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临床试验/NCT07285174
NCT07285174尚未招募不适用

Shanghai Lymphoma Clinical Cohort

Ruijin Hospital0 个研究点目标入组 1,000 人开始时间: 2025年12月18日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
1,000
主要终点
Progression Free Survival (PFS)

研究概览

简要总结

The aim of this study is to prospectively collect clinical information on patients with lymphoma, and to explore the best therapeutic strategies in the real-world population.

详细描述

Lymphoma is a common hematological malignancy. This study aims to prospectively collect clinical information on patients with lymphoma, including the distribution of involved sites, clinical and molecular characteristics of different lymphoma subtypes, clinical treatment protocols, and prognosis, to explore the best therapeutic strategies in the real-world population.

研究设计

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

入排标准

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

入选标准

  • Age ≥ 16 years (including 16 years old).
  • Patients newly diagnosed with non-Hodgkin lymphoma
  • Patients who have received systematic clinical treatment.
  • Patients with measurable lesions, at least containing one effective evaluation of efficacy.

排除标准

  • Patients who only receive supportive treatment.
  • Patients who cannot obtain effective evaluation data of efficacy.

结局指标

主要结局

Progression Free Survival (PFS)

时间窗: Baseline up to data cut-off (up to approximately 1 year)

Progression-Free Survival (PFS) will be defined from the date of starting therapy and the date of disease progression, relapse or death from any cause.

次要结局

  • Overall Survival (OS)(Baseline up to data cut-off (up to approximately 1 year))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Zhao Weili

Dean

Ruijin Hospital

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