Actively Recruiting

Age: 19Years - 74Years
All Genders
ID06796517

Risk Factor Analysis Study for the Efficacy Comparison Between Advanced Immunochemotherapy and Classical Immunochemotherapy: a Prospective Study for Relapsed/Refractory Lymphoma Patients

Led by Sung-Soo Park · Updated on 2025-01-28

72

Participants Needed

2

Research Sites

4 weeks

Total Duration

On this page

Sponsors

S

Sung-Soo Park

Lead Sponsor

Y

Yeouido St. Mary's Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are comparing advanced immunochemotherapy treatments with classical immunochemotherapy in patients with relapsed or refractory high grade B cell lymphoma. The study aims to find out if advanced therapies like CAR-T therapy, bispecific antibodies, and antibody-drug conjugates provide better survival outcomes than classical treatments such as proteasome inhibitors, immune modulatory drugs, and monoclonal antibodies. This observational study uses laboratory findings and electronic medical records to evaluate survival and treatment safety. Participants receive either advanced immunochemotherapy, including CAR-T therapy that modifies and expands their own T cells to target B cell antigens, bispecific antibodies which enhance immune activation without requiring cell modification, or antibody-drug conjugates that deliver targeted cytotoxic drugs to cancer cells. Alternatively, patients may receive classical immunochemotherapy treatments involving proteasome inhibitors, immune modulatory drugs, or monoclonal antibodies targeting specific cancer cell antigens. Treatments are not assigned by the study but observed as part of routine care. Throughout the study, researchers will monitor overall survival from the start of treatment or enrollment for up to 100 months, as well as progression-free survival. Data collection includes laboratory tests and review of medical records to assess outcomes and safety. Participation involves no intervention from the study team beyond data gathering, and the total observation period may extend up to several years to evaluate long-term effects.

CONDITIONS

Brief Title

Immunotherapy in Lymphoma

Who Can Participate

Age: 19Years - 74Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 19 to 74 years
  • Diagnosed with diffuse large B cell lymphoma, primary mediastinal large B cell lymphoma, high grade B cell lymphoma, or Burkitt lymphoma after January 2015
  • Have received immunochemotherapy for relapsed or refractory lymphoma
Not Eligible

You will not qualify if you...

  • Progression to acute leukemia
  • Development of solid tumor during treatment
  • Active infectious status such as acute pneumonia, viral infection, active hepatitis B, or active pulmonary tuberculosis

AI-Screening

AI-Powered 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)

Monitoring

Duration - Up to 100 months

Participants are observed to assess the outcomes of different immunochemotherapy treatments for lymphoma.

Regular visits according to treatment schedules

Trial Site Locations

Total: 2 locations

1

Seoul St. Mary Hospital

Seoul, South Korea, 06591

Actively Recruiting

2

Yeoido St. Mary Hospital

Seoul, South Korea, 07345

Actively Recruiting

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Research Team

S

Sung-Soo Park, MD. PhD.

Y

Young-Woo Jeon, MD. PhD.

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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