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dc.contributor.authorFernández Montes, Ana 
dc.contributor.authorGrávalos, Cristina
dc.contributor.authorPericay, Carles
dc.contributor.authorSafont, Ma José
dc.contributor.authorBenavides, Manuel
dc.contributor.authorÉlez, Elena
dc.contributor.authorGarcía-Alfonso, Pilar
dc.contributor.authorGarcía-Paredes, Beatriz
dc.contributor.authorCarrato, Alfredo
dc.contributor.authorAranda, Enrique
dc.date.accessioned2022-03-23T08:55:21Z
dc.date.available2022-03-23T08:55:21Z
dc.date.issued2020
dc.identifier.issn1533-0028
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/32507561es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/16374
dc.description.abstractColorectal cancer (CRC) is a public health problem: it is the third most common cancer in men (746,000 new cases/year) and the second in women (614,000 new cases/year), representing the second leading cause of death by cancer worldwide. The survival of patients with metastatic CRC (mCRC) has increased prominently in recent years, reaching a median of 25 to 30 months. A growing number of patients with mCRC are candidates to receive a treatment in third line or beyond, although the optimal drug regimen and sequence are still unknown. In this situation of refractoriness, there are several alternatives: (1) To administer sequentially the 2 oral drugs approved in this indication: trifluridine/tipiracil and regorafenib, which have shown a statistically significant benefit in progression-free survival and overall survival with a different toxicity profile. (2) To administer cetuximab or panitumumab in treatment-naive patients with RAS wild type, which is increasingly rare because these drugs are usually indicated in first- or second-line. (3) To reuse drugs already administered that were discontinued owing to toxicity or progression (oxaliplatin, irinotecan, fluoropyrimidine, antiangiogenics, anti-epidermal growth factor receptor [if RAS wild-type]). High-quality evidence is limited, but this strategy is often used in routine clinical practice in the absence of alternative therapies especially in patients with good performance status. (4) To use specific treatments for very selected populations, such as trastuzumab/lapatinib in mCRC human epidermal growth factor receptor 2-positive, immunotherapy in microsatellite instability, intrahepatic therapies in limited disease or primarily located in the liver, although the main recommendation is to include patients in clinical trials.en
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.meshMicrosatellite Instability*
dc.subject.meshClinical Trials as Topic*
dc.subject.meshHumans*
dc.subject.meshExpert Testimony*
dc.subject.meshDrug Resistance*
dc.subject.meshColorectal Neoplasms*
dc.subject.meshPatient Selection*
dc.titleCurrent Options for Third-line and Beyond Treatment of Metastatic Colorectal Cancer. Spanish TTD Group Expert Opinion.en
dc.typeJournal Articlees
dc.authorsophosFernández-Montes, Ana;Grávalos, Cristina;Pericay, Carles;Safont, Ma José;Benavides, Manuel;Élez, Elena;García-Alfonso, Pilar;García-Paredes, Beatriz;Carrato, Alfredo;Aranda, Enrique
dc.identifier.doi10.1016/j.clcc.2020.04.003
dc.identifier.pmid32507561
dc.identifier.sophos36768
dc.issue.number3es
dc.journal.titleClinical Colorectal Canceres
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Ourense, Verín e O Barco de Valdeorras - Complexo Hospitalario Universitario de Ourense::Oncoloxía médicaes
dc.relation.publisherversionhttps://www.clinical-colorectal-cancer.com/article/S1533-0028(20)30049-9/pdfes
dc.rights.accessRightsopenAccess
dc.subject.decsinestabilidad de microsatélites*
dc.subject.decsresistencia a medicamentos*
dc.subject.decsensayos clínicos como asunto*
dc.subject.decsselección de los pacientes*
dc.subject.decshumanos*
dc.subject.decstestimonio experto*
dc.subject.decsneoplasias colorrectales*
dc.subject.keywordCHUOes
dc.typefidesArtículo de Revisiónes
dc.typesophosArtículo de Revisiónes
dc.volume.number19es


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