Abstract 71P
Background
Male breast cancer, comprising approximately 1% of all breast cancer cases, often leads to the exclusion of male patients as a criterion in clinical trials. While the efficacy of Cyclin-dependent kinases 4 and 6 (CDK 4/6) inhibitors has been established in metastatic hormone receptor-positive (HR+) and human epidermal growth factor receptor 2-negative (HER2-) breast cancer in women, limited data exist on their effectiveness in male patients. We aimed to evaluate the efficacy and safety of palbociclib or ribociclib in male patients with breast cancer.
Methods
Our study is a multicenter, retrospective study.We included male patients with HR+ and HER2-metastatic breast cancer who received palbociclib or ribociclib as first-line treatment. Our primary endpoints were PFS, overall response rates (ORR), and drug-related adverse effects.
Results
A total of 46 male patients from 27 institutions were enrolled. The median age at initiation of CDK 4/6 inhibitors was 63.64 ± 13.69 years, with a median follow-up of 21.33 (95% CI: 14.92-27.74) months. The ORR were 84% for palbociclib and 76.2% for ribociclib. The mPFS for the entire cohort was 28.06 months (95% CI: 18.70-37.42). No significant difference in PFS was observed between palbociclib and ribociclib (mPFS: 24.46 months (95% CI: 11.51-37.42) vs 28.33 months (95% CI: 14.77-41.88), respectively; p=0.211). No new adverse events were reported.
Conclusions
Our study demonstrates that palbociclib and ribociclib are effective and safe options for first-line treatment in male patients with HR+/HER2- metastatic breast cancer. However, further prospective studies are warranted to establish their efficacy in this population.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Hacettepe University School of Medicine, GO/22732.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.