the mutation. Additionally, CTC number at 12 months was identified as an independent prognostic biomarker for tumor progression and cancer specific survival (CSS). Ten (63%) progressive patients showed an increment of CTC number with a median anticipation period of four months compared with imaging techniques.

CONCLUSIONS

The TERT c.-124C > T mutation could be considered a biomarker of aggressivity. CTC enumeration is a useful tool for identifying MIBC patients at high risk of progression and CSS after RC and for detecting tumor progression earlier than imaging techniques.

摘要

目的

目前的临床预后因素还不够准确,无法识别和监测接受根治性膀胱切除术 (RC) 后进展风险高的肌层浸润性膀胱癌 (MIBC) 患者。在这里,我们确定了肿瘤和循环肿瘤细胞 (CTC) 计数中的基因改变,以找到对 RC 后 MIBC 管理有用的生物标志物。

方法

纳入 39 例接受 RC 的 MIBC 患者。对肿瘤组织 DNA 进行下一代测序分析。在 RC 前、RC 后 1、4 和 12 个月采集血液,从中分离 CTCs。

结果

16 例(41%)患者在中位时间 8.5 个月时进展,其中 11 例(69%)患者携带 TERT c.-124C > T 突变。所有携带 TERT c.-124C > T 突变的进展患者在 RC 后 12 个月的 CTC 数量明显增加,与未携带突变的患者相比。此外,CTC 数量在 12 个月时被确定为肿瘤进展和癌症特异性生存 (CSS) 的独立预后生物标志物。与影像学技术相比,10 例(63%)进展患者的 CTC 数量增加,中位预期时间为 4 个月。

结论

TERT c.-124C > T 突变可被视为侵袭性的生物标志物。CTC 计数是一种有用的工具,可以识别 RC 后进展风险和 CSS 高的 MIBC 患者,并比影像学技术更早地检测肿瘤进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/291c/9279241/c01be1ee40b3/345_2022_4061_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/291c/9279241/54bbfa588290/345_2022_4061_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/291c/9279241/c01be1ee40b3/345_2022_4061_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/291c/9279241/54bbfa588290/345_2022_4061_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/291c/9279241/c01be1ee40b3/345_2022_4061_Fig2_HTML.jpg

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