Galimberti M, Polchi P, Lucarelli G, Giardini C, Baronciani D, Angelucci E, Politi P
Divisione Ematologica di Muraglia, Centro Trapianto Midollo Osseo Ospedale di Pesaro, Italy.
Transplantation. 1988 Mar;45(3):566-9. doi: 10.1097/00007890-198803000-00013.
This study compares the efficacy of 2 posttransplant immunosuppressive regimens for prevention of graft-versus-host disease (GVHD). Forty-four patients, ages 8-15 years, with homozygous beta thalassemia received marrow allografts from HLA-identical siblings following an ablative regimen of busulfan and cyclophosphamide. Twenty-two patients received cyclosporine (CsA) alone and 22 received cyclosporine, cyclophosphamide, and methotrexate for prophylaxis against GVHD. Two who received CsA alone have died (1 of graft rejection and 1 of acute GVHD) as did 4 patients who received 3 drugs (1 of rejection, 1 of acute GVHD, 1 of infection and cardiac failure before engraftment, and 1 of acute respiratory failure before engraftment). One patient in each group rejected the transplant and survives with thalassemia. The probability of developing acute GVHD was 41% for the CsA group and 15% for the 3-drug group (P = less than 0.05). Patients receiving CsA alone had a probability of event-free survival of 86% compared to 77% in the group receiving 3 drugs (P = 0.40) with a followup of 209-706 days. Although the study showed a decrease in the incidence of GVHD in recipients of the more intensive prophylactic regimen, this study was terminated since it was apparent that even if larger numbers of patients were studied it would be difficult to demonstrate a significant survival advantage with the use of this drug regimen.
本研究比较了两种移植后免疫抑制方案预防移植物抗宿主病(GVHD)的疗效。44例8至15岁的纯合子β地中海贫血患者,在接受白消安和环磷酰胺清髓方案后,接受了来自HLA相合同胞的骨髓移植。22例患者单独接受环孢素(CsA)治疗,22例患者接受环孢素、环磷酰胺和甲氨蝶呤预防GVHD。单独接受CsA治疗的患者中有2例死亡(1例死于移植排斥,1例死于急性GVHD),接受三种药物治疗的患者中有4例死亡(1例死于排斥,1例死于急性GVHD,1例在植入前死于感染和心力衰竭,1例在植入前死于急性呼吸衰竭)。每组各有1例患者移植失败,存活下来并患有地中海贫血。CsA组发生急性GVHD的概率为41%,三联药物组为15%(P<0.05)。单独接受CsA治疗的患者无事件生存率为86%,而接受三种药物治疗的患者为77%(P = 0.40),随访时间为209至706天。尽管该研究表明更强化预防方案的接受者中GVHD的发生率有所降低,但该研究已终止,因为很明显,即使研究更多患者,使用该药物方案也难以证明有显著的生存优势。