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临床试验/ITMCTR2022000101
ITMCTR2022000101尚未招募1 期

Clinical study of jianpiyishen granules and Western medicine in the treatment of fragile DLBCL in the elderly

Guang'anmen Hospital0 个研究点开始时间: 待定最近更新:

试验速览

阶段
1 期
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational study

入排标准

年龄范围
60 至 110(—)
性别
All

入选标准

  • 1. Patients with CD20-positive initial treatment of large B-cell lymphoma with pathological diagnosis;
  • 2. Age = 60 years old, male or female;
  • 3. Ann Arbor/Cotswords Phase I-IV;
  • 4. CGA assessment of patients before treatment, and elderly vulnerable patients who are not suitable for standardized therapy must meet one of the following criteria: 1) ADL < 5 points; 2) IADL < 6 points; 3) 1 grade 3 to 4 comorbidities (or 8 grade 2 comorbidities> in the MCIRS-G score; 4) Patients with an age = 80 years old need to meet: ADL =5, or IADL =7, or 0-1 in the MCIRS-G score of grade 3 to 4 (or > 5 grade 2 complications);
  • 5. The expected survival period is more than 6 months;
  • 6. Alanine aminotransferase (AST)= 2.5×ULN, alanine aminotransferase (ALT)=2.5×ULN, serum creatinine Cr=1.5×ULN;
  • 7. Volunteer to participate in this study and sign an informed consent form.

排除标准

  • 1. Those who have a previous history of blood or non-hematologic tumors undergoing chemoradiotherapy;
  • 2. In the past 5 years, there is a history of malignant tumors other than skin squamous cell carcinoma, skin basal cell carcinoma, and cervical carcinoma in situ;
  • 3. Patients with central nervous system involvement;
  • 4. There is a serious infection that is not controlled;
  • 5. Have other uncontrolled diseases and the researcher believes that it is not suitable for joiners;
  • 6. Participating in other clinical studies;
  • 7. Persons infected with COVID-19(excluding cured patients);
  • 8. Patients with poor adherence.

研究者

发起方
Guang'anmen Hospital

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