Cost-benefit analysis of biomarker-driven early detection of pancreatic cancer in individuals with new-onset diabetes

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Stefanova, Irena and Thompson, Nathan and Stott, Martyn and Oldfield, Lucy and Hanson, Robert and van der Meer, Robert and Palmer, Daniel and Greenhalf, William and Halloran, Christopher and Costello, Eithne (2024) Cost-benefit analysis of biomarker-driven early detection of pancreatic cancer in individuals with new-onset diabetes. In: 56th European Pancreatic Club (EPC) Meeting, 2024-06-26 - 2024-06-29, Auditorio de Galicia.

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Abstract

Introduction: Pancreatic adenocarcinoma (PDAC) is associated with a poor 5-year survival rate of 7-10% and a low incidence (13.3 in 100,000 people). Population-wide screening using current modalities is not feasible. However, screening of high-risk groups is recommended. By the time of PDAC diagnosis, ~85% of patients have glucose dysregulation and 40-65% have diabetes, the majority of which is new-onset (NOD< 3 years). In effect, NOD is a warning sign for the development of PDAC. For 10% of individuals in the NOD high-risk cohort diabetes is a result of pancreatic disease, of which 10% is PDAC-related diabetes. The United Kingdom Early Detection Initiative for pancreatic cancer (UK-EDI) study is establishing resources and undertaking research aimed at detecting pancreatic cancer in the NOD high-risk group. It is currently investigating plasma biomarker panels which differentiate between type 2 and type-3c diabetes which could facilitate PDAC screening in individuals with NOD. Evaluating key factors in a biomarker’s value could aid its refinement and development into an economically viable screening solution. Aim: To undertake cost-benefit analysis of biomarker-driven PDAC screening in NOD. Methods: Markov state-transition decision model: assessing the downstaging benefits of new screening policies over a 5-year period; focused on individuals with NOD >50 years, if screened for PDAC using a novel biomarker signature; comparison of biomarker-driven screening cohort to standard care pathway. Health-related quality of life utility weights - taken from the most recent literature. Average treatment costs for each health state - taken from NHS Cost Collection 2021-2022 and recent literature. Included are the cost of operation, intensive care stay, physiotherapy, diabetes care, chemotherapy (neoadjuvant and adjuvant, endoscopy/interventional radiology services, dietitian care, palliative care and hepatobiliary and oncology appointments. Calculation of: Incremental cost-effectiveness ratios; Net benefits; Willingness-to-pay threshold per Quality-Adjusted Life Year (QALY) of £30,000. One-way and multi-way sensitivity analysis, to allow for parameter uncertainty and determine critical factors for cost effectiveness. Results: Biomarker-driven screening for PDAC in NOD can be cost effective (costing £28,617.33 per QALY), provided that: screening is targeted at high-risk patients with NOD (1% risk threshold group); biomarker performance is high (sensitivity and specificity at 90% or above); biomarker costs are sufficiently low (around £45/test); At least 35% of PDAC cases detected through screening have resectable-stage disease. The most influential factors were: biomarker specificity and sensitivity, incidence in target population and resectable PDAC treatment cost. Future direction: UK-EDI will continue to progress its resource building (including NOD cohort and questionnaire data) in parallel with developing its biomarker pipeline to facilitate biomarker-driven screening of NOD for PDAC. Cost benefit analysis will be a consistent key component of this work. Conclusions: Cost-benefit analysis plays an essential part in biomarker discovery because it informs key stake holders regarding relevant factors in biomarker value. This is essential component of their translation into a real-world practical application. Screening the high-risk NOD group for PDAC becomes cost-effective when an optimal biomarker signature can be selected. Acknowledgements: We are grateful for the support provided by Cancer Research UK, Pancreatic Cancer UK, Liverpool ECMC, and TRANSPAN COST Action CA21116 (European Cooperation in Science and Technology) for funding to attend this conference. Collaborations: This work is undertaken in collaboration with Management Science at the University of Strathclyde (Glasgow, UK) and the UK Early Detection Initiative for pancreatic cancer (led by Liverpool).

ORCID iDs

Stefanova, Irena, Thompson, Nathan, Stott, Martyn, Oldfield, Lucy, Hanson, Robert, van der Meer, Robert ORCID logoORCID: https://orcid.org/0000-0002-9442-1628, Palmer, Daniel, Greenhalf, William, Halloran, Christopher and Costello, Eithne;
CORE (COnnecting REpositories)