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A phase III trial comparing CHOP to PMitCEBO with or without G-CSF in patients aged 60 plus with aggressive non-Hodgkin's lymphoma
The management of older patients with aggressive non-Hodgkin's lymphoma presents a challenge to the physician. Age is a poor prognostic indicator, due to reduced ability to tolerate and maintain dose-intensive chemotherapy. Generally, older patients demonstrate a lower response rate, reduced su...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3216418/ https://www.ncbi.nlm.nih.gov/pubmed/16508640 http://dx.doi.org/10.1038/sj.bjc.6602975 |
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author | Burton, C Linch, D Hoskin, P Milligan, D Dyer, M J S Hancock, B Mouncey, P Smith, P Qian, W MacLennan, K Jack, A Webb, A Cunningham, D |
author_facet | Burton, C Linch, D Hoskin, P Milligan, D Dyer, M J S Hancock, B Mouncey, P Smith, P Qian, W MacLennan, K Jack, A Webb, A Cunningham, D |
author_sort | Burton, C |
collection | PubMed |
description | The management of older patients with aggressive non-Hodgkin's lymphoma presents a challenge to the physician. Age is a poor prognostic indicator, due to reduced ability to tolerate and maintain dose-intensive chemotherapy. Generally, older patients demonstrate a lower response rate, reduced survival and increased toxicity, although the majority of large randomised trials exclude older patients. This randomised trial was conducted in patients 60 years or over to compare CHOP (cyclophosphamide 750 mg m(−2), doxorubicin 50 mg m(−2), vincristine 1.4 mg m(−2), prednisolone 100 mg) with PMitCEBO (mitoxantrone 7 mg m(−2), cyclophosphamide 300 mg m(−2), etoposide 150 mg m(−2), vincristine 1.4 mg m(−2), bleomycin 10 mg m(−2) and prednisolone 50 mg). Due to the myelosuppressive nature of these regimens, patients were also randomised to the addition of G-CSF. The formal results of this trial with long-term follow-up are now reported. Data were analysed to assess efficacy and toxicity. Overall response rate was 84% in the CHOP arm and 83% in the PMitCEBO arm, with overall response rates of 83% for the use of G-CSF and 84% for no G-CSF. At median 44 months follow-up, there was no significant difference in failure-free, progression-free or overall survival between the CHOP and PMitCEBO arms. At 3 years, the actuarial failure-free survival was 44% in CHOP recipients and 42% in PMitCEBO recipients and the 3-year actuarial overall survival was 46% and 45% respectively. There was no significant difference in the failure-free, progression-free or overall survival with the addition of G-CSF. |
format | Online Article Text |
id | pubmed-3216418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-32164182011-11-16 A phase III trial comparing CHOP to PMitCEBO with or without G-CSF in patients aged 60 plus with aggressive non-Hodgkin's lymphoma Burton, C Linch, D Hoskin, P Milligan, D Dyer, M J S Hancock, B Mouncey, P Smith, P Qian, W MacLennan, K Jack, A Webb, A Cunningham, D Br J Cancer Clinical Study The management of older patients with aggressive non-Hodgkin's lymphoma presents a challenge to the physician. Age is a poor prognostic indicator, due to reduced ability to tolerate and maintain dose-intensive chemotherapy. Generally, older patients demonstrate a lower response rate, reduced survival and increased toxicity, although the majority of large randomised trials exclude older patients. This randomised trial was conducted in patients 60 years or over to compare CHOP (cyclophosphamide 750 mg m(−2), doxorubicin 50 mg m(−2), vincristine 1.4 mg m(−2), prednisolone 100 mg) with PMitCEBO (mitoxantrone 7 mg m(−2), cyclophosphamide 300 mg m(−2), etoposide 150 mg m(−2), vincristine 1.4 mg m(−2), bleomycin 10 mg m(−2) and prednisolone 50 mg). Due to the myelosuppressive nature of these regimens, patients were also randomised to the addition of G-CSF. The formal results of this trial with long-term follow-up are now reported. Data were analysed to assess efficacy and toxicity. Overall response rate was 84% in the CHOP arm and 83% in the PMitCEBO arm, with overall response rates of 83% for the use of G-CSF and 84% for no G-CSF. At median 44 months follow-up, there was no significant difference in failure-free, progression-free or overall survival between the CHOP and PMitCEBO arms. At 3 years, the actuarial failure-free survival was 44% in CHOP recipients and 42% in PMitCEBO recipients and the 3-year actuarial overall survival was 46% and 45% respectively. There was no significant difference in the failure-free, progression-free or overall survival with the addition of G-CSF. Nature Publishing Group 2006-03-27 2006-02-28 /pmc/articles/PMC3216418/ /pubmed/16508640 http://dx.doi.org/10.1038/sj.bjc.6602975 Text en Copyright © 2006 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This 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 license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license 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 license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Study Burton, C Linch, D Hoskin, P Milligan, D Dyer, M J S Hancock, B Mouncey, P Smith, P Qian, W MacLennan, K Jack, A Webb, A Cunningham, D A phase III trial comparing CHOP to PMitCEBO with or without G-CSF in patients aged 60 plus with aggressive non-Hodgkin's lymphoma |
title | A phase III trial comparing CHOP to PMitCEBO with or without G-CSF in patients aged 60 plus with aggressive non-Hodgkin's lymphoma |
title_full | A phase III trial comparing CHOP to PMitCEBO with or without G-CSF in patients aged 60 plus with aggressive non-Hodgkin's lymphoma |
title_fullStr | A phase III trial comparing CHOP to PMitCEBO with or without G-CSF in patients aged 60 plus with aggressive non-Hodgkin's lymphoma |
title_full_unstemmed | A phase III trial comparing CHOP to PMitCEBO with or without G-CSF in patients aged 60 plus with aggressive non-Hodgkin's lymphoma |
title_short | A phase III trial comparing CHOP to PMitCEBO with or without G-CSF in patients aged 60 plus with aggressive non-Hodgkin's lymphoma |
title_sort | phase iii trial comparing chop to pmitcebo with or without g-csf in patients aged 60 plus with aggressive non-hodgkin's lymphoma |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3216418/ https://www.ncbi.nlm.nih.gov/pubmed/16508640 http://dx.doi.org/10.1038/sj.bjc.6602975 |
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