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Pharmacokinetics, safety, and tolerability of olaparib and temozolomide for recurrent glioblastoma: results of the phase I OPARATIC trial
Author(s) -
Catherine Hanna,
Kathreena M. Kurian,
Karin Williams,
Colin Watts,
Alan Jackson,
Ross Carruthers,
Karen Strathdee,
Garth Cruickshank,
Laurence Dunn,
Sara Erridge,
Lisa Godfrey,
Sarah Jefferies,
Catherine McBain,
Rebecca Sleigh,
Alex McCormick,
Marc Pittman,
Sarah Halford,
Anthony J. Chalmers
Publication year - 2020
Publication title -
neuro-oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.005
H-Index - 125
eISSN - 1523-5866
pISSN - 1522-8517
DOI - 10.1093/neuonc/noaa104
Subject(s) - olaparib , tolerability , medicine , temozolomide , parp inhibitor , oncology , pharmacokinetics , pharmacology , cancer research , chemotherapy , adverse effect , poly adp ribose polymerase , chemistry , biochemistry , polymerase , gene
The poly(ADP-ribose) polymerase (PARP) inhibitor olaparib potentiated radiation and temozolomide (TMZ) chemotherapy in preclinical glioblastoma models but brain penetration was poor. Clinically, PARP inhibitors exacerbate the hematological side effects of TMZ. The OPARATIC trial was conducted to measure penetration of recurrent glioblastoma by olaparib and assess the safety and tolerability of its combination with TMZ.

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