Our findings suggest that clinically significant OATP1B-mediated interactions are not anticipated with CDK4/6 inhibitors, either as victims or perpetrators, which supports ongoing clinical trials investigating the co-administration of CDK4/6 inhibitors with OATP1B substrates and inhibitors.
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Drabison et al. (Tue,) studied this question.
www.synapsesocial.com/papers/69d894ce6c1944d70ce05b3d — DOI: https://doi.org/10.1007/s00280-026-04877-x
Thomas Drabison
E. H. Ahmed
Nathan Colasanti
Cancer Chemotherapy and Pharmacology
The Ohio State University
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