Nash R A, Antin J H, Karanes C, Fay J W, Avalos B R, Yeager A M, Przepiorka D, Davies S, Petersen F B, Bartels P, Buell D, Fitzsimmons W, Anasetti C, Storb R, Ratanatharathorn V
Clinical Research Division, Fred Hutchinson Cancer Research Center, and the Department of Medicine, University of Washington, Seattle, WA, USA.
Blood. 2000 Sep 15;96(6):2062-8.
After the transplantation of unmodified marrow from human leukocyte antigen-matched unrelated donors receiving cyclosporine (CSP) and methotrexate (MTX), the incidence of acute graft-versus-host disease (GVHD) is greater than 75%. Tacrolimus is a macrolide compound that, in previous preclinical and clinical studies, was effective in combination with MTX for the prevention of acute GVHD. Between March 1995 and September 1996, 180 patients were randomized in a phase 3, open-label, multicenter study to determine whether tacrolimus combined with a short course of MTX (n = 90), more than CSP and a short course of MTX (n = 90), would reduce the incidence of acute GVHD after marrow transplantation from unrelated donors. There was a significant trend toward decreased severity of acute GVHD across all grades (P =.005). Based on the Kaplan-Meier estimate, the probability of grade II-IV acute GVHD in the tacrolimus group (56%) was significantly lower than in the CSP group (74%; P =.0002). Use of glucocorticoids for the management of GVHD was significantly lower with tacrolimus than with CSP (65% vs 81%, respectively; P =. 019). The number of patients requiring dialysis in the first 100 days was similar (tacrolimus, 9; CSP, 8). Overall and relapse-free survival rates for the tacrolimus and CSP arms at 2 years was 54% versus 50% (P =.46) and 47% versus 42% (P =.58), respectively. The combination of tacrolimus and MTX after unrelated donor marrow transplantation significantly decreased the risk for acute GVHD than did the combination of CSP and MTX, with no significant increase in toxicity, infections, or leukemia relapse.
在接受环孢素(CSP)和甲氨蝶呤(MTX)治疗的人类白细胞抗原匹配的无关供体的未修饰骨髓移植后,急性移植物抗宿主病(GVHD)的发生率大于75%。他克莫司是一种大环内酯类化合物,在先前的临床前和临床研究中,与MTX联合使用对预防急性GVHD有效。在1995年3月至1996年9月期间,180名患者被随机纳入一项3期、开放标签、多中心研究,以确定他克莫司联合短疗程MTX(n = 90)是否比CSP联合短疗程MTX(n = 90)能降低无关供体骨髓移植后急性GVHD的发生率。所有分级的急性GVHD严重程度均有显著降低趋势(P =.005)。根据Kaplan-Meier估计,他克莫司组II-IV级急性GVHD的发生率(56%)显著低于CSP组(74%;P =.0002)。他克莫司用于治疗GVHD的糖皮质激素使用量显著低于CSP(分别为65%和81%;P =.019)。前100天需要透析的患者数量相似(他克莫司组9例,CSP组8例)。他克莫司组和CSP组2年时的总生存率和无复发生存率分别为54%对50%(P =.46)和47%对42%(P =.58)。无关供体骨髓移植后他克莫司与MTX联合使用比CSP与MTX联合使用显著降低了急性GVHD的风险,且毒性、感染或白血病复发无显著增加。