Hargrave Darren, Bartels Ute, Bouffet Eric
Department of Paediatric Oncology, Royal Marsden Hospital, Sutton, Surrey, UK.
Lancet Oncol. 2006 Mar;7(3):241-8. doi: 10.1016/S1470-2045(06)70615-5.
Diffuse intrinsic brainstem gliomas constitute 15-20% of all CNS tumours in children, and are the main cause of death in children with brain tumours. Many clinical trials have been done over the past three decades, but survival has remained static. More than 90% of children die within 2 years of diagnosis, and conventional fractionated radiation remains the standard treatment. However, median survival differs substantially between clinical trials, suggesting a survival benefit with some strategies. We appraised the consistency between protocols in terms of eligibility criteria, definition and assessment of response and progression, statistical design, and endpoints. Study designs varied substantially, which could explain the differences in outcome, and no treatment has shown a benefit over conventional radiotherapy. However, consistency between protocols (eg, eligibility criteria and outcome measures) is important to measure the progress in management of diffuse pontine gliomas.
弥漫性脑桥内生型胶质瘤占儿童中枢神经系统肿瘤的15% - 20%,是儿童脑肿瘤的主要死因。在过去三十年里进行了许多临床试验,但生存率一直没有变化。超过90%的儿童在诊断后2年内死亡,传统的分次放疗仍然是标准治疗方法。然而,不同临床试验之间的中位生存期差异很大,这表明某些治疗策略可能带来生存益处。我们从纳入标准、反应和进展的定义及评估、统计设计和终点等方面评估了各试验方案之间的一致性。研究设计差异很大,这可能解释了结果的差异,而且没有哪种治疗方法比传统放疗更具优势。然而,试验方案之间的一致性(如纳入标准和结果测量)对于衡量弥漫性脑桥胶质瘤治疗进展很重要。