Actively Recruiting

Age: 0 - 17Years
All Genders
ID05937828

French National Cohort of Patients With Pediatric-onset of Autoimmune Cytopenia (OBS'CEREVANCE Cohort)

Led by University Hospital, Bordeaux · Updated on 2023-07-10

3500

Participants Needed

9

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying pediatric-onset autoimmune cytopenias, including Immune Thrombocytopenia (ITP), Autoimmune Hemolytic Anemia (AIHA), and Evans Syndrome, which involves two or three combined cytopenias. These rare diseases cause the immune system to destroy blood cells. This observational cohort study, coordinated by the CEREVANCE Rare Disease Centre and involving 30 French pediatric hematologic centers, aims to understand long-term health outcomes, genetic factors, and treatment effects in these patients. The study collects detailed data over many years on patients diagnosed before age 18 with these autoimmune cytopenias. It includes monitoring disease characteristics, treatment histories, adverse reactions, and immune-related symptoms. The cohort supports care, education, and research missions by maintaining an unbiased database that tracks health and treatment responses, including targeted therapies. Participants are followed regularly with health assessments every six months up to age 19, documenting treatments, side effects, and disease events. This long-term follow-up helps researchers describe disease progression and treatment impact. Data collected include genetic information and clinical outcomes, supporting research into the underlying causes and management of these rare pediatric autoimmune blood disorders.

CONDITIONS

Brief Title

OBS'CEREVANCE: French Cohort of Pediatric Autoimmune Cytopenia

Who Can Participate

Age: 0 - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of Immune Thrombocytopenia (ITP), Autoimmune Hemolytic Anemia (AIHA), or Evans Syndrome
  • Onset of disease before 18 years of age
Not Eligible

You will not qualify if you...

  • Opposition of legal representative to participation or data collection

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Long-term Monitoring

Duration - Up to 19 years

Participants are observed over many years to collect data on health outcomes, treatment responses, and adverse events related to pediatric autoimmune cytopenias.

Visits every 6 months after baseline

Trial Site Locations

Total: 9 locations

1

CHU Amiens Picardie Service d' Onco-Immuno-Hématologie Pédiatrique

Amiens, France

Actively Recruiting

2

CHU d'Angers Unité d'Hémato-Oncologie Pédiatrique

Angers, France

Actively Recruiting

3

BESANCON CHU de Besançon Hôpital Jean MINJOZ Unité d'Hémato-Oncologie Pédiatrique, Pédiatrie 1

Besançon, France

Actively Recruiting

4

CHU de Bordeaux - Unité d'Hématologie et d'Oncologie pédiatrique

Bordeaux, France

Actively Recruiting

5

CHU BREST Hôpital Morvan Unité d'Onco-Hématologie

Brest, France

Actively Recruiting

6

CHU de Caen Unité d'Onco-Hématologie

Caen, France

Actively Recruiting

7

CHU de Clermont Ferrand

Clermont-Ferrand, France

Actively Recruiting

8

APHP Hôpital Bicêtre Service de Pédiatrie générale

Paris, France

Actively Recruiting

9

CH de Cornouaille Service de Pédiatrie

Quimper, France

Actively Recruiting

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Research Team

N

Nathalie ALADJIDI, MD

A

Aurore Capelli

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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Published Research Related To This Trial

Benefits of rituximab as a second-line treatment for autoimmune haemolytic anaemia in children: a prospective French cohort study.

Stéphane Ducassou, Guy Leverger, Helder Fernandes...

https://pubmed.ncbi.nlm.nih.gov/28444729

Treatment with cyclosporin in auto-immune cytopenias in children: The experience from the French cohort OBS'CEREVANCE.

Mathilde Penel Page, Yves Bertrand, Helder Fernandes...

https://pubmed.ncbi.nlm.nih.gov/29756344

Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes.

Jérôme Hadjadj, Nathalie Aladjidi, Helder Fernandes...

https://pubmed.ncbi.nlm.nih.gov/30940614

Second-line treatment trends and long-term outcomes of 392 children with chronic immune thrombocytopenic purpura: the French experience over the past 25 years.

Stéphane Ducassou, Anne Gourdonneau, Helder Fernandes...

https://pubmed.ncbi.nlm.nih.gov/32130726

Prospective Evaluation of the First Option, Second-Line Therapy in Childhood Chronic Immune Thrombocytopenia: Splenectomy or Immunomodulation.

Stéphane Ducassou, Helder Fernandes, Hélène Savel...

https://pubmed.ncbi.nlm.nih.gov/33340549

Long term follow-up of pediatric-onset Evans syndrome: broad immunopathological manifestations and high treatment burden.

Thomas Pincez, Helder Fernandes, Thierry Leblanc...

https://pubmed.ncbi.nlm.nih.gov/33440924