<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(1)</volume><submitter>Graziosi A</submitter><pubmed_abstract>&lt;h4>Background&lt;/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.&lt;h4>Methods&lt;/h4>Four databases with English-language restriction were searched </pubmed_abstract><journal>Systematic reviews</journal><pagination>36</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12859863</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Pharmacokinetic interactions and clinical implications of PPIs and CDKIs in breast cancer: a systematic review and meta-analysis.</pubmed_title><pmcid>PMC12859863</pmcid><pubmed_authors>Graziosi A</pubmed_authors><pubmed_authors>Pani A</pubmed_authors><pubmed_authors>Fornasari D</pubmed_authors><pubmed_authors>Nani A</pubmed_authors><pubmed_authors>Schianchi A</pubmed_authors><pubmed_authors>Del Re M</pubmed_authors><pubmed_authors>Pane R</pubmed_authors><pubmed_authors>Basso M</pubmed_authors><pubmed_authors>Melis M</pubmed_authors><pubmed_authors>Giossi R</pubmed_authors><pubmed_authors>Danesi R</pubmed_authors><pubmed_authors>Avantaggiato M</pubmed_authors><pubmed_authors>Tinazzo E</pubmed_authors><pubmed_authors>Canella M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pharmacokinetic interactions and clinical implications of PPIs and CDKIs in breast cancer: a systematic review and meta-analysis.</name><description>&lt;h4>Background&lt;/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.&lt;h4>Methods&lt;/h4>Four databases with English-language restriction were searched </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-11T05:32:17.616Z</modification><creation>2026-06-11T03:08:30.303Z</creation></dates><accession>S-EPMC12859863</accession><cross_references><pubmed>41462352</pubmed><doi>10.1186/s13643-025-03046-0</doi></cross_references></HashMap>