<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>3</volume><submitter>Hohloch K</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Dose escalation and modification of CHOP has improved the prognosis of patients with aggressive lymphoma; even in the rituximab era, dose escalation for high-risk patients is exploited and frequently limited by drug toxicity. Idarubicin (Id) is a 4-demethoxy anthracycline analogue of daunorubicin with activity against lymphoma and has been reported to cause less cardiotoxicity than other anthracylines. The aim of this study was to replace doxorubicine with idarubicin in the CHOEP regimen and to find the maximum tolerable dose (MTD) of idarubicin based on hematotoxicity.&lt;h4>Patients and methods&lt;/h4>Between 11/96 and 09/98, 64 patients (pts) aged 18-75 yrs (pts. 18-60, LDH not elevated, >60 years all risk groups) with newly diagnosed aggressive lymphoma received 6 cycles o</pubmed_abstract><journal>SpringerPlus</journal><pagination>5</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3890437</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Significant dose Escalation of Idarubicin in the treatment of aggressive Non- Hodgkin Lymphoma leads to increased hematotoxicity without improvement in efficacy in comparison to standard CHOEP-14: 9-year follow up results of the CIVEP trial of the DSHNHL.</pubmed_title><pmcid>PMC3890437</pmcid><pubmed_authors>Zwick C</pubmed_authors><pubmed_authors>Pfreundschuh M</pubmed_authors><pubmed_authors>Kaiser U</pubmed_authors><pubmed_authors>Hasenclever D</pubmed_authors><pubmed_authors>Hohloch K</pubmed_authors><pubmed_authors>Feller AC</pubmed_authors><pubmed_authors>Engert A</pubmed_authors><pubmed_authors>Hoffkes HG</pubmed_authors><pubmed_authors>Mesters R</pubmed_authors><pubmed_authors>Kroschinsky F</pubmed_authors><pubmed_authors>Ziepert M</pubmed_authors><pubmed_authors>German High-Grade Non-Hodgkin´s Lymphoma Study Group (DSHNHL)</pubmed_authors><pubmed_authors>Loffler M</pubmed_authors><pubmed_authors>Trumper L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Significant dose Escalation of Idarubicin in the treatment of aggressive Non- Hodgkin Lymphoma leads to increased hematotoxicity without improvement in efficacy in comparison to standard CHOEP-14: 9-year follow up results of the CIVEP trial of the DSHNHL.</name><description>&lt;h4>Background&lt;/h4>Dose escalation and modification of CHOP has improved the prognosis of patients with aggressive lymphoma; even in the rituximab era, dose escalation for high-risk patients is exploited and frequently limited by drug toxicity. Idarubicin (Id) is a 4-demethoxy anthracycline analogue of daunorubicin with activity against lymphoma and has been reported to cause less cardiotoxicity than other anthracylines. The aim of this study was to replace doxorubicine with idarubicin in the CHOEP regimen and to find the maximum tolerable dose (MTD) of idarubicin based on hematotoxicity.&lt;h4>Patients and methods&lt;/h4>Between 11/96 and 09/98, 64 patients (pts) aged 18-75 yrs (pts. 18-60, LDH not elevated, >60 years all risk groups) with newly diagnosed aggressive lymphoma received 6 cycles o</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Jan</publication><modification>2025-04-04T21:13:54.144Z</modification><creation>2019-03-27T01:19:56Z</creation></dates><accession>S-EPMC3890437</accession><cross_references><pubmed>24455463</pubmed><doi>10.1186/2193-1801-3-5</doi></cross_references></HashMap>