<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Puvvada SD</submitter><funding>NIH/NCI Community Oncology Research Program</funding><funding>Bristol-Myers Squibb</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>National Clinical Trials Network</funding><pagination>686-91</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5125530</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>174(5)</volume><pubmed_abstract>Double hit lymphoma (DHL) and double protein-expressing (MYC, BCL2) lymphomas (DPL) fare poorly with R-CHOP (rituximab + cyclophosphamide, doxorubicin, vincristine, prednisolone); consolidative autologous stem cell transplant (ASCT) may improve outcomes. S9704, a phase III randomized study of CHOP +/-R with or without ASCT enabled evaluation of intensive consolidation. Immunohistochemistry (IHC) identified 27 of 198 patients (13·6%) with MYC overexpression; 20 (74%) harboured concurrent BCL2 overexpression. Four had DHL and 16 had DPL only. With median 127 months follow-up, there is a trend favouring outcomes after ASCT in DPL and MYC protein overexpressing patients, whereas all DHL patients have died irrespective of ASCT.</pubmed_abstract><journal>British journal of haematology</journal><pubmed_title>Outcomes of MYC-associated lymphomas after R-CHOP with and without consolidative autologous stem cell transplant: subset analysis of randomized trial intergroup SWOG S9704.</pubmed_title><pmcid>PMC5125530</pmcid><funding_grant_id>CA180835</funding_grant_id><funding_grant_id>UG1 CA189860</funding_grant_id><funding_grant_id>CA189872</funding_grant_id><funding_grant_id>UG1 CA189954</funding_grant_id><funding_grant_id>UG1 CA189953</funding_grant_id><funding_grant_id>UG1 CA189854</funding_grant_id><funding_grant_id>UG1 CA189952</funding_grant_id><funding_grant_id>CA189822</funding_grant_id><funding_grant_id>UG1 CA189872</funding_grant_id><funding_grant_id>P30 CA060553</funding_grant_id><funding_grant_id>CA180819</funding_grant_id><funding_grant_id>CA189804</funding_grant_id><funding_grant_id>U10 CA180835</funding_grant_id><funding_grant_id>U10 CA180838</funding_grant_id><funding_grant_id>CA189808</funding_grant_id><funding_grant_id>UG1 CA189957</funding_grant_id><funding_grant_id>CA180888</funding_grant_id><funding_grant_id>CA180821</funding_grant_id><funding_grant_id>CA180846</funding_grant_id><funding_grant_id>CA180801</funding_grant_id><funding_grant_id>U10 CA180819</funding_grant_id><funding_grant_id>CA180820</funding_grant_id><funding_grant_id>CA180863</funding_grant_id><funding_grant_id>CA189860</funding_grant_id><funding_grant_id>CA189953</funding_grant_id><funding_grant_id>CA189854</funding_grant_id><funding_grant_id>UG1 CA189822</funding_grant_id><funding_grant_id>CA189952</funding_grant_id><funding_grant_id>U10 CA180863</funding_grant_id><funding_grant_id>U10 CA180820</funding_grant_id><funding_grant_id>CA189954</funding_grant_id><funding_grant_id>CA189957</funding_grant_id><funding_grant_id>U10 CA180801</funding_grant_id><funding_grant_id>U10 CA180846</funding_grant_id><funding_grant_id>UG1 CA189808</funding_grant_id><funding_grant_id>U10 CA180821</funding_grant_id><funding_grant_id>U10 CA180888</funding_grant_id><funding_grant_id>UG1 CA189804</funding_grant_id><pubmed_authors>Leblanc M</pubmed_authors><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Couban S</pubmed_authors><pubmed_authors>Shea TC</pubmed_authors><pubmed_authors>Friedberg JW</pubmed_authors><pubmed_authors>Puvvada SD</pubmed_authors><pubmed_authors>Rimsza LM</pubmed_authors><pubmed_authors>Marcellus D</pubmed_authors><pubmed_authors>Cook JR</pubmed_authors><pubmed_authors>Leonard JP</pubmed_authors><pubmed_authors>Stiff PJ</pubmed_authors><pubmed_authors>Kahl B</pubmed_authors><pubmed_authors>Winter JN</pubmed_authors><pubmed_authors>Smith SM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Outcomes of MYC-associated lymphomas after R-CHOP with and without consolidative autologous stem cell transplant: subset analysis of randomized trial intergroup SWOG S9704.</name><description>Double hit lymphoma (DHL) and double protein-expressing (MYC, BCL2) lymphomas (DPL) fare poorly with R-CHOP (rituximab + cyclophosphamide, doxorubicin, vincristine, prednisolone); consolidative autologous stem cell transplant (ASCT) may improve outcomes. S9704, a phase III randomized study of CHOP +/-R with or without ASCT enabled evaluation of intensive consolidation. Immunohistochemistry (IHC) identified 27 of 198 patients (13·6%) with MYC overexpression; 20 (74%) harboured concurrent BCL2 overexpression. Four had DHL and 16 had DPL only. With median 127 months follow-up, there is a trend favouring outcomes after ASCT in DPL and MYC protein overexpressing patients, whereas all DHL patients have died irrespective of ASCT.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Sep</publication><modification>2025-04-18T20:51:55.459Z</modification><creation>2019-03-27T02:29:59Z</creation></dates><accession>S-EPMC5125530</accession><cross_references><pubmed>27072903</pubmed><doi>10.1111/bjh.14100</doi></cross_references></HashMap>