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Adverse health events and late mortality after pediatric allogeneic hematopoietic SCT-two decades of longitudinal follow-up

机译:小儿同种异体造血干细胞移植后的不良健康事件和晚期死亡率-纵向随访二十年

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Treatment-related late toxicities after pediatric allogeneic hematopoietic SCT (allo-HSCT) are increasingly important as long-term survival has become an expected outcome for many transplanted children and adolescents. In a retrospective cohort study, we assessed long-term health outcomes in 204 allo-HSCT survivors transplanted in childhood or adolescence (<20 years) between 1978 through 2000 after a median follow-up time of 12 (range 4-28) years. Data on conditioning regimen, adverse health events (AE) and growth and hormonal substitutions (hormone replacement therapies (HRTs)) were obtained from medical records. AEs were graded retrospectively according to Common Terminology Criteria for Adverse Events v3.0. Late deaths (>= 48 months after allo-HSCT) were evaluated separately. Multivariate analysis demonstrated that chronic GVHD (P<0.000) and longer follow-up time (P<0.05) correlated with AEs, whereas CY-based conditioning was inversely correlated (P<0.002). TBI and longer follow-up duration predicted more severe AEs (P<0.001 and P<0.001, respectively). HRTs were more frequent after TBI. Diabetes type II, dyslipidemia and hypertension were detected in 9, 7 and 7% of the survivors, respectively. Late deaths (n = 22) were most frequently due to pulmonary failure (n = 7), followed by secondary malignancy (n = 5). The occurrence of AEs after pediatric allo-HSCT is high and likely to increase during extended follow-up, particularly in patients who have received TBI.
机译:小儿同种异体造血干细胞移植(allo-HSCT)后与治疗有关的后期毒性变得越来越重要,因为长期存活已成为许多移植儿童和青少年的预期结果。在一项回顾性队列研究中,我们评估了中位随访时间为12年(4至28岁)的1978年至2000年之间,在1978年至2000年之间儿童或青少年期(<20岁)移植的204名同种HSCT幸存者的长期健康结果。有关调理方案,不良健康事件(AE)以及生长和激素替代(激素替代疗法(HRT))的数据均来自医疗记录。根据不良事件通用术语标准v3.0对不良事件进行回顾性分级。晚期死亡(> -HSCT后> = 48个月)分别进行评估。多变量分析表明,慢性GVHD(P <0.000)和较长的随访时间(P <0.05)与不良事件相关,而基于CY的条件则呈负相关(P <0.002)。 TBI和更长的随访时间预示着更严重的不良事件(分别为P <0.001和P <0.001)。 TBI后HRT更为频繁。分别在9、7和7%的幸存者中发现了II型糖尿病,血脂异常和高血压。晚期死亡(n = 22)最常归因于肺衰竭(n = 7),其次是继发性恶性肿瘤(n = 5)。小儿同种异体造血干细胞移植术后不良事件的发生率很高,并且在延长的随访期间可能增加,特别是在接受TBI的患者中。

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