Cristelli M P, Tedesco-Silva H, Medina-Pestana J O, Franco M F
Transplant Division, Hospital do Rim e Hipertensão, UNIFESP, São Paulo, SP, Brazil.
Transpl Infect Dis. 2013 Aug;15(4):369-78. doi: 10.1111/tid.12095. Epub 2013 May 22.
Debate is increasing on whether mycophenolic acid (MPA) provides survival benefits comparable to azathioprine (AZA) after renal transplantation.
This retrospective cohort study compared safety and efficacy of AZA (n = 662) vs. MPA (n = 267) in low-immunologic-risk kidney transplant recipients (KTR) receiving tacrolimus (TAC) and steroids between 1998 and 2007. Primary outcomes were treatment discontinuation and infection. Secondary endpoints included survival free from biopsy-proven acute rejection, graft loss, death, and renal function.
The 5-year survival free of treatment discontinuation was higher in the MPA compared to the AZA group (74.1% vs. 60.3%, P < 0.001). MPA was discontinued exclusively because of adverse events (16.4%), while AZA was discontinued primarily for lack of efficacy (21.2%). In univariable analysis, MPA was associated with higher incidence of total (561.5 vs. 667.5 episodes/1000 person-year, P < 0.001), bacterial (167 vs. 158 episodes/1000 person-years, P = 0.001), and viral infections (83.2 vs. 100.4 episodes/1000 person-years, P = 0.001), but this association was not confirmed in multivariable analysis. Over 29% of viral infections in the AZA group occurred after conversion to MPA. A high incidence of tuberculosis was observed (2.9 episodes/1000 person-years) with a higher incidence (but not a statistically significant difference) in the AZA group. No significant differences were found in patient survival (90% vs. 89%, P = 0.78) or graft survival (81% vs. 77.7%, P = 0.08), but infection accounted for >50% of all deaths.
The type of antimetabolite, AZA or MPA, was not independently associated with any safety or efficacy outcome 5 years after transplantation, suggesting that AZA is still a viable option for low-risk KTR receiving TAC and steroids.
关于肾移植后霉酚酸(MPA)是否能提供与硫唑嘌呤(AZA)相当的生存益处的争论日益激烈。
这项回顾性队列研究比较了1998年至2007年间接受他克莫司(TAC)和类固醇治疗的低免疫风险肾移植受者(KTR)中,AZA组(n = 662)和MPA组(n = 267)的安全性和有效性。主要结局是治疗中断和感染。次要终点包括无活检证实的急性排斥反应的生存期、移植物丢失、死亡和肾功能。
MPA组5年无治疗中断的生存率高于AZA组(74.1%对60.3%,P < 0.001)。MPA仅因不良事件而停药(16.4%),而AZA主要因缺乏疗效而停药(21.2%)。在单变量分析中,MPA与总感染(561.5对667.5次/1000人年,P < 0.001)、细菌感染(167对158次/1000人年)和病毒感染(83.2对100.4次/1000人年,P = 0.001)的发生率较高相关,但在多变量分析中这种相关性未得到证实。AZA组超过29%的病毒感染发生在转换为MPA之后。观察到结核病的发生率较高(2.9次/1000人年),AZA组的发生率更高(但无统计学显著差异)。患者生存率(90%对89%,P = 0.78)或移植物生存率(81%对77.7%,P = 0.08)无显著差异,但感染占所有死亡的比例超过50%。
移植后5年,抗代谢物的类型(AZA或MPA)与任何安全性或有效性结局均无独立相关性,这表明对于接受TAC和类固醇治疗的低风险KTR,AZA仍是一个可行的选择。