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High‐dose Methotrexate plus temozolomide with or without rituximab in patients with untreated primary central nervous system lymphoma: A retrospective study from China

The purpose of this retrospective study was to compare the efficacy and toxicity of high‐dose methotrexate plus temozolomide (MT regimen) and rituximab plus MT (RMT regimen) in patients with untreated primary central nervous system lymphoma (PCNSL). A total of 62 patients with untreated PCNSL were e...

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Autores principales: Chen, Cui, Sun, Peng, Cui, Juan, Yan, Shumei, Chen, Hao, Xia, Yi, Bi, Xiwen, Liu, Panpan, Wang, Yu, Yang, Hang, Nie, Man, Zhang, Xue‐Wen, Jiang, Wenqi, Li, Zhi‐Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488123/
https://www.ncbi.nlm.nih.gov/pubmed/30821418
http://dx.doi.org/10.1002/cam4.1906
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author Chen, Cui
Sun, Peng
Cui, Juan
Yan, Shumei
Chen, Hao
Xia, Yi
Bi, Xiwen
Liu, Panpan
Wang, Yu
Yang, Hang
Nie, Man
Zhang, Xue‐Wen
Jiang, Wenqi
Li, Zhi‐Ming
author_facet Chen, Cui
Sun, Peng
Cui, Juan
Yan, Shumei
Chen, Hao
Xia, Yi
Bi, Xiwen
Liu, Panpan
Wang, Yu
Yang, Hang
Nie, Man
Zhang, Xue‐Wen
Jiang, Wenqi
Li, Zhi‐Ming
author_sort Chen, Cui
collection PubMed
description The purpose of this retrospective study was to compare the efficacy and toxicity of high‐dose methotrexate plus temozolomide (MT regimen) and rituximab plus MT (RMT regimen) in patients with untreated primary central nervous system lymphoma (PCNSL). A total of 62 patients with untreated PCNSL were enrolled between January 2005 and December 2015, with the median age of 53.5 years (range 29‐77).In this study, 32 patients received RMT as induction therapy, and 30 received MT. Objective responses were noted in 93.7% of the patients in the RMT group and in 69.0% of the patients in the MT group (P = 0.018), while complete responses were noted in 53.2% of the patients in the RMT group and 27.6% of the patients in the MT group (P < 0.001). The 2‐ and 5‐year PFS rates were 81.3% and 53.3%, respectively, for the RMT group and 46.5% and 29.1%, respectively, for the MT group (P = 0.019). The 2‐ and 5‐year overall survival (OS) rates were 82.3% and 82.3%, respectively, for the RMT group and 65.7% and 50.0%, respectively, for the MT group (P = 0.015). Multivariate analyses showed that therapeutic regimen (RMT vs MT) was an independent prognostic factor for PFS and OS. Our encouraging results suggest that the RMT regimen may be a feasible and safe therapeutic approach for first‐line treatment of PCNSL.
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spelling pubmed-64881232019-05-23 High‐dose Methotrexate plus temozolomide with or without rituximab in patients with untreated primary central nervous system lymphoma: A retrospective study from China Chen, Cui Sun, Peng Cui, Juan Yan, Shumei Chen, Hao Xia, Yi Bi, Xiwen Liu, Panpan Wang, Yu Yang, Hang Nie, Man Zhang, Xue‐Wen Jiang, Wenqi Li, Zhi‐Ming Cancer Med Clinical Cancer Research The purpose of this retrospective study was to compare the efficacy and toxicity of high‐dose methotrexate plus temozolomide (MT regimen) and rituximab plus MT (RMT regimen) in patients with untreated primary central nervous system lymphoma (PCNSL). A total of 62 patients with untreated PCNSL were enrolled between January 2005 and December 2015, with the median age of 53.5 years (range 29‐77).In this study, 32 patients received RMT as induction therapy, and 30 received MT. Objective responses were noted in 93.7% of the patients in the RMT group and in 69.0% of the patients in the MT group (P = 0.018), while complete responses were noted in 53.2% of the patients in the RMT group and 27.6% of the patients in the MT group (P < 0.001). The 2‐ and 5‐year PFS rates were 81.3% and 53.3%, respectively, for the RMT group and 46.5% and 29.1%, respectively, for the MT group (P = 0.019). The 2‐ and 5‐year overall survival (OS) rates were 82.3% and 82.3%, respectively, for the RMT group and 65.7% and 50.0%, respectively, for the MT group (P = 0.015). Multivariate analyses showed that therapeutic regimen (RMT vs MT) was an independent prognostic factor for PFS and OS. Our encouraging results suggest that the RMT regimen may be a feasible and safe therapeutic approach for first‐line treatment of PCNSL. John Wiley and Sons Inc. 2019-03-01 /pmc/articles/PMC6488123/ /pubmed/30821418 http://dx.doi.org/10.1002/cam4.1906 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Chen, Cui
Sun, Peng
Cui, Juan
Yan, Shumei
Chen, Hao
Xia, Yi
Bi, Xiwen
Liu, Panpan
Wang, Yu
Yang, Hang
Nie, Man
Zhang, Xue‐Wen
Jiang, Wenqi
Li, Zhi‐Ming
High‐dose Methotrexate plus temozolomide with or without rituximab in patients with untreated primary central nervous system lymphoma: A retrospective study from China
title High‐dose Methotrexate plus temozolomide with or without rituximab in patients with untreated primary central nervous system lymphoma: A retrospective study from China
title_full High‐dose Methotrexate plus temozolomide with or without rituximab in patients with untreated primary central nervous system lymphoma: A retrospective study from China
title_fullStr High‐dose Methotrexate plus temozolomide with or without rituximab in patients with untreated primary central nervous system lymphoma: A retrospective study from China
title_full_unstemmed High‐dose Methotrexate plus temozolomide with or without rituximab in patients with untreated primary central nervous system lymphoma: A retrospective study from China
title_short High‐dose Methotrexate plus temozolomide with or without rituximab in patients with untreated primary central nervous system lymphoma: A retrospective study from China
title_sort high‐dose methotrexate plus temozolomide with or without rituximab in patients with untreated primary central nervous system lymphoma: a retrospective study from china
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488123/
https://www.ncbi.nlm.nih.gov/pubmed/30821418
http://dx.doi.org/10.1002/cam4.1906
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