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Recruiting Observational

The Pathogenesis and Prognostic Factors of Lymphoma

NCT06203652 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2023-06-05
Last updated
2024-01-12

Condition(s) studied

LymphomaHodgkin LymphomaNon-hodgkin Lymphoma

Investigational drug(s) / intervention(s)

Real-world regimen

Real-world regimen: The final personalized management strategy is determined based on current conventional treatment options, physician and patient preferences.The following protocols: chemotherapy, immunochemotherapy,Anti-cd20 monoclonal antibody, BTKi and so on

Study summary

The aim of this study is to describe the clinical and genetic characteristics of Chinese lymphoma patients, and to explore the relationship between those characteristics and phatogenesis.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients with pathological diagnosis of lymphoma (including Hodgkin lymphoma and non-Hodgkin lyphoma, eg. THRLBCL, DLBCL, MZL, CLL/SLL...) from 2007 to 2027. * Patients with complete diagnostic, treatment and follow-up records. * Fully comprehension and signature of the informed consent form (ICF) for participation. Exclusion Criteria: * Those who refuse to use reliable methods of contraception during pregnancy, lactation or age-appropriate period. * Severe mental illness. * Patients deemed unsuitable for inclusion by the investigator.

Primary outcome measure(s)

  • OS — Baseline up to data cut-off (Up to approximately 20 years)
    Overall survival (OS) refers to the time from receiving the first dose to death from any cause

Trial sites (1)

FacilityCityRegionStatus
Zhongshan Hospital,Fudan University Shanghai Shanghai Municipality Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06203652 on ClinicalTrials.gov ↗ ← All trials in China