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dc.contributor.authorLluch Gómez, J.
dc.contributor.authorNúñez Álvarez, V.
dc.contributor.authorde la Torre-Hita, C.
dc.contributor.authorBernal Gómez, Marco
dc.contributor.authorCampini Bermejo, A.
dc.contributor.authorPerdomo Zaldívar, E.
dc.contributor.authorRodríguez Pérez, L.
dc.contributor.authorCalvete Candenas, J.
dc.contributor.authorMartínez Bautista, M.J.
dc.contributor.authorBenítez Rodríguez, E.
dc.contributor.authorBaena Cañada, José Manuel 
dc.contributor.otherMedicinaes_ES
dc.date.accessioned2023-11-20T11:28:32Z
dc.date.available2023-11-20T11:28:32Z
dc.date.issued2023-05-03
dc.identifier.issn2045-2322
dc.identifier.urihttp://hdl.handle.net/10498/29626
dc.description.abstractAdjuvant trastuzumab in HER2+ breast cancer reduces recurrence and mortality, and has been the standard treatment since 2006. The objective was to analyze health outcomes in the real world. Observational, retrospective study of patients with HER2+ breast cancer, stages I–III, treated with adjuvant trastuzumab in the past 15 years in only one center and for the first time in Spain. Survival was analyzed according to the number of cycles and cardiotoxicity. Two hundred and seventy-five HER2positive patients (18.60%) out of 1479 received adjuvant (73%) or neoadjuvant/adjuvant (26%) trastuzumab, concomitantly (90%) or sequentially (10%) with chemotherapy. The probability of overall and disease-free survival (OS and DFS) at 5 years was 0.93 (95% CI 0.89–0.96), and 0.88 (95% CI 0.83–0.92). The number of cases with a significant and asymptomatic decrease in ventricular ejection fraction and heart failure were 54 (19.64%) and 12 (4.36%), respectively. Sixty-eight patients (24.70%) received 16 or fewer cycles, especially those older than 65 (OR 0.371, 95% CI 0.152–0.903; p = 0.029) and with cardiotoxicity (OR 15.02, 95% CI 7.437–30.335; p < 0.001). The risk of cardiotoxicity was associated with having received radiotherapy (OR 0.0362, 95% CI 0.139–0.938; p = 0.037). Arterial hypertension (HR 0.361, 95% CI 0.151–0.863, p = 0.022), neoadjuvant treatment (HR 0.314, 95% CI 0.132–0.750, p = 0.009) and cardiotoxicity (HR 2.755, 95% CI 1.235–6.143, p = 0.013) maintained significant association with OS. Only neoadjuvant treatment maintained a significant association with DFS (HR 0.437, 95% CI 0.213–0.899, p = 0.024). The effectiveness of neoadjuvant and adjuvant trastuzumab can be considered comparable to those of clinical trials. In the real world, factors such as age, hypertension, radiotherapy, neoadjuvant treatment, and cardiotoxicity should be taken into consideration to optimize outcomes.es_ES
dc.formatapplication/pdfes_ES
dc.language.isoenges_ES
dc.publisherSpringeres_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceScientific Reports. Vol. 13, nº 1, December 2023, 7168es_ES
dc.subjectbreast canceres_ES
dc.subjectAdjuvant trastuzumabes_ES
dc.subjectRetrospective Studieses_ES
dc.titleReal world evidence of adjuvant trastuzumab in HER2 positive early breast canceres_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.description.physDesc13 páginases_ES
dc.identifier.doi10.1038/s41598-023-34429-9
dc.type.hasVersionVoRes_ES


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