ISRCTN88720356已完成3 期
A clinico-pathologic study of Primary Mediastinal B-cell lymphoma
Southampton University Hospitals NHS Trust (UK)0 个研究点目标入组 125 人开始时间: 2010年3月31日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 125
研究概览
简要总结
2014 results in: https://www.ncbi.nlm.nih.gov/pubmed/24799481 (added 10/09/2019) 2015 results in: https://www.ncbi.nlm.nih.gov/pubmed/26089397 (added 10/09/2019) 2018 results in: https://www.ncbi.nlm.nih.gov/pubmed/29720487 (added 10/09/2019)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Primary mediastinal diffuse large B-cell lymphoma, CD20 positive. Patients must have histological confirmation of the diagnosis, and in addition have a dominant mass within the anterior mediastinum.
- •2. No prior treatment of lymphoma. Patients may have received corticosteroids for up to 1 week for the relief of local compressive symptoms.
- •3. Any stage of disease
- •4. Age at least 18 years
- •5. Fit to receive chemotherapy with curative intent
- •6. Able and willing to give informed consent, and to undergo staging including PET scanning
- •7. Willingness to comply with an appropriate contraceptive method in women of childbearing potential or men
排除标准
- •1. Evidence of clinically significant cardiac disease, as defined by history of symptomatic ventricular arrhythmias, congestive heart failure or myocardial infarction within 12 months before study entry
- •2. Cardiac compromise due to local extension of lymphoma will not be an exclusion criterion in the absence of other cardiac disease
- •3. Impairment of bone marrow function (WBC < 3.0 x 10^9/L, ANC < 1.5 x 10^9/L, PLT < 100 x 10^9/L), unless due to involvement by lymphoma
- •4. Major impairment of renal function (serum creatinine > 2 x upper normal) or liver function (ASAT/ALAT > 2.5 x upper normal, total bilirubin > 2.5 x upper normal), unless due to lymphoma involvement
- •5. Known HIV infection. Patients will not be tested routinely.
- •6. Pregnant or lactating women
- •7. Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial
研究者
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