跳至主要内容
临床试验/EUCTR2007-006652-19-IT
EUCTR2007-006652-19-IT进行中(未招募)不适用

A Randomized Pilot Study on Central Nervous System (CNS) Prophylaxiswith Liposome-Encapsulated Cytarabine (DepoCyte) in a Population of Adult Patientswith Acute Lymphoblastic Leukemia (ALL) Treated with an Updated and Lineage-TargetedMinimal Residual Disease (MRD)-Oriented Postremission Strategy. - NILG-ALL 10/07

ILG0 个研究点开始时间: 2008年4月8日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

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

  • ALL Prospective Register
  • 1. Age 18+ years.
  • 2. Diagnosis of untreated ALL with B-/T-precursor phenotype or B/T-LL, either de novo or secondary to chemo-radiotherapy for other cancer.
  • 3. Signed informed consent.
  • Inclusion criteria
  • 1. Age 18-65 years.
  • 2. Diagnosis of untreated ALL with B-/T-precursor phenotype or B-cell lymphoblastic lymphoma (B-LL), either de novo or secondary to chemo-radiotherapy for other cancer.
  • 3. Full cytological, cytochemical, cytogenetic and immunobiological disease characterization by revised FAB, EGIL and WHO criteria.
  • 4. Bone marrow and peripheral blood sampling (ALL) or biopsy specimen (LL) for MRD study.
  • 5. ECOG performance status 0-2 or reversible ECOG 3 score following intensive care of complications.
  • 6. Signed informed consent.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • 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

  • 1. Diagnosis of B-ALL (FAB L3 ALL/Burkitt?s leukemia or lymphoma) and T-LL (T-cell lymphoblastic lymphoma).
  • 2. Down?s syndrome.
  • 3. Pre-existing, uncontrolled pathology such as cardiac disease (congestive/ischemic, acute myocardial infarction within the past 3 months, untreatable arrythmias, NYHA classes III and IV), severe liver disease with serum bilirubin >3 mg/dL and/or ALT >3 x upper normal limit (unless attributable to ALL/LL), kidney function impairment with serum creatinine >2 mg/dL (unless attributable to ALL/LL), and severe neurological or psychiatric disorder that impairs the patient?s ability to understand and sign the informed consent, or to cope with the intended treatment plan.
  • 4. Known HIV positive serology.
  • 5. Other active hematological or non-hematological cancer with life expectancy <1 year.
  • 6. Pregnancy (fertile women will be advised not to become pregnant while on treatment; and male patients to adopt contraceptive methods), unless therapeutic aborption/early discharge is carried out.

研究者

发起方
ILG

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