<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(8)</volume><submitter>Marin C</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Different liquid chromatography tandem mass spectrometry (LC-MS/MS) methods have been published for quantification of monoclonal antibodies (mAbs) in plasma but thus far none allowed the simultaneous quantification of several mAbs, including immune checkpoint inhibitors. We developed and validated an original multiplex LC-MS/MS method using a ready-to-use kit to simultaneously assay 7 mAbs (i.e., bevacizumab, cetuximab, ipilimumab, nivolumab, pembrolizumab, rituximab and trastuzumab) in plasma. This method was next cross-validated with respective reference methods (ELISA or LC-MS/MS).&lt;h4>Methods&lt;/h4>The mAbXmise kit was used for mAb extraction and full-length stable-isotope-labeled antibodies as internal standards. The LC-MS/MS method was fully validated following curren</pubmed_abstract><journal>Pharmaceuticals (Basel, Switzerland)</journal><pagination>796</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8401780</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cross-Validation of a Multiplex LC-MS/MS Method for Assaying mAbs Plasma Levels in Patients with Cancer: A GPCO-UNICANCER Study.</pubmed_title><pmcid>PMC8401780</pmcid><pubmed_authors>Ciccolini J</pubmed_authors><pubmed_authors>Lacarelle B</pubmed_authors><pubmed_authors>Thomas F</pubmed_authors><pubmed_authors>Millet A</pubmed_authors><pubmed_authors>Marin C</pubmed_authors><pubmed_authors>Blanchet B</pubmed_authors><pubmed_authors>Lebert D</pubmed_authors><pubmed_authors>Khoudour N</pubmed_authors><pubmed_authors>Bros P</pubmed_authors><pubmed_authors>Ternant D</pubmed_authors><pubmed_authors>Guitton J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cross-Validation of a Multiplex LC-MS/MS Method for Assaying mAbs Plasma Levels in Patients with Cancer: A GPCO-UNICANCER Study.</name><description>&lt;h4>Background&lt;/h4>Different liquid chromatography tandem mass spectrometry (LC-MS/MS) methods have been published for quantification of monoclonal antibodies (mAbs) in plasma but thus far none allowed the simultaneous quantification of several mAbs, including immune checkpoint inhibitors. We developed and validated an original multiplex LC-MS/MS method using a ready-to-use kit to simultaneously assay 7 mAbs (i.e., bevacizumab, cetuximab, ipilimumab, nivolumab, pembrolizumab, rituximab and trastuzumab) in plasma. This method was next cross-validated with respective reference methods (ELISA or LC-MS/MS).&lt;h4>Methods&lt;/h4>The mAbXmise kit was used for mAb extraction and full-length stable-isotope-labeled antibodies as internal standards. The LC-MS/MS method was fully validated following curren</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Aug</publication><modification>2026-05-02T03:19:51.7Z</modification><creation>2022-02-11T10:05:36.782Z</creation></dates><accession>S-EPMC8401780</accession><cross_references><pubmed>34451893</pubmed><doi>10.3390/ph14080796</doi></cross_references></HashMap>