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dc.contributor.authorAranda, E.
dc.contributor.authorPolo, E.
dc.contributor.authorCamps, C.
dc.contributor.authorCarrato, A.
dc.contributor.authorDiaz-Rubio, E.
dc.contributor.authorGuillem, V.
dc.contributor.authorLópez López, Rafael 
dc.contributor.authorAnton, A.
dc.date.accessioned2022-04-29T10:25:31Z
dc.date.available2022-04-29T10:25:31Z
dc.date.issued2020
dc.identifier.issn1699-048X
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/31974819es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/16590
dc.description.abstractPURPOSE: The primary aim of this retrospective study was to describe the treatment patterns according to the type of treatment received by patients with metastatic colorectal cancer (mCRC) in Spain. METHODS: This was a retrospective, observational, multicenter study performed by 33 sites throughout Spain that included consecutive patients aged 18 years or older who had received or were receiving treatment for mCRC. RESULTS: At the time of inclusion, of the 873 evaluable patients, 507 (58%) had received two lines, 235 (27%) had received three lines, 106 (12%) had received four lines, and the remaining patients had received up to ten lines. The most frequent chemotherapy schemes were the FOLFOX or CAPOX regimens (66%) for first-line treatment, FOLFOX, CAPOX or FOLFIRI (70%) for second-line treatment, and FOLFOX, FOLFIRI or other fluoropyrimidine-based regimens for third- and fourth-line (over 60%) treatment. Sixty percent of patients received targeted therapy as part of their first-line treatment, and this proportion increased up to approximately 70% of patients as part of the second-line of treatment. A relevant proportion of patients were treated with unknown KRAS, and especially the BRAF, mutation statuses. CONCLUSIONS: This study reveals inconsistencies regarding adherence to the recommendations of the ESMO guidelines for the management of mCRC in Spain. Improved adherence to the standard practice described in such guidelines for the determination of RAS and BRAF mutation statuses and the use of targeted therapies in first-line treatment should be considered to guarantee that patients can benefit from the best therapeutic approaches available.en
dc.rightsAtribución 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshMutation*
dc.subject.meshProto-Oncogene Proteins B-raf*
dc.subject.meshMiddle Aged*
dc.subject.meshHumans*
dc.subject.meshTreatment Outcome*
dc.subject.meshNeoplasm Metastasis*
dc.subject.meshProto-Oncogene Proteins p21(ras)*
dc.subject.meshRetrospective Studies*
dc.subject.meshAged*
dc.subject.meshMolecular Targeted Therapy*
dc.subject.meshColorectal Neoplasms*
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols*
dc.titleTreatment patterns for metastatic colorectal cancer in Spainen
dc.typeJournal Articlees
dc.authorsophosAranda, E.;Polo, E.;Camps, C.;Carrato, A.;Diaz-Rubio, E.;Guillem, V.;Lopez, R.;Anton, A.
dc.identifier.doi10.1007/s12094-019-02279-5
dc.identifier.pmid31974819
dc.identifier.sophos39493
dc.issue.number9es
dc.journal.titleClinical & Translational Oncologyes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostela::Oncoloxía médicaes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS)es
dc.page.initial1455es
dc.page.final1462es
dc.rights.accessRightsopenAccess
dc.subject.decsproteínas protooncogénicas p21(ras)*
dc.subject.decsmutación*
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada*
dc.subject.decsresultado del tratamiento*
dc.subject.decsanciano*
dc.subject.decsestudios retrospectivos*
dc.subject.decsmediana edad*
dc.subject.decsmetástasis neoplásica*
dc.subject.decshumanos*
dc.subject.decsterapia molecular selectiva*
dc.subject.decsproteínas protooncogénicas B-raf*
dc.subject.decsneoplasias colorrectales*
dc.subject.keywordCHUSes
dc.subject.keywordIDISes
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number22es


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Atribución 4.0 Internacional
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