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RECRUITING
NCT06362148

Circulating Tumor DNA in Peripheral T-cell Lymphomas

Sponsor: University of Aarhus

View on ClinicalTrials.gov

Summary

The aim of this study is to evaluate the feasibility of circulating tumor DNA (ctDNA) measurement in blood plasma for the applicability in prognostication, treatment evaluation and measurable residual disease (MRD) surveillance in a cohort of patients with newly diagnosed or relapsed/refractory peripheral T-cell lymphomas (PTCL).

Official title: Next-Generation Sequencing-based, Tumor- and Plasma-informed Droplet Digital PCR Assay for Detection of Circulating Tumor DNA in Peripheral T-cell Lymphomas

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

50

Start Date

2024-03-01

Completion Date

2030-12

Last Updated

2024-04-22

Healthy Volunteers

No

Interventions

DIAGNOSTIC_TEST

Tumor- and plasma-informed, next-generation sequencing (NGS)-based patient-specific droplet digital (dd)PCR assay

Blood sampling for circulating tumor DNA analysis at baseline, cycle 2 day 1, cycle 3 day 1, mid-treatment, end of induction/end of treatment, 100 day follow-up, 6 month, 12 month, 18 month and 24 month follow-up. Blood sampling will also be done in case of relapsing/refractory disease at any point prior to the abovementioned time points.

DIAGNOSTIC_TEST

18F-fludeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT)

FDG-PET/CT performed at baseline, mid-treatment, end of induction/end of treatment and 6 month, 12 month, 18 month and 24 month follow-up.

Locations (1)

Department of Hematology, Aarhus University Hospital

Aarhus, Central Jutland, Denmark