Zhang R, Zhou L
Department of Neurosurgery, Hua Shan Hospital, Shanghai Medical University, Shanghai 200040, China.
Chin Med J (Engl). 1999 Apr;112(4):297-301.
To elucidate the diagnosis, treatment and prognosis of medulloblastoma in both children and adults.
A retrospective review was conducted in 80 patients with medulloblastoma confirmed pathologically during the period of 1984 and 1995. Multivariate analysis and comparison were made of the therapeutic effects of operation, radiotherapy and chemotherapy as well as the survival period.
There were 42 males and 38 females with average age at diagnosis being 9.1 years in children and 25.1 years in adults. All patients were operated on to remove the tumour. Cerebral aqueduct re-opening was got through in 54 cases (67.5%), and Torkilsen's shunt was carried out at the same time for the rest patients. Seventeen patients had ventriculoperitoneal shunt, and 13 of them were performed after surgical excision of the tumour. Complete follow-up information was obtained in 61 patients (76%) for a period of 6 months to 14 years. During the follow-up, 27 patients received postoperative craniospinal irradiation, and 27 local radiation. Fourteen patients were subjected to adjuvant chemotherapy. The overall 5-year and 10-year survival rates were 50.5% and 27.89% respectively. The 5-year survival rate was higher in adults than in children (P < 0.05), whereas the 10-year survival rate was similar. Thirty-two patients died of relapse or metastasis between 6 months and 10 years after initial surgical therapy, and the mean recurrence time was 3.5 years.
Operation and postoperative regular radiotherapy were important therapeutic modalities for medulloblastoma. Total or subtotal removal of the tumour combined with craniospinal radiotherapy can improve patients' survival rate. The survival period of medulloblastoma patients is consistent with Collins' law, that is, the period of risk for survival is the age at initial diagnosis plus 9 months. Only few patients can gain long-term survival.
阐明儿童和成人髓母细胞瘤的诊断、治疗及预后情况。
对1984年至1995年间经病理确诊的80例髓母细胞瘤患者进行回顾性研究。对手术、放疗和化疗的治疗效果以及生存期进行多因素分析和比较。
男性42例,女性38例,儿童诊断时平均年龄为9.1岁,成人为25.1岁。所有患者均接受手术切除肿瘤。54例(67.5%)打通了脑导水管,其余患者同时进行了托尔基尔森分流术。17例患者行脑室腹腔分流术,其中13例在肿瘤手术切除后进行。61例患者(76%)获得了6个月至14年的完整随访信息。随访期间,27例患者接受了术后全脑脊髓照射,27例接受局部放疗。14例患者接受了辅助化疗。总体5年和10年生存率分别为50.5%和27.89%。成人5年生存率高于儿童(P<0.05),而10年生存率相似。32例患者在初次手术治疗后6个月至10年间死于复发或转移,平均复发时间为3.5年。
手术及术后规律放疗是髓母细胞瘤重要的治疗方式。肿瘤全切或次全切联合全脑脊髓放疗可提高患者生存率。髓母细胞瘤患者的生存期符合柯林斯定律,即生存危险期为初次诊断时的年龄加9个月。仅有少数患者能获得长期生存。