<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17</volume><submitter>Teng LC</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The influence of the breast as the primary site on the outcome of diffuse large B-cell lymphoma (DLBCL) and further changes in therapeutic strategies remain unclear. We aimed to compare the outcomes between primary breast and non-breast DLBCL and analyze the genetic profiles of some of the study cohorts using next-generation sequencing.&lt;h4>Methods&lt;/h4>This matched-pair study reviewed the medical records of 19 patients with stage I and II primary breast DLBCL diagnosed between January 2005 and December 2021 on the basis of the Wiseman and Liao criteria, and we used 1:4 propensity score matching to identify patients with non-breast DLBCL as the control group. The overall response rate, progression-free survival (PFS), and overall survival (OS) were the outcome measures.&lt;h4>Results&lt;/h4>Patients with primary breast and non-breast DLBCL had a 5-year PFS of 72.6% and 86.9%, respectively (&lt;i>P&lt;/i> = .206). These 2 groups also had comparable 5-year OS (86.9% vs 87.8%; &lt;i>P&lt;/i> = .772). The breast as the primary site was not associated with inferior PFS (hazard ratio [HR]: 2.14; 95% CI: 0.66-6.96; &lt;i>P&lt;/i> = .206) and OS (HR: 1.26; 95% CI: 0.27-5.93; &lt;i>P&lt;/i> = .772).&lt;h4>Conclusion&lt;/h4>Patients with primary breast DLBCL and those with non-breast DLBCL had comparable PFS and OS under rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) or R-CHOP-like regimens. Further investigations of the mutation profile, its clinical impact, potential central nervous system relapse, and prognosis of primary breast DLBCL are required.</pubmed_abstract><journal>Clinical Medicine Insights. Oncology</journal><pagination>11795549231203142</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10613402</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Clinical Features and Outcomes of Primary Breast Diffuse Large B-Cell Lymphoma: A Matched-Pair Study.</pubmed_title><pmcid>PMC10613402</pmcid><pubmed_authors>Chen MH</pubmed_authors><pubmed_authors>Liao YM</pubmed_authors><pubmed_authors>Chen TC</pubmed_authors><pubmed_authors>Teng LC</pubmed_authors><pubmed_authors>Gau JP</pubmed_authors><pubmed_authors>Hsiao TH</pubmed_authors><pubmed_authors>Yeh SP</pubmed_authors><pubmed_authors>Teng CJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical Features and Outcomes of Primary Breast Diffuse Large B-Cell Lymphoma: A Matched-Pair Study.</name><description>&lt;h4>Background&lt;/h4>The influence of the breast as the primary site on the outcome of diffuse large B-cell lymphoma (DLBCL) and further changes in therapeutic strategies remain unclear. We aimed to compare the outcomes between primary breast and non-breast DLBCL and analyze the genetic profiles of some of the study cohorts using next-generation sequencing.&lt;h4>Methods&lt;/h4>This matched-pair study reviewed the medical records of 19 patients with stage I and II primary breast DLBCL diagnosed between January 2005 and December 2021 on the basis of the Wiseman and Liao criteria, and we used 1:4 propensity score matching to identify patients with non-breast DLBCL as the control group. The overall response rate, progression-free survival (PFS), and overall survival (OS) were the outcome measures.&lt;h4>Results&lt;/h4>Patients with primary breast and non-breast DLBCL had a 5-year PFS of 72.6% and 86.9%, respectively (&lt;i>P&lt;/i> = .206). These 2 groups also had comparable 5-year OS (86.9% vs 87.8%; &lt;i>P&lt;/i> = .772). The breast as the primary site was not associated with inferior PFS (hazard ratio [HR]: 2.14; 95% CI: 0.66-6.96; &lt;i>P&lt;/i> = .206) and OS (HR: 1.26; 95% CI: 0.27-5.93; &lt;i>P&lt;/i> = .772).&lt;h4>Conclusion&lt;/h4>Patients with primary breast DLBCL and those with non-breast DLBCL had comparable PFS and OS under rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) or R-CHOP-like regimens. Further investigations of the mutation profile, its clinical impact, potential central nervous system relapse, and prognosis of primary breast DLBCL are required.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-22T13:38:40.675Z</modification><creation>2025-04-06T00:46:00.471Z</creation></dates><accession>S-EPMC10613402</accession><cross_references><pubmed>37905234</pubmed><doi>10.1177/11795549231203142</doi></cross_references></HashMap>