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dc.contributor.authorCastellano, Daniel
dc.contributor.authorMaroto, José Pablo
dc.contributor.authorEspinosa, Enrique
dc.contributor.authorGrande, Enrique
dc.contributor.authorBolós Fernández, Victoria
dc.contributor.authorLlinares, Julia
dc.contributor.authorEsteban, Emilio
dc.contributor.authorGonzález del Alba, Aránzazu
dc.contributor.authorCliment, Miguel Ángel
dc.contributor.authorArranz, José Ángel
dc.contributor.authorMéndez, María José
dc.contributor.authorFernández Parra, Eva
dc.contributor.authorAntón-Aparicio, Luis M.
dc.contributor.authorBayona, Cristina
dc.contributor.authorGallegos, Isabel
dc.contributor.authorGallardo, Enrique
dc.contributor.authorSamaniego, Luz
dc.contributor.authorGarcía Donas, Jesús
dc.date.accessioned2021-06-21T08:56:29Z
dc.date.available2021-06-21T08:56:29Z
dc.date.issued2017-08-28
dc.identifier.citationCastellano D, Maroto JP, Espinosa E, Grande E, Bolós MV, Llinares J, et al. Experience with Sunitinib in metastatic renal cell carcinoma (mRCC) patients: pooled analysis from 3 Spanish observational prospective studies. Expert Opin Drug Saf. 2018:17(6):573-579es_ES
dc.identifier.issn1474-0338
dc.identifier.urihttp://hdl.handle.net/2183/28112
dc.description.abstract[Abstract] Background: A pivotal, randomized, phase III trial demonstrated a statistically significant superiority of sunitinib over interferon-α in metastatic renal cell carcinoma (mRCC) patients. Objective: To evaluate the effectiveness and safety of sunitinib in patients with advanced or mRCC in routine clinical practice. Methods: Retrospective pooled analysis of clinical data from three observational and prospective studies carried out between 2007 and 2011 in 33 Spanish hospitals. Tumor response, Progression-free survival (PFS) and overall survival (OS), and main sunitinib-related toxicities were registered. Results: 224 patients were analyzed. Median PFS 10.6 months (95% CI: 9.02–12.25), median OS 21.9 months (95% CI: 17.2–26.6). Objective response rate (ORR) 43.8% (95% CI: 36.8–50.7). Median time to PR was 3.8 months (95% CI: 3.86–5.99) and to CR 8.2 months (95% CI: 4.75–9.77). The most common ≥ grade-3 AEs were asthenia/fatigue (18.7%), hand-foot syndrome (6.2%), hypertension (5.8%) and neutropenia (4.8%). Hand-foot syndrome, diarrhea and mucositis were confirmed as independent predictors for PFS and/or OS in a multivariate analysis (p < 0.05) Conclusions: Outcomes with sunitinib in daily clinical practice resemble those obtained in clinical trials. Long-term benefit with sunitinib is possible in advanced RCC patients but the appropriate management of toxicities is mandatory to enable patients to remain on treatment.es_ES
dc.language.isoenges_ES
dc.publisherTaylor & Francises_ES
dc.relation.urihttps://doi.org/10.1080/14740338.2017.1330410es_ES
dc.rightsThis is an accepted manuscript of an article published by Taylor & Francis in "Expert Opinion on Drug Safety", avaliable online at Taylor & Francis Online web.es_ES
dc.subjectEffectivenesses_ES
dc.subjectRoutine clinical practicees_ES
dc.subjectSafetyes_ES
dc.subjectSunitibes_ES
dc.titleExperience with Sunitinib in metastatic renal cell carcinoma (mRCC) patients: pooled analysis from 3 Spanish observational prospective studieses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessinfo:eu-repo/semantics/openAccesses_ES
UDC.journalTitleExpert Opinion on Drug Safetyes_ES
UDC.volume17es_ES
UDC.issue6es_ES
UDC.startPage573es_ES
UDC.endPage579es_ES


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