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National Cancer Institute - NCI Division of Cancer Treatment and ...

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Strategic Partnering to<br />

Evaluate <strong>Cancer</strong> Signatures<br />

Contacts:<br />

James W. Jacobson, Ph.D.<br />

301-402-4185, jacobsoj@mail.nih.gov<br />

Tracy Lively, Ph.D.<br />

301-496-1591, livelyt@mail.nih.gov<br />

The Strategic Partnering to Evaluate<br />

<strong>Cancer</strong> Signatures (SPECS) program<br />

consists <strong>of</strong> six grants that support<br />

multi-institutional, multidisciplinary<br />

32 32 ■ P R O G R A M A C C O M P L I S H M E N T S 2 0 0 6<br />

■ ■ ■<br />

The Strategic Partnering to Evaluate <strong>Cancer</strong> Signatures<br />

program supports research that bridges the gap<br />

between the discovery <strong>of</strong> molecular signatures<br />

<strong>and</strong> their integration into clinical practice.<br />

research teams. The SPECS program<br />

leverages <strong>NCI</strong>’s investment in cancer<br />

clinical trials, cancer centers, <strong>NCI</strong> intramural<br />

programs, <strong>and</strong> the Specialized<br />

Programs <strong>of</strong> Research Excellence (SPORE)<br />

program. The projects include collaborations<br />

with biotechnology companies,<br />

community hospitals, national laboratories,<br />

<strong>and</strong> academic institutions in the<br />

United States, Canada, <strong>and</strong> Europe.<br />

The SPECS initiative supports six large<br />

collaborative research groups that are<br />

exploring how information derived from<br />

comprehensive molecular analyses can be<br />

used to impact the care <strong>of</strong> cancer patients<br />

<strong>and</strong> ultimately improve outcomes. SPECS<br />

supports research that bridges the gap<br />

between the discovery <strong>of</strong> molecular signatures<br />

<strong>and</strong> their integration into clinical<br />

practice. Investigators are refining <strong>and</strong><br />

confirming both genomic <strong>and</strong> proteomic<br />

signatures that have already been shown<br />

to address clinical needs or questions.<br />

They are defining the critical components<br />

<strong>of</strong> the signatures <strong>and</strong> developing robust<br />

assays for measuring those components in<br />

the clinical setting. They will confirm that<br />

the modified signatures provide reproducible,<br />

reliable information that can potentially<br />

inform clinical decision-making. It is<br />

anticipated that the signatures developed<br />

in SPECS will lead to assays that are ready<br />

for validation in prospective clinical trials.

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