Department of Urology, Lenox Hill Hospital, Northwell Health, Zucker School of Medicine at Hofstra/Northwell, New York, United States; Department of Urology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Department of Surgery, Jackson Memorial Hospital, University of Miami Miller School of Medicine, Miami, United States; Miami Transplant Institute, Jackson Memorial Hospital, University of Miami Miller School of Medicine, Miami, United States; Department of Urology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Actas Urol Esp (Engl Ed). 2021 Jul-Aug;45(6):427-438. doi: 10.1016/j.acuroe.2020.09.009. Epub 2021 Jun 17.
Kidney transplantation is associated with an increased risk of bladder cancer; however guidelines have not been established on the management of bladder cancer after kidney transplantation.
A systematic literature review using PubMed was performed in accordance with the PRISMA statement to identify studies concerning the prevalence and survival of bladder cancer after kidney transplantation. The risk factors and management of bladder cancer after kidney transplantation were also reviewed and discussed.
A total of 41 studies, published between 1996 and 2018, reporting primary data on bladder cancer after kidney transplantation were identified. Marked heterogeneity in bladder cancer prevalence, time to diagnosis, non-muscle invasive/muscle-invasive bladder cancer prevalence, and survival was noted. Four studies, published between 2003 and 2017, reporting primary data on bladder cancer treated with Bacillus Calmette-Guérin (BCG) after kidney transplantation were identified. Disease-free survival, cancer-specific survival, and overall survival were similar between BCG studies (75-100%).
Carcinogen exposure that led to ESRD, BKV, HPV, immunosuppressive agents, and the immunosuppressed state likely contribute to the increased risk of bladder cancer after renal transplantation. Non-muscle invasive disease should be treated with transurethral resection. BCG can be safely used in transplant recipients and likely improves the disease course. Muscle-invasive disease should be treated with radical cystectomy, with special consideration to the dissection and urinary diversion choice. Chemotherapy and immune checkpoint inhibitors can be safely used in regionally advanced bladder cancer with potential benefit. mTOR inhibitors may reduce the risk of developing bladder cancer, and immunosuppression medications should be reduced if malignancy develops.
肾移植会增加膀胱癌的风险;然而,对于肾移植后膀胱癌的管理,尚未制定指南。
根据 PRISMA 声明,使用 PubMed 进行了系统的文献回顾,以确定关于肾移植后膀胱癌患病率和生存的研究。还回顾和讨论了肾移植后膀胱癌的危险因素和管理。
共确定了 41 项研究,发表时间为 1996 年至 2018 年,报告了肾移植后膀胱癌的原始数据。膀胱癌患病率、诊断时间、非肌肉浸润/肌肉浸润膀胱癌患病率和生存率存在显著异质性。还确定了 4 项研究,发表时间为 2003 年至 2017 年,报告了肾移植后用卡介苗(BCG)治疗膀胱癌的原始数据。肾移植后接受 BCG 治疗的患者无疾病生存率、癌症特异性生存率和总生存率相似(75-100%)。
导致 ESRD、BKV、HPV、免疫抑制剂和免疫抑制状态的致癌物暴露可能导致肾移植后膀胱癌风险增加。非肌肉浸润性疾病应采用经尿道切除术治疗。BCG 可安全用于移植受者,并且可能改善疾病过程。肌层浸润性疾病应采用根治性膀胱切除术治疗,特别要考虑解剖和尿流改道选择。化疗和免疫检查点抑制剂可安全用于局部晚期膀胱癌,具有潜在益处。mTOR 抑制剂可能降低发生膀胱癌的风险,如果发生恶性肿瘤,应减少免疫抑制药物。