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RECRUITING
NCT05440838

Identification of Factors Associated With Treatment Response in Patients With Polycythemia Vera, Essential Thrombocythemia, and Pre-myelofibrosis.

Sponsor: University Hospital, Angers

View on ClinicalTrials.gov

Summary

First-line treatment for patients with polycythemia vera, essential thrombocythemia, and pre-myelofibrosis is based on hydroxyurea or pegylated interferon. The objective of treatment is to prevent thrombotic complications and leukemic transformation. Despite overall good response rates, some patients do not respond to treatment and others lose their response over time. Both situations are associated with worse survival and there are to date no clear predictive factors for response although the existence of additional mutations seems unfavorable. In this exploratory study, we hypothesize that biological factors at diagnosis are associated with hematological response at 12 months. We will more specifically study the association between mutational profile, assessed by next-generation sequencing, and cytokine profile with hematological response. This study will help in identifying patients who will not respond to hydroxyurea or pegylated interferon and give the opportunity to try other treatments upfront, in the perspective of precision medicine. On the basic science side, this study will help in understanding the molecular and immunological factors involved in resistance to treatment.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

120

Start Date

2023-05-17

Completion Date

2032-02-17

Last Updated

2026-03-06

Healthy Volunteers

No

Interventions

DIAGNOSTIC_TEST

Next-generation sequencing

Next-generation sequencing and cytokine profile will be established in all patients before the start of treatment.

Locations (6)

Chu Angers

Angers, France

Chu Brest

Brest, France

Chu Nantes

Nantes, France

Chu Poitiers

Poitiers, France

Chu Rennes

Rennes, France

Chu Tours

Tours, France