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The economic evaluation of personalised oncology medicines: ethical challenges
Jan R R Lewis1, Wendy L Lipworth, Ian H Kerridge
1Centre for Values, Ethics and Law in Medicine, University of Sydney, Sydney, NSW, Australia. jlewis@med.usyd.edu.au.
Abstract:
Insights into the molecular drivers of cancer are providing opportunities for the development of new targeted treatments and more personalised approaches to cancer management. Drugs targeting mutant epidermal growth factor receptors, such as erlotinib and gefitinib, may provide more effective, safer and better tolerated treatment options compared with chemotherapy among appropriately selected patients with advanced non-small cell lung cancer (NSCLC). First-line access to these newer treatments remains unfunded after several considerations by the Pharmaceutical Benefits Advisory Committee and their assessment that these are not cost-effective treatments. We suggest that there may be evidentiary and ethical challenges associated with the assessment of the cost-effectiveness of personalised oncology medicines in Australia, and that a new approach is needed to determine the value and cost-effectiveness of personalised medicine.
Insights
Targeted cancer therapies like erlotinib and gefitinib offer better options for advanced non-small cell lung cancer (NSCLC). However, their cost-effectiveness assessment in Australia poses challenges, necessitating a new approach for personalized medicine evaluation.
Area of Science:
- Oncology
- Pharmacoeconomics
- Molecular Biology
Background:
- Molecular insights are driving personalized cancer treatments.
- Targeted therapies like erlotinib and gefitinib show promise for advanced non-small cell lung cancer (NSCLC).
- Current treatments may be surpassed by targeted drugs in efficacy, safety, and tolerability for selected patients.
Purpose of the Study:
- To examine the challenges in assessing the cost-effectiveness of personalized oncology medicines in Australia.
- To propose a new framework for evaluating the value of personalized medicine.
Main Methods:
- Review of current treatment guidelines and reimbursement decisions.
- Analysis of pharmacoeconomic assessment frameworks.
- Ethical considerations in personalized medicine evaluation.
Main Results:
- First-line access to targeted therapies for advanced NSCLC is currently unfunded in Australia.
- The Pharmaceutical Benefits Advisory Committee has deemed these treatments not cost-effective.
- Significant evidentiary and ethical challenges exist in current cost-effectiveness assessments.
Conclusions:
- A novel approach is required to accurately determine the value and cost-effectiveness of personalized oncology medicines.
- Current assessment methods may not adequately capture the benefits of targeted cancer therapies.
- Addressing these challenges is crucial for equitable patient access to innovative treatments.
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