{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["15(1)"],"submitter":["Graziosi A"],"pubmed_abstract":["<h4>Background</h4>Breast cancer is the fourth leading cause of cancer mortality worldwide. New drugs, such as cyclin-dependent kinase 4/6 inhibitors (CDKIs), increase the life expectancy of receptor-positive (HR+) and human epidermal growth factor receptor 2 negative (HER2-) breast cancer patients. This class acts to limit the G1/S transition in tumor cells, inducing tumor cell death. Owing to the basic nature of CDKIs, their solubilities are pH dependent and could be influenced by the concurrent use of acid-reducing agents such as proton pump inhibitors (PPIs). This meta-analysis aims to assess the impact of co-administering PPIs on the pharmacokinetics and clinical efficacy of CDKIs in breast cancer patients.<h4>Methods</h4>Four databases with English-language restriction were searched "],"journal":["Systematic reviews"],"pagination":["36"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12859863"],"repository":["biostudies-literature"],"pubmed_title":["Pharmacokinetic interactions and clinical implications of PPIs and CDKIs in breast cancer: a systematic review and meta-analysis."],"pmcid":["PMC12859863"],"pubmed_authors":["Graziosi A","Pani A","Fornasari D","Nani A","Schianchi A","Del Re M","Pane R","Basso M","Melis M","Giossi R","Danesi R","Avantaggiato M","Tinazzo E","Canella M"],"additional_accession":[]},"is_claimable":false,"name":"Pharmacokinetic interactions and clinical implications of PPIs and CDKIs in breast cancer: a systematic review and meta-analysis.","description":"<h4>Background</h4>Breast cancer is the fourth leading cause of cancer mortality worldwide. New drugs, such as cyclin-dependent kinase 4/6 inhibitors (CDKIs), increase the life expectancy of receptor-positive (HR+) and human epidermal growth factor receptor 2 negative (HER2-) breast cancer patients. This class acts to limit the G1/S transition in tumor cells, inducing tumor cell death. Owing to the basic nature of CDKIs, their solubilities are pH dependent and could be influenced by the concurrent use of acid-reducing agents such as proton pump inhibitors (PPIs). This meta-analysis aims to assess the impact of co-administering PPIs on the pharmacokinetics and clinical efficacy of CDKIs in breast cancer patients.<h4>Methods</h4>Four databases with English-language restriction were searched ","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Dec","modification":"2026-06-11T05:32:17.616Z","creation":"2026-06-11T03:08:30.303Z"},"accession":"S-EPMC12859863","cross_references":{"pubmed":["41462352"],"doi":["10.1186/s13643-025-03046-0"]}}