Abstract 307: The use of biospecimens in cancer population science research

Abstract

Abstract Background: Over the past two decades, researchers have increasingly used human biospecimens to help evaluate hypotheses related to disease risk, outcomes and treatment options. We conducted an analysis of the population science cancer research grants funded by NCI in order to gain a more comprehensive understanding of the biospecimens involved in those studies. Recognizing that there are many pre-existing collections of biospecimens, we investigated the cost and time efficiencies observed with studies involving the use of existing biospecimens versus collecting new specimens. Methods: Data available for 1,018 extramural, peer-reviewed grants (active as of July 2012) supported by the Division of Cancer Control and Population Sciences, (NCI Division that supports cancer control and population science extramural research grants) were analyzed. Results: 455 of the grants were determined to involve biospecimens. The most common specimen types included were DNA (66% of grants involved DNA), whole blood (51%), serum or plasma (40%), and tissue (39%). Grants that involved the use of existing biospecimens resulted in greater cost (serum/plasma studies were 4.2 times less expensive) and time efficiencies (1.4 times more publications per year resulted) than grants that collected new biospecimens. Conclusions: Clearly, there is an opportunity for NCI to promote future sharing. We are currently working to better catalogue our funded resources and make data available to the extramural community. Further work is being done to investigate possible trends based on year of grant award. Citation Format: Danielle M. Carrick, Eliza Mette, Brittany Hoyle, Scott D. Rogers, Elizabeth M. Gillanders, Sheri D. Schully, Leah E. Mechanic. The use of biospecimens in cancer population science research. [abstract]. In: Proceedings of the 105th Annual Meeting of the American Association for Cancer Research; 2014 Apr 5-9; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2014;74(19 Suppl):Abstract nr 307. doi:10.1158/1538-7445.AM2014-307