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Authors Puthiamadathil JM, Weinberg BA
Received 22 July 2017
Accepted for publication 5 September 2017
Published 3 October 2017 Volume 2017:9 Pages 461—469
DOI https://doi.org/10.2147/CMAR.S113320
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Colin Mak
Peer reviewer comments 2
Editor who approved publication: Professor Kenan Onel
Abstract: Patients
with metastatic colorectal cancer (mCRC) are surviving longer now than ever
before, but mortality rates are still high and more effective therapies are
clearly needed. For patients with disease that is refractory to
fluoropyrimidines, oxaliplatin, irinotecan, and biologic agents targeting the
vascular endothelial growth factor and epidermal growth factor receptor
pathways, novel treatment options trifluridine/tipiracil (TAS-102) and
regorafenib can be effective disease stabilizers. However, objective clinical
responses are rare and toxicities are manageable but common. In order to
tackle poor clinical responses to TAS-102, there is an ongoing effort to
effectively combine this drug with other agents, particularly those targeting
angiogenesis. Certain subpopulations appear to benefit more than others from
TAS-102; those that benefit often have underlying genetic defects in DNA repair
pathways and/or develop neutropenia. In this review, we focus on the role of
TAS-102 in the treatment of mCRC, including its use in combination with other
agents, potential predictive biomarkers of response to TAS-102, and possible
future directions.
Keywords: metastatic
colorectal cancer, trifluridine, tipiracil, TAS-102, regorafenib
摘要视频链接:Impact of TAS-102 in metastatic colorectal cancer