Ljungman P, Aschan J, Lewensohn-Fuchs I, Carlens S, Larsson K, Lönnqvist B, Mattsson J, Sparrelid E, Winiarski J, Ringdén O
Department of Hematology, Huddinge University Hospital, Karolinska Institutet, Sweden.
Transplantation. 1998 Nov 27;66(10):1330-4. doi: 10.1097/00007890-199811270-00012.
Several preventive strategies against cytomegalovirus (CMV) disease have been developed during the last decade. These have frequently been used in combination, and it has been difficult to identify each strategy's contribution.
Risk factors for CMV disease, death in CMV disease and transplant-related mortality were analyzed in 584 patients, who underwent a total of 594 allogeneic bone marrow transplants.
The overall probability of CMV disease was 8.9%. No seronegative patient who had a seronegative marrow donor developed CMV disease. The corresponding probabilities for seronegative patients with seropositive donors, seropositive patients with seronegative donors, and seropositive patients with seropositive donors were 5.4%, 13.7%, and 11.7%, respectively. In multivariate Cox models, the use of preemptive antiviral therapy and being CMV-seronegative reduced the risk for CMV disease, CMV-associated death, and transplant-related mortality (TRM). Patients who received unrelated or mismatched family donor transplants had increased risks for CMV disease, CMV-associated death, and TRM. Older age was a significant risk factor for CMV disease and TRM. A total of 258 patients who were monitored by polymerase chain reaction for CMV DNA were analyzed separately to assess whether addition of another CMV preventive strategy could give benefit. Patients who received mismatched or unrelated donor transplants had increased risk for CMV disease, death in CMV disease, and TRM. High-dose acyclovir prophylaxis or addition of intravenous immune globulin had no influence.
Preemptive therapy based on polymerase chain reaction for CMV DNA was associated with reduced risks for CMV disease, CMV-associated death, and TRM, whereas other prophylactic modalities did not give additional benefit.
在过去十年中,已开发出几种针对巨细胞病毒(CMV)疾病的预防策略。这些策略经常联合使用,因此很难确定每种策略的贡献。
对584例接受了总共594例异基因骨髓移植的患者分析了CMV疾病的危险因素、CMV疾病死亡情况以及移植相关死亡率。
CMV疾病的总体发生率为8.9%。接受血清学阴性骨髓供体的血清学阴性患者未发生CMV疾病。接受血清学阳性供体的血清学阴性患者、接受血清学阴性供体的血清学阳性患者以及接受血清学阳性供体的血清学阳性患者的相应发生率分别为5.4%、13.7%和11.7%。在多变量Cox模型中,采用抢先抗病毒治疗以及CMV血清学阴性可降低CMV疾病、CMV相关死亡和移植相关死亡率(TRM)的风险。接受无关或不匹配的家庭供体移植的患者发生CMV疾病、CMV相关死亡和TRM的风险增加。年龄较大是CMV疾病和TRM的重要危险因素。对总共258例通过聚合酶链反应监测CMV DNA的患者进行单独分析,以评估添加另一种CMV预防策略是否有益。接受不匹配或无关供体移植的患者发生CMV疾病、CMV疾病死亡和TRM的风险增加。高剂量阿昔洛韦预防或添加静脉注射免疫球蛋白没有影响。
基于聚合酶链反应检测CMV DNA的抢先治疗与降低CMV疾病、CMV相关死亡和TRM的风险相关,而其他预防方式并未带来额外益处。