Actively Recruiting

Age: 18Years +
All Genders
ID06550427

Early Assessment of Aggressive B-Cell Lymphoma Treatment Response and Prediction of Recurrence Using Phased Variant Analysis With Next-Generation Sequencing

Led by National Taiwan University Hospital · Updated on 2025-06-17

200

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Lymphoma, including large B-cell lymphoma (LBCL), is a common aggressive cancer affecting the lymphatic system. This research is focused on using a new method called phased variant analysis with next-generation sequencing to monitor circulating tumor DNA (ctDNA) in the blood. This approach aims to better understand how the lymphoma responds to treatment and to predict if the disease might come back, offering a potentially safer alternative to current imaging methods like CT and PET scans. The study is observational and involves collecting blood samples from participants diagnosed with lymphoma to analyze ctDNA using phased variant techniques. This advanced genetic testing looks at specific DNA mutations from tumor cells to track changes during treatment. The goal is to see how ctDNA levels correlate with early treatment outcomes over a period of up to 24 months or until death. Participants will be monitored through regular blood tests to measure ctDNA levels, alongside standard clinical assessments. Researchers will compare these results with disease progress and treatment response using clinical data. The main outcome measured is the relationship between ctDNA analyzed by phased variant and the early outcomes of lymphoma, helping to evaluate the effectiveness of this diagnostic approach while ensuring participant safety throughout the study duration.

CONDITIONS

Brief Title

Early Assessment of Lymphoma Treatment Response Using Phased Variant Analysis With Next-Generation Sequencing

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Pathology proven lymphoma
  • Age 18 years or older
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 24 months or until death

Participants undergo blood sample collection for ctDNA analysis using phased variant next-generation sequencing to assess lymphoma treatment response.

Periodic blood sample collections as scheduled by the study

Long-term Monitoring

Duration - Up to 24 months or until death

Participants are monitored for early outcomes of lymphoma and potential recurrence following ctDNA analysis.

Follow-up visits scheduled over the monitoring period

Trial Site Locations

Total: 1 location

1

National Taiwan University Hospital

Taipei, Taiwan

Actively Recruiting

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Research Team

T

Tai-Chung Huang, Ph.D

H

Huang

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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