par Becherini, Carlotta;Visani, Luca;Caini, Saverio;Bhattacharya, Indrani Subarna;Kirby, Anna A.M.;Nader Marta, Gustavo;Morgan, Gilberto;Salvestrini, Viola;Coles, Charlotte Elizabeth;Cortes, Javier;Curigliano, Giuseppe;de Azambuja, Evandro ;Harbeck, Nadia;Isacke, Clare Marie;Kaidar-Person, Orit;Marangoni, E.;Offersen, Birgitte;Rugo, Hope H.S.;Morandi, Andrea;Lambertini, Matteo Md Phd M.;Poortmans, Philipp;Livi, Lorenzo;Meattini, Icro
Référence Cancer treatment reviews, 119, 102586
Publication Publié, 2023-09
Référence Cancer treatment reviews, 119, 102586
Publication Publié, 2023-09
Article révisé par les pairs
Résumé : | The cyclin-dependent kinase 4 and 6 inhibitors (CDK4/6i) have become the standard of care for hormone receptor-positive (HR + ) and human epidermal growth factor receptor 2-negative (HER2-) metastatic breast cancer, improving survival outcomes compared to endocrine therapy alone. Abemaciclib and ribociclib, in combination with endocrine therapy, have demonstrated significant benefits in invasive disease-free survival for high-risk HR+/HER2- early breast cancer patients. Each CDK4/6i—palbociclib, ribociclib, and abemaciclib—exhibits distinct toxicity profiles. Radiation therapy (RT) can be delivered with a palliative or ablative intent, particularly using stereotactic body radiation therapy for oligometastatic or oligoprogressive disease. However, pivotal randomized trials lack information on concomitant CDK4/6i and RT, and existing preclinical and clinical data on the potential combined toxicities are limited and conflicting. As part of a broader effort to establish international consensus recommendations for integrating RT and targeted agents in breast cancer treatment, we conducted a systematic review and meta-analysis to evaluate the safety profile of combining CDK4/6i with palliative and ablative RT in both metastatic and early breast cancer settings. |