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Synchronous multiple primary tumors in patients with malignant lymphoma: a retrospective study
BACKGROUND: Synchronous multiple primary malignant tumors (sMPMTs) are sometimes diagnosed in patients with malignant lymphoma. We herein investigated the prognostic impact of sMPMT in lymphoma patients and the optimal treatment strategy. METHODS: Seventy-five patients with sMPMTs (5.8%) among 1285...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188225/ https://www.ncbi.nlm.nih.gov/pubmed/35690729 http://dx.doi.org/10.1186/s12885-022-09734-7 |
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author | Yagi, Yu Kanemasa, Yusuke Sasaki, Yuki Ohigashi, An Morita, Yuka Tamura, Taichi Nakamura, Shohei Kageyama, Akihiko Omuro, Yasushi Shimoyama, Tatsu |
author_facet | Yagi, Yu Kanemasa, Yusuke Sasaki, Yuki Ohigashi, An Morita, Yuka Tamura, Taichi Nakamura, Shohei Kageyama, Akihiko Omuro, Yasushi Shimoyama, Tatsu |
author_sort | Yagi, Yu |
collection | PubMed |
description | BACKGROUND: Synchronous multiple primary malignant tumors (sMPMTs) are sometimes diagnosed in patients with malignant lymphoma. We herein investigated the prognostic impact of sMPMT in lymphoma patients and the optimal treatment strategy. METHODS: Seventy-five patients with sMPMTs (5.8%) among 1285 patients with lymphoma newly diagnosed between August 2004 and April 2020 were enrolled. RESULTS: In patients with indolent lymphoma, those with sMPMTs had a worse prognosis than those without sMPMTs (5-year overall survival [OS]: 73.4% and 87.8%, respectively; P = 0.047). Among those with high and low tumor burden, the cumulative rate of death due to solid tumors was significantly higher in patients with sMPMTs than those without sMPMTs (high tumor burden: 26.7% vs. 1.6%, P < 0.001; low tumor burden: 12.7% vs. 1.0%, P = 0.003). The presence of sMPMTs did not have a significant impact on outcomes in patients with diffuse large B-cell lymphoma (DLBCL) (5-year OS: 65.4% and 66.9%, respectively; P = 0.74; 5-year progression-free survival [PFS]: 65.5% and 59.9%, respectively; P = 0.65). However, the cumulative rate of death from solid tumor in patients with sMPMTs was significantly higher than in patients without sMPMTs (5-year cumulative rate: 7.4% and 2.1%, respectively; P = 0.004). The treatment sequence did not have a significant effect on outcomes or the relative dose intensity of chemotherapy. CONCLUSIONS: In patients with indolent lymphoma, those with sMPMTs had a significantly worse prognosis than those without sMPMTs, mainly because of high mortality due to solid tumors. The presence of sMPMTs was not a significant prognostic factor in patients with DLBCL. It is important to assess the status and need for early treatment of each type of malignancy in patients with sMPMTs. |
format | Online Article Text |
id | pubmed-9188225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91882252022-06-12 Synchronous multiple primary tumors in patients with malignant lymphoma: a retrospective study Yagi, Yu Kanemasa, Yusuke Sasaki, Yuki Ohigashi, An Morita, Yuka Tamura, Taichi Nakamura, Shohei Kageyama, Akihiko Omuro, Yasushi Shimoyama, Tatsu BMC Cancer Research BACKGROUND: Synchronous multiple primary malignant tumors (sMPMTs) are sometimes diagnosed in patients with malignant lymphoma. We herein investigated the prognostic impact of sMPMT in lymphoma patients and the optimal treatment strategy. METHODS: Seventy-five patients with sMPMTs (5.8%) among 1285 patients with lymphoma newly diagnosed between August 2004 and April 2020 were enrolled. RESULTS: In patients with indolent lymphoma, those with sMPMTs had a worse prognosis than those without sMPMTs (5-year overall survival [OS]: 73.4% and 87.8%, respectively; P = 0.047). Among those with high and low tumor burden, the cumulative rate of death due to solid tumors was significantly higher in patients with sMPMTs than those without sMPMTs (high tumor burden: 26.7% vs. 1.6%, P < 0.001; low tumor burden: 12.7% vs. 1.0%, P = 0.003). The presence of sMPMTs did not have a significant impact on outcomes in patients with diffuse large B-cell lymphoma (DLBCL) (5-year OS: 65.4% and 66.9%, respectively; P = 0.74; 5-year progression-free survival [PFS]: 65.5% and 59.9%, respectively; P = 0.65). However, the cumulative rate of death from solid tumor in patients with sMPMTs was significantly higher than in patients without sMPMTs (5-year cumulative rate: 7.4% and 2.1%, respectively; P = 0.004). The treatment sequence did not have a significant effect on outcomes or the relative dose intensity of chemotherapy. CONCLUSIONS: In patients with indolent lymphoma, those with sMPMTs had a significantly worse prognosis than those without sMPMTs, mainly because of high mortality due to solid tumors. The presence of sMPMTs was not a significant prognostic factor in patients with DLBCL. It is important to assess the status and need for early treatment of each type of malignancy in patients with sMPMTs. BioMed Central 2022-06-11 /pmc/articles/PMC9188225/ /pubmed/35690729 http://dx.doi.org/10.1186/s12885-022-09734-7 Text en © The Author(s) 2022 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 | Research Yagi, Yu Kanemasa, Yusuke Sasaki, Yuki Ohigashi, An Morita, Yuka Tamura, Taichi Nakamura, Shohei Kageyama, Akihiko Omuro, Yasushi Shimoyama, Tatsu Synchronous multiple primary tumors in patients with malignant lymphoma: a retrospective study |
title | Synchronous multiple primary tumors in patients with malignant lymphoma: a retrospective study |
title_full | Synchronous multiple primary tumors in patients with malignant lymphoma: a retrospective study |
title_fullStr | Synchronous multiple primary tumors in patients with malignant lymphoma: a retrospective study |
title_full_unstemmed | Synchronous multiple primary tumors in patients with malignant lymphoma: a retrospective study |
title_short | Synchronous multiple primary tumors in patients with malignant lymphoma: a retrospective study |
title_sort | synchronous multiple primary tumors in patients with malignant lymphoma: a retrospective study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188225/ https://www.ncbi.nlm.nih.gov/pubmed/35690729 http://dx.doi.org/10.1186/s12885-022-09734-7 |
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