Hazar V, Kansoy S, Küpesiz A, Aksoylar S, Kantar M, Yeşilipek A
Department of Pediatric Hematology & Oncology, Akdeniz University Medical Faculty, Antalya, Turkey.
Bone Marrow Transplant. 2004 May;33(9):931-5. doi: 10.1038/sj.bmt.1704463.
Cytomegalovirus (CMV) disease remains an important cause of morbidity and mortality in patients undergoing hematopoietic stem cell transplantation (HSCT). We evaluated high-dose acyclovir (HDACV) and pre-emptive ganciclovir to prevent CMV disease in 76 children who underwent peripheral blood stem cell transplantation (PBSCT) and were at risk for CMV reactivation and disease (both recipient and donor seropositive) from May 1998 to April 2003. All received HDACV from day -9 to 6 months post transplant in conjunction with weekly CMV pp65 antigenemia monitoring. The incidence of antigenemia in this cohort was 19.7%, at a median of 22 days post-PBSCT. The frequencies were 26.4 and 4.4% in allogeneic and autologous groups, respectively (P=0.03). Patients with nonmalignant disease had higher CMV antigenemia than those with malignant disease (30.8 vs 8.1%, P=0.02). Age at PBSCT, sex, graft-versus-host disease (GVHD) prophylaxis regimen and presence of acute GVHD did not affect the risk of CMV antigenemia. None of the patients who had positive pp65 antigenemia developed CMV disease during the study period. We conclude that pp65 antigenemia-guided HDACV and pre-emptive ganciclovir may prevent CMV disease in children undergoing PBSCT.
巨细胞病毒(CMV)疾病仍然是接受造血干细胞移植(HSCT)患者发病和死亡的重要原因。我们评估了大剂量阿昔洛韦(HDACV)和抢先使用更昔洛韦,以预防1998年5月至2003年4月期间76例接受外周血干细胞移植(PBSCT)且有CMV再激活和疾病风险(受者和供者血清学均为阳性)的儿童发生CMV疾病。所有患者在移植后第-9天至6个月接受HDACV治疗,并每周进行CMV pp65抗原血症监测。该队列中抗原血症的发生率为19.7%,中位时间为PBSCT后22天。在异基因和自体组中的发生率分别为26.4%和4.4%(P=0.03)。非恶性疾病患者的CMV抗原血症高于恶性疾病患者(30.8%对8.1%,P=0.02)。PBSCT时的年龄、性别、移植物抗宿主病(GVHD)预防方案以及急性GVHD的存在均不影响CMV抗原血症的风险。在研究期间,pp65抗原血症呈阳性的患者均未发生CMV疾病。我们得出结论,pp65抗原血症指导下的HDACV和抢先使用更昔洛韦可能预防接受PBSCT儿童的CMV疾病。