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临床试验/NCT06150053
NCT06150053已完成不适用

Dose Dense Chemotherapy in Elderly Patients > 80 Years Old With DLBCL

University Hospital, Saarland1 个研究点 分布在 1 个国家目标入组 79 人开始时间: 2018年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
79
试验地点
1
主要终点
Progression-free survival (PFS)

研究概览

简要总结

Multi-center retrospective analysis of patients with DLBCL aged ≥80 years old treated with R-CHOP-14 compared to other regimens. Patient data including baseline characteristics, histology, dose intensity and treatment outcomes will be extracted from hospital medical electronic records. Relative dose intensity (RDI) will be calculated as the percentage of the dose intensity achieved divided by the intended dose intensity. Primary endpoints are overall (OS), progression-free (PFS) and event-free survival (EFS), defined as time from diagnosis to death, death or progression/relapse, progression/relapse or treatment discontinuation.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
80 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • histologically proven, untreated diffus large B-cell lymphoma (DLBCL)
  • diagnosis between 2005 - 2019
  • age ≥80 at diagnosis

排除标准

  • diagnosis revision at a later timepoint

结局指标

主要结局

Progression-free survival (PFS)

时间窗: through study completion, an average of 2 years

time from diagnosis to death or progression/relapse

Overall survival (OS) death or progression/relapse, progression/relapse or treatment discontinuation.

时间窗: through study completion, an average of 2 years

time from diagnosis to death

Event-free survival (EFS)

时间窗: through study completion, an average of 2 years

defined as time from diagnosis to death or progression/relapse or treatment discontinuation.

次要结局

  • Relative Dose intensity(within the treatment period, up to 36 weeks)

研究者

发起方
University Hospital, Saarland
申办方类型
Other
责任方
Principal Investigator
主要研究者

Konstantinos Christofyllakis

Consultant

University Hospital, Saarland

研究点 (1)

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