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临床试验/JPRN-jRCT1091220276
JPRN-jRCT1091220276已完成2 期

A phase II randomized controlled trial of WT1 peptide vaccine (DSP-7888) therapy in patients with childhood, adolescent and young adult soft tissue sarcoma.

未提供0 个研究点目标入组 24 人开始时间: 2017年2月17日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
24

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
ot applicable 至 < 30age old(—)
性别
All

入选标准

  • High risk rhabdomyosarcoma defined by JRS-II risk group classification.
  • 1. Rhabdomyosarcoma with distant metastasis at diagnosis.
  • 2. Alveolar rhabdomyosarcoma of unfaborable site origin with macroscopic residual disease at diagnosis.
  • Patients with rhabdomyosarcomamust be in complete remission or must have no FDG avid lesion at enrollment.
  • Non-rhabdomyosarcoma with features described below.
  • 3. grossly resected high grade tumor with diameter of 5cm or larger.
  • 4. localized tumor which is unresected at diagnosis.
  • 5. regional lymph node metastasis and/or distant metastasis at diagnosis except low grade tumor where all lesions are resected.
  • Patients with non-rhabdomyosarcoma soft tissue sarcoma must be in complete remission at enrollment.
  • 2) Enrollment within 120 days after last chemotherapy, surgery or irradiation.
  • 3) ECOG 0-2 (>=16 years old) or Lansky 50-100% (< 16 years old)
  • 4) Patients must have sufficient organ function.
  • 5) Age younger than 30 years old.
  • 6) All patients and/or their parents or legal guardians must sign a written informed consent.

排除标准

  • 1) patients with synchronous or metachronous concomitant malignancies
  • 2) patients receiving chemotherapy
  • 3) patients with uncontrollable complications
  • 4) patients with uncontrollable infection
  • 5) patients with severe psychotic disorder
  • 6) Female patients who are pregnant or patients considering pregnancy
  • 7) patients who have not agreed to use an effective contraceptive method.
  • 8) patients who plan to participate in other clinical trials with intervention during this clinical trial.
  • 9) Patients with any other inappropriate condition judged by physician

研究者

发起方
未提供

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