Study and Monitoring of Multiple Endocrine Neoplasia Type 1

Recruiting

• Conditions: MEN1

• Registration Number: NCT03966612
• Lead Sponsor: Centre Hospitalier Universitaire Dijon

Brief Summary

Multiple Endocrine Neoplasia Type I (MEN1) is a rare autosomal dominant disorder, predisposing sufferers to the development of endocrine tumors. The three most commont endocrine disorders of MEN1 are the secretory tumours of the parathyroid, pituitary gland and pancreas, in addition to which other tumours may be observed.

The diagnosis of MEN1 is essential for 1) appropriate therapeutic management of proven endocrine disorders, 2) screening for other endocrine and non-endocrine tumours, 3) family screening of affected relatives and 4) monitoring of patients who have been diagnosed. Undiagnosed MEN1 is one of the reasons for therapeutic failure in the management of endocrine damage. Detection is therefore of major importance, and any improvement in early diagnosis can improve management.

The natural history of the disease in all its clinical forms remains poorly understood, with published studies of selected or small populations. There are still clinical forms that are difficult to link to the syndrome. These clinical forms need to be specified in order to ensure optimal management. Only a large cohort will lead to the identification of the various forms of this condition and clarify its prognosis.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2019-01-11
• Study Start: 2019-04-05
• Study First Submitted QC: 2019-05-24
• Study First Posted: 2019-05-29
• Status Verified: 2024-07
• Last Update Submitted: 2024-07-26
• Last Update Posted: 2024-07-29
• Primary Completion: 2028-12
• Study Completion: 2029-11

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 1600

Inclusion Criteria

SYMPTOMATIC PATIENTS

• person (adult or minor) who has not opposed participation
• if the patient is a minor, the parents must not oppose their child's participation,
• at least two of the three main types of lesions (parathyroid, pancreas, pituitary gland)
• OR a known isolated tumor, main type or not, associated with the gene mutation of the NEM1 locus on chromosome 11q13
• OR an isolated tumor, main type or not, in an individual with a confirmed family history of NEM1

ASYMPTOMATIC PATIENTS WITH A MUTATION

• Presence of a characteristic mutation of NEM1

Exclusion Criteria

NA

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
risk of occurrence of each type of MEN1 related tumors	Through study completion, an average of 10 years	risk of occurrence of each type of MEN1 related tumors in patients with confirmed MEN-1
genotype-phenotype correlation : association of specific mutations (genotype) with the clinical manifestations (phenotype)	Through study completion, an average of 10 years
overall survival	Through study completion, an average of 10 years
specific survival and life expectancy	Through study completion, an average of 10 years
age at Men1 diagnosis globally and according to the initial presentation	Through study completion, an average of 10 years
treatment description of each type of MEN1 related tumors as well as their impact on survival and on disease control	Through study completion, an average of 10 years

Trial Locations

Locations (1)

CHU Dijon Bourgogne; 🇫🇷 Dijon, France