Clinical Features and Outcomes of Primary Breast Diffuse Large B-Cell Lymphoma: A Matched-Pair Study

Author:

Teng Ling-Chiao1,Liao Yu-Min2,Gau Jyh-Pyng3,Hsiao Tzu-Hung4567,Chen Tsung-Chih1,Chen Mei-Hui189,Yeh Su-Peng210,Teng Chieh-Lin Jerry111121314ORCID

Affiliation:

1. Division of Hematology/Medical Oncology, Department of Medicine, Taichung Veterans General Hospital, Taichung

2. Department of Hematology and Oncology, China Medical University Hospital, Taichung

3. Division of Hematology and Oncology, Department of Medicine, Taipei Medical University Hospital, Taipei City

4. Department of Medical Research, Taichung Veterans General Hospital, Taichung

5. Department of Chemical Engineering, National Tsing Hua University, Hsinchu

6. Department of Public Health, Fu Jen Catholic University, New Taipei City

7. Institute of Genomics and Bioinformatics, National Chung Hsing University, Taichung

8. Department of Nursing, Taichung Veterans General Hospital, Taichung

9. College of Nursing, Hung Kuang University, Taichung

10. School of Medicine, China Medical University, Taichung

11. Department of Post-Baccalaureate Medicine, College of Medicine, National Chung Hsing University, Taichung

12. Department of Life Science, Tunghai University, Taichung

13. School of Medicine, Chung Shan Medical University, Taichung

14. Ph.D. Program in Translational Medicine, National Chung Hsing University, Taichung

Abstract

Background: 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. Methods: 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. Results: Patients with primary breast and non-breast DLBCL had a 5-year PFS of 72.6% and 86.9%, respectively ( P = .206). These 2 groups also had comparable 5-year OS (86.9% vs 87.8%; P = .772). The breast as the primary site was not associated with inferior PFS (hazard ratio [HR]: 2.14; 95% CI: 0.66-6.96; P = .206) and OS (HR: 1.26; 95% CI: 0.27-5.93; P = .772). Conclusion: 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.

Publisher

SAGE Publications

Subject

Oncology

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