<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chen HY</submitter><funding>Innovative Research Group Project of the National Natural Science Foundation of China</funding><pagination>33</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7879534</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Although R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone) remains the standard chemotherapy regimen for diffuse large B cell lymphoma (DLBCL) patients, not all patients are responsive to the scheme, and there is no effective method to predict treatment response.&lt;h4>Methods&lt;/h4>We utilized 5hmC-Seal to generate genome-wide 5hmC profiles in plasma cell-free DNA (cfDNA) from 86 DLBCL patients before they received R-CHOP chemotherapy. To investigate the correlation between 5hmC modifications and curative effectiveness, we separated patients into training (n = 56) and validation (n = 30) cohorts and developed a 5hmC-based logistic regression model from the training cohort to predict the treatment response in the validation cohort.&lt;h4>Results&lt;/h4></pubmed_abstract><journal>Clinical epigenetics</journal><pubmed_title>5-Hydroxymethylcytosine profiles of cfDNA are highly predictive of R-CHOP treatment response in diffuse large B cell lymphoma patients.</pubmed_title><pmcid>PMC7879534</pmcid><funding_grant_id>81800195</funding_grant_id><funding_grant_id>31471299</funding_grant_id><funding_grant_id>81522046</funding_grant_id><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Xu N</pubmed_authors><pubmed_authors>He C</pubmed_authors><pubmed_authors>Li F</pubmed_authors><pubmed_authors>Chen L</pubmed_authors><pubmed_authors>Qin Y</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Xiao XB</pubmed_authors><pubmed_authors>Hong Y</pubmed_authors><pubmed_authors>He XH</pubmed_authors><pubmed_authors>Zhu HC</pubmed_authors><pubmed_authors>Chen HY</pubmed_authors><pubmed_authors>Yang P</pubmed_authors><pubmed_authors>Yang ZR</pubmed_authors><pubmed_authors>Pang M</pubmed_authors><pubmed_authors>Yan C</pubmed_authors><pubmed_authors>Jing HM</pubmed_authors><pubmed_authors>Lin J</pubmed_authors><pubmed_authors>Zhang WL</pubmed_authors></additional><is_claimable>false</is_claimable><name>5-Hydroxymethylcytosine profiles of cfDNA are highly predictive of R-CHOP treatment response in diffuse large B cell lymphoma patients.</name><description>&lt;h4>Background&lt;/h4>Although R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone) remains the standard chemotherapy regimen for diffuse large B cell lymphoma (DLBCL) patients, not all patients are responsive to the scheme, and there is no effective method to predict treatment response.&lt;h4>Methods&lt;/h4>We utilized 5hmC-Seal to generate genome-wide 5hmC profiles in plasma cell-free DNA (cfDNA) from 86 DLBCL patients before they received R-CHOP chemotherapy. To investigate the correlation between 5hmC modifications and curative effectiveness, we separated patients into training (n = 56) and validation (n = 30) cohorts and developed a 5hmC-based logistic regression model from the training cohort to predict the treatment response in the validation cohort.&lt;h4>Results&lt;/h4></description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Feb</publication><modification>2026-05-04T18:27:20.384Z</modification><creation>2021-02-21T10:46:59Z</creation></dates><accession>S-EPMC7879534</accession><cross_references><pubmed>33573703</pubmed><doi>10.1186/s13148-020-00973-8</doi></cross_references></HashMap>