Genetic Factors and Pheochromocytomas in Neoplasia Type 2

Genetic Modifying Factors and Pheochromocytomas in Multiple Endocrine Neoplasia Type 2

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT05158712

Acronym

NEM2A-Pheo

Enrollment

Registered

2021-12-15

Start date

2022-02-02

Completion date

2023-12-14

Last updated

2023-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neoplasia, Pheochromocytoma

Keywords

neoplasia, pheochromocytoma

Brief summary

Multiple endocrine neoplasia type 2A (MEN2A) is a rare syndrome associated with activating mutations in the RET proto-oncogene, combining medullary thyroid cancer in approximately 100% of cases and pheochromocytoma in 10-80% of cases. While it is accepted that the RET mutation causes variable penetrance of pheochromocytoma in the MEN2A patient population, there is no pathophysiological explanation for the phenotypic variability among patients with the same mutation, including within the same family. The aim of this study is to better characterise the genetic factors that may explain the variable penetrance of pheochromocytoma in MEN2. To this end, the investigatoes plan to perform a whole exome analysis in 2 families carrying the p. Cys634Arg mutation causing NEM2A, followed in Marseille by the principal investigator: the 1st family has 11 members all aged over 35 years, for which 8 are carriers of pheochromocytoma while 3 have not developed it (while their age is higher than the latest age of diagnosis of pheochromocytoma in this family); the 2nd family has 3 members (father and daughter with pheochromocytoma developed before 25 years; son without pheochromocytoma at an age of 42 years). The investigators believe that the analysis of these patients should allow the isolation of variants on genes potentially involved in the genesis of a pheochromocytoma in MEN2.

Interventions

None listed

Study design

Observational model

FAMILY_BASED

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Inclusion criteria

* Patient aged 18 years or older * Male or female patient * Patient followed in the investigating department for familial NEM2A C634R (multiple endocrine neoplasia type 2) with or without pheochromocytoma * Patient affiliated to or benefiting from a social security scheme * Patient having given his non-opposition to participate in this study * Patient who has given his consent for the genetic analysis carried out in the framework of the study * Patient able to understand the purpose of the study

Exclusion criteria

* Protected persons (articles L1121-5, L1121-6 and L121-8 of the Public Health Code): pregnant or breastfeeding women, persons deprived of their liberty, under guardianship or curator * Patients unable to understand the purpose of the study and the information note

Design outcomes

Primary

Measure	Time frame	Description
Genetic profile	Month 0	whole-exome analysis between patients with and without pheochromocytoma

Countries

France

Contacts

Primary ContactFrederic Castinetti

frederic.castinetti@ap-hm.fr0491384131

Outcome results