Gagnon Marie-France, Cardinal Héloïse, Emond Jean-Pierre, Latour Mathieu, Lemieux Bernard
Division of Hematology-Oncology, Department of Medicine, Centre Hospitalier de l'Université de Montréal, Montreal, QC, Canada.
Division of Nephrology, Department of Medicine, Centre Hospitalier de l'Université de Montréal, Montreal, QC, Canada.
Transplant Direct. 2019 Sep 19;5(10):e489. doi: 10.1097/TXD.0000000000000937. eCollection 2019 Oct.
It is unclear if immunosuppression increases the likelihood of malignant transformation of monoclonal gammopathy of undetermined significance (MGUS) and whether adverse renal outcomes in kidney transplant recipients with MGUS are more frequent.
We performed a retrospective cohort study of kidney transplant recipients at the Centre Hospitalier de l'Université de Montréal between 2000 and 2016.
Among 755 study participants, 13 (1.7%) were found to have MGUS before transplant. Two evolved to smoldering multiple myeloma and 2 presented paraprotein-induced allograft injury from light chain deposition disease. Forty-six patients developed posttransplant MGUS (2.5% 5-y cumulative incidence) of which 1 progressed to multiple myeloma and 1 experienced kidney allograft loss from light chain deposition disease. None of the patients with a malignant transformation or paraprotein-induced renal disease after transplantation had had a systematic workup before transplantation to exclude hematologic malignancies and paraprotein-related kidney injury. Nine posttransplant MGUS (21%) were transient. Multivariable analysis revealed that age at transplant (hazard ratio 1.05 per 1-y increase, 95% confidence intervals, 1.02-1.08) and prior cytomegalovirus infection (hazard ratio 2.22, 95% confidence intervals, 1.07-4.58) were associated with the development of MGUS after transplantation. Of 7 posttransplant lymphoproliferative disorders, none were preceded by MGUS.
Our results suggest that the identification of MGUS in a transplant candidate should lead to further investigations to exclude a plasma cell neoplasm and monoclonal gammopathy of renal significance before transplantation. MGUS arising after transplantation appears to carry a favorable evolution.
免疫抑制是否会增加意义未明的单克隆丙种球蛋白病(MGUS)发生恶性转化的可能性,以及MGUS肾移植受者出现不良肾脏结局的情况是否更常见尚不清楚。
我们对2000年至2016年期间蒙特利尔大学中心医院的肾移植受者进行了一项回顾性队列研究。
在755名研究参与者中,13人(1.7%)在移植前被发现患有MGUS。2人进展为冒烟型多发性骨髓瘤,2人出现轻链沉积病导致的副蛋白诱导的移植肾损伤。46名患者发生移植后MGUS(5年累积发病率为2.5%),其中1人进展为多发性骨髓瘤,1人因轻链沉积病导致移植肾丢失。移植后发生恶性转化或副蛋白诱导的肾脏疾病的患者在移植前均未进行系统检查以排除血液系统恶性肿瘤和副蛋白相关的肾脏损伤。9例移植后MGUS(21%)为短暂性。多变量分析显示,移植时年龄(每增加1岁风险比为1.05,95%置信区间为1.02 - 1.08)和既往巨细胞病毒感染(风险比为2.22,95%置信区间为1.07 - 4.58)与移植后MGUS的发生相关。在7例移植后淋巴增殖性疾病中,无一例先有MGUS。
我们的结果表明,在移植候选者中识别出MGUS应促使在移植前进行进一步检查,以排除浆细胞肿瘤和具有肾脏意义的单克隆丙种球蛋白病。移植后出现的MGUS似乎预后良好。