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dc.contributor.authorFeliú Batlle, Jaime 
dc.contributor.authorSafont, María José
dc.contributor.authorSalud, Antonieta T.
dc.contributor.authorLosa, Ferrán C.
dc.contributor.authorGarcía-Girón, Carlos
dc.contributor.authorBosch, Carles J A
dc.contributor.authorEscudero, Pilar
dc.contributor.authorLópez Manzanera, Rafael
dc.contributor.authorMadroñal, C.
dc.contributor.authorBolaños, Margarita
dc.contributor.authorGil, Mireia
dc.contributor.authorLlombart, Antonio C.
dc.contributor.authorCastro-Carpeño, J.
dc.contributor.authorGonzález Barón, Manuel
dc.contributor.otherUAM. Departamento de Medicinaes_ES
dc.date.accessioned2014-11-04T10:58:00Z
dc.date.available2014-11-04T10:58:00Z
dc.date.issued2010-05-01
dc.identifier.citationBritish Journal of Cancer 102.10 (2010): 1468 – 1473en_US
dc.identifier.issn0007-0920 (print)en_US
dc.identifier.issn1532-1827 (online)en_US
dc.identifier.urihttp://hdl.handle.net/10486/662397
dc.description.abstractBACKGROUND: The efficacy and safety of capecitabine and bevacizumab in elderly patients with metastatic colorectal cancer (mCRC) considered unsuitable for receiving first-line chemotherapy with an irinotecan or oxaliplatin-based combination were assessed in a phase II, open, multicentre, uncontrolled study. METHODS: Treatment consisted of capecitabine 1250 mgm 2 (or 950 mgm 2 for patients with a creatinine clearance of 30–50ml min 1) twice daily on days 1–14 and bevacizumab (7.5 mg kg 1) on day 1 every 3 weeks. RESULTS: A total of 59 patients aged X70 years with mCRC were enrolled. In an intention-to-treat analysis, the overall response rate was 34%, with 71% of patients achieving disease control. Median progression-free survival and overall survival were 10.8 months and 18 months, respectively. In all, 32 patients (54%) had grade 3/4 adverse events (AEs), the most common being hand–foot syndrome (19%), diarrhoea (9%) and deep venous thrombosis (7%). Four patients died because of treatment-related AEs. A relationship was detected between creatinine clearance p50 ml min 1 and the development of non-bevacizumab-related grade 3/4 AEs. The incidence of bevacizumab-associated AEs (hypertension, thromboembolic events and proteinuria) was consistent with that of previous reports in elderly patients. CONCLUSION: Bevacizumab combined with capecitabine represents a valid therapeutic alternative in elderly patients considered to be unsuitable for receiving polychemotherapy.en_US
dc.description.sponsorshipThis study was supported by Hoffmann-La Roche, Nutley, NJ, USA.en_US
dc.format.extent6 pag.en
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherNature Publishing Groupen_US
dc.relation.ispartofBritish journal of canceren_US
dc.rights© 2010 Cancer Research UKen_US
dc.subject.otherAgeden_US
dc.subject.otherBevacizumaben_US
dc.subject.otherCapecitabineen_US
dc.subject.otherColorectal neoplasmsen_US
dc.subject.otherNeoplasm metastasisen_US
dc.titleCapecitabine and bevacizumab as first-line treatment in elderly patients with metastatic colorectal canceren_US
dc.typearticleen
dc.subject.ecienciaMedicinaes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1038/sj.bjc.6605663es_ES
dc.identifier.doi10.1038/sj.bjc.6605663es_ES
dc.identifier.publicationfirstpage1468es_ES
dc.identifier.publicationissue10es_ES
dc.identifier.publicationlastpage1473es_ES
dc.identifier.publicationvolume102es_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.rights.cc© 2010 Cancer Research UKen_US
dc.rights.accessRightsopenAccessen
dc.authorUAMFeliú Batlle, Jaime (261277)
dc.authorUAMGonzález Barón, Manuel (259851)
dc.facultadUAMFacultad de Medicina
dc.institutoUAMInstituto de Investigación Sanitaria Hospital Universitario de La Paz (IdiPAZ)


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