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肾移植后基于FK506免疫抑制的前瞻性随机试验。

A prospective randomized trial of FK506-based immunosuppression after renal transplantation.

作者信息

Shapiro R, Jordan M L, Scantlebury V P, Vivas C, Fung J J, McCauley J, Randhawa P, Demetris A J, Irish W, Mitchell S

机构信息

Department of Surgery, Pittsburgh Transplantation Institute, University of Pittsburgh Medical Center, Pennsylvania 15213.

出版信息

Transplantation. 1995 Feb 27;59(4):485-90. doi: 10.1097/00007890-199559040-00007.

Abstract

A group of 204 adult patients was entered into a prospective, randomized trial comparing FK506/prednisone with FK506/azathioprine/prednisone after renal transplantation between August 1, 1991 and October 11, 1992. The purpose of the study was to see if the addition of azathioprine would reduce the incidence of rejection and improve graft survival. The recipient population was unselected, with 61 (30%) patients undergoing retransplantation, 37 (18%) having a panel-reactive antibody greater than 40%, and 33 (16%) over 60 years of age. The mean recipient age was 43.8 +/- 13.7 years (range 17.6-78). The mean donor age was 34.0 +/- 20.1 years (range 0.3-75); 13% of the cadaveric kidneys were from pediatric donors less than 3 years of age and were transplanted en bloc. The mean cold ischemia time was 31.4 +/- 8.4 hr. Living donors were the source of 13% of the kidneys. The mean follow-up was 22 +/- 4 months (range 12-29). Overall one-year actual patient survival was 94%. Overall one-year actual graft survival was 87%. Patients starting on double therapy had a one-year actual patient survival of 96% and a one-year actual graft survival of 92%. Patients starting on triple therapy had a one-year actual patient survival of 91% (P = ns compared with double therapy), and a one-year actual graft survival of 82% (P < 0.02, compared with double therapy). Overall results with first cadaver transplants included a one-year actual patient survival of 94% and one-year actual graft survival of 88%, with no differences between double and triple therapy. The overall incidence of rejection was 48%, with 54% in the double therapy group and 41% in the triple therapy group (P < .07). The incidence of steroid-resistant rejection requiring antilymphocyte therapy (OKT3 or ATGAM) was 13%, and was not different between the double and triple therapy groups. The mean serum creatinine was 1.8 +/- 0.8 mg/dl. The mean BUN was 33 +/- 21 mg/dl, with no significant difference between the therapy groups. The mean serum cholesterol was 192 +/- 49 mg/dl. A total of 56% of the patients are off prednisone, and 35% of the patients are not taking any antihypertensive medications. Other complications included cytomegalovirus--14%; new-onset diabetes--16% (half of which was reversible); and posttransplant lymphoproliferative disorder--1%.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

1991年8月1日至1992年10月11日期间,204例成年患者参与了一项前瞻性随机试验,比较肾移植后使用FK506/泼尼松与FK506/硫唑嘌呤/泼尼松的效果。该研究的目的是观察添加硫唑嘌呤是否会降低排斥反应的发生率并提高移植物存活率。接受者群体未经过筛选,其中61例(30%)患者接受再次移植,37例(18%)患者的群体反应性抗体大于40%,33例(16%)患者年龄超过60岁。接受者的平均年龄为43.8±13.7岁(范围17.6 - 78岁)。供者的平均年龄为34.0±20.1岁(范围0.3 - 75岁);13%的尸体肾来自年龄小于3岁的儿科供者,且是整块移植。平均冷缺血时间为31.4±8.4小时。13%的肾来自活体供者。平均随访时间为22±4个月(范围12 - 29个月)。总体一年实际患者存活率为94%。总体一年实际移植物存活率为87%。开始接受双重治疗的患者一年实际患者存活率为96%,一年实际移植物存活率为92%。开始接受三联治疗的患者一年实际患者存活率为91%(与双重治疗相比P = 无显著差异),一年实际移植物存活率为82%(与双重治疗相比P < 0.02)。首次尸体肾移植的总体结果包括一年实际患者存活率为94%,一年实际移植物存活率为88%,双重治疗和三联治疗之间无差异。排斥反应的总体发生率为48%,双重治疗组为54%,三联治疗组为41%(P < 0.07)。需要抗淋巴细胞治疗(OKT3或抗胸腺细胞球蛋白)的激素抵抗性排斥反应发生率为13%,双重治疗组和三联治疗组之间无差异。平均血清肌酐为1.8±0.8mg/dl。平均尿素氮为33±21mg/dl,治疗组之间无显著差异。平均血清胆固醇为192±49mg/dl。共有56%的患者停用泼尼松,35%的患者未服用任何抗高血压药物。其他并发症包括巨细胞病毒感染——14%;新发糖尿病——16%(其中一半是可逆的);以及移植后淋巴细胞增生性疾病——1%。(摘要截选至400字)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f127/2952527/c63b44637250/nihms238077f1.jpg

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