Clinical trial Recruiting at 1 site Interventional

See how common Muir-Torre syndrome is among people with Lynch syndrome

Official title: Determining the Prevalence of Muir-Torre Syndrome in Patients With Lynch Syndrome

Run by Centre Hospitalier Universitaire de Nīmes · NCT07201012 · Data updated 2026-11-12

This study tests how common Muir-Torre syndrome is in people with a confirmed Lynch syndrome.

More Lynch Syndrome trials

Quick facts

Study typeInterventional
SexAll
Enrollment150 (estimated)
SponsorCentre Hospitalier Universitaire de Nīmes
Academic / other
Locations1 site (Nîmes, Gard)
StatusRecruiting
StartedMarch 13, 2026
Main results expectedNovember 2026
Study endsDecember 2027
Registry record updatedJune 22, 2026
Trial IDNCT07201012 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are people with a confirmed germline alteration in MLH1, PMS2, MSH2, or MSH6 who are followed at CHU de Nîmes and can provide informed consent.

Probably not a fit

Patients without Lynch syndrome or without a confirmed MMR gene mutation may not benefit from the findings.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Researchers will enroll patients with genetically confirmed Lynch syndrome who are treated at CHU de Nîmes to determine how often Muir-Torre syndrome occurs. They will analyze skin and other tumors using immunohistochemistry and microsatellite instability testing to understand tumor patterns linked to the genetic syndrome. A biobank of skin and tumor samples will be created for retrospective and prospective analyses, including smears from skin lesions and healthy tissue. The study will also describe dermatological manifestations and monitor for new tumors as recommended by practice guidelines.

Why it matters

Potential benefit: If successful, the study could clarify how frequently Muir-Torre syndrome occurs in Lynch patients and improve screening and management for skin and visceral tumors.

How similar studies have gone: Prior work has established links between Lynch syndrome and Muir-Torre features, but prevalence in this specific population requires confirmation.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patient with a germline alteration of one of the MMR (MisMatch Repair) pathway genes (MLH1, PMS2, MSH2, MSH6) proven by constitutional genetic analysis (genetically authenticated Lynch syndrome).
* Patient followed at Nîmes University Hospital.
* Patient having given free and informed consent.
* Person affiliated to or benefiting from a social security scheme.

Exclusion Criteria:

* Person under court protection, guardianship or curatorship.
* A person who is unable to give consent.
* Person for whom it is impossible to give informed information.

Where it's running

  • CHU de Nîmes
    Nîmes, Gard, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.