| Literature DB >> 30439622 |
Kulsoom U Abdul1, Megan Houweling1, Fredrik Svensson2, Ravi S Narayan3, Fleur M G Cornelissen1, Asli Küçükosmanoglu1, Emmanouil Metzakopian4, Colin Watts5, David Bailey2, Tom Wurdinger1, Bart A Westerman6.
Abstract
Glioblastoma is the most common and malignant form of brain cancer, for which the standard treatment is maximal surgical resection, radiotherapy and chemotherapy. Despite these interventions, mean overall survival remains less than 15 months, during which extensive tumor infiltration throughout the brain occurs. The resulting metastasized cells in the brain are characterized by chemotherapy resistance and extensive intratumoral heterogeneity. An orthogonal approach attacking both intracellular resistance mechanisms as well as intercellular heterogeneity is necessary to halt tumor progression. For this reason, we established the WINDOW Consortium (Window for Improvement for Newly Diagnosed patients by Overcoming disease Worsening), in which we are establishing a strategy for rational selection and development of effective therapies against glioblastoma. Here, we overview the many challenges posed in treating glioblastoma, including selection of drug combinations that prevent therapy resistance, the need for drugs that have improved blood brain barrier penetration and strategies to counter heterogeneous cell populations within patients. Together, this forms the backbone of our strategy to attack glioblastoma.Entities:
Keywords: Blood brain barrier; Combination therapy; Glioblastoma; Small molecule drugs; Therapy resistance; Toxicity
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Year: 2018 PMID: 30439622 DOI: 10.1016/j.drup.2018.10.001
Source DB: PubMed Journal: Drug Resist Updat ISSN: 1368-7646 Impact factor: 18.500