<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Taylor SA</submitter><funding>Cancer Research UK</funding><funding>National Institute for Health Research (NIHR)</funding><funding>Wellcome Trust</funding><pagination>523-532</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6529610</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(6)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Whole-body magnetic resonance imaging (WB-MRI) could be an alternative to multi-modality staging of non-small-cell lung cancer (NSCLC), but its diagnostic accuracy, effect on staging times, number of tests needed, cost, and effect on treatment decisions are unknown. We aimed to prospectively compare the diagnostic accuracy and efficiency of WB-MRI-based staging pathways with standard pathways in NSCLC.&lt;h4>Methods&lt;/h4>The Streamline L trial was a prospective, multicentre trial done in 16 hospitals in England. Eligible patients were 18 years or older, with newly diagnosed NSCLC that was potentially radically treatable on diagnostic chest CT (defined as stage IIIb or less). Exclusion criteria were severe systemic disease, pregnancy, contraindications to MRI, or histologies </pubmed_abstract><journal>The Lancet. Respiratory medicine</journal><pubmed_title>Diagnostic accuracy of whole-body MRI versus standard imaging pathways for metastatic disease in newly diagnosed non-small-cell lung cancer: the prospective Streamline L trial.</pubmed_title><pmcid>PMC6529610</pmcid><funding_grant_id>13/122/01</funding_grant_id><funding_grant_id>EME/13/122/01</funding_grant_id><funding_grant_id>10/68/01</funding_grant_id><funding_grant_id>NF-SI-0512-10012</funding_grant_id><funding_grant_id>16463</funding_grant_id><funding_grant_id>NF-SI-0513-10019</funding_grant_id><funding_grant_id>ICA-CDRF-2017-03-053</funding_grant_id><pubmed_authors>Naaseri S</pubmed_authors><pubmed_authors>Clarke CS</pubmed_authors><pubmed_authors>McKirdy F</pubmed_authors><pubmed_authors>Win T</pubmed_authors><pubmed_authors>Woodrow L</pubmed_authors><pubmed_authors>Patel P</pubmed_authors><pubmed_authors>Sidhu HS</pubmed_authors><pubmed_authors>Patel U</pubmed_authors><pubmed_authors>Couture J</pubmed_authors><pubmed_authors>Phiri P</pubmed_authors><pubmed_authors>Jenkins I</pubmed_authors><pubmed_authors>Gibbons N</pubmed_authors><pubmed_authors>Prior K</pubmed_authors><pubmed_authors>Roehrig J</pubmed_authors><pubmed_authors>Russell P</pubmed_authors><pubmed_authors>Mohammed A</pubmed_authors><pubmed_authors>Beeston T</pubmed_authors><pubmed_authors>Adeniba R</pubmed_authors><pubmed_authors>Beare S</pubmed_authors><pubmed_authors>Prezzi D</pubmed_authors><pubmed_authors>Blakeway L</pubmed_authors><pubmed_authors>Birch D</pubmed_authors><pubmed_authors>Yu D</pubmed_authors><pubmed_authors>Piga W</pubmed_authors><pubmed_authors>Jayme A</pubmed_authors><pubmed_authors>Nagy Z</pubmed_authors><pubmed_authors>Lauigan R</pubmed_authors><pubmed_authors>Conteh V</pubmed_authors><pubmed_authors>Hameeduddin A</pubmed_authors><pubmed_authors>Nichols P</pubmed_authors><pubmed_authors>Green A</pubmed_authors><pubmed_authors>Bridgewater J</pubmed_authors><pubmed_authors>Bazari F</pubmed_authors><pubmed_authors>Beedham 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We aimed to prospectively compare the diagnostic accuracy and efficiency of WB-MRI-based staging pathways with standard pathways in NSCLC.&lt;h4>Methods&lt;/h4>The Streamline L trial was a prospective, multicentre trial done in 16 hospitals in England. Eligible patients were 18 years or older, with newly diagnosed NSCLC that was potentially radically treatable on diagnostic chest CT (defined as stage IIIb or less). Exclusion criteria were severe systemic disease, pregnancy, contraindications to MRI, or histologies </description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jun</publication><modification>2025-04-22T15:39:57.722Z</modification><creation>2019-07-01T13:54:12Z</creation></dates><accession>S-EPMC6529610</accession><cross_references><pubmed>31080129</pubmed><doi>10.1016/S2213-2600(19)30090-6</doi></cross_references></HashMap>