Cell-Free DNA as a Prognostic Biomarker for Monitoring Muscle-Invasive Bladder Cancer

被引:20
作者
Carrasco, Raquel [1 ,2 ,3 ]
Ingelmo-Torres, Mercedes [1 ,2 ]
Gomez, Ascension [1 ]
Trullas, Ramon [4 ]
Roldan, Fiorella L. [1 ,2 ,3 ]
Ajami, Tarek [1 ,2 ,3 ]
Moreno, Davinia [1 ]
Rodriguez-Carunchio, Leonardo [5 ,6 ]
Alcaraz, Antonio [1 ,2 ,7 ]
Izquierdo, Laura [1 ,2 ,7 ]
Mengual, Lourdes [1 ,2 ,3 ]
机构
[1] Hosp Clin Barcelona, Lab & Serv Urol, Barcelona 08036, Spain
[2] Inst Invest Biomed August Pi & Sunyer IDIBAPS, Genet & Tumors Urol, Barcelona 08036, Spain
[3] Univ Barcelona UB, Fac Med & Ciencies Salut, Dept Biomed, Barcelona 08036, Spain
[4] Inst Invest Biomed Barcelona IIBB CSIC IDIBAPS, Unitat Neurobiol, Barcelona 08036, Spain
[5] Hosp Clin Barcelona, Serv Anat Patol, Barcelona 08036, Spain
[6] Univ Vic Univ Cent Catalunya UVic UCC, Fac Med, Vic 08500, Spain
[7] Univ Barcelona UB, Fac Med & Ciencies Salut, Dept Cirurgia & Especialitats Medicoquirurg, Barcelona 08036, Spain
关键词
bladder cancer; cell-free DNA; circulating tumor DNA; droplet digital PCR; prognosis; MUTATIONS; RECURRENCE; DISEASE;
D O I
10.3390/ijms231911732
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell-free DNA (cfDNA) has recently emerged as a real-time biomarker for diagnosis, monitoring and prediction of therapy response in tumoral disease. Here, we evaluated cfDNA as a prognostic biomarker for monitoring muscle-invasive bladder cancer (MIBC) patients at different follow-up time points. Blood samples from 37 MIBC patients who underwent radical cystectomy (RC) were collected at cystectomy and 1, 4, 12 and 24 months later. Plasma cfDNA amount and fragmentation patterns were determined. Four mutations were analyzed in cfDNA to detect circulating tumor DNA (ctDNA) during patient follow-up. During a median follow-up of 36 months, 46% of patients progressed; median time to progression was 10 months. cfDNA levels and ctDNA status four months after RC were identified as independent prognostic biomarkers of tumor progression (HR 5.290; p = 0.033) and cancer-specific survival (HR 4.199; p = 0.038), respectively. Furthermore, ctDNA clearance four months after RC was significantly associated with patients' clinical outcomes. In conclusion, cfDNA levels and ctDNA status four months after RC have prognostic implications in MIBC patients. In addition, cfDNA monitoring is useful to predict patient outcomes after RC. cfDNA analysis in the clinical setting could greatly improve MIBC patient management.
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页数:12
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