Safety and efficacy of cyclin-dependent kinase inhibitor rechallenge following ribociclib-induced limiting hypertransaminasemia
Jesús Fuentes-Antrás,
Alicia de Luna,
Alfonso López de Sá,
Alberto Ocaña,
José Ángel García-Sáenz,
Fernando Moreno
Affiliations
Jesús Fuentes-Antrás
Breast Cancer Unit, Department of Medical Oncology, San Carlos University Hospital, Madrid, Spain; Corresponding author.
Alicia de Luna
Breast Cancer Unit, Department of Medical Oncology, San Carlos University Hospital, Madrid, Spain
Alfonso López de Sá
Breast Cancer Unit, Department of Medical Oncology, San Carlos University Hospital, Madrid, Spain
Alberto Ocaña
Breast Cancer Unit, Department of Medical Oncology, San Carlos University Hospital, Madrid, Spain; Experimental Therapeutics and Translational Oncology Unit, Department of Medical Oncology, San Carlos University Hospital, Madrid, Spain
José Ángel García-Sáenz
Breast Cancer Unit, Department of Medical Oncology, San Carlos University Hospital, Madrid, Spain
Fernando Moreno
Breast Cancer Unit, Department of Medical Oncology, San Carlos University Hospital, Madrid, Spain
Cyclin-dependent kinase inhibitors (CDKIs) and endocrine therapy (ET) are the corner-stone of systemic therapy for patients with hormone-positive (HR+) HER2-negative metastatic breast cancer (MBC). However, limited data exist regarding rechallenge treatment strategies with CDKIs after limiting toxicity. In this report, we provide evidence of the safety and efficacy of sequential treatment with palbociclib or abemaciclib in 6 HR+/HER- MBC patients who experienced grade ≥3 ribociclib-induced hypertransaminasemia. Until results from large observational or randomized studies are communicated, empirical evidence may help make individualized decisions on CDKI rechallenge beyond ribociclib-induced unacceptable liver toxicity.