Molecular Screening for Lynch Syndrome in Southern Denmark

Vejle Hospital2,000 enrolled

Overview

A clinically applicably strategy for molecular screening for Lynch Syndrome has been implemented in the Region of Southern Denmark. Based on sequential analysis with immunohistochemistry and methylation analysis, patients with possible hereditary colorectal cancer are identified. These patients are offered genetic risk assessment and counselling. The study hypothesis is that molecular screening will identify more patients with Lynch Syndrome than the family history alone. Prospective data collection is performed using established clinical databases.

Study Type

OBSERVATIONAL

Enrollment

2,000

Conditions

Colorectal Cancer Lynch Syndrome HNPCC

Interventions

ObservationOTHER

Observation

Eligibility

Sex: ALL

Medical Language ↔ Plain English

Inclusion Criteria: * Histological diagnosis of colorectal adenocarcinoma * Diagnosed at one of the five departments of pathology in the region Exclusion Criteria: * None

Locations (7)

Department of Pathology

Esbjerg, Denmark

Department of Clinical Genetics

Odense, Denmark

Department of Pathology

Odense, Denmark

Department of Pahology

Svendborg, Denmark

Data from ClinicalTrials.gov

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