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Researchers Receive Grants from NCCN Oncology Research Program Funded Through GlaxoSmithKline


The National Comprehensive Cancer Network® (NCCN®) Oncology Research Program (ORP) recently awarded research grants to investigators following a review of proposals submitted in response to the NCCN Dabrafenib and Trametinib Request for Proposals. These grants were made possible through a $4-million research grant from GlaxoSmithKline to scientifically evaluate and define clinical effectiveness of dabrafenib (GSK2118436) and trametinib (GSK1120212) in treatment of advanced melanoma and other advanced cancers.


FORT WASHINGTON, PA – The National Comprehensive Cancer Network® (NCCN®) Oncology Research Program (ORP) recently awarded 11 research grants to investigators following a review of proposals submitted in response to the NCCN Dabrafenib and Trametinib Request for Proposals. These grants were made possible through a $4-million research grant from GlaxoSmithKline to scientifically evaluate the clinical effectiveness of dabrafenib (GSK2118436) and trametinib (GSK1120212) in treatment of advanced melanoma and other cancers.

The NCCN ORP is pleased to have the opportunity to work with GlaxoSmithKline on the dabrafenib and trametinib research projects, said Diane Paul, MS, RN, Vice President, NCCN ORP. These 11 new studies – bringing the total ORP clinical trials to more than 70 – afford the NCCN Member Institutions and their investigators the opportunity to identify breakthroughs in various cancer settings, and determine whether these drugs can improve patient outcomes.

According to GlaxoSmithKline: Dabrafenib (GSK2118436) is an investigational, orally bioavailable, selective RAF kinase inhibitor (BRAF). Activating mutations in BRAF are present in approximately 50 percent of melanoma and approximately eight percent of all cancers. The mutation appears to have a direct role in activating the mitogen-activated protein (MAP) kinase pathway, which controls processes such as cell proliferation, differentiation, survival, and apoptosis (cell death).

Trametinib (GSK1120212) is also an investigational, orally bioavailable inhibitor of mitogen-activated extracellular signal regulated kinase 1 (MEK1) and MEK2. MEK proteins are key components of the extracellular signal-related kinase (ERK) pathway, which is commonly hyper-activated in tumor cells. Constant and unregulated activation of this pathway has been implicated in many cancers. MEK 1/2 are thought to play a role in the activation of key signaling pathways that regulate cell growth.
The following proposals for dabrafenib have been awarded funding:

The following proposals for trametinib have been awarded funding:

The awardees responded to a Request for Proposals issued by the NCCN ORP to the 21 NCCN Member Institutions. Submissions were peer reviewed by the NCCN Dabrafenib and Trametinib Scientific Review Committees. The awardees were selected based on several key criteria, including scientific merit, existing data, and the types of studies necessary to further evaluate the activity of dabrafenib and trametinib.

The NCCN ORP is organized to obtain funding to support scientifically meritorious research projects at NCCN Member Institutions. Policies and standards for the program were set by the NCCN Investigator Steering Committee, a group comprised of senior research physicians appointed by each NCCN Member Institution. The NCCN ORP has received more than $36 million in research grants from major pharmaceutical companies to support investigator-initiated trials. These trials explore new venues of clinical investigation that answer important scientific questions. Studies evaluate combinations and sequencing regimens of drugs, drug resistance, mechanisms of action of specific agents, or explore extended uses for scientific agents.

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