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在接受依维莫司治疗且减少钙调磷酸酶抑制剂暴露或接受当前标准治疗的肾移植受者中,伤口愈合不良事件:来自 24 个月 TRANSFORM 研究的见解。

Wound healing adverse events in kidney transplant recipients receiving everolimus with reduced calcineurin inhibitor exposure or current standard-of-care: insights from the 24-month TRANSFORM study.

机构信息

Department of Surgery, Fondazione Policlinico Universitario A. Gemelli, IRCCS , Rome, Italy.

Department of Surgery, The Comprehensive Transplant Center, The Ohio State University, Wexner Medical Center , Columbus, OH, USA.

出版信息

Expert Opin Drug Saf. 2020 Oct;19(10):1339-1348. doi: 10.1080/14740338.2020.1792441. Epub 2020 Jul 20.

Abstract

OBJECTIVES

In TRANSFORM, kidney transplant recipients received either everolimus in combination with reduced-exposure calcineurin inhibitor (EVR+rCNI) at standard EVR pre-dose concentrations of 3-8 ng/mL or mycophenolic acid plus standard-exposure CNI (MPA+sCNI). The authors analyzed the incidence of wound healing adverse events (WHAEs) over the 2-year study period 15.

METHODS

Patients were randomized to either EVR+rCNI or MPA+sCNI, both combined with induction therapy and steroids 19.

RESULTS

The safety population consisted of 2,026 patients (EVR+rCNI: 1,014, MPA+sCNI: 1,012). The proportion of patients with at least 1 WHAE was comparable between EVR+rCNI and MPA+sCNI treatment groups [20.6% vs. 17.3%; risk ratio (RR): 1.19; 95% confidence interval (CI): 0.99, 1.43] at month 24. The numerical difference between EVR+rCNI and MPA+sCNI was mainly caused by an increased proportion of EVR patients with lymphocele and wound dehiscence [7.5% vs. 5.1% (RR: 1.46; 95% CI: 1.04, 2.05) and 3.9% vs. 1.8% (RR: 2.22; 95%CI: 1.28, 3.84), respectively] 20.

CONCLUSION

The immediate introduction of EVR+rCNI after kidney transplantation was associated with an overall comparable incidence of WHAEs versus current standard-of-care over the 24-month study period. There was an increased relative risk of experiencing lymphocele and wound dehiscence but the absolute risks were rather low in both groups 21.

CT.GOV IDENTIFIER: NCT01950819.

摘要

目的

在 TRANSFORM 研究中,肾移植受者接受依维莫司联合低剂量钙调磷酸酶抑制剂(EVR+rCNI,EVR 预剂量浓度为 3-8ng/ml)或吗替麦考酚酯联合标准剂量钙调磷酸酶抑制剂(MPA+sCNI)治疗。本研究分析了为期 2 年的研究期间伤口愈合不良事件(WHAEs)的发生率 15。

方法

患者被随机分为 EVR+rCNI 或 MPA+sCNI 组,均联合诱导治疗和类固醇治疗 19。

结果

安全性人群包括 2026 例患者(EVR+rCNI 组 1014 例,MPA+sCNI 组 1012 例)。EVR+rCNI 和 MPA+sCNI 治疗组在第 24 个月时至少发生 1 次 WHAE 的患者比例相似[20.6%比 17.3%;风险比(RR):1.19;95%置信区间(CI):0.99,1.43]。EVR+rCNI 组与 MPA+sCNI 组之间的数值差异主要是由于接受 EVR 治疗的患者中,淋巴囊肿和伤口裂开的比例增加[7.5%比 5.1%(RR:1.46;95%CI:1.04,2.05)和 3.9%比 1.8%(RR:2.22;95%CI:1.28,3.84)] 20。

结论

与当前的标准治疗相比,肾移植后立即开始 EVR+rCNI 治疗在 24 个月的研究期间总体上与 WHAEs 的发生率相当。接受 EVR 治疗的患者发生淋巴囊肿和伤口裂开的相对风险增加,但两组的绝对风险均较低 21。

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