Multicentre Study to Determine the Cardiotoxicity of R-CHOP (Rituximab, Cyclophosphamide, Doxorubicin, Vincristin and Prednisolone) Compared to R-COMP (Rituximab, Cyclophosphamide, Liposomal Doxorubicin, Vincristin and Prednisolone) in Patients With Diffuse Large B-Cell Lymphoma (NHL-14)
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 94
- 试验地点
- 10
- 主要终点
- Reduction of cardiotoxicity in the R-COMP arm versus R-CHOP
研究概览
简要总结
Diffuse large B-cell lymphoma is the most prevalent subgroup within malignant lymphoma. Clinical benefit has been shown for the treatment with cyclophosphamide, doxorubicin, vincristin and prednisolone (CHOP regimen); this could be further improved recently by the addition of rituximab (R-CHOP), a monoclonal antibody.
Improved response and overall survival rates make it necessary to evaluate late toxicities of the therapy regimens. Cardiotoxicity is a known risk factor of specific chemotherapies, with 7% patients being affected if doxorubicin cumulative doses are under 550mg/sqm. Retrospective data analyses indicate that this incidence of cardiotoxicity may be higher under combination chemotherapy. Liposomal doxorubicin has been shown to have lower cardiotoxic effects and at the same time equivalent or higher efficacy compared to conventional doxorubicin.
The aim of this study is to evaluate alternative regimens for the treatment of diffuse large B-cell lymphoma, substituting liposomal doxorubicin (R-COMP) for conventional doxorubicin (R-CHOP).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Histologically confirmed, CD20 positive, diffuse large B-cell lymphoma (DLCL)
- •measurable disease according to international criteria
- •male or female
- •age 18 years and above
- •written informed consent
排除标准
- •myocardial infarction within 6 months prior to study entry
- •cardiac insufficiency NYHA grade 3 or 4
- •previous treatment with chemotherapy or radiotherapy
- •CNS involvement of the disease
- •positive for HIV
- •WHO Performance Index 3 or 4
- •secondary malignoma
- •concurrent disease that prohibits chemotherapy
- •known hypersensitivity towards the study interventions or their constituents
- •neutropenia or thrombopenia
研究组 & 干预措施
R-COMP
Treatment with Rituximab, Cyclophosphamide, liposomal Doxorubicin, Vincristin and Prednisolone
干预措施: Cyclophosphamide (Drug)
R-CHOP
Treatment with Rituximab, Cyclophosphamide, Doxorubicin, Vincristin and Prednisolone
干预措施: Rituximab (Drug)
R-CHOP
Treatment with Rituximab, Cyclophosphamide, Doxorubicin, Vincristin and Prednisolone
干预措施: Cyclophosphamide (Drug)
R-CHOP
Treatment with Rituximab, Cyclophosphamide, Doxorubicin, Vincristin and Prednisolone
干预措施: Doxorubicin (Drug)
R-CHOP
Treatment with Rituximab, Cyclophosphamide, Doxorubicin, Vincristin and Prednisolone
干预措施: Vincristin (Drug)
R-CHOP
Treatment with Rituximab, Cyclophosphamide, Doxorubicin, Vincristin and Prednisolone
干预措施: Prednisolone (Drug)
R-COMP
Treatment with Rituximab, Cyclophosphamide, liposomal Doxorubicin, Vincristin and Prednisolone
干预措施: Rituximab (Drug)
R-COMP
Treatment with Rituximab, Cyclophosphamide, liposomal Doxorubicin, Vincristin and Prednisolone
干预措施: liposomal Doxorubicin (Drug)
R-COMP
Treatment with Rituximab, Cyclophosphamide, liposomal Doxorubicin, Vincristin and Prednisolone
干预措施: Vincristin (Drug)
R-COMP
Treatment with Rituximab, Cyclophosphamide, liposomal Doxorubicin, Vincristin and Prednisolone
干预措施: Prednisolone (Drug)
结局指标
主要结局
Reduction of cardiotoxicity in the R-COMP arm versus R-CHOP
时间窗: Study duration
次要结局
- Significance of serial NT-proBNP measurements for determination of anthracycline-dependent cardiotoxicity(Study Duration)
- Feasibility of evaluation with Haematopoietic Cell Transplantation Comorbidity Index (HCT-CI)(Study duration)
- Rate of Complete Responses(At end of treatment)
- Difference in Overall Survival at 3 and 5 yrs(5 years)
- Difference in Event-free Survival at 3 and 5 yrs(5 years)
- Difference in Progression-free Survival at 3 and 5 yrs(5 years)
- Difference in cause-specific death(5 years)