Abstract

Adjuvant 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.

Details

Title
Real world evidence of adjuvant trastuzumab in HER2 positive early breast cancer
Author
Lluch-Gómez, J. 1 ; Núñez-Álvarez, V. 1 ; de la Torre-Hita, C. 1 ; Bernal-Gómez, M. 1 ; Campini-Bermejo, A. 1 ; Perdomo-Zaldívar, E. 1 ; Rodríguez-Pérez, L. 1 ; Calvete-Candenas, J. 1 ; Martínez-Bautista, M. J. 2 ; Benítez-Rodríguez, E. 3 ; Baena-Cañada, J. M. 1   VIAFID ORCID Logo 

 Hospital Universitario Puerta del Mar (HUPM), Medical Oncology Department, Cádiz, Spain (GRID:grid.411342.1) (ISNI:0000 0004 1771 1175); Instituto de Investigación e Innovación Biomédica de Cádiz (INIBiCA) [Institute for Biomedica Research and Innovation], Cádiz, Spain (GRID:grid.512013.4) 
 Instituto de Investigación e Innovación Biomédica de Cádiz (INIBiCA) [Institute for Biomedica Research and Innovation], Cádiz, Spain (GRID:grid.512013.4); Hospital Universitario Puerta del Mar (HUPM), Pharmacy Unit, Cádiz, Spain (GRID:grid.411342.1) (ISNI:0000 0004 1771 1175) 
 Instituto de Investigación e Innovación Biomédica de Cádiz (INIBiCA) [Institute for Biomedica Research and Innovation], Cádiz, Spain (GRID:grid.512013.4); Hospital Universitario Puerta del Mar, Preventive Medicine Department, Cádiz, Spain (GRID:grid.411342.1) (ISNI:0000 0004 1771 1175) 
Pages
7168
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2808773447
Copyright
© The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.