<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Gristina V</submitter><funding>Piano Nazionale di Ripresa e Resilienza (PNRR) project - Italian Network of excellence for advanced diagnosis (INNOVA)</funding><pagination>1422-1435</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12077285</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(5)</volume><pubmed_abstract>Extracellular vesicle (EV) monitoring can complement clinical assessment of cancer response. In this study, patients with advanced non-small cell lung cancer (NSCLC) undergoing osimertinib, alectinib, pembrolizumab or platinum-based chemotherapy ± pembrolizumab were enrolled. EVs were characterized using Bradford assay to quantify the circulating cell-free EV protein content (cfEV), and dynamic light scattering to assess Rayleigh ratio excess at 90°, z-averaged hydrodynamic diameter and polydispersity index. A total of 135 plasma samples from 27 patients were collected at baseline (T0) and at the first radiological restaging (T1). A ∆cfEV &lt; 20% was associated with improved median progression-free survival (mPFS) in responders versus non-responders. Specifically, cfEV responders on pembroli</pubmed_abstract><journal>Molecular oncology</journal><pubmed_title>On-treatment dynamics of circulating extracellular vesicles in the first-line setting of patients with advanced non-small cell lung cancer: the LEXOVE prospective study.</pubmed_title><pmcid>PMC12077285</pmcid><funding_grant_id>PNC-E3-2022-23683266 PNC-HLS-DA (C43C22001630001)</funding_grant_id><pubmed_authors>Bazan Russo TD</pubmed_authors><pubmed_authors>Taverna S</pubmed_authors><pubmed_authors>Carreca AP</pubmed_authors><pubmed_authors>Troncone G</pubmed_authors><pubmed_authors>Santini D</pubmed_authors><pubmed_authors>Galvano A</pubmed_authors><pubmed_authors>Manno M</pubmed_authors><pubmed_authors>Bono M</pubmed_authors><pubmed_authors>Raccosta S</pubmed_authors><pubmed_authors>Barraco N</pubmed_authors><pubmed_authors>Pepe F</pubmed_authors><pubmed_authors>Badalamenti G</pubmed_authors><pubmed_authors>Bazan V</pubmed_authors><pubmed_authors>Incorvaia L</pubmed_authors><pubmed_authors>Malapelle U</pubmed_authors><pubmed_authors>Pisapia P</pubmed_authors><pubmed_authors>Russo A</pubmed_authors><pubmed_authors>Gristina V</pubmed_authors></additional><is_claimable>false</is_claimable><name>On-treatment dynamics of circulating extracellular vesicles in the first-line setting of patients with advanced non-small cell lung cancer: the LEXOVE prospective study.</name><description>Extracellular vesicle (EV) monitoring can complement clinical assessment of cancer response. In this study, patients with advanced non-small cell lung cancer (NSCLC) undergoing osimertinib, alectinib, pembrolizumab or platinum-based chemotherapy ± pembrolizumab were enrolled. EVs were characterized using Bradford assay to quantify the circulating cell-free EV protein content (cfEV), and dynamic light scattering to assess Rayleigh ratio excess at 90°, z-averaged hydrodynamic diameter and polydispersity index. A total of 135 plasma samples from 27 patients were collected at baseline (T0) and at the first radiological restaging (T1). A ∆cfEV &lt; 20% was associated with improved median progression-free survival (mPFS) in responders versus non-responders. Specifically, cfEV responders on pembroli</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 May</publication><modification>2026-07-15T08:30:02.995Z</modification><creation>2026-07-01T03:11:58.785Z</creation></dates><accession>S-EPMC12077285</accession><cross_references><pubmed>39780749</pubmed><doi>10.1002/1878-0261.13737</doi></cross_references></HashMap>