Effectiveness and safety of palbociclib and ribociclib as treatment for metastatic breast cancer in a Costa Rican Hospital from 2017 to 2022
Palbociclib y ribociclib en cáncer de mama
DOI:
https://doi.org/10.51481/amc.v66i4.1434Keywords:
Breast neoplasms, Costa Rica, mortality, palbociclib, ribociclibAbstract
Aim: To describe and compare the effectiveness and safety of palbociclib and ribociclib with endocrine therapy as treatment for metastatic breast cancer.
Methods: A cohort study was carried out with all patients employing palbociclib or ribociclib as treatment for hormone receptor positive, human epidermal growth factor receptor 2 negative (HR+/HER2-) breast cancer, during June 2017 and December 2022 at Hospital San Juan de Dios, San José, Costa Rica. A retrospective review was performed to obtain clinical variables from medical files. Progression-free survival (PFS) and overall survival (OS) were calculated through Kaplan-Meier method. The effectiveness and safety outcomes were compared through the log-rank test and chi-squared, respectively.
Results: During the study period a total of 125 patients were identified using palbociclib (n=81), or ribociclib (n=44), as first line (n=98) or subsequent therapy (n=27) for metastatic breast cancer. For patients receiving palbociclib or ribociclib as first-line therapy, median PFS was 23.5 months (95% Confidence Interval (95%CI): 17.3-39.6 months), and median OS was 32.4 months (95% CI: 20.6-61.3 months), with no differences between both therapies (PFS Hazard ratio: 0.68; 95%CI: 0.41-1.16, p=0.15). A total of 13 patients (10.5%) had to reduce treatment dose due to persistent side effects, with hematological adverse reactions as the most frequent side effects (anemia: 35%, neutropenia: 28%).
Conclusions: There were no significant differences between palbociclib and ribociclib with endocrine therapy as first or further lines of therapy for metastatic HR+/HER2- breast cancer.
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