Goodrich J M, Mori M, Gleaves C A, Du Mond C, Cays M, Ebeling D F, Buhles W C, DeArmond B, Meyers J D
Fred Hutchinson Cancer Research Center, Seattle, WA 98104.
N Engl J Med. 1991 Dec 5;325(23):1601-7. doi: 10.1056/NEJM199112053252303.
Cytomegalovirus (CMV) infection is a major cause of morbidity and mortality after allogeneic bone marrow transplantation. We conducted a controlled trial of ganciclovir for the early treatment of CMV infection in asymptomatic recipients of bone marrow transplants whose surveillance cultures for CMV became positive.
Bone marrow--allograft recipients who were seropositive for CMV antibodies or who received seropositive marrow were screened for CMV excretion by culture of throat swabs, blood, urine, or bronchoalveolar-lavage fluid. In this double-blind trial, 72 patients who had marrow engraftment and were excreting virus were randomly assigned to receive either placebo or ganciclovir (5 mg per kilogram of body weight twice a day for one week, followed by 5 mg per kilogram per day) for the first 100 days after transplantation. Patients were followed for the development of biopsy-confirmed CMV disease, ganciclovir-related toxicity, and survival.
Between assignment to the study drug and day 100 after transplantation, CMV disease developed in only 1 of the 37 patients assigned to receive ganciclovir (3 percent), but in 15 of the 35 patients assigned to receive placebo (43 percent, P less than 0.00001). The ganciclovir recipients had rapid suppression of virus excretion; 85 percent had negative cultures after one week of treatment, as compared with 44 percent of the placebo group (P = 0.001). The principal toxic reaction was neutropenia; 11 ganciclovir recipients had an absolute neutrophil count below 0.75 x 10(9) per liter, as compared with 3 placebo recipients (P = 0.052). Treatment was discontinued in 11 ganciclovir recipients and 1 placebo recipient because of neutropenia (P = 0.003). After treatment was stopped, the neutrophil count recovered in all patients. Overall survival was significantly greater in the ganciclovir group than in the placebo group both 100 days and 180 days after transplantation (P = 0.041 and 0.027, respectively).
Early treatment with ganciclovir in patients with positive surveillance cultures reduces the incidence of CMV disease and improves survival after allogeneic bone marrow transplantation.
巨细胞病毒(CMV)感染是异基因骨髓移植后发病和死亡的主要原因。我们进行了一项关于更昔洛韦的对照试验,用于早期治疗CMV监测培养呈阳性的无症状骨髓移植受者的CMV感染。
对CMV抗体血清阳性或接受血清阳性骨髓的骨髓移植受者,通过咽拭子、血液、尿液或支气管肺泡灌洗液培养筛查CMV排泄情况。在这项双盲试验中,72例骨髓已植入且正在排出病毒的患者被随机分配,在移植后的前100天接受安慰剂或更昔洛韦(5毫克/千克体重,每日2次,共1周,随后5毫克/千克体重,每日1次)治疗。对患者进行随访,观察活检确诊的CMV疾病的发生、更昔洛韦相关毒性及生存情况。
在分配研究药物至移植后第100天期间,分配接受更昔洛韦治疗的37例患者中仅1例发生CMV疾病(3%),而分配接受安慰剂治疗的35例患者中有15例发生(43%,P<0.00001)。接受更昔洛韦治疗的患者病毒排泄迅速得到抑制;治疗1周后85%的患者培养结果为阴性,而安慰剂组为44%(P = 0.001)。主要毒性反应为中性粒细胞减少;11例接受更昔洛韦治疗的患者绝对中性粒细胞计数低于0.75×10⁹/L,而接受安慰剂治疗的患者有3例(P = 0.052)。11例接受更昔洛韦治疗的患者和1例接受安慰剂治疗的患者因中性粒细胞减少而停药(P = 0.003)。停药后,所有患者的中性粒细胞计数均恢复。在移植后100天和180天,更昔洛韦组的总体生存率均显著高于安慰剂组(分别为P = 0.041和0.027)。
对监测培养呈阳性的患者早期使用更昔洛韦治疗可降低异基因骨髓移植后CMV疾病的发生率并提高生存率。