Publication: A multicenter, phase I, pharmacokinetic study of osimertinib in cancer patients with normal renal function or severe renal impairment.
dc.contributor.author | Vishwanathan, Karthick | |
dc.contributor.author | Sanchez-Simon, Inmaculada | |
dc.contributor.author | Keam, Bhumsuk | |
dc.contributor.author | Penel, Nicolas | |
dc.contributor.author | de Miguel-Luken, Maria | |
dc.contributor.author | Weilert, Doris | |
dc.contributor.author | Mills, Andrew | |
dc.contributor.author | Marotti, Marcelo | |
dc.contributor.author | Johnson, Martin | |
dc.contributor.author | Ravaud, Alain | |
dc.date.accessioned | 2023-02-09T09:35:54Z | |
dc.date.available | 2023-02-09T09:35:54Z | |
dc.date.issued | 2020 | |
dc.description.abstract | Osimertinib is a third-generation, irreversible, oral epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI) that potently and selectively inhibits both EGFR-TKI sensitizing and EGFR T790M and has demonstrated efficacy in non-small cell lung cancer (NSCLC) central nervous system metastases. In this phase I study, we assessed the effects of normal renal function (NRF) and severe renal impairment (SRI) on the pharmacokinetics (PK) of osimertinib in patients with solid tumors. Part A: patients with NRF (creatinine clearance [CrCL] ≥90 mL/min), and SRI, (CrCL | |
dc.identifier.doi | 10.1002/prp2.613 | |
dc.identifier.essn | 2052-1707 | |
dc.identifier.pmc | PMC7307240 | |
dc.identifier.pmid | 32567817 | |
dc.identifier.pubmedURL | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307240/pdf | |
dc.identifier.unpaywallURL | https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/prp2.613 | |
dc.identifier.uri | http://hdl.handle.net/10668/15791 | |
dc.issue.number | 4 | |
dc.journal.title | Pharmacology research & perspectives | |
dc.journal.titleabbreviation | Pharmacol Res Perspect | |
dc.language.iso | en | |
dc.organization | Hospital Universitario Virgen del Rocío | |
dc.page.number | e00613 | |
dc.pubmedtype | Clinical Trial, Phase I | |
dc.pubmedtype | Journal Article | |
dc.pubmedtype | Multicenter Study | |
dc.pubmedtype | Research Support, Non-U.S. Gov't | |
dc.rights | Attribution 4.0 International | |
dc.rights.accessRights | open access | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject | epidermal growth factor receptors | |
dc.subject | kidney | |
dc.subject | non-small cell lung cancer | |
dc.subject | osimertinib | |
dc.subject | pharmacokinetics | |
dc.subject | renal disposition | |
dc.subject | tyrosine kinase inhibitors | |
dc.subject.mesh | Acrylamides | |
dc.subject.mesh | Administration, Oral | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Aged, 80 and over | |
dc.subject.mesh | Aniline Compounds | |
dc.subject.mesh | Antineoplastic Agents | |
dc.subject.mesh | Area Under Curve | |
dc.subject.mesh | Female | |
dc.subject.mesh | Hepatic Insufficiency | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Kidney Function Tests | |
dc.subject.mesh | Male | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Neoplasms | |
dc.subject.mesh | Protein Kinase Inhibitors | |
dc.subject.mesh | Severity of Illness Index | |
dc.title | A multicenter, phase I, pharmacokinetic study of osimertinib in cancer patients with normal renal function or severe renal impairment. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 8 | |
dspace.entity.type | Publication |
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