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髓母细胞瘤患儿的甲状腺功能减退:3600 cGy与2340 cGy颅脊髓放疗的比较

Hypothyroidism in children with medulloblastoma: a comparison of 3600 and 2340 cGy craniospinal radiotherapy.

作者信息

Paulino Arnold C

机构信息

Department of Radiation Oncology, The University of Iowa College of Medicine, University of Iowa Health Care and Children's Hospital of Iowa, Iowa City, IA, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2002 Jul 1;53(3):543-7. doi: 10.1016/s0360-3016(02)02744-x.

Abstract

PURPOSE

To determine if low-dose craniospinal irradiation (2340 cGy) with chemotherapy is associated with a lower incidence of hypothyroidism compared to standard dose (3600 cGy) with or without chemotherapy in children with medulloblastoma.

PATIENTS AND METHODS

Between 1980 and 1999, 32 patients < or =20 years old survived after craniospinal irradiation with or without chemotherapy. Twenty patients received 3600 cGy craniospinal irradiation (CSI), whereas 12 had 2340 cGy CSI; all patients received a posterior fossa boost to a total dose 5040-5580 cGy. The median ages at the time of CSI for those receiving 2340 cGy and 3600 cGy were 7.2 and 10.2 years, respectively. Chemotherapy (CT) was employed in 22 children. All children who received 2340 cGy had CT consisting of vincristine, CCNU, and either cisplatin or cyclophosphamide. Ten of 20 (50%) patients receiving 3600 cGy had CT; the most common regimen was vincristine, CCNU, and prednisone. Serum-free thyroxine and thyroid-stimulating hormone concentrations were measured in all children at variable times after radiotherapy. Thyroid-stimulating hormone responses to i.v. thyrotrophin-releasing hormone were assessed in those suspected of having central hypothyroidism. Median follow-up for children receiving 2340 cGy was 5 years (range: 2-11.2 years), whereas for those receiving 3600 cGy, follow-up was 12.5 years (range: 2.4-20 years).

RESULTS

Eighteen patients (56%) developed hypothyroidism at a median time after radiotherapy of 41 months (range: 10 months to 18 years). Primary hypothyroidism was more common than central hypothyroidism (38% and 19%). All 7 children <5 years developed hypothyroidism, whereas 9 of 15 (60%) ages 5-10 and 2 of 10 (20%) age >10 years had hypothyroidism (p < 0.001). Hypothyroidism was documented in 10 of 12 (83%) who had 2340 cGy + CT, 6 of 10 (60%) who had 3600 cGy + CT, and 2 of 10 (20%) who had 3600 cGy without CT (p < 0.025).

CONCLUSIONS

Current treatment regimens consisting of chemotherapy and 2340 cGy craniospinal irradiation followed by a posterior fossa boost for medulloblastoma do not show a reduction of hypothyroidism. Young age and use of chemotherapy were associated with a higher incidence of hypothyroidism.

摘要

目的

确定与接受标准剂量(3600 cGy)联合或不联合化疗相比,低剂量全脑脊髓照射(2340 cGy)联合化疗治疗髓母细胞瘤患儿时,甲状腺功能减退的发生率是否更低。

患者与方法

1980年至1999年间,32例年龄≤20岁的患者在接受全脑脊髓照射联合或不联合化疗后存活。20例患者接受3600 cGy全脑脊髓照射(CSI),而12例接受2340 cGy CSI;所有患者均接受后颅窝加量照射,总剂量达5040 - 5580 cGy。接受2340 cGy和3600 cGy照射时的中位年龄分别为7.2岁和10.2岁。22例儿童接受了化疗(CT)。所有接受2340 cGy照射的儿童化疗方案包括长春新碱、洛莫司汀以及顺铂或环磷酰胺。接受3600 cGy照射的20例患者中有10例(50%)接受了化疗;最常见的化疗方案是长春新碱、洛莫司汀和泼尼松。在放疗后的不同时间对所有儿童测定血清游离甲状腺素和促甲状腺激素浓度。对怀疑有中枢性甲状腺功能减退的患儿评估促甲状腺激素对静脉注射促甲状腺激素释放激素的反应。接受2340 cGy照射儿童的中位随访时间为5年(范围:2 - 11.2年),而接受3600 cGy照射儿童的随访时间为12.5年(范围:2.4 - 20年)。

结果

18例患者(56%)在放疗后中位时间41个月(范围:10个月至18年)出现甲状腺功能减退。原发性甲状腺功能减退比中枢性甲状腺功能减退更常见(分别为38%和19%)。所有7例年龄<5岁的儿童均出现甲状腺功能减退,而15例年龄5 - 10岁的儿童中有9例(60%)以及10例年龄>10岁的儿童中有2例(20%)出现甲状腺功能减退(p<0.001)。接受2340 cGy + CT的12例患者中有10例(83%)记录有甲状腺功能减退,接受3600 cGy + CT的10例患者中有6例(60%)以及接受3600 cGy未接受CT的10例患者中有2例(20%)出现甲状腺功能减退(p<0.025)。

结论

目前用于髓母细胞瘤的化疗联合2340 cGy全脑脊髓照射后再行后颅窝加量照射的治疗方案未显示甲状腺功能减退发生率降低。年龄小和使用化疗与甲状腺功能减退发生率较高相关。

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