RecruitingNCT07472972

Dynamic Individualized Risk Profiling of Patients With Relapsed/Refractory Lymphoid Malignancies and CD19-CAR T Cell Therapy (INTeRCePT 2.0)


Sponsor

University of Zurich

Enrollment

50 participants

Start Date

Jun 20, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

The INTeRCePT 2 study aims to develop a predictive assay to determine which patients with B cell lymphoma are most likely to respond to CAR T cell therapy. This assay combines five components for longitudinal profiling of each patient. The goal of the trial is that the assay can be completed (feasibility). This comprehensive assay integrates five key components including circulating tumor DNA (CAPPseq), inflammation markers from peripheral blood tests (InflaMIX), PET CT imaging parameters, immune cell profiles (flow cytometry), and performance status (ECOG). Ultimately, this tool could improve treatment selection, and guide more personalized therapy decisions for lymphoma patients receiving CAR T cells.


Eligibility

Plain Language Summary

Simplified for easier understanding

This study is closely monitoring patients with a type of blood cancer (B-cell lymphoma) who are receiving a specialized treatment called CAR T cell therapy — where a patient's own immune cells are modified in the lab to fight cancer. Researchers want to learn more about why some patients respond better than others by collecting blood and biopsy samples at different stages. **You may be eligible if...** - You are 18 years or older - You have been diagnosed with relapsed or refractory B-cell lymphoma (cancer that has come back or stopped responding to treatment) - You are already planned to receive CAR T cell therapy as part of your standard care - You are willing to donate blood and tissue samples at scheduled visits **You may NOT be eligible if...** - You have a condition that prevents you from receiving CAR T cell therapy (e.g., active infection, pregnancy) - You have another medical or psychological condition that would prevent you from completing study procedures - You are unwilling or unable to follow the study protocol Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(1)

Universityhospital Zurich, Department of Medical Oncology and Hematology

Zurich, Canton of Zurich, Switzerland

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NCT07472972


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