Sequencing of treatment in metastatic colorectal cancer: Where to fit the target?

dc.contributor.authorTemraz, Sally N.
dc.contributor.authorMukherji, Deborah M.
dc.contributor.authorShamseddine, Ali I.
dc.contributor.departmentInternal Medicine
dc.contributor.departmentDivision of Hematology Oncology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:43:09Z
dc.date.available2025-01-24T11:43:09Z
dc.date.issued2014
dc.description.abstractColorectal cancer is a lethal disease if not discovered early. Even though appropriate screening and preventive strategies are in place in many countries, a significant number of patients are still diagnosed at late stages of the disease. The management of metastatic colorectal cancer remains a significant clinical challenge to oncologists worldwide. While cytotoxic regimens constitute the main treatment of choice in this patient population, addition of the five biologics (bevacizumab, cetuximab, aflibercept, panitumumab and regorafenib) to these regimens has improved clinical outcomes. The most commonly used cytotoxic regimens include doublet combinations (FOLFOX/XELOX or FOLFIRI). Many clinical trials have been published and others are underway to compare the biologic agents with one another in order to prove the superiority of one regimen over another. Metastatic colorectal cancer patients have many treatment options; however, the optimal use and sequence of targeted agents remain to be determined. This review entails concise and updated clinical data on the management of metastatic colorectal cancer. The aim of the review is to determine where to fit the five biologic targets into the treatment algorithm of metastatic colorectal cancer patients and to derive treatment sequences that would achieve best clinical outcome based on the current available data. © 2014 Baishideng Publishing Group Co., Limited. All rights reserved.
dc.identifier.doihttps://doi.org/10.3748/wjg.v20.i8.1993
dc.identifier.eid2-s2.0-84894589497
dc.identifier.pmid24616571
dc.identifier.urihttp://hdl.handle.net/10938/30218
dc.language.isoen
dc.publisherBaishideng Publishing Group Co
dc.relation.ispartofWorld Journal of Gastroenterology
dc.sourceScopus
dc.subjectAnti-epithelial growth factor receptor
dc.subjectAnti-vascular endothelial growth factor
dc.subjectChemotherapy
dc.subjectMetastatic colorectal cancer
dc.subjectTreatment sequence
dc.subjectAlgorithms
dc.subjectAngiogenesis inhibitors
dc.subjectAntibodies, monoclonal
dc.subjectAntibodies, monoclonal, humanized
dc.subjectAntineoplastic combined chemotherapy protocols
dc.subjectCamptothecin
dc.subjectClinical trials as topic
dc.subjectColorectal neoplasms
dc.subjectDisease progression
dc.subjectDrug administration schedule
dc.subjectFluorouracil
dc.subjectHumans
dc.subjectLeucovorin
dc.subjectNeoplasm metastasis
dc.subjectOrganoplatinum compounds
dc.subjectPhenylurea compounds
dc.subjectPyridines
dc.subjectReceptors, vascular endothelial growth factor
dc.subjectRecombinant fusion proteins
dc.subjectAflibercept
dc.subjectBevacizumab
dc.subjectCapecitabine
dc.subjectCetuximab
dc.subjectFluoropyrimidine
dc.subjectFolinic acid
dc.subjectIrinotecan
dc.subjectOxaliplatin
dc.subjectPanitumumab
dc.subjectRegorafenib
dc.subjectAngiogenesis inhibitor
dc.subjectAntineoplastic agent
dc.subjectCarbanilamide derivative
dc.subjectHybrid protein
dc.subjectMonoclonal antibody
dc.subjectPlatinum complex
dc.subjectPyridine derivative
dc.subjectVasculotropin receptor
dc.subjectArticle
dc.subjectColorectal cancer
dc.subjectControlled clinical trial (topic)
dc.subjectDrug dose regimen
dc.subjectHuman
dc.subjectMeta analysis (topic)
dc.subjectPhase 2 clinical trial (topic)
dc.subjectPhase 3 clinical trial (topic)
dc.subjectRandomized controlled trial (topic)
dc.subjectAlgorithm
dc.subjectAnalogs and derivatives
dc.subjectClinical trial (topic)
dc.subjectDisease course
dc.subjectDrug administration
dc.subjectMetastasis
dc.titleSequencing of treatment in metastatic colorectal cancer: Where to fit the target?
dc.typeArticle

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