Marr K A, Seidel K, Slavin M A, Bowden R A, Schoch H G, Flowers M E, Corey L, Boeckh M
Fred Hutchinson Cancer Research Center and the University of Washington, Seattle, WA 98109-1024, USA.
Blood. 2000 Sep 15;96(6):2055-61.
Two randomized, placebo-controlled trials previously showed that fluconazole (400 mg/d) administered prophylactically decreases the incidence of candidiasis in blood and marrow transplant (BMT) recipients. However, there exists conflicting data regarding the optimal duration of fluconazole administration, specifically whether prophylaxis through acute graft-versus-host disease (GVHD) results in improved survival in allograft recipients. Reported here are the results of long-term follow-up and a detailed analysis of invasive candidiasis and candidiasis-related death in 300 patients who received fluconazole (400 mg/d) or placebo for 75 days after BMT at the Fred Hutchinson Cancer Research Center. Patients in both treatment arms were compared for survival, causes of death, and the incidence of invasive fungal infections early (less than 110 days) and late (more than 110 days) after BMT. After 8 years of follow-up, survival is significantly better in fluconazole recipients compared with placebo recipients (68 of 152 vs 41 of 148, P =.0001). The overall incidence of invasive candidiasis was increased in patients who received placebo compared with fluconazole (30 of 148 vs 4 of 152, P <.001). More patients who received placebo died with candidiasis early (13 of 148 vs 1 of 152, P =.001) and late (8 of 96 vs 1 of 121, P =.0068) after BMT. The incidence of severe GVHD involving the gut was higher in patients who did not receive fluconazole (20 of 143 vs 8 of 145, P =.02), and fewer patients who received fluconazole died with this complication. Thus, administration of fluconazole (400 mg/d) for 75 days after BMT appears to be associated with decreased gut GVHD, a persistent protection against disseminated candidal infections and candidiasis-related death, resulting in an overall survival benefit in allogeneic BMT recipients.
两项随机、安慰剂对照试验先前表明,预防性给予氟康唑(400毫克/天)可降低血液和骨髓移植(BMT)受者念珠菌病的发病率。然而,关于氟康唑给药的最佳持续时间,特别是通过急性移植物抗宿主病(GVHD)进行预防是否能提高同种异体移植受者的生存率,存在相互矛盾的数据。本文报告了弗雷德·哈钦森癌症研究中心300例BMT后接受氟康唑(400毫克/天)或安慰剂治疗75天的患者的长期随访结果以及对侵袭性念珠菌病和念珠菌病相关死亡的详细分析。比较了两个治疗组患者BMT后早期(少于110天)和晚期(超过110天)的生存率、死亡原因以及侵袭性真菌感染的发生率。经过8年的随访,氟康唑治疗组患者的生存率明显高于安慰剂治疗组(152例中的68例对148例中的41例,P = 0.0001)。与氟康唑治疗组相比,接受安慰剂治疗的患者侵袭性念珠菌病的总体发病率有所增加(148例中的30例对152例中的4例,P < 0.001)。更多接受安慰剂治疗的患者在BMT后早期(148例中的13例对152例中的1例,P = 0.001)和晚期(96例中的8例对121例中的1例,P = 0.0068)死于念珠菌病。未接受氟康唑治疗的患者发生涉及肠道的严重GVHD的发生率较高(143例中的20例对145例中的8例,P = 0.02),接受氟康唑治疗的患者死于这种并发症的较少。因此,BMT后给予氟康唑(400毫克/天)75天似乎与肠道GVHD的减少、对播散性念珠菌感染和念珠菌病相关死亡的持续保护有关,从而使同种异体BMT受者的总体生存受益。