ORIGINAL RESEARCH article
Front. Pharmacol.
Sec. Drugs Outcomes Research and Policies
Volume 16 - 2025 | doi: 10.3389/fphar.2025.1532022
The unexploited potential of data systems tracking medicines utilization: An opportunity to improve access to oncology combination therapies
Provisionally accepted- 1KU Leuven, Leuven, Belgium
- 2Oxford Population Health, University of Oxford, Oxford, United Kingdom
- 3Global Oncology Policy, Merck, Rahway, New Jersey, United States
- 4Swedish Institute for Health Economics, Lund, Sweden
- 5Karolinska Institutet (KI), Solna, Stockholm, Sweden
- 6Charles River Associates, London, United Kingdom
- 7Graduate School of Health, Faculty of Health, University of Technology Sydney, Sydney, New South Wales, Australia
- 8Department of Pharmacology, Therapeutics and Toxicology, Autonomous University of Barcelona, Barcelona, Spain
- 9Charles River Associates, Brussels, Belgium
- 10Pharmacoepidemiology Unit, Claude Bernard University Lyon 1, Lyon, France
- 11Charles River Associates, Cambridge, United Kingdom
- 12Aquantic AG, Zeiningen, Switzerland
- 13Postgraduate School of Health Economics and Management (ALTEMS), Catholic University of the Sacred Heart, Rome, Italy
- 14Strathclyde Institute of Pharmacy and Biomedical Sciences, Faculty of Science, University of Strathclyde, Glasgow, Scotland, United Kingdom
- 15Department of Public Health Pharmacy and Management, School of Pharmacy, Sefako Makgatho Health Sciences University, Pretoria, South Africa
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Background: While progress has been made in oncology treatments, including the introduction of combination therapies, barriers affect patient access. There are approaches that could improve access including combination-specific pricing that allow the price to reflect whether a product is used in monotherapy or in combination. The feasibility of this solution requires data on the utilization of combination therapies.Aim: To investigate the ability of data systems across Belgium, England, France, Italy, Spain, Sweden, Switzerland and Australia to track drug utilization of combination therapies, particularly in oncology.Methods: A targeted literature review was conducted to investigate the attributes of the key data systems. One-on-one semi-structured interviews were subsequently conducted with country experts to validate the research, who were screened based on their expertise and knowledge of the respective data and reimbursement systems in their countries, followed by an advisory board to align on policy recommendations. Country-specific and cross-border insights were gathered from nine experts across these countries.Results: There are data systems that routinely collect medicine utilization data across seven European countries and Australia. These datasets can potentially be leveraged to track the utilization of combination therapies. Where available, administrative data systems, such as reimbursement claims data, can be leveraged, though other types of systems, such as product registries, may be more suitable in some countries, emphasizing the need to consider country-specific nuances. Using existing data systems is likely to be less resource-intensive than setting up a novel system for this application. While viable sources of data exist in most countries, many need improving to fully harness their tracking potential. There are several common areas where improvement is needed to track combination therapies effectively. These include data quality, access for different stakeholders, minimizing the burden of data entry and management, and increasing support from national authorities to foster multi-stakeholder engagement. Conclusion: While most countries possess data systems that could serve as a foundation for tracking combination oncology therapies, these systems require optimization and proper implementation. Our core recommendation is for policymakers to explore the expansion and enhancement of data infrastructures.
Keywords: oncology combination therapies1, individual patient-level healthcare data2, utilization tracking3, pricing and reimbursement4, pharmaceutical policy5, Europe6, Australia7
Received: 21 Nov 2024; Accepted: 30 Jun 2025.
Copyright: © 2025 Simoens, Dodwell, Hartevelt, Lindgren, Pistollato, Pont, Pontes, Roediger, Sablek, Van Ganse, Wang, Wenger, Wilsdon, Xoxi and Godman. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Steven Simoens, KU Leuven, Leuven, Belgium
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.