Cargando…

First- and second-line treatment strategies for hormone-receptor (HR)-positive HER2-negative metastatic breast cancer: A real-world study

BACKGROUND: Endocrine therapy (ET) plus cyclin-dependent-kinases 4/6 inhibitors (CDK4/6i) represents the standard treatment for luminal-metastatic breast cancer (MBC). However, prospective head-to-head comparisons are still lacking for 1st line (L) options, and it is still crucial to define the best...

Descripción completa

Detalles Bibliográficos
Autores principales: Basile, Debora, Gerratana, Lorenzo, Corvaja, Carla, Pelizzari, Giacomo, Franceschin, Giorgia, Bertoli, Elisa, Palmero, Lorenza, Zara, Diego, Alberti, Martina, Buriolla, Silvia, Da Ros, Lucia, Bonotto, Marta, Mansutti, Mauro, Spazzapan, Simon, Cinausero, Marika, Minisini, Alessandro Marco, Fasola, Gianpiero, Puglisi, Fabio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053791/
https://www.ncbi.nlm.nih.gov/pubmed/33812267
http://dx.doi.org/10.1016/j.breast.2021.02.015
Descripción
Sumario:BACKGROUND: Endocrine therapy (ET) plus cyclin-dependent-kinases 4/6 inhibitors (CDK4/6i) represents the standard treatment for luminal-metastatic breast cancer (MBC). However, prospective head-to-head comparisons are still lacking for 1st line (L) options, and it is still crucial to define the best strategy between 1st and 2nd L. MATERIALS AND METHODS: 717 consecutive luminal-MBC pts treated between 2008 and 2020 were analyzed at the Oncology Department of Aviano and Udine, Italy. Differences about survival outcomes (OS, PFS and PPS) were tested by log-rank test. The attrition rate (AR) between 1st and 2ndL was calculated. RESULTS: At 1(st)L, pts were treated with ET (49%), chemotherapy (CT) (31%) and ET-CDKi (20%) while, at 2(nd)L, 33% received ET, 33% CT and 8% ET-CDKi. Overall AR was 10%, 7% for CT, 8% for ET and 17% for ET-CDKi. By multivariate analysis, 1(st)L ET-CDK4/6i showed a better mPFS1 and OS. Moreover, 2(nd)L ET-CDK4/6i demonstrated better mPFS2 compared to ET and CT. Notably, 1(st)L ET-CDKi resulted in higher mPFS than 2ndL ET-CDKi. Intriguingly, 1(st)L ET-CDK4/6i was associated with worse mPPS compared to CT and ET. Secondarily, 1(st)L ET-CDK4/6i followed by CT had worse OS compared to 1(st)L ET-CDK4/6i followed by ET. Notably, none of baseline characteristics at 2(nd)L influenced 2(nd)L treatment choice (ET vs. CT) after ET-CDKi. CONCLUSION: Our real-world data demonstrated that ET-CDKi represents the best option for 1(st)L luminal-MBC compared to ET and CT. Also, the present study pointed out that 2(nd)L ET, potentially combined with other molecules, could be a feasible option after CDK4/6i failure, postponing CT on later lines.