Kapriniotis Konstantinos, Tzelves Lazaros, Lazarou Lazaros, Mitsogianni Maria, Mitsogiannis Iraklis
Department of Urology, Whipps Cross University Hospital, London E11 1NR, UK.
2nd Department of Urology, Sismanogleio Hospital, National and Kapodistrian University of Athens (NKUA), 115 27 Athens, Greece.
Biomedicines. 2024 Apr 21;12(4):921. doi: 10.3390/biomedicines12040921.
Current management of non-metastatic muscle invasive bladder cancer (MIBC) includes radical cystectomy and cisplatin-based neoadjuvant chemotherapy (NAC), offers a 5-year survival rate of approximately 50% and is associated with significant toxicities. A growing body of evidence supports the role of liquid biopsies including circulating tumour DNA (ctDNA) as a prognostic and predictive marker that could stratify patients according to individualised risk of progression/recurrence. Detectable ctDNA levels prior to radical cystectomy have been shown to be correlated with higher risk of recurrence and worse overall prognosis after cystectomy. In addition, ctDNA status after NAC/neoadjuvant immunotherapy is predictive of the pathological response to these treatments, with persistently detectable ctDNA being associated with residual bladder tumour at cystectomy. Finally, detectable ctDNA levels post-cystectomy have been associated with disease relapse and worse disease-free (DFS) and overall survival (OS) and might identify a population with survival benefit from adjuvant immunotherapy.
非转移性肌肉浸润性膀胱癌(MIBC)的当前治疗方法包括根治性膀胱切除术和顺铂新辅助化疗(NAC),其5年生存率约为50%,且伴有明显的毒性。越来越多的证据支持包括循环肿瘤DNA(ctDNA)在内的液体活检作为一种预后和预测标志物的作用,它可以根据个体进展/复发风险对患者进行分层。根治性膀胱切除术之前可检测到的ctDNA水平已被证明与更高的复发风险以及膀胱切除术后更差的总体预后相关。此外,NAC/新辅助免疫治疗后的ctDNA状态可预测这些治疗的病理反应,持续可检测到的ctDNA与膀胱切除术中残留膀胱肿瘤相关。最后,膀胱切除术后可检测到的ctDNA水平与疾病复发以及更差的无病生存期(DFS)和总生存期(OS)相关,并且可能识别出从辅助免疫治疗中获益的人群。