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05 Brain Cancer

$18,675P30FY2020CANIH

University Of Tx Md Anderson Can Ctr, Houston TX

Investigators

Linked publications, trials & patents

Trial NCT07407920Trial NCT07349641Trial NCT06651580Trial NCT05681026Trial NCT05223036Trial NCT05078866Trial NCT05057312Trial NCT05054296Trial NCT05044546Trial NCT05023967Trial NCT05011045Trial NCT04875728Trial NCT04870645Trial NCT04810091Trial NCT04751422Trial NCT04740164Trial NCT04668300Trial NCT04615013Trial NCT04505267Trial NCT04484909Trial NCT04483349Trial NCT04481204Trial NCT04474301Trial NCT04458610Trial NCT04447222Trial NCT04435691Trial NCT04430725Trial NCT04407247Trial NCT04373720Trial NCT04317781Trial NCT04311723Trial NCT04310826Trial NCT04310397Trial NCT04265430Trial NCT04257045Trial NCT04256941Trial NCT04239989Trial NCT04239976Trial NCT04239157Trial NCT04236882Trial NCT04228042Trial NCT04220827Trial NCT04220775Trial NCT04220008Trial NCT04219969Trial NCT04219904Trial NCT04216732Trial NCT04216563Trial NCT04216524Trial NCT04216472Trial NCT04215029Trial NCT04200534Trial NCT04199026Trial NCT04196972Trial NCT04189783Trial NCT04189770Trial NCT04189757Trial NCT04188418Trial NCT04188405Trial NCT04186884Trial NCT04186832Trial NCT04185337Trial NCT04181463Trial NCT04171622Trial NCT04171219Trial NCT04171037Trial NCT04169763Trial NCT04169737Trial NCT04169542Trial NCT04160052Trial NCT04151082Trial NCT04150939Trial NCT04140487Trial NCT04135326Trial NCT04134208Trial NCT04132843Trial NCT04132505Trial NCT04132440Trial NCT04129138Trial NCT04128748Trial NCT04128501Trial NCT04127721Trial NCT04125914Trial NCT04119037Trial NCT04106843Trial NCT04106245Trial NCT04090619Trial NCT04090567Trial NCT04087057Trial NCT04083378Trial NCT04082572Trial NCT04074746Trial NCT04066894Trial NCT04062305Trial NCT04062266Trial NCT04058964Trial NCT04054245Trial NCT04054167Trial NCT04054154Trial NCT04053517

Abstract

PROJECT SUMMARY/ABSTRACT The Brain Cancer Program (BCP), a multidisciplinary basic, translational, and clinical research program, includes 86 members (36 primary and 50 associate). Leadership is provided by physician-scientists: Amy Heimberger and Frederick Lang, both neurosurgeons; Juan Fueyo-Margareto, a laboratory-based investigator; and John de Groot, a neuro-oncologist. The overall goal of the BCP is to identify the genetic and molecular determinants of primary and metastatic brain tumor formation and progression and to use this knowledge to improve the survival and quality of life of patients through specifically targeted biological and small-molecule therapies. The program has 3 specific aims. Aim 1: To develop effective viral and immunotherapeutic treatment strategies that exploit glioblastoma heterogeneity. Aim 2: To determine how to optimize targeted approaches for central nervous system tumors. Aim 3: To define factors that promote the development of central nervous system metastases, devise strategies to prevent their formation, develop early detection or identify at-risk patients, and prioritize optimal therapeutic approaches. The BCP's annual direct peer-reviewed funding is $5.7M, including a Brain Cancer SPORE. Of the total peer-reviewed funding, $2.1M (37%) is from NCI grants, and $3.6M is from other peer-reviewed sources. BCP members have authored 703 publications in peer-reviewed journals over the past 6 years, of which 362 (51%) were intra-programmatic, 170 (24%) were inter-programmatic, and 485 (69%) involved external collaborations. Forty-one percent of publications have appeared in journals with IF >5, and 13% have appeared in journals with IF >10, including Nature, Cancer Cell, Mol Cell, Lancet Oncol, J Clin Oncol, J Natl Cancer Inst, J Clin Invest, and Nat Genet. Accomplishments include major contributions to The Cancer Genome Atlas and key leadership roles in the international glioblastoma Adaptive Global Innovative Learning Environment Bayesian Clinical Trial. During the last grant period, members of the BCP made important contributions in evaluating transcriptome plasticity and radiation resistance in glioblastoma stem cells (GSCs) (Bhat et al, Cancer Cell, 2013) and the roles of Quaking in self-renewal and preventing terminal differentiation of GSCs (Hu J et al, Proc Natl Acad Sci USA, 2013; Shingu et al, Nat Genet, 2017), WNT5a in driving GSC differentiation into endothelial-like cells that support invasive glioblastoma cells (Hu B et al, Cell, 2016), and PKM2 in altering cell metabolism and cell-cycle progression with the Cancer Biology and Metastasis Program (Yang et al, Mol Cell, 2012; Yang et al, Cell, 2012; Jiang Y et al, Mol Cell, 2014; Jiang Y et al, Nat Commun, 2014). Another important advance by BCP members is the use of stereotactic radiosurgery after brain metastasis resection as an alternative to whole-brain radiotherapy, which has influenced the standard of care for these patients nationally (Mahajan A et al, Lancet Oncol, 2017). We have seen a 50% decrease in the use of whole- brain irradiation at The University of Texas MD Anderson Cancer Center.

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