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Title

A conceptually new treatment approach for relapsed glioblastoma: Coordinated undermining of survival paths with nine repurposed drugs (CUSP9) by the International Initiative for Accelerated Improvement of Glioblastoma Care

AuthorsKast, Richard E.; Muñoz Sáez, M.; Halatsch, Marc-Eric
KeywordsTemozolomide
Disulfiram
Cytokines
Captopril
Auranofin
Artesunate
Aprepitant
Sertraline
Neurokinin
Glioblastoma
Ketoconazole
Nelfinavir
Angiotensin
Issue Date2013
PublisherImpact Journals
CitationOncotarget 4(4): 502-530 (2013)
AbstractTo improve prognosis in recurrent glioblastoma we developed a treatment protocol based on a combination of drugs not traditionally thought of as cytotoxic chemotherapy agents but that have a robust history of being well-tolerated and are already marketed and used for other non-cancer indications. Focus was on adding drugs which met these criteria: a) were pharmacologically well characterized, b) had low likelihood of adding to patient side effect burden, c) had evidence for interfering with a recognized, well-characterized growth promoting element of glioblastoma, and d) were coordinated, as an ensemble had reasonable likelihood of concerted activity against key biological features of glioblastoma growth. We found nine drugs meeting these criteria and propose adding them to continuous low dose temozolomide, a currently accepted treatment for relapsed glioblastoma, in patients with recurrent disease after primary treatment with the Stupp Protocol. The nine adjuvant drug regimen, Coordinated Undermining of Survival Paths, CUSP9, then are aprepitant, artesunate, auranofin, captopril, copper gluconate, disulfiram, ketoconazole, nelfinavir, sertraline, to be added to continuous low dose temozolomide. We discuss each drug in turn and the specific rationale for use- how each drug is expected to retard glioblastoma growth and undermine glioblastoma’s compensatory mechanisms engaged during temozolomide treatment. The risks of pharmacological interactions and why we believe this drug mix will increase both quality of life and overall survival are reviewed.
DescriptionKast, Richard E. et al.
Publisher version (URL)http://doi.org/10.18632/oncotarget.969
URIhttp://hdl.handle.net/10261/142759
DOI10.18632/oncotarget.969
Identifiersissn: 1949-2553
Appears in Collections:(IBIS) Artículos
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