Padovani Laetitia, Sunyach Marie-Pierre, Perol David, Mercier Cedric, Alapetite Claire, Haie-Meder Christine, Hoffstetter Sylvette, Muracciole Xavier, Kerr Christine, Wagner Jean-Philippe, Lagrange Jean-Léon, Maire Jean-Philippe, Cowen Didier, Frappaz Didier, Carrie Christian
Department of Radiation Oncology, Hôpital de la Timone, Marseille, France.
Int J Radiat Oncol Biol Phys. 2007 Jun 1;68(2):433-40. doi: 10.1016/j.ijrobp.2006.12.030.
To assess prognostic factors for adults with medulloblastoma in a multicenter, retrospective study.
Data were collected by file review or mail inquiry for 253 adults treated between 1975 to 2004. Radiologists or surgeons assessed disease characteristics, such as volume and extension. Patients were classified as having either high- or standard-risk disease. Prognostic factors were analyzed.
Median patient age was 29 years. Median follow-up was 7 years. Radiotherapy was delivered in 246 patients and radiochemotherapy in 142. Seventy-four patients relapsed. Respective 5- and 10-year overall survival rates were 72% and 55%. Univariate analysis showed that survival significantly correlated with metastasis, postsurgical performance status, brainstem involvement, involvement of the floor of the fourth ventricle (V4), and radiation dose to the spine and to the posterior cerebral fossa (PCF). By multivariate analysis, brainstem, V4 involvement, and dose to the PCF were negative prognostic factors. In the standard-risk subgroup there was no overall survival difference between patients treated with axial doses of >or=34 Gy and patients treated with craniospinal doses <34 Gy plus chemotherapy.
We report the largest series of medulloblastoma in adults. Prognostic factors were similar to those observed in children. Results suggest that patients with standard-risk disease could be treated with radiochemotherapy, reducing doses to the craniospinal area, maintaining at least 50 Gy to the PCF. The role of chemotherapy for this group is still unclear. A randomized study should be performed to confirm these results, but because frequency is very low, such a study would be difficult.
在一项多中心回顾性研究中评估成人髓母细胞瘤的预后因素。
通过查阅病历或邮件询问收集了1975年至2004年间接受治疗的253例成人患者的数据。放射科医生或外科医生评估疾病特征,如肿瘤体积和范围。患者被分为高危或标准风险疾病。对预后因素进行分析。
患者中位年龄为29岁。中位随访时间为7年。246例患者接受了放疗,142例接受了放化疗。74例患者复发。5年和10年总生存率分别为72%和55%。单因素分析显示,生存与转移、术后功能状态、脑干受累、第四脑室底(V4)受累以及脊柱和后颅窝(PCF)的放射剂量显著相关。多因素分析显示,脑干、V4受累和PCF剂量是不良预后因素。在标准风险亚组中,轴向剂量≥34 Gy的患者与颅脊髓剂量<34 Gy加化疗的患者之间总生存率无差异。
我们报告了最大系列的成人髓母细胞瘤病例。预后因素与儿童中观察到的相似。结果表明,标准风险疾病的患者可以接受放化疗,减少颅脊髓区域的剂量,PCF至少维持50 Gy。化疗对该组患者的作用仍不清楚。应进行随机研究以证实这些结果,但由于发病率很低,这样的研究将很困难。