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临床试验/EUCTR2011-003769-14-IT
EUCTR2011-003769-14-IT进行中(未招募)不适用

R-CHOP-14 or R-CHOP-21 & consolidation PET–oriented radiotherapy (RT) in diffuse large B cell lymphoma (DLBCL) patients with low risk profile according to age-adjusted IPI (0 with bulky or 1)

Fondazione Italiana Linfomi ONLUS0 个研究点开始时间: 2012年3月7日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(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
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Age 18-80 years
  • Patients aged > 70 years with FIT profile according to VGM
  • Histological diagnosis of DLBCL (CD20+), follicular lymphoma grade IIIB, T-cell rich large B cell lymphoma
  • aaIPI=1 +/- bulky and aaIPI=0 with bulky (>7.5 cm)
  • ECOG-PS < 3 unless due to lymphoma
  • Ventricular ejection fraction = 50%
  • Biochemical, renal and hepatic tests within normal range
  • Negative HIV and HBV tests. In case of HBcAb positive and HBsAb +/-, which is indicative of a past infection (occult carriers) the subject can be included, but antiviral prophylaxis with lamivudine must be given from the beginning of treatment until 12 months after treatment completion. Anti-HCV positive patients can be included in the absence of viral replication (HVR-RNA absent or less than 500 copies/ml.
  • Written informed consent
  • Life-expectancy > 3 months
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 92
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 20

排除标准

  • CD20 negative B-cell lymphoma;
  • Lymphoblastic lymphoma or Burkitt’s lymphoma;
  • Primary Mediastinal B-cell Lymphoma;
  • Grade I, II, IIIa Follicular Lymphoma, Lymphocytic/Lymphoplasmacytic, Marginal, Mantle Lymphoma;
  • T cell Lymphoma (any histotype);
  • Patients aged > 80 years and < 18 years;
  • Age-adjusted IPI= 0 (with no bulky disease);
  • PS > 3 if not related to lymphoma;
  • Patient already treated with chemotherapy, RT, immunotherapy (with the exception of therapies specified in the study protocol);
  • Creatinine >1.4 mg/dl or creatinine clearance <60 ml/min;
  • AST/ALT or Bilirubin >2.5 times normal limit, unless the alteration is due to lymphoma;
  • Clinically significant cardiopathies or cardiovascular disease (e.g. uncontrolled hypertension, uncontrolled multifocal cardiac arrhythmias);
  • Ventricular ejection fraction < 50%;
  • Pulmonary pathologies (e.g. BPCO, pulmonary fibrosis, TBC etc);
  • Concurrent thrombohemolytic disease;
  • HIV positivity;
  • Positive serology for HBV (HBsAg+) and HCV positivity in presence of replication marks;
  • CNS localization disease;
  • Malignancy during last 3 years, except from carcinoma in situ of the cervix, basal cell skin carcinoma or early stage prostate cancer or DCIS (good prognosis) treated only with surgery;
  • Inability of the patient to give her/his informed consent;
  • Drug addiction or alcoholism;
  • Pregnancy or breast-feeding women.

研究者

发起方
Fondazione Italiana Linfomi ONLUS

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