...
首页> 外文期刊>Pediatric blood & cancer >The UK Experience of a Treatment Strategy for Pediatric Metastatic Medulloblastoma Comprising Intensive Induction Chemotherapy, Hyperfractionated Accelerated Radiotherapy and Response Directed High Dose Myeloablative Chemotherapy or Maintenance Chemotherapy (Milan Strategy)
【24h】

The UK Experience of a Treatment Strategy for Pediatric Metastatic Medulloblastoma Comprising Intensive Induction Chemotherapy, Hyperfractionated Accelerated Radiotherapy and Response Directed High Dose Myeloablative Chemotherapy or Maintenance Chemotherapy (Milan Strategy)

机译:英国对小儿转移性髓母细胞瘤的治疗策略的经验,包括密集诱导化学疗法,超分割加速放疗和响应定向大剂量清髓性化学疗法或维持性化学疗法(米兰策略)

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Background. Historically, the 5-year overall survival (OS) for metastatic medulloblastoma (MMB) was less than 40%. The strategy of post-operative induction chemotherapy (IC) followed by hyper-fractionated accelerated radiotherapy (HART) and response directed high dose chemotherapy (HDC) was reported in a single center study to improve 5-year OS to 73%. We report outcomes of this strategy in UK. Methods. Questionnaires were sent to all 20 UK pediatric oncology primary treatment centers to collect retrospective data on delivered treatment, toxicity and survival with this strategy in children aged 3-19 years with MMB. Results. Between February 2009 and October 2011, 34 patients fulfilled the entry criteria of the original study. The median age was 7 years (range 3-15). Median interval from surgery to HART was 109 versus 85 days in the original series. The incidence of grade 3 or 4 hematological toxicities with IC and HDC was 83-100%. All 16 patients who achieved complete response by the end of the regimen remain in remission but only three of 18 patients with lesser responses are still alive (P<0.0001). With a median follow-up of 45 months for survivors, the estimated 3-year OS is 56% (95% CI 38, 71). This result is outside the 95% CI of the original study results and encompasses the historical survival result of 40%. Conclusion. Within the limits of statistical significance, we did not replicate the improved survival results reported in the original series. The reasons include differences in patient sub-groups and protocol administration. International randomized phase III studies are needed. (C) 2015 Wiley Periodicals, Inc.
机译:背景。从历史上看,转移性髓母细胞瘤(MMB)的5年总生存率(OS)不到40%。在一项单中心研究中报告了术后诱导化疗(IC)继之以超分割加速放疗(HART)和反应定向高剂量化疗(HDC)的策略,该策略可将5年OS改善至73%。我们在英国报告了该策略的成果。方法。将问卷调查表发送给所有20个英国儿科肿瘤科一级治疗中心,以收集有关3-19岁MMB儿童采用该策略的治疗,毒性和生存率的回顾性数据。结果。在2009年2月至2011年10月之间,有34位患者符合原始研究的入组标准。中位年龄为7岁(范围3-15)。从手术到HART的中位间隔为109天,而原始系列为85天。 IC和HDC对3或4级血液学毒性的发生率为83-100%。到方案结束时已完全缓解的所有16名患者仍处于缓解状态,但18名缓解较轻的患者中只有3名仍然活着(P <0.0001)。对幸存者进行的中位随访期为45个月,估计3年OS为56%(95%CI 38,71)。该结果超出了原始研究结果的95%CI,涵盖了40%的历史生存率结果。结论。在统计学意义的范围内,我们没有复制原始系列中报道的改善的生存结果。原因包括患者亚组和方案管理的差异。需要国际随机III期研究。 (C)2015威利期刊公司

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号