Cargando…
A meta-analysis of CAG (cytarabine, aclarubicin, G-CSF) regimen for the treatment of 1029 patients with acute myeloid leukemia and myelodysplastic syndrome
The regimen of cytarabine, aclarubicin and G-CSF (CAG) has been widely used in China and Japan for treatment of acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). We searched literature on CAG between 1995 and 2010 and performed a meta-analysis to determine its overall efficacy using a...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3230125/ https://www.ncbi.nlm.nih.gov/pubmed/22082134 http://dx.doi.org/10.1186/1756-8722-4-46 |
_version_ | 1782218037993144320 |
---|---|
author | Wei, Guoqing Ni, Wanmao Chiao, Jen-wei Cai, Zhen Huang, He Liu, Delong |
author_facet | Wei, Guoqing Ni, Wanmao Chiao, Jen-wei Cai, Zhen Huang, He Liu, Delong |
author_sort | Wei, Guoqing |
collection | PubMed |
description | The regimen of cytarabine, aclarubicin and G-CSF (CAG) has been widely used in China and Japan for treatment of acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). We searched literature on CAG between 1995 and 2010 and performed a meta-analysis to determine its overall efficacy using a random-effects or fixed-effects model. Thirty five trials with a total of 1029 AML (n = 814) and MDS (n = 215) patients were included for analysis. The CR rate of AML (57.9%) was significantly higher than that of MDS (45.7%) (p < 0.01). No difference in CR was noted between the new (56.7%) and relapsed/refractory AML (60.1%) (p > 0.05). The CR rate was also significantly higher in patients with favorable (64.5%) and intermediate (69.6%) karyotypes than those with unfavorable one (29.5%) (p < 0.05). Remarkably, the CR rate of CAG was significantly higher than those of non-CAG regimens (odds ratio 2.43). CAG regimen was well tolerated, with cardiotoxicity in 2.3% and early death in 5.2% of the cases. In conclusion, CAG regimen was an effective and safe regimen for the treatment of AML, and may be more effective than non-CAG regimens. Randomized controlled trials are strongly recommended to evaluate its efficacy and safety in comparison with the current standard treatment. |
format | Online Article Text |
id | pubmed-3230125 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32301252011-12-05 A meta-analysis of CAG (cytarabine, aclarubicin, G-CSF) regimen for the treatment of 1029 patients with acute myeloid leukemia and myelodysplastic syndrome Wei, Guoqing Ni, Wanmao Chiao, Jen-wei Cai, Zhen Huang, He Liu, Delong J Hematol Oncol Research The regimen of cytarabine, aclarubicin and G-CSF (CAG) has been widely used in China and Japan for treatment of acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). We searched literature on CAG between 1995 and 2010 and performed a meta-analysis to determine its overall efficacy using a random-effects or fixed-effects model. Thirty five trials with a total of 1029 AML (n = 814) and MDS (n = 215) patients were included for analysis. The CR rate of AML (57.9%) was significantly higher than that of MDS (45.7%) (p < 0.01). No difference in CR was noted between the new (56.7%) and relapsed/refractory AML (60.1%) (p > 0.05). The CR rate was also significantly higher in patients with favorable (64.5%) and intermediate (69.6%) karyotypes than those with unfavorable one (29.5%) (p < 0.05). Remarkably, the CR rate of CAG was significantly higher than those of non-CAG regimens (odds ratio 2.43). CAG regimen was well tolerated, with cardiotoxicity in 2.3% and early death in 5.2% of the cases. In conclusion, CAG regimen was an effective and safe regimen for the treatment of AML, and may be more effective than non-CAG regimens. Randomized controlled trials are strongly recommended to evaluate its efficacy and safety in comparison with the current standard treatment. BioMed Central 2011-11-14 /pmc/articles/PMC3230125/ /pubmed/22082134 http://dx.doi.org/10.1186/1756-8722-4-46 Text en Copyright ©2011 Wei et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Wei, Guoqing Ni, Wanmao Chiao, Jen-wei Cai, Zhen Huang, He Liu, Delong A meta-analysis of CAG (cytarabine, aclarubicin, G-CSF) regimen for the treatment of 1029 patients with acute myeloid leukemia and myelodysplastic syndrome |
title | A meta-analysis of CAG (cytarabine, aclarubicin, G-CSF) regimen for the treatment of 1029 patients with acute myeloid leukemia and myelodysplastic syndrome |
title_full | A meta-analysis of CAG (cytarabine, aclarubicin, G-CSF) regimen for the treatment of 1029 patients with acute myeloid leukemia and myelodysplastic syndrome |
title_fullStr | A meta-analysis of CAG (cytarabine, aclarubicin, G-CSF) regimen for the treatment of 1029 patients with acute myeloid leukemia and myelodysplastic syndrome |
title_full_unstemmed | A meta-analysis of CAG (cytarabine, aclarubicin, G-CSF) regimen for the treatment of 1029 patients with acute myeloid leukemia and myelodysplastic syndrome |
title_short | A meta-analysis of CAG (cytarabine, aclarubicin, G-CSF) regimen for the treatment of 1029 patients with acute myeloid leukemia and myelodysplastic syndrome |
title_sort | meta-analysis of cag (cytarabine, aclarubicin, g-csf) regimen for the treatment of 1029 patients with acute myeloid leukemia and myelodysplastic syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3230125/ https://www.ncbi.nlm.nih.gov/pubmed/22082134 http://dx.doi.org/10.1186/1756-8722-4-46 |
work_keys_str_mv | AT weiguoqing ametaanalysisofcagcytarabineaclarubicingcsfregimenforthetreatmentof1029patientswithacutemyeloidleukemiaandmyelodysplasticsyndrome AT niwanmao ametaanalysisofcagcytarabineaclarubicingcsfregimenforthetreatmentof1029patientswithacutemyeloidleukemiaandmyelodysplasticsyndrome AT chiaojenwei ametaanalysisofcagcytarabineaclarubicingcsfregimenforthetreatmentof1029patientswithacutemyeloidleukemiaandmyelodysplasticsyndrome AT caizhen ametaanalysisofcagcytarabineaclarubicingcsfregimenforthetreatmentof1029patientswithacutemyeloidleukemiaandmyelodysplasticsyndrome AT huanghe ametaanalysisofcagcytarabineaclarubicingcsfregimenforthetreatmentof1029patientswithacutemyeloidleukemiaandmyelodysplasticsyndrome AT liudelong ametaanalysisofcagcytarabineaclarubicingcsfregimenforthetreatmentof1029patientswithacutemyeloidleukemiaandmyelodysplasticsyndrome AT weiguoqing metaanalysisofcagcytarabineaclarubicingcsfregimenforthetreatmentof1029patientswithacutemyeloidleukemiaandmyelodysplasticsyndrome AT niwanmao metaanalysisofcagcytarabineaclarubicingcsfregimenforthetreatmentof1029patientswithacutemyeloidleukemiaandmyelodysplasticsyndrome AT chiaojenwei metaanalysisofcagcytarabineaclarubicingcsfregimenforthetreatmentof1029patientswithacutemyeloidleukemiaandmyelodysplasticsyndrome AT caizhen metaanalysisofcagcytarabineaclarubicingcsfregimenforthetreatmentof1029patientswithacutemyeloidleukemiaandmyelodysplasticsyndrome AT huanghe metaanalysisofcagcytarabineaclarubicingcsfregimenforthetreatmentof1029patientswithacutemyeloidleukemiaandmyelodysplasticsyndrome AT liudelong metaanalysisofcagcytarabineaclarubicingcsfregimenforthetreatmentof1029patientswithacutemyeloidleukemiaandmyelodysplasticsyndrome |