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临床试验/NCT04516655
NCT04516655Unknown2 期

A Phase II, Single-arm Trail of Chidamide Combined With Rituximab and High-dose Methotrexate in Previously Untreated Patients With Primary Central Nervous System Lymphoma

Fudan University0 个研究点目标入组 51 人开始时间: 2020年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
入组人数
51
主要终点
CR rate

研究概览

简要总结

This study will evaluate the efficacy, safety and patient reported outcomes of chidamide 20 mg biw PO day1-14 and rituximab 375 mg/m2 IV given on day 1 and methotrexate 3.5g/m2 IV given on day 2 of every 21-day cycle for 6 cycles in untreated patients with primary central nervous system lymphoma.

The primary study endpoint will be complete response (CR) rate as assessed by the investigator. The hypothesis is previously untreated patients with primary central nervous system lymphoma could achieve a CR rate of 80% with C-R-HDMTX.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ECOG Performance Status of 0, 1, or 2
  • Previously untreated patients with primary central nervous system lymphoma with pathologically confirm
  • At least one bi-dimensionally measurable lesion, defined as >1.0 cm in its longest dimension as measured by MRI
  • Signed written Informed Consent Form
  • hematologic function,defined as follows:
  • Hemoglobin ³ 9.0 g/dL without packed RBC transfusion during 14 days before first treatment
  • ANC ³ 1,000/µL
  • Platelet count ³ 80,000/µL
  • Adequate liver and kidney function function,defined as follows:
  • Serum AST and ALT≤ 2.5 *ULN ,Total bilirubin ≤ 1.5 * ULN Serum creatinine clearance ≥ 50 mL/min (using Cockcroft-Gault formula)

排除标准

  • Evidence of extracranial involvement (such as testis and breast) and secondary CNS involvement
  • Evidence of pleural fluid, ascites and pericardial effusion
  • History or presence of prolonged QTc interval in ECG, QTc interval>470ms in female and >450ms in male
  • History of other malignancy in 5 years
  • Positive test results for hepatitis C, HIV and RPR.
  • Positive test results for chronic hepatitis B infection (defined as positive hepatitis B surface antigen [HBsAg] serology) Patients with occult or prior hepatitis B infection (defined as positive total hepatitis B core antibody and negative HBsAg) may be included if hepatitis B virus (HBV) DNA is less than 10E4 at the time of screening.
  • Pregnancy or lactation or intending to become pregnant during study
  • Prior organ transplantation
  • Known active bacterial, viral, fungal, mycobacterial, parasitic, or other infection at study enrollment or significant infections within 2 weeks before the start of Cycle
  • Evidence of significant, uncontrolled, epilepsy

研究组 & 干预措施

C-R-MTX

Experimental

chidamide 20 mg biw PO day1-14 and rituximab 375 mg/m2 IV given on day 1 and methotrexate 3.5g/m2 IV given on day 2 of every 21-day cycle for 6 cycles

干预措施: chidamide combined with rituximab and high-dose methotrexate (Drug)

结局指标

主要结局

CR rate

时间窗: up to 18 weeks

CR rate of the lesion of previously untreated patients with primary central nervous system lymphoma according to the international collaborative evaluation criteria for central nervous system lymphoma (2005)with Enhanced MRI every 2 cycles

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Fangfang Lv, MD

Principal Investigator

Fudan University

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