<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>89(6)</volume><submitter>Vermunt MAC</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Recently, docetaxel treatment of metastatic prostate cancer patients shifted towards the hormone-sensitive stage of the disease. There are contradictive reports on differences in toxicity of docetaxel in metastatic hormone-sensitive prostate cancer (mHSPC) and metastatic castration-resistant prostate cancer (mCRPC) patients. Possible differences in toxicity might be attributed to different pharmacokinetics (PK) in the two patient populations.&lt;h4>Methods&lt;/h4>Patients with mCRPC or mHSPC and a standard indication for docetaxel treatment were included in the study. All patients had suppressed serum testosterone levels (≤ 0.5 ng/mL or 1.73 nmol/L). Venous blood samples were obtained at the first docetaxel treatment, until 48 h after infusion. Plasma concentrations of docetaxel,</pubmed_abstract><journal>Cancer chemotherapy and pharmacology</journal><pagination>785-793</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9135852</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Comparison of docetaxel pharmacokinetics between castration-resistant and hormone-sensitive metastatic prostate cancer patients.</pubmed_title><pmcid>PMC9135852</pmcid><pubmed_authors>Vermunt MAC</pubmed_authors><pubmed_authors>Rosing H</pubmed_authors><pubmed_authors>Bergman AM</pubmed_authors><pubmed_authors>van Nuland M</pubmed_authors><pubmed_authors>Beijnen JH</pubmed_authors><pubmed_authors>van der Heijden LT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparison of docetaxel pharmacokinetics between castration-resistant and hormone-sensitive metastatic prostate cancer patients.</name><description>&lt;h4>Purpose&lt;/h4>Recently, docetaxel treatment of metastatic prostate cancer patients shifted towards the hormone-sensitive stage of the disease. There are contradictive reports on differences in toxicity of docetaxel in metastatic hormone-sensitive prostate cancer (mHSPC) and metastatic castration-resistant prostate cancer (mCRPC) patients. Possible differences in toxicity might be attributed to different pharmacokinetics (PK) in the two patient populations.&lt;h4>Methods&lt;/h4>Patients with mCRPC or mHSPC and a standard indication for docetaxel treatment were included in the study. All patients had suppressed serum testosterone levels (≤ 0.5 ng/mL or 1.73 nmol/L). Venous blood samples were obtained at the first docetaxel treatment, until 48 h after infusion. Plasma concentrations of docetaxel,</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2025-04-04T11:28:52.154Z</modification><creation>2025-04-04T11:28:52.154Z</creation></dates><accession>S-EPMC9135852</accession><cross_references><pubmed>35467095</pubmed><doi>10.1007/s00280-022-04433-3</doi></cross_references></HashMap>