<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhou S</submitter><funding>Natural Science Foundation of Chongqing Innovation Group Science Program</funding><funding>Military Clinical Medical Innovation Project of Xinqiao hospital</funding><funding>National Natural Science Foundation of China</funding><funding>Chongqing Science and Health Joint Medical Research Major Project</funding><funding>Translational Research Grant of NCRCH</funding><pagination>96-105</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11226560</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>120(1)</volume><pubmed_abstract>The conditioning regimen is an important part of autologous hematopoietic stem cell transplantation (ASCT). We explored the efficacy and safety of an optimized BEAC (adjusted-dose, intermediate-dose cytarabine and reduced-dose cyclophosphamide, AD-BEAC) conditioning regimen for non-Hodgkin lymphoma (NHL). A total of 141 NHL patients received AD-BEAC or a standard-dose BEAC (SD-BEAC) conditioning regimen from January 2007 to December 2017, and 104 patients were included in the study after 1:1 propensity matching. The 5-year overall survival (OS) and progression free survival (PFS) rates were significantly higher with AD-BEAC than with SD-BEAC (82.7% vs. 67.3%, P = 0.039; 76.9% vs. 57.7%, P = 0.039). Transplant-related mortality (TRM) was 3.8% in both the AD-BEAC and SD-BEAC groups. The AD-BEAC group had lower incidence of oral ulcers and cardiotoxicity than the SD-BEAC group. An optimized BEAC conditioning regimen is an effective conditioning regimen for ASCT in NHL with acceptable toxicity, that is more effective and safer than a standard BEAC conditioning regimen.</pubmed_abstract><journal>International journal of hematology</journal><pubmed_title>Optimized BEAC conditioning regimen improves clinical outcomes of autologous hematopoietic stem cell transplantation in non-Hodgkin lymphomas.</pubmed_title><pmcid>PMC11226560</pmcid><funding_grant_id>82070208</funding_grant_id><funding_grant_id>2021WWB05</funding_grant_id><funding_grant_id>2022ZDXM025</funding_grant_id><funding_grant_id>No. 81970162</funding_grant_id><funding_grant_id>2021JSLC0003</funding_grant_id><funding_grant_id>cstc2021jcyj-cxttX0001</funding_grant_id><funding_grant_id>2022DBXM003</funding_grant_id><funding_grant_id>2020ZKZC02</funding_grant_id><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Lin S</pubmed_authors><pubmed_authors>Zhou S</pubmed_authors><pubmed_authors>Li F</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Gao L</pubmed_authors><pubmed_authors>Ma X</pubmed_authors><pubmed_authors>Xiang X</pubmed_authors><pubmed_authors>Rao J</pubmed_authors><pubmed_authors>Zeng Y</pubmed_authors><pubmed_authors>Dong S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Optimized BEAC conditioning regimen improves clinical outcomes of autologous hematopoietic stem cell transplantation in non-Hodgkin lymphomas.</name><description>The conditioning regimen is an important part of autologous hematopoietic stem cell transplantation (ASCT). We explored the efficacy and safety of an optimized BEAC (adjusted-dose, intermediate-dose cytarabine and reduced-dose cyclophosphamide, AD-BEAC) conditioning regimen for non-Hodgkin lymphoma (NHL). A total of 141 NHL patients received AD-BEAC or a standard-dose BEAC (SD-BEAC) conditioning regimen from January 2007 to December 2017, and 104 patients were included in the study after 1:1 propensity matching. The 5-year overall survival (OS) and progression free survival (PFS) rates were significantly higher with AD-BEAC than with SD-BEAC (82.7% vs. 67.3%, P = 0.039; 76.9% vs. 57.7%, P = 0.039). Transplant-related mortality (TRM) was 3.8% in both the AD-BEAC and SD-BEAC groups. The AD-BEAC group had lower incidence of oral ulcers and cardiotoxicity than the SD-BEAC group. An optimized BEAC conditioning regimen is an effective conditioning regimen for ASCT in NHL with acceptable toxicity, that is more effective and safer than a standard BEAC conditioning regimen.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2025-04-04T12:54:06.477Z</modification><creation>2025-04-04T12:54:06.477Z</creation></dates><accession>S-EPMC11226560</accession><cross_references><pubmed>38587693</pubmed><doi>10.1007/s12185-024-03755-7</doi></cross_references></HashMap>