Le Q T, Weil M D, Wara W M, Lamborn K R, Prados M D, Edwards M S, Gutin P H
Department of Radiation Oncology, University of California, San Francisco 94143-0226, USA.
Cancer J Sci Am. 1997 Jul-Aug;3(4):238-45.
This analysis aimed to review the experience in the management of adult medulloblastoma at the University of California, San Francisco, and to identify important prognostic factors for survival and posterior fossa control.
We performed a retrospective review of 34 adult patients, age > or = 15, with cerebellar medulloblastoma treated with radiotherapy at the University of California, San Francisco from 1970 to 1994. All patients underwent a surgical procedure (complete resection in 17, subtotal resection in 10, and biopsy alone in seven), followed by craniospinal irradiation. Most patients treated after 1979 also received chemotherapy. Twenty were classified as poor-risk due to either incomplete resection or evidence of disease outside of the posterior fossa at diagnosis.
The 5-year posterior fossa control and overall survival rates were 61% and 58%, respectively. The majority of relapses occurred in the posterior fossa (14 of 17). Multivariate analysis revealed that age (favoring older patients), gender (favoring female patients), and extent of disease at diagnosis (favoring localized disease) were important prognostic factors for posterior fossa control. There was a trend toward improved posterior fossa control with higher radiation dose to the posterior fossa in patients with a complete resection. Gender and extent of disease at presentation were significant prognostic factors for survival. The 5-year survival rates were 92% for female patients versus 40% for male patients, and 67% for patients with localized disease versus 25% for those with disseminated disease. The prognosis following recurrence was poor; all died of the disease.
Survival for adult medulloblastoma was comparable to its pediatric counterpart. In patients with localized disease at presentation, gender (favoring female patients) and age (favoring older patients) were important prognostic factors for posterior fossa control and survival. In patients with disseminated disease at presentation, the prognosis is poor, and innovative therapy is needed to improve survival.
本分析旨在回顾加利福尼亚大学旧金山分校治疗成人髓母细胞瘤的经验,并确定生存和后颅窝控制的重要预后因素。
我们对1970年至1994年在加利福尼亚大学旧金山分校接受放疗的34例年龄≥15岁的小脑髓母细胞瘤成年患者进行了回顾性研究。所有患者均接受了手术(17例全切,10例次全切,7例仅活检),随后进行全脑全脊髓照射。1979年后治疗的大多数患者还接受了化疗。20例因手术切除不完全或诊断时后颅窝外有疾病证据而被归类为高危患者。
5年后颅窝控制率和总生存率分别为61%和58%。大多数复发发生在后颅窝(17例中的14例)。多因素分析显示,年龄(年长患者更有利)、性别(女性患者更有利)和诊断时疾病范围(局限性疾病更有利)是后颅窝控制的重要预后因素。全切患者后颅窝接受更高辐射剂量有改善后颅窝控制的趋势。性别和就诊时疾病范围是生存的重要预后因素。女性患者5年生存率为92%,男性患者为40%;局限性疾病患者为67%,播散性疾病患者为25%。复发后的预后很差;所有患者均死于该疾病。
成人髓母细胞瘤的生存率与儿童患者相当。就诊时为局限性疾病的患者,性别(女性患者更有利)和年龄(年长患者更有利)是后颅窝控制和生存的重要预后因素。就诊时为播散性疾病的患者,预后很差,需要创新疗法来提高生存率。