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2015 ; 10
(2
): 199-213
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gab.com Text
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Regorafenib as a single-agent in the treatment of patients with gastrointestinal
tumors: an overview for pharmacists
#MMPMID25213039
Rey JB
; Launay-Vacher V
; Tournigand C
Target Oncol
2015[Jun]; 10
(2
): 199-213
PMID25213039
show ga
Regorafenib (BAY 73-4506, StivargaŽ Bayer HealthCare Pharmaceutical Inc) is an
oral multikinase inhibitor with a distinct and wide-ranging profile of tyrosine
kinase inhibition, resulting in antiangiogenic and antiproliferative properties
in tumors. Single-agent regorafenib administered as a 160-mg daily dose for the
first 21 days of a 28-day cycle is approved for use in patients with pretreated
metastatic colorectal cancer (mCRC) and gastrointestinal stromal tumor (GIST)
progressing on imatinib and sunitinib, following publication of data from the
phase III CORRECT and GRID studies respectively. Regorafenib is currently under
phase III investigation in patients with hepatocellular carcinoma and is in
several phase II studies in patients with gastrointestinal (GI) tumors. This
review describes the clinical development of regorafenib in patients with GI
cancers, and highlights the key issues important for the modern day clinical
pharmacist who forms part of the multidisciplinary team ensuring safe and
effective delivery of the drug to the patient. This information is considered of
particular importance to the clinical pharmacist for the future development of
regorafenib in this treatment setting.