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临床试验/EUCTR2007-001478-10-PL
EUCTR2007-001478-10-PL进行中(未招募)1 期

CWS-2007-HR: A randomised phase-III trial of the Cooperative Weichteilsarkom Studiengruppe for localised high-risk Rhabdomyosarcoma and localised Rhabdomyosarcoma-like Soft Tissue Sarcoma in children, adolescents, and young adults. - CWS-2007-HR

niversitätsklinikum Tübingen0 个研究点目标入组 320 人开始时间: 2012年8月8日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
320

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • written informed consent for registration, randomisation, data
  • collection/transfer, and tumour material asservation available
  • pathologically (including molecular pathology) proven diagnosis of
  • rhabdomyosarcoma (RMS) or RMS-like soft tissue sarcoma (STS) and
  • tumour material available for pathology review
  • age > 6 months and <18 years at the time of randomisation
  • Rhabdomyosarcoma of the High Risk” Group, i.e.:
  • - RME, N0, M0, IRS II&III, >5 cm or >10 years in EXT, HN-PM, OTH, UG-BP
  • - RME, N1, M0, any IRS-group, any size or age
  • - RMA, NO, M0, any IRS-group, any size or age
  • (exception: paratesticular RMA are not eligible)
  • Rhabdomyosarcoma of the Very High Risk” Group, i.e.:
  • - RMA, N1, MO, IRS II&III, any size or age
  • - localised high-risk RMS-like Soft Tissue Sarcoma, i.e.:
  • - EES, pPNET, UDS: any N, M0, any IRS-group, any size or age
  • - SySa, any N, M0, any size or age
  • (exception: SySa IRSI&II, not T2b, N0, M0 are not eligible)
  • no pre-existing illness preventing treatment
  • no previous malignant tumours
  • available for long term follow up through the treating centre
  • in remission at the time of randomisation after standard multimodal therapy
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 15
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • pregnant or lactating women
  • other medical condition precluding treatment with protocol
  • (e.g. HIV, psychiatric disorder, etc.)
  • for sexually active females and males in Arm B (O-TIE treatment): refusal to use effective contraception (e.g. oral, IUD)

研究者

发起方
niversitätsklinikum Tübingen

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