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dc.contributor.author | Gil-Raga, Mireia | es_ES |
dc.contributor.author | Jantus-Lewintre, Eloisa | es_ES |
dc.contributor.author | Gallach-Garcia, Sandra | es_ES |
dc.contributor.author | Giner-Bosch, Vicent | es_ES |
dc.contributor.author | Frangi-Caregnato, Alejandro Federico | es_ES |
dc.contributor.author | Safont-Aguilera, María José | es_ES |
dc.contributor.author | Garde-Noguera, Javier | es_ES |
dc.contributor.author | Zorraquino-Pina, Estefanía | es_ES |
dc.contributor.author | García-Martínez, Marisa | es_ES |
dc.contributor.author | Camps-Herrero, Carlos | es_ES |
dc.date.accessioned | 2020-02-16T21:01:48Z | |
dc.date.available | 2020-02-16T21:01:48Z | |
dc.date.issued | 2018 | es_ES |
dc.identifier.issn | 1699-048X | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/137018 | |
dc.description.abstract | [EN] PurposeAfter surgical resection, an ample prognosis variability among stages is observed. Multiple prognostic factors are individually studied and some CRC classifiers have been proposed. Not one have been implemented into clinical practice.Methods/patientsWe classified 105 patients with resected CRC (stage I-III) into five molecular subtypes using BRAF(V600E) and RAS (KRAS; NRAS) status, and the expression of DNA mismatch repair (MMR) proteins (MLH1 and MSH2). Clinicopathological features and DFS) of distincts groups were evaluated.Results and conclusionsRAS and BRAF(V600E) mutations were detected in 43.8 and 11.4% of patients, respectively. 19% of tumours had lack of expression of any MMR proteins reflecting a system deficiency (dMMR). Patients with any RAS mutation had lower DFS that patients with RAS wild type (wt) (40.23 vs 45.26months; p value=0.035). Of a total of five molecular subtypes, three were MMR proficient (pMMR): RAS mutated (39%), BRAF(V600E) mutated (6.7%) and RAS/BRAF(V600E) wt (35.2%); and two were dMMR: BRAF(V600E) mutated (4.8%) and BRAF(V600E) wt (14.3%). Left side tumours were more frequently observed in pMMR/RAS and BRAF(V600E) wt subtype, and right side tumours in dMMR subtypes. Among the three pMMR subtypes, a benefit survival was observed for patients without any mutation in BRAF(v600E) or RAS oncogenes (median of DFS=45.5 vs 40.98months in RAS mutated group; p=0.084 and vs 34.13 in BRAF(v600E) mutated group; p=0.031). Molecular classification using these biomarkers can be useful to identify groups with differences in prognosis. | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | Springer-Verlag | es_ES |
dc.relation.ispartof | Clinical & Translational Oncology | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.subject | Colorectal cancer | es_ES |
dc.subject | Prognostic factor | es_ES |
dc.subject | Molecular subtypes | es_ES |
dc.subject.classification | BIOLOGIA CELULAR | es_ES |
dc.subject.classification | ESTADISTICA E INVESTIGACION OPERATIVA | es_ES |
dc.title | Molecular subtypes in early colorectal cancer associated with clinical features and patient prognosis | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1007/s12094-018-1874-8 | es_ES |
dc.rights.accessRights | Cerrado | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Departamento de Estadística e Investigación Operativa Aplicadas y Calidad - Departament d'Estadística i Investigació Operativa Aplicades i Qualitat | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Departamento de Biotecnología - Departament de Biotecnologia | es_ES |
dc.description.bibliographicCitation | Gil-Raga, M.; Jantus-Lewintre, E.; Gallach-Garcia, S.; Giner-Bosch, V.; Frangi-Caregnato, AF.; Safont-Aguilera, MJ.; Garde-Noguera, J.... (2018). Molecular subtypes in early colorectal cancer associated with clinical features and patient prognosis. Clinical & Translational Oncology. 20(11):1422-1429. https://doi.org/10.1007/s12094-018-1874-8 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://doi.org/10.1007/s12094-018-1874-8 | es_ES |
dc.description.upvformatpinicio | 1422 | es_ES |
dc.description.upvformatpfin | 1429 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 20 | es_ES |
dc.description.issue | 11 | es_ES |
dc.relation.pasarela | S\373614 | es_ES |
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