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Published on: April 23, 2015
The Cancer Drugs Fund in Practice and Under the New Framework
Celia Sabry-Grant1, Kinga Malottki2, Alexander Diamantopoulos2
1Symmetron Limited, 8 Devonshire Square, London, EC2M 4PL, UK. csabrygrant@symmetron.net.
The Cancer Drugs Fund (CDF) allows patient access to treatments before routine availability. Data collection for cancer drugs often exceeds recommendations, ensuring patient benefit while awaiting further evidence.
Area of Science:
- Health economics and outcomes research
- Oncology drug access and reimbursement
- Health technology assessment
Background:
- The Cancer Drugs Fund (CDF) was established in 2010 to enhance patient access to novel cancer treatments.
- Stricter budgeting rules were implemented in 2016, requiring treatments to demonstrate cost-effectiveness potential based on collected data.
Purpose of the Study:
- To examine the process and criteria for evaluating cancer treatments under the revised CDF framework.
- To assess the extent of data collection for treatments included in the CDF.
Main Methods:
- Analysis of CDF list, UK National Institute for Health and Care Excellence (NICE), and Scottish Medicines Consortium documents (dated May 10, 2018).
- Data collection focused on drug indications, reasons for CDF inclusion, data collection methods, incremental cost-effectiveness ratios (ICERs), and Scottish recommendations.
Main Results:
- Twelve drugs were approved for 17 indications, with 12 for end-of-life care. Common cancers included non-small-cell lung, urothelial, lymphocytic leukaemia, and multiple myeloma.
- Companies' ICERs were typically lower than those from committees and evidence review groups.
- Drugs were listed on the CDF for 6-42 months (majority ≥18 months), with overall survival data frequently collected.
Conclusions:
- Data collection for overall survival often surpassed the recommended two years, indicating extended patient access to potentially beneficial drugs.
- The CDF appears to facilitate early patient access to cancer drugs, potentially bridging the gap before routine availability.
- Study limitations include reliance on published data and a small dataset.
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