Kumar Lachi Pavan, Deepa Syed Fayaz Ahmed J, Moinca I, Suresh P, Naidu K V J R
Department of Radiation Oncology, Nizams Institute of Medical Sciences, Hyderabad, Telangana, India.
Asian J Neurosurg. 2015 Jan-Mar;10(1):50. doi: 10.4103/1793-5482.151516.
Medulloblastoma is a common malignancy in the pediatric population, accounting for 25% of all childhood brain tumors and relatively uncommon in adults. This review was to investigate treatment outcome and prognostic factors after treatment of medulloblastoma.
A total of 53 patients with histological confirmed medulloblastoma cases treated at our institute between 2006 and 2012 were included in the study. Demographic variables, clinical variables, radiological findings and treatment details with respect to age, sex, signs and symptoms, location of tumor, extent of surgical resection, histopathology type, radiotherapy dose, follow-up period and outcomes were recorded. Survival was analyzed by using these parameters.
Thirty-one (58.5%) patients were pediatric (<14 years), and 22 (41.5%) patients were adults (≥14 years). Duration of symptoms were <3 months in 19 (36%) and more than 3 months in 34 (64%) patients. Tumor resection was performed in all patients with gross total resection in 8 (15%) patients, near total resection in 34 (64%) patients and subtotal resection in 11 (21%) patients. All patients underwent postoperative craniospinal irradiation (CSI) delivering a median craniospinal dose of 36 Gy with additional boosts to the posterior fossa up to 54 Gy. Median overall survival was 50 months for the total group whereas 36 months for pediatric age group and 70 months for adult group. Desmoplastic histology showed an improved outcome compared with other histologies with a median survival of 71 months compared with that of classical medulloblastoma histology being 36 months and other histologies shown a median survival of 34 only.
Treatment of medulloblastoma with surgery and CSI yields long survival rates in both children and adults. Adult age group and desmoplastic histology were associated with a favorable outcome.
髓母细胞瘤是儿科人群中常见的恶性肿瘤,占所有儿童脑肿瘤的25%,在成人中相对少见。本综述旨在研究髓母细胞瘤治疗后的治疗结果和预后因素。
本研究纳入了2006年至2012年期间在我院接受组织学确诊的53例髓母细胞瘤患者。记录了患者的人口统计学变量、临床变量、放射学检查结果以及治疗细节,包括年龄、性别、体征和症状、肿瘤位置、手术切除范围、组织病理学类型、放疗剂量、随访时间和结果。利用这些参数进行生存分析。
31例(58.5%)患者为儿童(<14岁),22例(41.5%)患者为成人(≥14岁)。19例(36%)患者症状持续时间<3个月,34例(64%)患者症状持续时间超过3个月。所有患者均接受了肿瘤切除术,其中8例(15%)患者实现了全切,34例(64%)患者接近全切,11例(21%)患者次全切除。所有患者均接受了术后全脑脊髓照射(CSI),全脑脊髓中位剂量为36 Gy,后颅窝额外加量至54 Gy。全组患者的中位总生存期为50个月,儿童年龄组为36个月,成人组为70个月。促纤维增生型组织学表现出比其他组织学更好的预后,中位生存期为71个月,而经典型髓母细胞瘤组织学的中位生存期为36个月,其他组织学的中位生存期仅为34个月。
手术和CSI治疗髓母细胞瘤在儿童和成人中均能产生较长的生存率。成人年龄组和促纤维增生型组织学与良好的预后相关。