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髓母细胞瘤的超分割全脑全脊髓放疗

Hyperfractionated craniospinal radiation in medulloblastoma.

作者信息

Marymont M H, Geohas J, Tomita T, Strauss L, Brand W N, Mittal B B

机构信息

Radiation Oncology Center, Northwestern Memorial Hospital, Chicago, IL 60611, USA.

出版信息

Pediatr Neurosurg. 1996;24(4):178-84. doi: 10.1159/000121035.

Abstract

From 1986 to 1991, 13 patients at Northwestern Memorial Hospital were entered onto a pilot study designed to test the feasibility of treating children with medulloblastoma (11 patients) or primitive neuroectodermal tumors of the cerebral hemispheres (2 patients) with hyperfractionated craniospinal radiotherapy (HFxRT). Follow-up times ranged from 10 to 96 months with a median of 53 months. The patients were prospectively divided among three treatment arms depending on prior treatment history, if any, and degree of surgical resection. The 3 patients in group I had undergone gross total resection of the primary site, receiving 64.8 Gy to the primary site and 31.2 Gy directed to the craniospinal axis (CSA). Of these 3 patients, patient 1 had residual disease in the thoracic spine at T-10. The 8 patients in group II, who had gross residual disease remaining at the primary site, received 72 Gy to the primary site and 34 Gy to the CSA. Five of these eight patients in group II also received 8-in-1 chemotherapy. The 2 patients in group III had already failed chemotherapy and were then treated with 60 Gy to the primary site and 26 Gy to the CSA. Of the 11 patients in groups I and II, 7 of the 11 (64%) have never recurred. Two of the three group-I patients have not recurred, and 5 of the 7 group-II patients have not recurred. In addition, patient 7 (group II) remains alive after salvage with bone marrow transplant, following a local failure bordering the tentorium. Unfortunately, neither of the group-III patients could be salvaged with HFxRT. Acute/subacute toxicities included 7 cases of external auditory canal or skin desquamation, 2 cases of postradiation somnolence, and 1 case each of poor wound healing and neutropenia. Chronic toxicities included hypothyroidism in 2 patients and growth problems in 2 patients. Neuropsychologic complications affected only the 3 youngest patients in the study. Three patients developed neurologic sequelae attributed to radiation, including 1 with progressive urinary incontinence, 1 who developed a transient ischemic attack, and 1 who became progressively ataxic. Our research, although based on a small number of patients, suggests that hyperfractionated radiation therapy to craniospinal access is feasible and that the survival results are favorable. This treatment strategy should be further explored in a phase-III randomized trial.

摘要

1986年至1991年期间,西北纪念医院的13名患者参与了一项初步研究,该研究旨在测试对患有髓母细胞瘤的儿童(11例)或大脑半球原始神经外胚层肿瘤的儿童(2例)进行超分割全脑全脊髓放疗(HFxRT)的可行性。随访时间从10个月至96个月不等,中位数为53个月。根据既往治疗史(如有)和手术切除程度,患者被前瞻性地分为三个治疗组。第一组的3例患者已对原发部位进行了全切,原发部位接受64.8 Gy照射,全脑全脊髓轴(CSA)接受31.2 Gy照射。在这3例患者中,患者1在胸10水平的胸椎有残留病灶。第二组的8例患者,原发部位有肉眼可见的残留病灶,原发部位接受72 Gy照射,CSA接受34 Gy照射。第二组的这8例患者中有5例还接受了8合1化疗。第三组的2例患者化疗已经失败,随后原发部位接受60 Gy照射,CSA接受26 Gy照射。在第一组和第二组的11例患者中,11例中有7例(64%)从未复发。第一组的3例患者中有2例未复发,第二组的7例患者中有5例未复发。此外,患者7(第二组)在小脑幕附近局部复发后,经骨髓移植挽救后仍然存活。不幸的是,第三组的2例患者均不能通过HFxRT挽救。急性/亚急性毒性反应包括7例外耳道或皮肤脱屑、2例放疗后嗜睡,以及各1例伤口愈合不良和中性粒细胞减少。慢性毒性反应包括2例甲状腺功能减退和2例生长问题。神经心理并发症仅影响研究中年龄最小的3例患者。3例患者出现了归因于放疗的神经后遗症,包括1例进行性尿失禁、1例发生短暂性脑缺血发作和1例逐渐出现共济失调。我们的研究虽然基于少数患者,但表明对全脑全脊髓通路进行超分割放射治疗是可行的,且生存结果良好。这种治疗策略应在III期随机试验中进一步探索。

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