KCT0003887招募中未知
Prospective, multicenter, randomized ,open-labeled, phase III study comparing high-dose intravenous methotrexate versus intrathecal methotrexate for the prophylaxis of CNS relapse in diffuse large B cell lymphoma
Chonnam National University Hospital Hwasun Hospital0 个研究点目标入组 205 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 205
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 18(Year) 至 79(Year)(—)
- 性别
- All
入选标准
- •Aged =18 years <80
- •Newly diagnosed DLBCL
- •High risk of CNS recurrence at diagnosis:
- •i)Age-adjusted IPI (aaIPI) = 2 or IPI = 4
- •ii)involvement of >1 extranodal sites plus an elevated LDH
- •iii) involvement of high-risk locations including bone marrow, nasal or paranasal sinuses,
- •testis, epidural disease (paravertebral or vertebra), breast, liver, adrenal or kidney
- •Estimated life expectancy of more than 3 months
- •ECOG performance status of 2 or lower, Karnofsky scale > 60
- •Adequate cardiac function (EF>45%) on echocardiogram or Heart scan (MUGA scan)
- •80 years of age and over or patient who could be not treated with conventional treatment due to poor general condition.
排除标准
- •Prior chemotherapy treatment for other previous cancer
- •Evidence of CNS involvement at baseline: presented with primary DLBCL of CNS, or concurrent CNS and systemic involvement by DLBCL at diagnosis
- •Lymphoma in patients with human immunodeficiency virus
- •Presence of significant uncontrolled active infection or HBV/HCV carrier patients
- •Presence of uncontrolled bleeding
- •Pregnant or lactating women
- •Patients taking monoamine oxidase inhibitors (MAOIs) will be excluded from the study, because of the risk of severe drug interactions
- •Any coexisting major illness or organ failure
- •Have any acute, subacute or chronic peripheral nerve or spinal cord in grade, at the time of inclusion, greater than or equal to 2 (NCI CTCAE v4.0).
- •Patients with psychiatric disorder or mental deficiency severe as to make compliance with the treatment unlike, and making informed consent impossible
研究者
相似试验
进行中(未招募)
1 期
Prospective, multicenter, randomized, open-label, parallel-group controlled phase 3 study of tacrolimus minimization in kidney transplant recipients selected according to the AGORA algorithm for their low immunological risk and medium-term graft failurekidney transplantationCTIS2022-502624-44-00Centre Hospitalier Universitaire De Nantes332
进行中(未招募)
不适用
Prospective, randomized, multi-center, open label phase III study to evaluate the efficacy and safety of immunosuppression following a heart-beating cadaveric renal transplantation based on the use of rabbit anti-T-lymphocyte serum, tacrolimus and mycophenolate, free of concomitant corticosteroids from the start of immunosuppression - IBERICArenal transplantationEUCTR2005-004431-21-PTFresenius Biotech GmbH160
进行中(未招募)
3 期
A clinical trial to study the effects of two drugs, R-TPR-026 andAranesp® in patients for correction of anemia due to Chronic Kidney DiseaseCTRI/2013/09/004005Reliance Life sciences Pvt Ltd104
进行中(未招募)
3 期
A clinical trial to study the effects of two drugs, R-TPR-023 and Avastinâ?¢ in patients with Metastatic colorectal cancerCTRI/2013/05/003699Reliance Life sciences Pvt Ltd105
进行中(未招募)
3 期
A clinical trial to study the effects of two drugs, R-TPR-016 and Herceptin® in patients with Metastatic HER2-Overexpressing Breast CancerCTRI/2013/04/003549Reliance Life sciences Pvt Ltd
