Halberg F E, Wara W M, Fippin L F, Edwards M S, Levin V A, Davis R L, Prados M B, Wilson C B
Dept. of Radiation Oncology, School of Medicine, University of California, San Francisco 94143.
Int J Radiat Oncol Biol Phys. 1991 Apr;20(4):651-4. doi: 10.1016/0360-3016(91)90004-n.
At the University of California, San Francisco, 65 children with medulloblastoma of the posterior fossa were treated postoperatively with craniospinal irradiation; the dose to the posterior fossa was 54 Gy. The 26 children initially treated had only radiation therapy, receiving 30 to 40 Gy to the spine and 40 to 50 Gy to the brain. Subsequently, 39 children were treated with low-dose craniospinal irradiation and chemotherapy; 24 to 30 Gy was directed to the whole brain and 24 to 26 Gy to the spinal axis. Chemotherapy generally consisted of procarbazine just before, and hydroxyurea during, radiation therapy. Poor-risk and good-risk patients (defined by tumor resection less than 75% or greater than 75%, positive or negative myelogram, positive or negative cerebrospinal fluid analysis, age less than or greater than 2 years, respectively) were evenly distributed between the low-dose and high-dose craniospinal radiation therapy groups. Median follow-up was 51 months (range, 24 to 228 months). Kaplan-Meier actuarial survival for all patients was 73% at 5 years, 70% at 10 years. Freedom from disease progression was 68% at 5 years, 65% at 10 years. Whereas poor-risk patients treated with low-dose craniospinal irradiation and chemotherapy had a 5-year survival of 58% and a 5-year freedom from disease progression of 39%, those figures in the comparable good-risk patients were 83% and 77%, respectively. For both good-risk and poor-risk patients, the posterior fossa was the primary site of recurrence. Tumors recurred in the frontal region, probably under blocks, in three patients receiving low-dose irradiation and in two receiving the higher dose. Reducing the dose of whole-brain and spinal irradiation and giving chemotherapy did not result in a higher rate of recurrence in the brain or spinal cord. Intellectual and social function appeared better in patients receiving the lower dose. We did not study whether chemotherapy benefitted good-risk patients. Craniospinal axis irradiation at a lower dose than conventionally used does not compromise local control or survival in patients with medulloblastoma, and may reduce toxicity.
在加利福尼亚大学旧金山分校,65名患有后颅窝髓母细胞瘤的儿童术后接受了全脑脊髓放疗;后颅窝的剂量为54 Gy。最初接受治疗的26名儿童仅接受放射治疗,脊柱接受30至40 Gy的照射,脑部接受40至50 Gy的照射。随后,39名儿童接受了低剂量全脑脊髓放疗及化疗;全脑照射剂量为24至30 Gy,脊髓轴照射剂量为24至26 Gy。化疗通常包括放疗前使用丙卡巴肼以及放疗期间使用羟基脲。预后不良和预后良好的患者(分别定义为肿瘤切除率小于75%或大于75%、脊髓造影阳性或阴性、脑脊液分析阳性或阴性、年龄小于或大于2岁)在低剂量和高剂量全脑脊髓放疗组中分布均匀。中位随访时间为51个月(范围为24至228个月)。所有患者的Kaplan-Meier精算生存率在5年时为73%,在10年时为70%。无疾病进展生存率在5年时为68%,在10年时为65%。接受低剂量全脑脊髓放疗及化疗的预后不良患者5年生存率为58%,5年无疾病进展生存率为39%,而在具有可比性的预后良好患者中,这两个数字分别为83%和77%。对于预后良好和预后不良的患者,后颅窝都是复发的主要部位。接受低剂量照射的3名患者和接受高剂量照射的2名患者在额叶区域(可能在遮挡部位下方)出现肿瘤复发。降低全脑和脊髓照射剂量并给予化疗并未导致脑或脊髓复发率升高。接受较低剂量治疗的患者智力和社会功能似乎更好。我们没有研究化疗对预后良好患者是否有益。与传统使用的剂量相比,较低剂量的全脑脊髓轴照射不会影响髓母细胞瘤患者的局部控制或生存率,并且可能降低毒性。