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临床试验/NL-OMON28081
NL-OMON28081招募中不适用

Phase III study comparing R-CODOX-M/R-IVAC versus dose-adjusted EPOCH-R (DA-EPOCH-R) for patients with newly diagnosed high risk Burkitt lymphoma

Stichting Hemato-Oncologie voor Volwassenen Nederland (HOVON) P/a HOVON Data CenterErasmus MC Cancer Institute, Clinical Trial CenterP.O. Box 20403000 CA RotterdamTel: 010 4391568Fax: 010 4391028e-mail: hdc@erasmusmc.nl0 个研究点目标入组 260 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
260

研究概览

简要总结

ot yet for this trial.

研究设计

研究类型
Interventional

入排标准

入选标准

  • First diagnosis of high risk Burkitt lymphoma (sporadic and
  • HIV associated), histologically confirmed according to the
  • WHO classification 2008. Upon its availability the WHO 2016
  • classification should be used, to replace the WHO 2008
  • classification;

排除标准

  • - All histopathological diagnoses other than Burkitt
  • lymphoma according to the WHO classification 2008,
  • irrespective of the presence of a MYC rearrangement. Upon
  • its availability the WHO 2016 classification should be used, to
  • replace the WHO 2008 classification;

研究者

发起方
Stichting Hemato-Oncologie voor Volwassenen Nederland (HOVON) P/a HOVON Data CenterErasmus MC Cancer Institute, Clinical Trial CenterP.O. Box 20403000 CA RotterdamTel: 010 4391568Fax: 010 4391028e-mail: hdc@erasmusmc.nl

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