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临床试验/JPRN-UMIN000000829
JPRN-UMIN000000829已完成2 期

Dose-adjusted EPOCH therapy for the previously untreated patients of advanced peripheral T-cell lymphoma

West Japan Hematology Oncology Group0 个研究点目标入组 42 人开始时间: 2007年9月22日最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
42

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
15years-old 至 79years-old(—)
性别
All

入选标准

  • (1)Histological confirmed
  • Anaplastic large cell lymphoma (ALCL) or
  • Angioimmunoblastic T-cell lymphoma (AILT) or
  • Peripheral T-cell lymphoma, unspecified (PTCL-u).
  • (2) Clinical stage of II, III, IV by Ann Arbor classification.
  • (3) Bidimensionally measurable disease
  • (4) Age: between 15 and 79.
  • (5) Performance Status: between 0 and 2.
  • (6) No organ dysfuction; neutrophil count >=1000/ml, platelet count >=75000/ml, ASTand ALT level <=3 times the upper limit of the normal range, total bilirubin level <= 2.0 mg/dl, serum creatinin level <= 2.0mg/dl, Resting ejection fraction >= 50% by UCG. SaO2 >=90% or PaO2 >=60 mmHg in room air.
  • (7) No prior chemotherapy, radiotherapy
  • (8) Understanding and agreement of written informed consent.

排除标准

  • 1) Uncontrollable active infection
  • 2) Complication; uncontrollable hypertension or DM, liver cirrhosis, interstitial pneumonia, pulmonary fibrosis.
  • 3) Positive for HIV antibody or HBs antigen.
  • 4) Have an active cancer.
  • 5) Pregnant or nursing.
  • 6) Psycological disorder like schizophrenia.
  • 7) A patient who was judged as inappropriate for the trial

研究者

发起方
West Japan Hematology Oncology Group

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