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The Cancer Drugs Fund in Practice and Under the New Framework

  • Celia Sabry-GrantEmail author
  • Kinga Malottki
  • Alexander Diamantopoulos
Original Research

Abstract

Background

The Cancer Drugs Fund (CDF) was established in 2010 to improve access to treatments not routinely available. Having widely overspent, stricter budgeting rules were introduced in 2016. The CDF can now only include treatments with potential to be cost effective once sufficient data are collected.

Objectives

Our objective was to explore the process and criteria used for consideration of treatments under the new CDF framework and to describe the extent of evidence collection.

Methods

We identified CDF list, UK National Institute for Health and Care Excellence (NICE) and Scottish Medicines Consortium documents (10 May 2018). Data were collected on drugs and indications, reasons for inclusion in the CDF, data collection, incremental cost-effectiveness ratios (ICERs), and corresponding recommendations for Scotland.

Results

In total, 12 drugs were listed on the CDF in 17 indications, 12 of which were considered end-of-life care. The most common cancers were non-small-cell lung (n = 4), urothelial (n = 3), lymphocytic leukaemia (n = 2) and multiple myeloma (n = 2). The companies’ ICERs were generally lower than those from the committee and the evidence review group. Drugs were included in the CDF for 6–42 months, with the majority included for ≥18 months. Data were frequently collected on overall survival (n = 16) and progression-free survival (n = 5) using NHS systems and, frequently, ongoing trials.

Conclusions

Data collection frequently included overall survival and exceeded the 2 years recommended in the CDF strategy. It appears the CDF is allowing patients access to drugs long before they may become available for routine use. Our results are limited by the availability of published information and the small dataset.

Notes

Acknowledgements

The authors thank Arianna Gentilini and Marta Giulia Viola for comments on the data synthesis.

Author Contributions

CSG, KM and AD designed the study, CSG carried out and KM checked the accuracy of identification of relevant cases and data collection, CSG, KM and AD undertook the synthesis and interpretation of the data. CSG and KM drafted the manuscript and all authors approved the final version.

Compliance with Ethical Standards

Funding

No sources of funding were used to conduct this study or prepare this manuscript.

Conflicts of interest

C. Sabry-Grant, K. Malottki and A. Diamantopoulos have no conflicts of interest that are directly relevant to the content of this article.

Data Availability

The data that support the findings of this study are available from the corresponding author upon reasonable request.

Supplementary material

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Supplementary material 1 (DOCX 26 kb)
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Supplementary material 2 (DOCX 26 kb)
40273_2019_793_MOESM3_ESM.xlsx (18 kb)
Supplementary material 3 (XLSX 17 kb)
40273_2019_793_MOESM4_ESM.docx (20 kb)
Supplementary material 4 (DOCX 19 kb)

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Copyright information

© Springer Nature Switzerland AG 2019

Authors and Affiliations

  1. 1.Symmetron LimitedLondonUK

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