跳至主要内容
临床试验/ISRCTN88720356
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

发起方
Southampton University Hospitals NHS Trust (UK)

相似试验