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临床试验/CTRI/2020/12/030005
CTRI/2020/12/030005尚未招募未知

Prospective evaluation of patients with primary CNS Lymphoma undergoing high dose consolidation chemotherapy with LACE.

Tata Memorial Centre0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • 1. Patients with histologically proven PCNSL and planned for ASCT
  • 2. Age > 18 years and less than 65 years
  • 3. ECOG PS <4
  • 4.Adequate bone marrow function with absolute leukocytes > 2000/mm3, neutrophil count (ANC) > 1000/mm3, hemoglobin > 8 g/dl and platelets > 100 000/mm3
  • 5.Adequate liver function with Serum SGOT/AST or SGPT/ALT < 3.0 X Upper Limit of Normal ULN ; bilirubin < 1.5 X LNS
  • 6. Creatinine clearance > 60 ml/min.
  • 7.Adequate cardiac function (LVEF more than 45%)
  • 8.Adequate lung function (DLCO more than 50%)
  • 9. Able to understand and sign informed consent

排除标准

  • Chemo-refractory disease
  • 2.HIV infection
  • 3.Active hepatitis B or C
  • 4.Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form.

研究者

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