Clari Roberta, Tarella Corrado, Giraudi Roberta, Torazza Maria Cristina, Gallo Ester, Lavacca Antonio, Fop Fabrizio, Mella Alberto, Dolla Caterina, Biancone Luigi
Department of Medical Sciences, Division of Nephrology Dialysis and Transplantation, Renal Transplantation Center 'A. Vercellone', Città della Salute e della Scienza Hospital and University of Turin, Turin, Italy.
Nephrology Unit, ASL TO5, Chieri, TO, Italy.
Clin Kidney J. 2020 Sep 18;14(1):317-324. doi: 10.1093/ckj/sfaa105. eCollection 2021 Jan.
Management of patients with oncohaematological disorders such as monoclonal gammopathy of undetermined significance (MGUS) is a frequent problem in pre-transplant work-up. Insights on disease progression and long-term functional outcomes are still lacking in this setting.
This was a retrospective analysis on all patients with MGUS who underwent kidney transplant (KT) at our centre between 1 January 2000 and 31 December 2017 (cases, = 65). Patients were matched with a control group (KTs with similar characteristics but without history of haematological disease, controls, = 1079). Primary endpoints were graft and patient survival; secondary endpoints were causes of graft failure, patient death, occurrence of allograft rejection, post-transplant neoplasia (not correlated to previous disorder) and/or infectious episodes.
The MGUS and control groups had a similar mean age [60 (29-79) versus 55.2 (19.3-79.5) years, respectively] and percentage of males (69.2% versus 64.6%, respectively). Median follow-up time since KT was 3.5 years (0-14) in cases and 8.3 years (0-14.9) in controls. All MGUS patients underwent KT following extensive multidiscliplinary investigations. No differences were found between cases and controls regarding patient and graft survival or post-transplant complications except for lower incidence of infections (58.7% versus 69.8%, P = 0.019) and increased use of mTOR inhbitors (30.3% versus 14.7%, P = 0.001) in MGUS. MGUS isotype did not influence graft and patient survival. The absence of difference in patients and graft survival was also confirmed in an adjunctive analysis where MGUS were compared with controls (ratio 1:2) matched for recipient age, gender, number of transplantations and transplant period.
Patients with MGUS may undergo KT without significantly increased risks of complications, provided that appropriate diagnostic procedures are carefully followed. Multidiscipline-based studies are crucial for establishing well designed pre- and post-transplant protocols for the best management of patients with coexisting MGUS and end-stage renal disease.
对患有血液肿瘤疾病(如意义未明的单克隆丙种球蛋白病,MGUS)的患者进行管理是移植前检查中经常遇到的问题。目前在这种情况下,对于疾病进展和长期功能结局仍缺乏相关见解。
这是一项对2000年1月1日至2017年12月31日期间在本中心接受肾移植(KT)的所有MGUS患者的回顾性分析(病例组,n = 65)。将患者与对照组(具有相似特征但无血液系统疾病史的肾移植患者,对照组,n = 1079)进行匹配。主要终点是移植物和患者的生存率;次要终点是移植物失败的原因、患者死亡、同种异体移植排斥反应的发生、移植后肿瘤形成(与先前疾病无关)和/或感染事件。
MGUS组和对照组的平均年龄相似[分别为60(29 - 79)岁和55.2(19.3 - 79.5)岁],男性比例也相似(分别为69.2%和64.6%)。肾移植后的中位随访时间,病例组为3.5年(0 - 14年),对照组为8.3年(0 - 14.9年)。所有MGUS患者在经过广泛的多学科检查后接受了肾移植。病例组和对照组在患者和移植物生存率或移植后并发症方面未发现差异,但MGUS患者的感染发生率较低(58.7%对69.8%,P = 0.019),mTOR抑制剂的使用增加(30.3%对14.7%,P = 0.001)。MGUS的亚型不影响移植物和患者的生存率。在一项辅助分析中,将MGUS患者与按受者年龄、性别、移植次数和移植时间匹配的对照组(比例1:2)进行比较,也证实了患者和移植物生存率无差异。
只要仔细遵循适当的诊断程序,MGUS患者进行肾移植时并发症风险不会显著增加。基于多学科的研究对于制定精心设计的移植前和移植后方案以最佳管理合并MGUS和终末期肾病的患者至关重要。