{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["17"],"submitter":["Teng LC"],"pubmed_abstract":["<h4>Background</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.<h4>Methods</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.<h4>Results</h4>Patients with primary breast and non-breast DLBCL had a 5-year PFS of 72.6% and 86.9%, respectively (<i>P</i> = .206). These 2 groups also had comparable 5-year OS (86.9% vs 87.8%; <i>P</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; <i>P</i> = .206) and OS (HR: 1.26; 95% CI: 0.27-5.93; <i>P</i> = .772).<h4>Conclusion</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."],"journal":["Clinical Medicine Insights. Oncology"],"pagination":["11795549231203142"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10613402"],"repository":["biostudies-literature"],"pubmed_title":["Clinical Features and Outcomes of Primary Breast Diffuse Large B-Cell Lymphoma: A Matched-Pair Study."],"pmcid":["PMC10613402"],"pubmed_authors":["Chen MH","Liao YM","Chen TC","Teng LC","Gau JP","Hsiao TH","Yeh SP","Teng CJ"],"additional_accession":[]},"is_claimable":false,"name":"Clinical Features and Outcomes of Primary Breast Diffuse Large B-Cell Lymphoma: A Matched-Pair Study.","description":"<h4>Background</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.<h4>Methods</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.<h4>Results</h4>Patients with primary breast and non-breast DLBCL had a 5-year PFS of 72.6% and 86.9%, respectively (<i>P</i> = .206). These 2 groups also had comparable 5-year OS (86.9% vs 87.8%; <i>P</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; <i>P</i> = .206) and OS (HR: 1.26; 95% CI: 0.27-5.93; <i>P</i> = .772).<h4>Conclusion</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.","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023","modification":"2025-04-22T13:38:40.675Z","creation":"2025-04-06T00:46:00.471Z"},"accession":"S-EPMC10613402","cross_references":{"pubmed":["37905234"],"doi":["10.1177/11795549231203142"]}}