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肾移植患者中基于抗胸腺细胞球蛋白连续给药与间断给药的诱导治疗比较:疗效及长期安全性

Comparison of induction based on continuous vs discontinuous administration of antithymocyte globulins in renal transplant patients: efficacy and long-term safety.

作者信息

Esposito L, Kamar N, Durand D, Rostaing L

机构信息

Department of Nephrology, Dialysis and Multiorgan Transplantation, CHU Rangueil Toulouse, France.

出版信息

Transplant Proc. 2005 Mar;37(2):892-4. doi: 10.1016/j.transproceed.2004.12.267.

DOI:10.1016/j.transproceed.2004.12.267
PMID:15848567
Abstract

UNLABELLED

This retrospective study sought to compare two modes of administration of antithymocyte globulin (RATG) after renal transplantation.

METHODS

Before 1993, group I patients (n = 93) received fixed doses of RATG (1 mg/kg per day) for 8 consecutive days. Thereafter, RATG was either continued at the same dose for 15 days, in cases of delayed graft function, or was infused every other day at the same dose until serum creatinine level became <150 micromol/L. After 1993, group II patients (n = 66) received RATG at full dose (1 mg/kg per day) during the first 3 days and thereafter the doses were adjusted to target a CD2 T-cell count <50/mm3. Both groups received steroids, azathioprine, and cyclosporine. The mean follow-up after transplantation was 117 +/- 31 months in group I and 93 +/- 19 months in group II.

RESULTS

The RATG cumulative dose and consequently cost were significantly higher among group I than group II patients. Long-term patient and graft survival were similar in both groups. The rate of acute graft-rejection episodes was significantly higher among group I than group II patients. At 7 years posttransplantation, the serum creatinine level and creatinine clearance were similar in the two groups. The rate of cytomegalovirus infection, as well as the cumulative incidence of severe infections and cancers were also similar in both groups. Among the cancers, skin neoplasms represented 30% in group I and 26% in group II (P = ns).

CONCLUSION

Adjusting RATG doses according to the CD2 lymphocyte count is safe, and a less expensive than using full doses.

摘要

未标注

本回顾性研究旨在比较肾移植后抗胸腺细胞球蛋白(兔抗人胸腺细胞球蛋白,RATG)的两种给药方式。

方法

1993年前,I组患者(n = 93)连续8天接受固定剂量的RATG(每日1mg/kg)。此后,对于移植肾功能延迟的患者,RATG以相同剂量继续使用15天,或者每隔一天以相同剂量输注,直至血清肌酐水平<150μmol/L。1993年后,II组患者(n = 66)在最初3天接受全剂量的RATG(每日1mg/kg),此后调整剂量以使CD2 T细胞计数<50/mm³。两组均接受类固醇、硫唑嘌呤和环孢素治疗。I组移植后的平均随访时间为117±31个月,II组为93±19个月。

结果

I组患者的RATG累积剂量及相应费用显著高于II组患者。两组的长期患者和移植物存活率相似。I组患者的急性移植排斥反应发生率显著高于II组患者。移植后7年,两组的血清肌酐水平和肌酐清除率相似。两组的巨细胞病毒感染率以及严重感染和癌症的累积发生率也相似。在癌症中,皮肤肿瘤在I组中占30%,在II组中占26%(P = 无显著差异)。

结论

根据CD2淋巴细胞计数调整RATG剂量是安全的,且比使用全剂量成本更低。

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PLoS One. 2009;4(3):e4709. doi: 10.1371/journal.pone.0004709. Epub 2009 Mar 5.