Patient decision aids in mainstreaming genetic testing for women with ovarian cancer: A prospective cohort study

Author:

Sobocan Monika1,Chandrasekaran Dhivya2,Sideris Michail13,Blyuss Oleg14,Fierheller Caitlin1,Kalra Ashwin1,Sia Jacqueline1,Miller Rowan E.5,Mills‐Baldock Tina6,Crusz Shanthini M.5,Sun Li1,Evans Olivia1,Robbani Sadiyah1,Jenkins Lucy A.7,Ahmed Munaza7,Kumar Ajith7,Quigley Mary6,Lockley Michelle8,Faruqi Asma9,Casey Laura9,Brockbank Elly3,Phadnis Saurabh3,Trevisan Giorgia9,Singh Naveena9,Legood Rosa10,Manchanda Ranjit1310ORCID

Affiliation:

1. Wolfson Institute of Population Health, Barts CRUK Cancer Centre Queen Mary University of London London UK

2. Department of Gynaecological Oncology University College London Hospital London UK

3. Department of Gynaecological Oncology Barts Health NHS Trust London UK

4. Department of Pediatrics and Pediatric Infectious Diseases Institute of Child´s Health Sechenov First Moscow State Medical University (Sechenov University) Moscow Russia

5. Department of Medical Oncology Barts Health NHS Trust London UK

6. Department of Medical Oncology, Barking Havering and Redbridge University Hospitals Essex UK

7. North East Thames Regional Genetics Service Great Ormond Street Hospital London UK

8. Barts Cancer Institute Queen Mary University of London London UK

9. Department of Pathology Barts Health NHS Trust London UK

10. Department of Health Services Research and Policy London School of Hygiene and Tropical Medicine London UK

Abstract

AbstractObjectiveTo evaluate patient preference for short (gist) or detailed/extensive decision aids (DA) for genetic testing at ovarian cancer (OC) diagnosis.DesignCohort study set within recruitment to the Systematic Genetic Testing for Personalised Ovarian Cancer Therapy (SIGNPOST) study (ISRCTN: 16988857).SettingNorth‐East London Cancer Network (NELCN) population.Population/SampleWomen with high‐grade non‐mucinous epithelial OC.MethodsA more detailed DA was developed using patient and stakeholder input following the principles/methodology of IPDAS (International Patients Decision Aids Standards). Unselected patients attending oncology clinics evaluated both a pre‐existing short and a new long DA version and then underwent mainstreaming genetic testing by a cancer clinician. Appropriate inferential descriptive and regression analyses were undertaken.Main outcome measuresSatisfaction, readability, understanding, emotional well‐being and preference for long/short DA.ResultsThe mean age of patients was 66 years (interquartile range 11), and 85% were White British ethnicity. Of the participants, 74% found DAs helpful/useful in decision‐making. Women reported higher levels of satisfaction (86% versus 58%, p < 0.001), right amount of information provided (76.79% versus49.12%, p < 0.001) and improved understanding (p < 0.001) with the long DA compared with the short DA. There was no statistically significant difference in emotional outcomes (feeling worried/concerned/reassured/upset) between ‘short’ and ‘long’ DA; 74% of patients preferred the long DA and 24% the short DA. Patients undergoing treatment (correlation coefficient (coef) = 0.603; 95% CI 0.165–1.041, p = 0.007), those with recurrence (coef = 0.493; 95% CI 0.065–0.92, p = 0.024) and older women (coef = 0.042; 95% CI 0.017–0.066, p = 0.001) preferred the short DA. Ethnicity did not affect outcomes or overall preference for long/short DA.ConclusionsA longer DA in OC patients has higher satisfaction without increasing emotional distress. Older women and those undergoing treatment/recurrence prefer less extensive information, whereas those in remission preferred a longer DA.

Funder

Barts Charity

Rosetrees Trust

Publisher

Wiley

Subject

Obstetrics and Gynecology

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