Universal tumor screening for lynch syndrome: perspectives of patients regarding willingness and informed consent

Author:

Subramonian Anusree1ORCID,Smith Doug2,Dicks Elizabeth1,Dawson Lesa34ORCID,Borgaonkar Mark5ORCID,Etchegary Holly1ORCID

Affiliation:

1. Clinical Epidemiology, Faculty of Medicine, Memorial University, St John's, NL, Canada

2. Patient Partner, St. John's, NL, Canada

3. Gynecologic Oncology, Women's Health & Genetics, Faculty of Medicine, Memorial University, St John's, NL, Canada

4. Women’s Health and Genetics, Eastern Health, St John's NL, Canada

5. Gastroenterology, Faculty of Medicine, Memorial University, St John's, NL, Canada

Abstract

Aim: Lynch Syndrome is associated with a significant risk of colorectal carcinoma (CRC) and other cancers. Universal tumor screening is a strategy to identify high-risk individuals by testing all CRC tumors for molecular features suggestive of Lynch Syndrome. Patient interest in screening and preferences for consent have been underexplored. Methods: A postal survey was administered to CRC patients in a Canadian province. Results: Most patients (81.4%) were willing to have tumors tested if universal tumor screening were available and were willing to discuss test results with family members and healthcare professionals. The majority (62.6%) preferred informed consent be obtained prior to screening. Conclusion: Patients were supportive of universal screening. They expected consent to be obtained, contrary to current practice across Canada and elsewhere.

Publisher

Future Medicine Ltd

Subject

Pharmacology,Molecular Medicine,General Medicine

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