Sato J, Ninomiya T, Tsuda Y, Komazawa M, Nagata K, Iwai A, Nishikawa K, Maeda H, Ohmiya A, Ohta M
Department of Pediatrics, University of Tokushima, Japan.
Int J Hematol. 1992 Dec;56(3):205-12.
Growth patterns were surveyed in 303 children with acute lymphoblastic leukemia who had remained in continuous first complete remission for a minimum of 1 year (median 3 years). Chemotherapy was given for 3 years, and central nervous system prophylaxis consisted of cranial irradiation at a total dose of 18 Gy or intravenous high-dose methotrexate (1.5-6 g/m2 for three to six doses). Intensive chemotherapy, including cyclophosphamide, doxorubicin, and cytosine arabinoside was given to children with high-risk features. Two of 205 children with low- or intermediate-risk features and 13 of 98 children with high-risk features showed a decrease in the growth rate of less than -2 SD. In 14 of these 15 patients, the age at onset was over 9 years and growth failure became most predominant in the prepubertal period: ten of these children showed a tendency toward delayed pubertal development, but eight showed later catch-up growth with pubertal maturation after completion of chemotherapy. Thus, chemotherapy appeared to contribute temporarily to the growth failure and gonadal impairment that occurred in the prepubertal period. No obvious correlation between the administered cranial irradiation and growth failure was found, but further study with a longer follow-up will be necessary to determine the long-term effects of irradiation on subsequent growth patterns in children.
对303例急性淋巴细胞白血病患儿的生长模式进行了调查,这些患儿持续首次完全缓解至少1年(中位时间为3年)。化疗持续3年,中枢神经系统预防措施包括总剂量为18 Gy的颅脑照射或静脉注射大剂量甲氨蝶呤(1.5 - 6 g/m²,分三至六剂)。具有高危特征的儿童接受了强化化疗,包括环磷酰胺、阿霉素和阿糖胞苷。205例低危或中危特征患儿中有2例,98例高危特征患儿中有13例生长速率下降小于 -2标准差。在这15例患者中的14例中,发病年龄超过9岁,生长发育迟缓在青春期前最为明显:其中10例儿童有青春期发育延迟的倾向,但8例在化疗结束后随着青春期成熟出现了后期追赶生长。因此,化疗似乎暂时导致了青春期前出现的生长发育迟缓以及性腺损害。未发现所给予的颅脑照射与生长发育迟缓之间存在明显相关性,但需要进行更长时间随访的进一步研究,以确定照射对儿童后续生长模式的长期影响。