Saran F H, Driever P H, Thilmann C, Mose S, Wilson P, Sharpe G, Adamietz I A, Böttcher H D
Department of Radiotherapy, Johann Wolfgang Goethe-University, Frankfurt/Main, Germany.
Int J Radiat Oncol Biol Phys. 1998 Dec 1;42(5):959-67. doi: 10.1016/s0360-3016(98)00262-4.
Very young children with medulloblastoma are considered to have a worse prognosis than older children. As radiotherapy remains an important part of the treatment, the adverse prognosis could be due to inadequate radiation treatment rather than biological factors. We analyzed the published literature to examine the impact of radiotherapy on survival in this group.
A Medline search was performed and we reviewed studies of treatment of medulloblastoma where radiotherapy was delivered using megavoltage equipment and the minimum follow-up allowed the calculation of 5-year survival rates.
Thirty-nine studies were published between 1979 and 1996 with a treatment including craniospinal irradiation and boost to the posterior fossa. Eleven studies comprising 1366 patients analyzed survival by age at diagnosis. Eight of 11 studies showed a worse 5-year survival for the younger patient group which reached statistical significance in two. There is also a suggestion of a higher proportion of children with metastatic disease at presentation in the very young age group. The usual policy in younger children was to give a lower dose of radiotherapy to the craniospinal axis (CSA) and posterior fossa (PF) with reduction of dose in the range of 15 to 25% compared to standard treatment. As dose reduction to the posterior fossa is associated with worse survival and local recurrence is the predominant site of failure, the major determinant of worse survival in very young children with medulloblastoma may be suboptimal radiotherapy. Protocols including postoperative chemotherapy with delayed, omitted, or only local tumor irradiation do not reach survival rates of protocols with standard radiotherapy, also suggesting a continued importance for irradiation.
Very young children with medulloblastoma have a worse prognosis than older children. Inadequate radiation dose and technique to the primary tumor region may be a major contributing factor. Current chemotherapeutic regimes alone are not sufficient to compensate for reduced radiation doses and volumes.
髓母细胞瘤患儿被认为比大龄儿童预后更差。由于放射治疗仍是治疗的重要组成部分,不良预后可能是由于放射治疗不足而非生物学因素所致。我们分析已发表的文献,以研究放射治疗对该组患儿生存的影响。
进行了医学文献数据库检索,并回顾了使用兆伏级设备进行放射治疗的髓母细胞瘤治疗研究,且最短随访时间允许计算5年生存率。
1979年至1996年间发表了39项研究,其治疗包括全脑全脊髓照射并加量照射后颅窝。11项研究(共1366例患者)按诊断时年龄分析生存率。11项研究中的8项显示较年轻患者组5年生存率更差,其中2项具有统计学意义。还有迹象表明,极年幼组患儿就诊时转移性疾病的比例更高。较年幼患儿的通常治疗策略是给予全脑全脊髓轴(CSA)和后颅窝(PF)较低剂量的放射治疗,与标准治疗相比,剂量降低幅度在15%至25%之间。由于后颅窝剂量降低与较差的生存率相关,且局部复发是主要的失败部位,髓母细胞瘤极年幼患儿生存率较差的主要决定因素可能是次优的放射治疗。包括术后化疗且延迟、省略或仅局部肿瘤照射的方案未达到标准放射治疗方案的生存率,这也表明放射治疗仍然很重要。
髓母细胞瘤极年幼患儿的预后比大龄儿童更差。原发肿瘤区域放射剂量和技术不足可能是一个主要促成因素。目前单独的化疗方案不足以弥补放射剂量和体积的减少。