Nakamura Miwa, Ohba Takashi, Sasaki Rumi, Saito Fumitaka, Yamaguchi Munekage, Motohara Takeshi, Mabe Hiroyo, Lu Xi, Katabuchi Hidetaka, Kondoh Eiji
Department of Obstetrics and Gynecology, Faculty of Life Sciences, Kumamoto University, 1-1-1, Honjo, Chuo-Ku, Kumamoto City, Kumamoto, 860-8556, Japan.
Department of Pediatrics, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Int J Clin Oncol. 2023 Nov;28(11):1563-1572. doi: 10.1007/s10147-023-02405-y. Epub 2023 Aug 30.
Hypogonadism is a significant late complication in childhood cancer survivors (CCS). The aim of this study was to elucidate the advantages and limitations of estrogen replacement therapy (ERT) for CCS with hypogonadism.
Seventeen CCS were divided into two groups: gonadal hypogonadism (GH) group (n = 8) and central hypogonadism (CH) group (n = 9). Pearson correlation coefficients were used to investigate the impact of cancer management on final height, bone density, and uterine development.
Seven of GH group had hematologic malignancies, and all of them underwent total body irradiation before bone marrow transplantation. The GH group showed significant positive correlations between the onset age of disease treatment and final height (p < 0.05, R = 0.712) and uterine size following ERT (p < 0.05, R = 0.775). All CCS in the CH group had brain tumors, and seven of them received chemotherapy. There were trends towards positive and negative correlations between the onset age of disease treatment and final height (p = 0.09, R = 0.598) or uterine size (p = 0.07, R = - 0.669), respectively. A negative correlation trend was observed between the age at ERT initiation and final height (p = 0.07, R = - 0.769) or bone density (p = 0.18, R = - 0.626) in six CH patients who received growth hormone therapy. Five CCS in both groups experienced osteoporosis, despite receiving ERT.
Individualized management strategies beyond ERT are essential to reduce long-term complications in CCS with hypogonadism, considering the type and timing of cancer treatment.
性腺功能减退是儿童癌症幸存者(CCS)中一种重要的晚期并发症。本研究的目的是阐明雌激素替代疗法(ERT)对性腺功能减退的CCS的优缺点。
17例CCS被分为两组:性腺性性腺功能减退(GH)组(n = 8)和中枢性性腺功能减退(CH)组(n = 9)。采用Pearson相关系数研究癌症治疗对最终身高、骨密度和子宫发育的影响。
GH组7例患有血液系统恶性肿瘤,均在骨髓移植前接受了全身照射。GH组疾病治疗开始年龄与最终身高(p < 0.05,R = 0.712)以及ERT后子宫大小之间存在显著正相关(p < 0.05,R = 0.775)。CH组所有CCS均患有脑肿瘤,其中7例接受了化疗。疾病治疗开始年龄与最终身高(p = 0.09,R = 0.598)或子宫大小(p = 0.07,R = -0.669)之间分别存在正相关和负相关趋势。在6例接受生长激素治疗的CH患者中,ERT开始年龄与最终身高(p = 0.07,R = -0.769)或骨密度(p = 0.18,R = -0.626)之间观察到负相关趋势。两组中有5例CCS尽管接受了ERT仍发生了骨质疏松。
考虑到癌症治疗的类型和时机,除ERT外的个体化管理策略对于减少性腺功能减退的CCS的长期并发症至关重要。