Bresters Dorine, Emons Joyce A M, Nuri Nardin, Ball Lynne M, Kollen Wouter J W, Hannema Sabine E, Bakker-Steeneveld Johanna D J, van der Bom Johanna G, Oostdijk Wilma
Leiden University Medical Center (LUMC), Willem-Alexander Children's Hospital, Leiden, The Netherlands.
Pediatr Blood Cancer. 2014 Nov;61(11):2048-53. doi: 10.1002/pbc.25162. Epub 2014 Aug 11.
Ovarian insufficiency (OI) and infertility are common and devastating late effects of cancer treatment and hematopoietic stem cell transplantation (HSCT). In children, gonadal insufficiency may subsequently lead to abnormal pubertal development. The aim of this study was to assess the cumulative incidence of OI and the need for hormonal induction of pubertal development after HSCT in childhood. We additionally assessed HSCT-related risk factors for OI.
A single center cohort study was undertaken of female patients transplanted during childhood, surviving at least 2 years post-HSCT and who were at least 10 years old at initiation of the study. Of 141 eligible patients, 109 were included and hormone levels and clinical data of these patients during follow-up were collected. Risk factors for OI were analyzed by multivariate Cox regression analysis.
Cumulative incidence of OI was 56% at a median follow-up of 7.2 years. Eight patients, initially diagnosed with OI, showed recovery of ovarian function over time. Hormonal induction of puberty was necessary in 44% of females who were pre-pubertal or pubertal at HSCT. In multivariate analysis, more advanced pubertal stage at HSCT was associated with OI. We found a trend for an association of busulfan with OI in patients conditioned with chemotherapy only.
The incidence of OI after HSCT was high and associated with more advanced pubertal stage at HSCT. Almost half of the females who were pre-pubertal or pubertal at HSCT required hormonal induction of pubertal development.
卵巢功能不全(OI)和不孕是癌症治疗及造血干细胞移植(HSCT)常见且严重的晚期影响。在儿童中,性腺功能不全随后可能导致青春期发育异常。本研究的目的是评估儿童HSCT后OI的累积发生率以及青春期发育激素诱导的必要性。我们还评估了与HSCT相关的OI危险因素。
对童年期接受移植、HSCT后存活至少2年且在研究开始时至少10岁的女性患者进行了单中心队列研究。在141名符合条件的患者中,纳入了109名,并收集了这些患者随访期间的激素水平和临床数据。通过多变量Cox回归分析分析OI的危险因素。
在中位随访7.2年时,OI的累积发生率为56%。最初诊断为OI的8名患者随着时间推移卵巢功能恢复。在HSCT时处于青春期前或青春期的女性中,44%需要进行青春期激素诱导。在多变量分析中,HSCT时青春期阶段越高级与OI相关。在仅接受化疗预处理的患者中,我们发现白消安与OI存在关联趋势。
HSCT后OI的发生率很高,且与HSCT时更高级的青春期阶段相关。在HSCT时处于青春期前或青春期的女性中,近一半需要进行青春期发育的激素诱导。