Jaing T H, Hung I J, Yang C P, Wang H S, Hung P C
Department of Pediatrics, Chang-Gung Memorial Hospital, Taipei, Taiwan, R.O.C.
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1995 Jul-Aug;36(4):279-85.
The medical records of 63 patients with histologically-confirmed medulloblastoma were reviewed. From these, the clinical features and treatment outcome of 49 patients were available for analysis. Following tumor resections, 44 patients were given craniospinal radiation therapy with local boosts to the posterior fossa and other macroscopically involved areas. Twenty patients received chemotherapy: 17 as postoperative adjuvant or salvage therapies, and 3 as preradiation chemotherapy. The postoperative early death occurred in two patients. The projected 5-year survival and recurrence-free survival rate of the overall group and the 41 patients who had completed radiotherapy were 61%, 70% and 50%, 57%, respectively. Two significant favorable factors were identified: complete tumor resection and combination radiotherapy. A better five-year survival rate was found in patients who had complete tumor resection (78% vs 19%); with combination radiotherapy the rate was 70% vs 0%.
回顾了63例经组织学确诊为髓母细胞瘤患者的病历。从中选取49例患者的临床特征及治疗结果进行分析。肿瘤切除术后,44例患者接受了颅脊髓放射治疗,并对后颅窝及其他肉眼可见受累区域进行局部加量照射。20例患者接受了化疗:17例作为术后辅助治疗或挽救性治疗,3例作为放疗前化疗。2例患者术后早期死亡。整个组以及41例完成放疗患者的预计5年生存率和无复发生存率分别为61%、70%和50%、57%。确定了两个显著的有利因素:肿瘤完全切除和联合放疗。肿瘤完全切除的患者5年生存率更高(78%对19%);接受联合放疗的患者生存率为70%,未接受联合放疗的患者生存率为0%。