Tufts Clinical and Translational Science Institute, Tufts University, Boston, Massachusetts, USA.
Biol Blood Marrow Transplant. 2011 Jul;17(7):1012-7. doi: 10.1016/j.bbmt.2010.10.025. Epub 2010 Oct 25.
Although the use of nonmyeloablative (NMA) hematopoietic stem cell transplantation (HSCT) regimens has expanded in the past decade, little data exist to support antiviral prophylaxis to prevent herpes zoster (HZ) in recipients who are seropositive for varicella-zoster virus in this population. The present study examined the clinical features, incidence, and risk factors for HZ in a homogeneous cohort of NMA allogeneic HSCT recipients. We conducted a retrospective cohort study assessing all patients who underwent sibling NMA HSCT at Maisonneuve-Rosemont Hospital (Montreal) between July 2000 and December 2008. All patients received the same conditioning regimen, immunoprophylaxis, and graft-versus-host disease therapy. The diagnosis of HZ was defined clinically. Factors associated with HZ were identified using a Cox proportional hazards model. A total of 179 patients were followed for a median of 33 months (interquartile range, 21-59). HZ developed in 66 patients (37%) at a median of 8.3 months post-HSCT; the incidence rate was 175 cases/1000 person-years. The estimated cumulative HZ incidence was 27% at 1 year, 36% at 2 years, and 44% at 3 years. Thoracic dermatomes were most frequently involved (30%); dissemination occurred in 5 patients. No deaths resulted from HZ, but 23% of patients developed postherpetic neuralgia. In multivariate analysis, reactivation of cytomegalovirus and herpes simplex virus was associated with a reduced likelihood of HZ (hazard ratio, 0.54 and 0.33, respectively). Antiviral prophylaxis or treatment for cytomegalovirus and herpes simplex virus reactivations were protective against HZ. The incidence of HZ in our cohort of NMA HSCT recipients is similar to the incidence reported in HSCT recipients who received a myeloablative conditioning regimen. Given the observed high risk, we conclude that recommendations for antiviral prophylaxis should apply, at least for the first year, to the NMA HSCT population as well.
尽管在过去十年中,非清髓性(NMA)造血干细胞移植(HSCT)方案的应用已经扩大,但在该人群中,针对血清水痘带状疱疹病毒阳性的接受者,预防带状疱疹(HZ)的抗病毒预防的数据很少。本研究检查了同质 NMA 同种异体 HSCT 受者队列中 HZ 的临床特征、发生率和危险因素。我们进行了一项回顾性队列研究,评估了 2000 年 7 月至 2008 年 12 月期间在 Maisonneuve-Rosemont 医院(蒙特利尔)接受同胞 NMA HSCT 的所有患者。所有患者均接受相同的预处理方案、免疫预防和移植物抗宿主病治疗。HZ 的诊断通过临床定义。使用 Cox 比例风险模型确定与 HZ 相关的因素。共有 179 例患者接受了中位 33 个月(四分位距,21-59)的随访。HSCT 后中位 8.3 个月时,66 例(37%)患者出现 HZ;发病率为 175 例/1000 人年。估计 1 年、2 年和 3 年的累积 HZ 发生率分别为 27%、36%和 44%。胸皮节最常受累(30%);5 例发生播散。没有因 HZ 而死亡,但 23%的患者出现带状疱疹后神经痛。多变量分析显示,巨细胞病毒和单纯疱疹病毒的再激活与 HZ 的可能性降低相关(风险比分别为 0.54 和 0.33)。抗病毒预防或治疗巨细胞病毒和单纯疱疹病毒再激活可预防 HZ。我们的 NMA HSCT 受者队列中 HZ 的发生率与接受清髓性预处理方案的 HSCT 受者报告的发生率相似。鉴于观察到的高风险,我们得出结论,至少在第一年,NMA HSCT 人群也应该推荐抗病毒预防。