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白血病骨髓移植后的生长与发育

Growth and development following marrow transplantation for leukemia.

作者信息

Sanders J E, Pritchard S, Mahoney P, Amos D, Buckner C D, Witherspoon R P, Deeg H J, Doney K C, Sullivan K M, Appelbaum F R

出版信息

Blood. 1986 Nov;68(5):1129-35.

PMID:3533180
Abstract

One hundred forty-two patients between the ages of 1 and 17 years who survived disease-free more than 1 year after marrow transplantation for hematologic malignancy had growth and development evaluations from one to 14 years posttransplant (median 4 years). Prior to transplant all children received multiagent chemotherapy and 55 also received central nervous system irradiation, but none had growth and development evaluations. Marrow transplant preparation included high-dose chemotherapy and total body irradiation (TBI) given as a single dose of 9.2 to 10.0 Gy (79 patients) or as fractionated doses of 2.0 to 2.25 Gy/d for six to seven days (63 patients). After transplant abnormal thyroid function was present in 39%. Stimulated 11-desoxycortisol levels were subnormal in 24% of patients evaluated. Growth hormone (GH) deficiency was present in 17 of 25 children who received previous cranial irradiation. Partial GH deficiency was present in 4 of 25 who received previous cranial irradiation and in 6 of 18 who had not received cranial irradiation. Height velocity was decreased in all patients. After transplant, height was significantly influenced by chronic graft-v-host disease and single-dose TBI. Sixty-eight percent had delayed development of secondary sexual characteristics. Gonadal failure occurred in nearly all who were postpubertal at transplant. While it is not possible to determine how many of these endocrine abnormalities occurred as a result of treatment administered prior to transplantation, these data do demonstrate that children who become long-term survivors after marrow transplantation for hematologic malignancy have endocrine abnormalities that adversely affect growth and development.

摘要

142例年龄在1至17岁之间、因血液系统恶性肿瘤接受骨髓移植后无病存活超过1年的患者,在移植后1至14年(中位时间4年)接受了生长发育评估。移植前,所有儿童均接受了多药化疗,55例还接受了中枢神经系统照射,但均未进行生长发育评估。骨髓移植预处理包括大剂量化疗和全身照射(TBI),79例患者接受单次剂量9.2至10.0 Gy照射,63例患者接受分剂量2.0至2.25 Gy/d、持续6至7天的照射。移植后,39%的患者出现甲状腺功能异常。在接受评估的患者中,24%的患者刺激后11-脱氧皮质醇水平低于正常。在25例曾接受颅脑照射的儿童中,17例存在生长激素(GH)缺乏。在25例曾接受颅脑照射的儿童中,4例存在部分GH缺乏,在18例未接受颅脑照射的儿童中,6例存在部分GH缺乏。所有患者的身高增长速度均下降。移植后,身高受到慢性移植物抗宿主病和单次剂量TBI的显著影响。68%的患者第二性征发育延迟。几乎所有移植时已进入青春期后的患者均发生性腺功能衰竭。虽然无法确定这些内分泌异常中有多少是移植前治疗导致的,但这些数据确实表明,因血液系统恶性肿瘤接受骨髓移植后成为长期存活者的儿童存在内分泌异常,这些异常对生长发育产生了不利影响。

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