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. 2017 Jul;6(3):167-177.
doi: 10.2217/cns-2017-0014. Epub 2017 Jul 18.

CNS Anticancer Drug Discovery and Development: 2016 conference insights

Affiliations

CNS Anticancer Drug Discovery and Development: 2016 conference insights

Victor A Levin et al. CNS Oncol. 2017 Jul.

Abstract

CNS Anticancer Drug Discovery and Development, 16-17 November 2016, Scottsdale, AZ, USA The 2016 second CNS Anticancer Drug Discovery and Development Conference addressed diverse viewpoints about why new drug discovery/development focused on CNS cancers has been sorely lacking. Despite more than 70,000 individuals in the USA being diagnosed with a primary brain malignancy and 151,669-286,486 suffering from metastatic CNS cancer, in 1999, temozolomide was the last drug approved by the US FDA as an anticancer agent for high-grade gliomas. Among the topics discussed were economic factors and pharmaceutical risk assessments, regulatory constraints and perceptions and the need for improved imaging surrogates of drug activity. Included were modeling tumor growth and drug effects in a medical environment in which direct tumor sampling for biological effects can be problematic, potential new drugs under investigation and targets for drug discovery and development. The long trajectory and diverse impediments to novel drug discovery, and expectation that more than one drug will be needed to adequately inhibit critical intracellular tumor pathways were viewed as major disincentives for most pharmaceutical/biotechnology companies. While there were a few unanimities, one consensus is the need for continued and focused discussion among academic and industry scientists and clinicians to address tumor targets, new drug chemistry, and more time- and cost-efficient clinical trials based on surrogate end points.

Keywords: academia; chemotherapy; gliomas; medulloblastoma; neuro-oncology; pharmaceutical industry.

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Conflict of interest statement

Financial & competing interests disclosure

Funding for the second CADDDC meeting was provided by Genentech, Bristol-Myers Squibb, AbbVie Inc., Pershing Square Sohn Cancer Research Alliance and Agios Pharmaceuticals. Because this manuscript is a meeting summary, we do not believe that there is a specific conflict of interest for any of the authors. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.

No writing assistance was utilized in the production of this manuscript.

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