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In 2016, four new anticancer drugs were approved by the FDA, and a further 12 existing agents were approved for 14 additional indications. Each one of these drugs is associated with
important clinical benefits, but at an average monthly cost of ∼US$9,000. Here, I discuss the cost–benefit considerations related to these treatments and contemplate future economic
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local taxes which are calculated during checkout ADDITIONAL ACCESS OPTIONS: * Log in * Learn about institutional subscriptions * Read our FAQs * Contact customer support REFERENCES * Savage,
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http://micromedex.com/products/product-suites/clinical-knowledge/redbook (2017). Download references AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Department of Medical Oncology, Brighton
and Sussex University Hospitals, Eastern Road, BN2 5BE, Brighton, UK Philip Savage Authors * Philip Savage View author publications You can also search for this author inPubMed Google
Scholar CORRESPONDING AUTHOR Correspondence to Philip Savage. ETHICS DECLARATIONS COMPETING INTERESTS The author declares no competing financial interests. POWERPOINT SLIDES POWERPOINT SLIDE
FOR TABLE 1 RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Savage, P. Approvals in 2016: cost–benefit challenges of new anticancer agents. _Nat Rev
Clin Oncol_ 14, 133–134 (2017). https://doi.org/10.1038/nrclinonc.2017.12 Download citation * Published: 20 February 2017 * Issue Date: March 2017 * DOI:
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