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Primary breast double-hit lymphoma management and outcomes: a real-world multicentre experience

BACKGROUND: Primary breast double-hit lymphoma (PB-DHL) is a rare, highly aggressive malignancy that poses challenges regarding accurate diagnosis and selecting optimal treatment regimens. METHODS: We retrospectively reviewed 48 cases of patients diagnosed with PB-DHL in six academic centres between...

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Autores principales: Zhang, Tingting, Zhang, Yuanfeng, Fei, Hairong, Shi, Xue, Wang, Liang, Wang, Peijun, Yu, Jie, Shen, Yuyan, Feng, Sizhou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8447786/
https://www.ncbi.nlm.nih.gov/pubmed/34535141
http://dx.doi.org/10.1186/s12935-021-02198-y
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author Zhang, Tingting
Zhang, Yuanfeng
Fei, Hairong
Shi, Xue
Wang, Liang
Wang, Peijun
Yu, Jie
Shen, Yuyan
Feng, Sizhou
author_facet Zhang, Tingting
Zhang, Yuanfeng
Fei, Hairong
Shi, Xue
Wang, Liang
Wang, Peijun
Yu, Jie
Shen, Yuyan
Feng, Sizhou
author_sort Zhang, Tingting
collection PubMed
description BACKGROUND: Primary breast double-hit lymphoma (PB-DHL) is a rare, highly aggressive malignancy that poses challenges regarding accurate diagnosis and selecting optimal treatment regimens. METHODS: We retrospectively reviewed 48 cases of patients diagnosed with PB-DHL in six academic centres between June 2014 and June 2020 in China. Study-specific data were recorded, including treatment options, therapeutic evaluation, prognostic factors and relapse patterns, and the overall survival (OS) and progression-free survival (PFS) were evaluated. RESULTS: In total, 48 patients were enrolled, with 14 patients treated with DA-EPOCH-R/MA (rituximab, dose-adjusted etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, alternating with high-dose methotrexate and cytarabine), 18 patients treated with DA-EPOCH-R (rituximab, dose-adjusted etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin), and 16 patients treated with R-HyperCVAD (rituximab, hyperfractionated cyclophosphamide, vincristine, doxorubicin, dexamethasone, alternating with cytarabine plus methotrexate). The overall 5-year OS and PFS rates were 41.7% (95% confidence interval [CI], 27.6–56.8%) and 37.5% (95% CI, 24.0–52.6%), respectively. Of the three treatment regimens, the 5-year OS was higher in DA-EPOCH-R/MA group than in the DA-EPOCH-R or R-HyperCVAD subgroups (57.1% vs. 38.9% vs. 31.3%; P = 0.016), as was the 5-year PFS (50.0% vs. 38.9% vs. 25.0%; P = 0.035). Autologous stem cell transplantation (ASCT) prolonged the OS and PFS compared with non-ASCT patients (5-year OS: 72.2% vs. 23.3%; P < 0.001; 5-year PFS: 72.2% vs. 16.7 %, P < 0.001). Multivariate analysis identified tumour size, risk stratification, treatment with DA-EPOCH-R/MA, breast irradiation, and ASCT as significant prognostic factors. CONCLUSIONS: DA-EPOCH-R/MA is a promising regimen for PB-DHL, and breast irradiation yields complementary benefits for prognosis. ASCT significantly decreased disease relapse, providing a potential curative PB-DHL intervention and justifying ASCT as first-line therapy for young patients. More effective treatment strategies for PB-DHL patients remain encouraging. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-021-02198-y.
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spelling pubmed-84477862021-09-20 Primary breast double-hit lymphoma management and outcomes: a real-world multicentre experience Zhang, Tingting Zhang, Yuanfeng Fei, Hairong Shi, Xue Wang, Liang Wang, Peijun Yu, Jie Shen, Yuyan Feng, Sizhou Cancer Cell Int Primary Research BACKGROUND: Primary breast double-hit lymphoma (PB-DHL) is a rare, highly aggressive malignancy that poses challenges regarding accurate diagnosis and selecting optimal treatment regimens. METHODS: We retrospectively reviewed 48 cases of patients diagnosed with PB-DHL in six academic centres between June 2014 and June 2020 in China. Study-specific data were recorded, including treatment options, therapeutic evaluation, prognostic factors and relapse patterns, and the overall survival (OS) and progression-free survival (PFS) were evaluated. RESULTS: In total, 48 patients were enrolled, with 14 patients treated with DA-EPOCH-R/MA (rituximab, dose-adjusted etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, alternating with high-dose methotrexate and cytarabine), 18 patients treated with DA-EPOCH-R (rituximab, dose-adjusted etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin), and 16 patients treated with R-HyperCVAD (rituximab, hyperfractionated cyclophosphamide, vincristine, doxorubicin, dexamethasone, alternating with cytarabine plus methotrexate). The overall 5-year OS and PFS rates were 41.7% (95% confidence interval [CI], 27.6–56.8%) and 37.5% (95% CI, 24.0–52.6%), respectively. Of the three treatment regimens, the 5-year OS was higher in DA-EPOCH-R/MA group than in the DA-EPOCH-R or R-HyperCVAD subgroups (57.1% vs. 38.9% vs. 31.3%; P = 0.016), as was the 5-year PFS (50.0% vs. 38.9% vs. 25.0%; P = 0.035). Autologous stem cell transplantation (ASCT) prolonged the OS and PFS compared with non-ASCT patients (5-year OS: 72.2% vs. 23.3%; P < 0.001; 5-year PFS: 72.2% vs. 16.7 %, P < 0.001). Multivariate analysis identified tumour size, risk stratification, treatment with DA-EPOCH-R/MA, breast irradiation, and ASCT as significant prognostic factors. CONCLUSIONS: DA-EPOCH-R/MA is a promising regimen for PB-DHL, and breast irradiation yields complementary benefits for prognosis. ASCT significantly decreased disease relapse, providing a potential curative PB-DHL intervention and justifying ASCT as first-line therapy for young patients. More effective treatment strategies for PB-DHL patients remain encouraging. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-021-02198-y. BioMed Central 2021-09-17 /pmc/articles/PMC8447786/ /pubmed/34535141 http://dx.doi.org/10.1186/s12935-021-02198-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Primary Research
Zhang, Tingting
Zhang, Yuanfeng
Fei, Hairong
Shi, Xue
Wang, Liang
Wang, Peijun
Yu, Jie
Shen, Yuyan
Feng, Sizhou
Primary breast double-hit lymphoma management and outcomes: a real-world multicentre experience
title Primary breast double-hit lymphoma management and outcomes: a real-world multicentre experience
title_full Primary breast double-hit lymphoma management and outcomes: a real-world multicentre experience
title_fullStr Primary breast double-hit lymphoma management and outcomes: a real-world multicentre experience
title_full_unstemmed Primary breast double-hit lymphoma management and outcomes: a real-world multicentre experience
title_short Primary breast double-hit lymphoma management and outcomes: a real-world multicentre experience
title_sort primary breast double-hit lymphoma management and outcomes: a real-world multicentre experience
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8447786/
https://www.ncbi.nlm.nih.gov/pubmed/34535141
http://dx.doi.org/10.1186/s12935-021-02198-y
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