Bushhouse S, Ramsay N K, Pescovitz O H, Kim T, Robison L L
Minnesota Department of Health, University of Minnesota, Minneapolis.
Am J Pediatr Hematol Oncol. 1989 Summer;11(2):134-40.
Longitudinal height data from 46 pediatric bone marrow transplant (BMT) patients, including 18 with aplastic anemia (AA), 19 with acute nonlymphoblastic leukemia (ANLL), and 9 with acute lymphoblastic leukemia (ALL), were analyzed to assess growth posttransplantation. Patients were prepared for BMT with high-dose cyclophosphamide followed by 7.5 Gy single-dose irradiation; AA patients received total lymphoid irradiation (TLI), and leukemia patients received total body irradiation (TBI). AA patients demonstrated reduced height posttransplant as reflected in a negative mean standard deviation score. The observed reduction was statistically significant only at 3 years following transplant. In contrast, leukemia patients showed a significant loss in relative height that was first visible at 1 year post-BMT and continued until at least 4 years post-BMT. Mean growth velocities in the leukemia patients were significantly below median for the 3 years following transplant. With a median follow-up of 4 years, antithymocyte globulin plus steroids in combination with methotrexate as graft vs. host prophylaxis was associated with less severe growth suppression than methotrexate alone, while there were no significant associations between growth during the first 2 years following transplant and prepubertal status at transplant (as defined by age), graft vs. host disease, thyroid or gonadal function, or previous therapies received by the leukemia patients. Children undergoing marrow transplantation, particularly those receiving TBI, are at significant risk of subsequent growth suppression.
分析了46例儿科骨髓移植(BMT)患者的纵向身高数据,其中包括18例再生障碍性贫血(AA)患者、19例急性非淋巴细胞白血病(ANLL)患者和9例急性淋巴细胞白血病(ALL)患者,以评估移植后的生长情况。患者接受大剂量环磷酰胺预处理,随后进行7.5 Gy单次照射;AA患者接受全身淋巴照射(TLI),白血病患者接受全身照射(TBI)。AA患者移植后身高降低,平均标准差评分为负值。观察到的身高降低仅在移植后3年具有统计学意义。相比之下,白血病患者的相对身高显著降低,在BMT后1年首次可见,并持续至BMT后至少4年。移植后3年,白血病患者的平均生长速度显著低于中位数。中位随访4年,抗胸腺细胞球蛋白加类固醇联合甲氨蝶呤作为移植物抗宿主病预防措施,与单独使用甲氨蝶呤相比,生长抑制较轻,而移植后前2年的生长与移植时的青春期前状态(按年龄定义)、移植物抗宿主病、甲状腺或性腺功能,或白血病患者先前接受的治疗之间无显著关联。接受骨髓移植的儿童,尤其是接受TBI的儿童,随后发生生长抑制的风险很高。