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High-intensity chemotherapy improved the prognosis of patients with high-grade B-cell lymphoma

OBJECTIVE: High-grade B-cell lymphoma (HGBL) is highly aggressive and has a poor prognosis. METHODS: The clinical data of 76 patients with High-grade B-cell lymphoma treated in our lymphoma center from July 2016 to April 2020 were analyzed retrospectively. The clinical features, treatment and progno...

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Autores principales: Chen, Yanfang, Cai, Qing, Chang, Yu, Zhang, Mingzhi, Li, Zhaoming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816475/
https://www.ncbi.nlm.nih.gov/pubmed/36618391
http://dx.doi.org/10.3389/fimmu.2022.1047115
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author Chen, Yanfang
Cai, Qing
Chang, Yu
Zhang, Mingzhi
Li, Zhaoming
author_facet Chen, Yanfang
Cai, Qing
Chang, Yu
Zhang, Mingzhi
Li, Zhaoming
author_sort Chen, Yanfang
collection PubMed
description OBJECTIVE: High-grade B-cell lymphoma (HGBL) is highly aggressive and has a poor prognosis. METHODS: The clinical data of 76 patients with High-grade B-cell lymphoma treated in our lymphoma center from July 2016 to April 2020 were analyzed retrospectively. The clinical features, treatment and prognosis of patients with two types of high-grade B-cell lymphoma were compared and analyzed. RESULTS: Among 76 patients with high-grade B-cell lymphoma, 44 cases (57.9%) were high-grade B-cell lymphoma, accompanied by MYC and Bcl-2 and/or Bcl-6 rearrangement (HGBLR) patients, and 32 cases (42.1%) were HGBL, NOS patients. The bone marrow infiltration, IPI (international prognostic index), Ann Arbor stage (III/IV), extranodal disease are more likely to occur in HGBLR group (P <0.05). Survival analysis of patients showed that overall survival (OS) and progression free survival (PFS) in HGBLR group were significantly shorter than those in HGBL, NOS group (median OS: 21 months vs not reached, P=0. 022; median PFS: 5 months vs 12 months, P = 0. 001). Further analysis demonstrated that, as compared with R-CHOP regimen, patients with HGBL who received high-intensity chemotherapy regimens (DA-EPOCH-R, R-CODOX-M/IVAC and R-Hyper-CVAD) had longer OS (median OS, 16 months vs not reached, P=0. 007) and PFS (median PFS, 5 months vs 11 months, P<0.001). Moreover, mu1tivariate ana1ysis showed that high-intensity chemotherapy regimens were independent risk factors for both PFS (P =0.001, HR: 0.306, 95% CI: 0.153–0.610) and OS (P =0.004, HR: 0.262, 95% CI: 0.105–0.656) in patients with HGBL. CONCLUSIONS: HGBLR patients have worse prognosis than patients with HGBL, NOS. High-intensity chemotherapy may improve the prognosis of patients with HGBL.
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spelling pubmed-98164752023-01-07 High-intensity chemotherapy improved the prognosis of patients with high-grade B-cell lymphoma Chen, Yanfang Cai, Qing Chang, Yu Zhang, Mingzhi Li, Zhaoming Front Immunol Immunology OBJECTIVE: High-grade B-cell lymphoma (HGBL) is highly aggressive and has a poor prognosis. METHODS: The clinical data of 76 patients with High-grade B-cell lymphoma treated in our lymphoma center from July 2016 to April 2020 were analyzed retrospectively. The clinical features, treatment and prognosis of patients with two types of high-grade B-cell lymphoma were compared and analyzed. RESULTS: Among 76 patients with high-grade B-cell lymphoma, 44 cases (57.9%) were high-grade B-cell lymphoma, accompanied by MYC and Bcl-2 and/or Bcl-6 rearrangement (HGBLR) patients, and 32 cases (42.1%) were HGBL, NOS patients. The bone marrow infiltration, IPI (international prognostic index), Ann Arbor stage (III/IV), extranodal disease are more likely to occur in HGBLR group (P <0.05). Survival analysis of patients showed that overall survival (OS) and progression free survival (PFS) in HGBLR group were significantly shorter than those in HGBL, NOS group (median OS: 21 months vs not reached, P=0. 022; median PFS: 5 months vs 12 months, P = 0. 001). Further analysis demonstrated that, as compared with R-CHOP regimen, patients with HGBL who received high-intensity chemotherapy regimens (DA-EPOCH-R, R-CODOX-M/IVAC and R-Hyper-CVAD) had longer OS (median OS, 16 months vs not reached, P=0. 007) and PFS (median PFS, 5 months vs 11 months, P<0.001). Moreover, mu1tivariate ana1ysis showed that high-intensity chemotherapy regimens were independent risk factors for both PFS (P =0.001, HR: 0.306, 95% CI: 0.153–0.610) and OS (P =0.004, HR: 0.262, 95% CI: 0.105–0.656) in patients with HGBL. CONCLUSIONS: HGBLR patients have worse prognosis than patients with HGBL, NOS. High-intensity chemotherapy may improve the prognosis of patients with HGBL. Frontiers Media S.A. 2022-12-23 /pmc/articles/PMC9816475/ /pubmed/36618391 http://dx.doi.org/10.3389/fimmu.2022.1047115 Text en Copyright © 2022 Chen, Cai, Chang, Zhang and Li https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Chen, Yanfang
Cai, Qing
Chang, Yu
Zhang, Mingzhi
Li, Zhaoming
High-intensity chemotherapy improved the prognosis of patients with high-grade B-cell lymphoma
title High-intensity chemotherapy improved the prognosis of patients with high-grade B-cell lymphoma
title_full High-intensity chemotherapy improved the prognosis of patients with high-grade B-cell lymphoma
title_fullStr High-intensity chemotherapy improved the prognosis of patients with high-grade B-cell lymphoma
title_full_unstemmed High-intensity chemotherapy improved the prognosis of patients with high-grade B-cell lymphoma
title_short High-intensity chemotherapy improved the prognosis of patients with high-grade B-cell lymphoma
title_sort high-intensity chemotherapy improved the prognosis of patients with high-grade b-cell lymphoma
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816475/
https://www.ncbi.nlm.nih.gov/pubmed/36618391
http://dx.doi.org/10.3389/fimmu.2022.1047115
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