Division of Infectious Diseases, Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA.
Pediatric Immunocompromised Host Program, Division of Infectious Diseases, Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA.
Transpl Infect Dis. 2021 Apr;23(2):e13505. doi: 10.1111/tid.13505. Epub 2020 Nov 29.
Adenovirus disease (ADVd) is a significant burden in pediatric hematopoietic stem cell transplant (HSCT) recipients. However, current knowledge of risk factors associated with poor clinical outcome and the effectiveness of antiviral therapy are not well understood. This study determined the relationship between transplant characteristics and risk of ADVd and also compared time to resolution of disease between pediatric patients who did and did not receive antiviral therapy.
We conducted a retrospective, single-center cohort study of pediatric patients undergoing HSCT at Duke University (2005-2016). Cases of ADVd were defined a priori using a classification tool. Cox proportional hazards (CPH) regression models were used to compare the hazard of ADVd between HSCT recipients differing by type of transplant and type of conditioning regimen. The hazard of time to resolution of ADVd by antiviral therapy (cidofovir, brincidofovir, both, or neither) was compared.
Ninety-three of 830 subjects had ADVd post-HSCT (11.2%). Umbilical cord transplant (UCT) recipients had 2.30 (95% CI 1.57, 6.90, P = .002) higher hazard of developing ADVd compared to non-cord allogeneic transplants, and 6.30 higher (95% CI 2.70, 19.61, P < .001) hazard compared to autologous transplants. Subjects who did not receive antiviral therapy experienced earlier resolution of ADVd compared to subjects who received therapy, even after adjusting for subjects with disseminated disease (HR [95% CI]: 3.75 [1.57, 8.93], P = .003).
Pediatric UCT recipients are at a higher risk for ADVd. Antiviral therapy was not associated with an earlier resolution of ADVd, even in patients with higher disease burden.
腺病毒病(ADVd)是儿科造血干细胞移植(HSCT)受者的重大负担。然而,目前对与不良临床结局相关的风险因素以及抗病毒治疗的有效性的了解并不充分。本研究确定了移植特征与 ADVd 风险之间的关系,并比较了接受和未接受抗病毒治疗的儿科患者疾病缓解时间。
我们对杜克大学(2005-2016 年)进行的儿科 HSCT 患者进行了回顾性、单中心队列研究。ADVd 病例是使用分类工具预先定义的。使用 Cox 比例风险(CPH)回归模型比较不同类型移植和不同类型预处理方案的 HSCT 受者 ADVd 的风险。比较抗病毒治疗(cidofovir、brincidofovir、两者或两者都不)对 ADVd 缓解时间的风险。
830 例患者中有 93 例(11.2%)在 HSCT 后发生 ADVd。与非脐带同种异体移植相比,脐带移植(UCT)受者 ADVd 的发生风险高 2.30 倍(95%CI 1.57,6.90,P=0.002),与自体移植相比,风险高 6.30 倍(95%CI 2.70,19.61,P<0.001)。与接受治疗的患者相比,未接受抗病毒治疗的患者 ADVd 更早得到缓解,即使在调整了播散性疾病的患者后也是如此(HR[95%CI]:3.75[1.57,8.93],P=0.003)。
儿科 UCT 受者 ADVd 的风险较高。抗病毒治疗与 ADVd 的更早缓解无关,即使在疾病负担较高的患者中也是如此。