<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Romano A</submitter><funding>Associazione Italiana per la Ricerca sul Cancro</funding><pagination>8735-8746</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7724487</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(23)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The neutrophil to lymphocyte ratio (NLR) and the lymphocyte to monocyte ratio (LMR) can reflect both the myeloid dysfunction and T-cell immune suppression and have prognostic significance.&lt;h4>Methods&lt;/h4>In 771 newly diagnosed advanced-stage Hodgkin Lymphoma (HL) patients we evaluated the baseline values of NLR and LMR as predictors of clinical outcome. According to the multicenter prospective phase II GITIL-HD0607 trial, all patients received two ABVD courses and if PET-2 negative received four additional ABVD cycles while if PET-2-positive patients were randomized to either BEACOPP escalated (Be) plus BEACOPP baseline (Bb) (4 + 4 courses) or Be + Bb (4 + 4) and Rituximab. PET scans were centrally reviewed by an expert panel by Blinded Independent Central Review.&lt;h4>Res</pubmed_abstract><journal>Cancer medicine</journal><pubmed_title>The neutrophil to lymphocyte ratio (NLR) and the presence of large nodal mass are independent predictors of early response: A subanalysis of the prospective phase II PET-2-adapted HD0607 trial.</pubmed_title><pmcid>PMC7724487</pmcid><funding_grant_id>IG2013</funding_grant_id><pubmed_authors>Biggi A</pubmed_authors><pubmed_authors>Zanotti R</pubmed_authors><pubmed_authors>Trentin L</pubmed_authors><pubmed_authors>Gini G</pubmed_authors><pubmed_authors>Gallamini A</pubmed_authors><pubmed_authors>Patti C</pubmed_authors><pubmed_authors>Corradini P</pubmed_authors><pubmed_authors>Schiavotto C</pubmed_authors><pubmed_authors>Cantonetti M</pubmed_authors><pubmed_authors>Tarella C</pubmed_authors><pubmed_authors>Picardi M</pubmed_authors><pubmed_authors>Gavarotti P</pubmed_authors><pubmed_authors>Bolis S</pubmed_authors><pubmed_authors>Viero P</pubmed_authors><pubmed_authors>Massimo Gianni A</pubmed_authors><pubmed_authors>Cimminiello M</pubmed_authors><pubmed_authors>Chauvie S</pubmed_authors><pubmed_authors>Rossi A</pubmed_authors><pubmed_authors>Di Raimondo F</pubmed_authors><pubmed_authors>La Nasa G</pubmed_authors><pubmed_authors>Viviani S</pubmed_authors><pubmed_authors>Zoli V</pubmed_authors><pubmed_authors>Rambaldi A</pubmed_authors><pubmed_authors>Romano A</pubmed_authors><pubmed_authors>Pavoni C</pubmed_authors><pubmed_authors>Parvis G</pubmed_authors><pubmed_authors>Ferreri AJM</pubmed_authors></additional><is_claimable>false</is_claimable><name>The neutrophil to lymphocyte ratio (NLR) and the presence of large nodal mass are independent predictors of early response: A subanalysis of the prospective phase II PET-2-adapted HD0607 trial.</name><description>&lt;h4>Background&lt;/h4>The neutrophil to lymphocyte ratio (NLR) and the lymphocyte to monocyte ratio (LMR) can reflect both the myeloid dysfunction and T-cell immune suppression and have prognostic significance.&lt;h4>Methods&lt;/h4>In 771 newly diagnosed advanced-stage Hodgkin Lymphoma (HL) patients we evaluated the baseline values of NLR and LMR as predictors of clinical outcome. According to the multicenter prospective phase II GITIL-HD0607 trial, all patients received two ABVD courses and if PET-2 negative received four additional ABVD cycles while if PET-2-positive patients were randomized to either BEACOPP escalated (Be) plus BEACOPP baseline (Bb) (4 + 4 courses) or Be + Bb (4 + 4) and Rituximab. PET scans were centrally reviewed by an expert panel by Blinded Independent Central Review.&lt;h4>Res</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Dec</publication><modification>2026-05-03T05:05:33.607Z</modification><creation>2021-02-20T10:55:05Z</creation></dates><accession>S-EPMC7724487</accession><cross_references><pubmed>33155754</pubmed><doi>10.1002/cam4.3396</doi></cross_references></HashMap>