Gonadal failure among female patients after hematopoietic stem cell transplantation for non-malignant diseases

IF 1 Q4 ENDOCRINOLOGY & METABOLISM
Akito Sutani, Yuichi Miyakawa, Atsumi Tsuji‐Hosokawa, Risa Nomura, Ryuichi Nakagawa, Keisuke Nakajima, M. Maru, Y. Aoki, K. Takasawa, M. Takagi, K. Imai, K. Kashimada, T. Morio
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引用次数: 4

Abstract

Abstract. In addition to malignant diseases, hematopoietic stem cell transplantation (HSCT) is also a vital option as a curative therapy for non-malignant diseases, such as immunodeficiency, and other hematological disorders. Not only for malignant diseases, but for non-malignant diseases, cytotoxic therapy of conditioning regimens are associated with high risks of adverse effects; however, clinical details regarding the long term outcomes of cytotoxic therapy for non-malignant diseases are not documented yet. To clarify the endocrinological consequences of pediatric HSCT for non-malignant disease patients, we conducted a retrospective analysis. From 1983 to 2014, 75 patients that underwent HSCT for non-malignant diseases were selected for this study. Of these, 23 patients (19 men, 4 women) were continuously followed up in our institute, with regular health check-ups for late effects. Based on a multiple linear regression analysis, the glucocorticoid treatment duration for chronic graft-versus-host disease (cGVHD) and the conditioning regimen were found to be independent predictors of growth retardation. All four female patients developed hypogonadism, and required hormone replacement therapy. The conditioning regimen for the four female patients with hypogonadism was based on the use of alkylating agents, and two female patients were treated with a reduced-intensity conditioning (RIC) regimen. Our study revealed that even the RIC regimen was toxic for the gonads in female patients, and that the survivors of both non-malignant and malignant diseases should be followed up carefully after pediatric HSCT.
非恶性疾病女性患者造血干细胞移植后性腺功能衰竭
摘要除了恶性疾病外,造血干细胞移植(HSCT)也是治疗非恶性疾病(如免疫缺陷和其他血液系统疾病)的重要选择。不仅对于恶性疾病,对于非恶性疾病,条件治疗方案的细胞毒性治疗也与不良反应的高风险相关;然而,关于非恶性疾病细胞毒性治疗的长期结果的临床细节尚未记录在案。为了阐明儿科HSCT对非恶性疾病患者的内分泌影响,我们进行了回顾性分析。从1983年到2014年,本研究选择了75名因非恶性疾病接受HSCT的患者。其中,23名患者(19名男性,4名女性)在我们的研究所接受了持续随访,并定期对晚期影响进行健康检查。基于多元线性回归分析,发现慢性移植物抗宿主病(cGVHD)的糖皮质激素治疗持续时间和调理方案是生长迟缓的独立预测因素。所有四名女性患者均出现性腺功能减退,需要激素替代治疗。四名患有性腺功能减退症的女性患者的调理方案是基于烷基化剂的使用,两名女性患者接受了低强度调理(RIC)方案的治疗。我们的研究表明,即使是RIC方案也对女性患者的性腺有毒,非恶性和恶性疾病的幸存者在儿童HSCT后应仔细随访。
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来源期刊
Clinical Pediatric Endocrinology
Clinical Pediatric Endocrinology ENDOCRINOLOGY & METABOLISM-
CiteScore
2.40
自引率
7.10%
发文量
34
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