Hill Garick, Chauvenet Allen R, Lovato James, McLean Thomas W
Department of Pediatrics, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
Pediatrics. 2005 Oct;116(4):e525-9. doi: 10.1542/peds.2005-0219.
The varicella-zoster virus (VZV) continues to be a dangerous pathogen to immunocompromised children. Children with acute lymphoblastic leukemia (ALL) are treated with intermittent steroid therapy. This study was undertaken to examine the relationship between steroid therapy for ALL and severity of varicella infection.
We performed a retrospective review of patients who were on Pediatric Oncology Group Protocol 9201 and had a history of varicella infection. Pediatric Oncology Group 9201 is a phase III study for the treatment of children with lesser risk ALL diagnosed between 1992 and 1999. Cases of varicella were coded 1 to 5 on the basis of severity: grade 1 caused minimal to no symptoms, grade 2 caused mild to moderate symptoms that did not require hospitalization, grade 3 caused symptoms severe enough to require hospitalization and intravenous acyclovir, grade 4 caused severe disease that had complications or that required intensive care, and grade 5 resulted in death.
Of 697 enrolled patients, 110 (15.8%) developed primary varicella; 59% of these were male. For analysis, disease grade was dichotomized into nonsevere (grades 1 and 2) and severe (grades 3, 4, and 5). Of the 110 patients, 56 had nonsevere disease; 54 had severe disease, including 2 deaths. Of the patients whose varicella was diagnosed within 3 weeks of receipt of prednisone, 70% had severe infection, whereas only 44% of those who had not received prednisone within 3 weeks had severe infection. The odds ratio for having a severe infection within 3 weeks of prednisone versus >3 weeks is 2.9 (95% confidence interval: 1.1-7.9). By multivariate analysis, older age at ALL diagnosis, years from ALL diagnosis to VZV diagnosis, and VZV diagnosis within the 4-week period of interest (during or within 3 weeks of prednisone therapy) all were independently associated with an increased risk for severe infection.
This study represents the largest study to date of varicella in children with ALL and provides convincing evidence that prednisone therapy during the VZV incubation period significantly increases the risk for developing severe varicella infection. In addition, older age is associated with more severe infection. Despite the varicella vaccine and a dropping incidence of primary infections, VZV remains a dangerous pathogen for pediatric patients with ALL. With the possible exception of induction therapy, patients who are on ALL therapy and are exposed to varicella should have steroid therapy delayed until after the VZV incubation period. These findings may have implications for other diseases that are treated with corticosteroids.
水痘带状疱疹病毒(VZV)对免疫功能低下的儿童仍然是一种危险的病原体。急性淋巴细胞白血病(ALL)患儿接受间歇性类固醇治疗。本研究旨在探讨ALL的类固醇治疗与水痘感染严重程度之间的关系。
我们对参加儿童肿瘤学组方案9201且有水痘感染病史的患者进行了回顾性研究。儿童肿瘤学组9201是一项针对1992年至1999年间诊断为低风险ALL的儿童进行治疗的III期研究。根据严重程度将水痘病例编码为1至5级:1级引起轻微至无症状,2级引起轻度至中度症状且无需住院,3级引起严重到需要住院和静脉注射阿昔洛韦的症状,4级引起有并发症或需要重症监护的严重疾病,5级导致死亡。
在697名登记患者中,110名(15.8%)发生原发性水痘;其中59%为男性。为了进行分析,将疾病分级分为非严重(1级和2级)和严重(第3、4和5级)。在这110名患者中,56名患有非严重疾病;54名患有严重疾病,包括2例死亡。在接受泼尼松治疗后3周内诊断出水痘的患者中,70%有严重感染,而在3周内未接受泼尼松治疗的患者中只有44%有严重感染。泼尼松治疗后3周内发生严重感染与>3周的比值比为2.9(95%置信区间:1.1 - 7.9)。通过多变量分析,ALL诊断时年龄较大、从ALL诊断到VZV诊断的年数以及在感兴趣的4周期间(泼尼松治疗期间或治疗后3周内)诊断出VZV均与严重感染风险增加独立相关。
本研究是迄今为止关于ALL患儿水痘的最大规模研究,并提供了令人信服的证据,即VZV潜伏期的泼尼松治疗显著增加了发生严重水痘感染的风险。此外,年龄较大与更严重的感染相关。尽管有水痘疫苗且原发性感染发病率下降,但VZV对ALL儿科患者仍然是一种危险的病原体。除诱导治疗可能例外,接受ALL治疗且接触水痘的患者应将类固醇治疗推迟至VZV潜伏期之后。这些发现可能对其他用皮质类固醇治疗的疾病有影响。