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Recruiting NCT04088422

Cell Free DNA in Mature B-cell Lymphoma

Observational Mature B-Cell Lymphoma

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: peripheral blood collection.
Who it may be relevant to
Registry conditions: Mature B-Cell Lymphoma. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Prospective, Observational Study on Cell Free DNA Genotyping as a Tool to Inform Mature B-cell Lymphoma Management

Overview

The purpose of this study is to assess whether plasma cell free DNA is an accurate tool that can early and dynamically inform on treatment outcome and an accessible source of tumor DNA to track tumor clonal evolution.

Interventions

  • Procedure peripheral blood collection
    peripheral blood collection at treatment start, interm PET/CT, end of treatment PET/CT, one-year and two-year follow-up and or progression or relapse

Primary outcome measures

  • progression free survival [Time frame: 2-year]
Secondary outcome measures (2)
  • overall survival [Time frame: 2-year]
  • Complete Response rate [Time frame: 6 weeks after treatment]

Eligibility criteria

Inclusion criteria

  • Documented diagnosis of mature B-cell tumor according to WHO 2008 criteria
  • 18 years or older

Exclusion criteria

  • Chemotherapy before
  • Other tumors

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Ruijin hospital — Shanghai

Identifiers

NCT: NCT04088422 · cfDNA

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗