Przepiorka D, Ippoliti C, Panina A, Goodrich J, Giralt S, van Besien K, Mehra R, Deisseroth A B, Andersson B, Luna M
University of Texas M.D. Anderson Cancer Center, Department of Hematology, Houston.
Bone Marrow Transplant. 1994 Apr;13(4):461-4.
To determine if ganciclovir given three times per week post-transplant is tolerable and effective for prevention of cytomegalovirus (CMV) infection in recipients of T cell-depleted marrow from related or unrelated donors, we have used ganciclovir 2.5 mg/kg iv three times daily on days -8 to -2 and 5 or 6 mg/kg iv 3 times per week from engraftment to day 100 as CMV prophylaxis for 51 adults who were CMV-seropositive or had seropositive donors. All patients received iv immunoglobulin 500 mg/kg weekly and CMV-negative or filtered blood products. Blood and urine were tested for CMV at weekly intervals through day 100. All patients received ganciclovir pre-transplant. Ten patients did not receive ganciclovir post-transplant (5 deaths, 3 graft failure, 1 renal failure, 1 required foscarnet). The median time to initiation of ganciclovir was 27 days (range 17-59 days) and the median duration of therapy was 51 days (range 5-83 range). Twelve patients had dose reductions (3 neutropenia and 9 renal insufficiency). Seven patients died before day 100, 2 had indications to change to foscarnet, 15 discontinued ganciclovir because of neutropenia and 17 completed the full ganciclovir course through day 100. G- or GM-CSF was given to 29 patients with neutrophils < 1.5 x 10(9)/l (10 had neutrophils < 0.5 x 10(9)/l) but only 12 of them could continue full-dose ganciclovir. Bacteremia occurred in 12 of the neutropenic patients. At day 120, the actuarial rate of CMV infection was 58% (95% CI 42-74%) and that of CMV disease was 36% (95% CI 21-51%).(ABSTRACT TRUNCATED AT 250 WORDS)
为确定移植后每周三次给予更昔洛韦预防巨细胞病毒(CMV)感染对接受来自相关或无关供体的T细胞去除骨髓移植受者是否耐受且有效,我们对51名CMV血清学阳性或供体血清学阳性的成年患者,在移植前8至2天每天静脉注射更昔洛韦2.5mg/kg,共3次,移植后从植入至第100天每周静脉注射5或6mg/kg,共3次,作为CMV预防措施。所有患者每周接受静脉注射免疫球蛋白500mg/kg以及CMV阴性或经过滤的血液制品。在第100天前每周检测血液和尿液中的CMV。所有患者移植前均接受更昔洛韦治疗。10名患者移植后未接受更昔洛韦治疗(5例死亡,3例移植失败,1例肾衰竭,1例需要膦甲酸钠治疗)。开始使用更昔洛韦的中位时间为27天(范围17 - 59天),中位治疗持续时间为51天(范围5 - 83天)。12名患者减少了剂量(3例中性粒细胞减少和9例肾功能不全)。7名患者在第100天前死亡,2例有改用膦甲酸钠的指征,15例因中性粒细胞减少停用更昔洛韦,17例至第100天完成了整个更昔洛韦疗程。29名中性粒细胞<1.5×10⁹/L的患者接受了G - 或GM - CSF治疗(10名患者中性粒细胞<0.5×10⁹/L),但其中只有12名患者能够继续使用全剂量更昔洛韦。12名中性粒细胞减少患者发生了菌血症。在第120天,CMV感染的精算发生率为58%(95%可信区间42 - 74%),CMV疾病的发生率为36%(95%可信区间21 - 51%)。(摘要截断于250字)