Clinico-immunological Characterization and Immune Tolerance Breakdown in CV2-autoimmunity

NCT ID: NCT06620913

Last Updated: 2024-10-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

232 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-05-01

Study Completion Date

2026-05-01

Brief Summary

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Paraneoplastic neurological syndromes are rare syndromes caused by the remote effects of cancer. They have an immune-mediated pathogenesis, yet the underlying mechanisms are not fully elucidated. CV2/Collapsin response-mediator protein 5 (CRMP5)-IgG paraneoplastic neurological syndrome is characterized by heterogeneous clinical presentations, affecting both central and peripheral nervous system, and the most frequently associate tumor is small cell lung carcinoma. Central nervous system involvement along with CSF and neuroimaging findings have not been fully described in the literature in CV2/CRMP5 patients. Unraveling the complexities of CV2/CRMP5 paraneoplastic neurological syndrome is critical to improve diagnosis, treatment, and patients' care. Our intention is to perform a comprehensive analysis of the clinical characteristics and instrumental investigations of a large cohort of CV2/CRMP5 patients.

Detailed Description

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Conditions

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CV2 Autoimmunity

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Patients with CV2 Abs

Patients harboring CV2 Abs and a paraneoplastic neurological syndromes.

Description of clinical, immunological and tumor features of patients harboring CV2 Abs

Intervention Type OTHER

This is a non-interventional study involving clinical data and biological samples (DNA and tumors block). Demographic and clinical data already collected in the database of the French Reference Center on PNS will be reviewed. The diagnostic tests performed to detect CV2-Abs in the patients already included in the database of the French Reference Center on PNS will be retrospectively analyzed.

Interventions

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Description of clinical, immunological and tumor features of patients harboring CV2 Abs

This is a non-interventional study involving clinical data and biological samples (DNA and tumors block). Demographic and clinical data already collected in the database of the French Reference Center on PNS will be reviewed. The diagnostic tests performed to detect CV2-Abs in the patients already included in the database of the French Reference Center on PNS will be retrospectively analyzed.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient with paraneoplastic neurological syndromes
* Patient with CV2 antibody in sera and/or CSF

Exclusion Criteria

* Patient with no data
* Patient without neurological disorder
* Patient without CV2 antibody in sera/CSF
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hospices Civils de Lyon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pr Jérôme Honnorat, Pr

Role: PRINCIPAL_INVESTIGATOR

Centre de référence des syndromes neurologiques paranéoplasiques et encéphalites auto-immunes, Lyon, France.

Locations

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Hôpital Neurologique Pierre Wertheimer / Groupement Hospitalier Est

Bron, , France

Site Status

Countries

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France

Other Identifiers

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24-5225

Identifier Type: -

Identifier Source: org_study_id

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