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Improvement of outcomes of an escalated high‐dose methotrexate-based regimen for patients with newly diagnosed primary central nervous system lymphoma: a real-world cohort study

PURPOSE: High‐dose methotrexate (HD‐MTX)-based chemotherapy regimen is the first-line treatment of primary central nervous system lymphoma (PCNSL). At present, doses of MTX in the range of 3.5–8 g/m(2) are frequently used. However, the optimal dose of methotrexate for PCNSL remains controversial. Th...

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Autores principales: Li, Qing, Ma, Jingjing, Ma, Yan, Lin, Zhiguang, Kang, Hui, Chen, Bobin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8349527/
https://www.ncbi.nlm.nih.gov/pubmed/34377030
http://dx.doi.org/10.2147/CMAR.S322467
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author Li, Qing
Ma, Jingjing
Ma, Yan
Lin, Zhiguang
Kang, Hui
Chen, Bobin
author_facet Li, Qing
Ma, Jingjing
Ma, Yan
Lin, Zhiguang
Kang, Hui
Chen, Bobin
author_sort Li, Qing
collection PubMed
description PURPOSE: High‐dose methotrexate (HD‐MTX)-based chemotherapy regimen is the first-line treatment of primary central nervous system lymphoma (PCNSL). At present, doses of MTX in the range of 3.5–8 g/m(2) are frequently used. However, the optimal dose of methotrexate for PCNSL remains controversial. The purpose of this real-world study was to compare the efficacy and toxicity of HD-MTX in patients with untreated PCNSL. METHODS: Immunocompetent adults with newly diagnosed PCNSL between January 2015 and December 2018 were investigated and followed up to June 2019. All patients’ initial treatments were based on HD‐MTX chemotherapy regimens. RESULTS: A total of 73 patients were reviewed. For patients who received HD-MTX at 8 g/m(2) vs.3.5 g/m(2), the complete response (CR) rates were 68.29% vs 43.75% (p = 0.03), and the median PFS times were 17.7 months vs 9.05 months (HR=0.455, 95% CI 0.239–0.865, p=0.016). There was no significant difference in OS between the two groups. Serious adverse effects were uncommon and clinically manageable. CONCLUSION: There is a correlation of treatment response and clinical outcomes between the dosage of MTX in initial induction therapy in newly diagnosed PCNSL. MTX dose of 8 g/m(2) provided a higher CR rate and PFS benefits with acceptable adverse effects.
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spelling pubmed-83495272021-08-09 Improvement of outcomes of an escalated high‐dose methotrexate-based regimen for patients with newly diagnosed primary central nervous system lymphoma: a real-world cohort study Li, Qing Ma, Jingjing Ma, Yan Lin, Zhiguang Kang, Hui Chen, Bobin Cancer Manag Res Original Research PURPOSE: High‐dose methotrexate (HD‐MTX)-based chemotherapy regimen is the first-line treatment of primary central nervous system lymphoma (PCNSL). At present, doses of MTX in the range of 3.5–8 g/m(2) are frequently used. However, the optimal dose of methotrexate for PCNSL remains controversial. The purpose of this real-world study was to compare the efficacy and toxicity of HD-MTX in patients with untreated PCNSL. METHODS: Immunocompetent adults with newly diagnosed PCNSL between January 2015 and December 2018 were investigated and followed up to June 2019. All patients’ initial treatments were based on HD‐MTX chemotherapy regimens. RESULTS: A total of 73 patients were reviewed. For patients who received HD-MTX at 8 g/m(2) vs.3.5 g/m(2), the complete response (CR) rates were 68.29% vs 43.75% (p = 0.03), and the median PFS times were 17.7 months vs 9.05 months (HR=0.455, 95% CI 0.239–0.865, p=0.016). There was no significant difference in OS between the two groups. Serious adverse effects were uncommon and clinically manageable. CONCLUSION: There is a correlation of treatment response and clinical outcomes between the dosage of MTX in initial induction therapy in newly diagnosed PCNSL. MTX dose of 8 g/m(2) provided a higher CR rate and PFS benefits with acceptable adverse effects. Dove 2021-08-04 /pmc/articles/PMC8349527/ /pubmed/34377030 http://dx.doi.org/10.2147/CMAR.S322467 Text en © 2021 Li et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Li, Qing
Ma, Jingjing
Ma, Yan
Lin, Zhiguang
Kang, Hui
Chen, Bobin
Improvement of outcomes of an escalated high‐dose methotrexate-based regimen for patients with newly diagnosed primary central nervous system lymphoma: a real-world cohort study
title Improvement of outcomes of an escalated high‐dose methotrexate-based regimen for patients with newly diagnosed primary central nervous system lymphoma: a real-world cohort study
title_full Improvement of outcomes of an escalated high‐dose methotrexate-based regimen for patients with newly diagnosed primary central nervous system lymphoma: a real-world cohort study
title_fullStr Improvement of outcomes of an escalated high‐dose methotrexate-based regimen for patients with newly diagnosed primary central nervous system lymphoma: a real-world cohort study
title_full_unstemmed Improvement of outcomes of an escalated high‐dose methotrexate-based regimen for patients with newly diagnosed primary central nervous system lymphoma: a real-world cohort study
title_short Improvement of outcomes of an escalated high‐dose methotrexate-based regimen for patients with newly diagnosed primary central nervous system lymphoma: a real-world cohort study
title_sort improvement of outcomes of an escalated high‐dose methotrexate-based regimen for patients with newly diagnosed primary central nervous system lymphoma: a real-world cohort study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8349527/
https://www.ncbi.nlm.nih.gov/pubmed/34377030
http://dx.doi.org/10.2147/CMAR.S322467
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