TY - JOUR
T1 - Patient Preferences for Hepatocellular Carcinoma Surveillance Parameters
AU - Woolen, Sean A.
AU - Singal, Amit G.
AU - Davenport, Matthew S.
AU - Troost, Jonathan P.
AU - Khalatbari, Shokoufeh
AU - Mittal, Sukul
AU - Siddiqui, Sehar
AU - Fobar, Austin
AU - Morris, Jason
AU - Odewole, Mobolaji
AU - Tapper, Elliot B.
AU - Pillai, Anjana
AU - Parikh, Neehar D.
N1 - Funding Information:
Conflicts of Interest These authors disclose the following: Amit G. Singal has served on advisory boards and as a consultant for Wako Diagnostics, Roche, Exact Sciences, Glycotest, and Bayer. Matthew Davenport has received unrelated royalties from Wolters Kluwer. Jonathan Troost owns stocks in Procter & Gamble and General Electric. Elliot Tapper has served as a consultant for Novartis, Axcella, Kaleido, Mallinckrodt, and Allergan; and on advisory boards for Mallinckrodt, Novo Nordisk, Takeda, and Rebiotix. Anjana Pillai has served on the Speakers Bureau for Simply Speaking Hepatitis and on the medical advisory board for Exelixis, Eisai, and Genentech. Neehar D. Parikh has served as a consultant for Bristol Myers Squibb, Exact Sciences, Eli Lilly, Freenome has served on advisory boards of Genentech, Eisai, Bayer, Exelixis, Wako/Fujifilm and has received research funding from Bayer, Target Pharmasolutions, Exact Sciences, and Glycotest. Funding Amit G. Singal's research is supported in part by National Institutes of Health U01 CA230694, R01 212008, and R01 MD12565. Neehar D. Parikh's research is supported in part by U01 CA230669. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Funding Information:
Funding Amit G. Singal’s research is supported in part by National Institutes of Health U01 CA230694, R01 212008, and R01 MD12565. Neehar D. Parikh’s research is supported in part by U01 CA230669. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Publisher Copyright:
© 2022 AGA Institute
PY - 2022/1
Y1 - 2022/1
N2 - Background and Aims: Professional societies recommend abdominal ultrasound (US) with or without alpha fetoprotein (AFP) for hepatocellular cancer (HCC) surveillance; however, there are several emerging surveillance modalities, including abbreviated MRI and blood-based biomarker panels. Most studies have focused on provider perspectives for surveillance logistics, but few have assessed patient preferences. We aimed to measure preferences among patients with cirrhosis regarding HCC surveillance modalities. Methods: We conducted a choice-based conjoint survey to patients with cirrhosis at four institutions. Participants were provided 15 scenarios in which they were asked to choose surveillance modalities based on five test attributes: benefits, i.e. sensitivity for early HCC (range: 35-95%), physical harm, i.e. false positives requiring additional testing (range: 10-40%), financial harm, i.e. out-of-pocket costs (range: $10-100), test logistics and convenience, i.e. duration of testing (range: 10-60 min). Hierarchical Bayes discrete choice conjoint analysis was used to derive attribute importance, and preference shares were determined by simulation. Results: In total 91% (182/199) of approached patients consented to participate in the study and 98% (n=179) successfully completed the survey. Surveillance benefits (importance: 51.3%, 95%CI: 49.0-53.4%) were valued more than risk of physical harm (importance: 7.6%, 95%CI 7.0-8.2%), financial harm (importance: 15.2%, 95%CI 14.0-16.3%), convenience (importance: 9.3%, 95%CI 8.5-10.1%) and test logistics (importance: 16.7%, 95%CI 15.4-18.1%). Based on simulations including all possible tests, patients preferred abbreviated MRI (29.0%), MRI (23.3%), or novel blood-based biomarkers (20.9%) to ultrasound alone (3.4%) or with AFP (8.8%). Conclusions: Patients with cirrhosis prioritize early HCC detection over potential surveillance-related harms or inconvenience.
AB - Background and Aims: Professional societies recommend abdominal ultrasound (US) with or without alpha fetoprotein (AFP) for hepatocellular cancer (HCC) surveillance; however, there are several emerging surveillance modalities, including abbreviated MRI and blood-based biomarker panels. Most studies have focused on provider perspectives for surveillance logistics, but few have assessed patient preferences. We aimed to measure preferences among patients with cirrhosis regarding HCC surveillance modalities. Methods: We conducted a choice-based conjoint survey to patients with cirrhosis at four institutions. Participants were provided 15 scenarios in which they were asked to choose surveillance modalities based on five test attributes: benefits, i.e. sensitivity for early HCC (range: 35-95%), physical harm, i.e. false positives requiring additional testing (range: 10-40%), financial harm, i.e. out-of-pocket costs (range: $10-100), test logistics and convenience, i.e. duration of testing (range: 10-60 min). Hierarchical Bayes discrete choice conjoint analysis was used to derive attribute importance, and preference shares were determined by simulation. Results: In total 91% (182/199) of approached patients consented to participate in the study and 98% (n=179) successfully completed the survey. Surveillance benefits (importance: 51.3%, 95%CI: 49.0-53.4%) were valued more than risk of physical harm (importance: 7.6%, 95%CI 7.0-8.2%), financial harm (importance: 15.2%, 95%CI 14.0-16.3%), convenience (importance: 9.3%, 95%CI 8.5-10.1%) and test logistics (importance: 16.7%, 95%CI 15.4-18.1%). Based on simulations including all possible tests, patients preferred abbreviated MRI (29.0%), MRI (23.3%), or novel blood-based biomarkers (20.9%) to ultrasound alone (3.4%) or with AFP (8.8%). Conclusions: Patients with cirrhosis prioritize early HCC detection over potential surveillance-related harms or inconvenience.
KW - HCC
KW - Harms
KW - Screening
KW - Sensitivity
UR - http://www.scopus.com/inward/record.url?scp=85103724935&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85103724935&partnerID=8YFLogxK
U2 - 10.1016/j.cgh.2021.02.024
DO - 10.1016/j.cgh.2021.02.024
M3 - Article
C2 - 33618022
AN - SCOPUS:85103724935
SN - 1542-3565
VL - 20
SP - 204-215.e6
JO - Clinical Gastroenterology and Hepatology
JF - Clinical Gastroenterology and Hepatology
IS - 1
ER -