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Prognostic Significance of Mixed-Lineage Leukemia (MLL) Gene Detected by Real-Time Fluorescence Quantitative PCR Assay in Acute Myeloid Leukemia

BACKGROUND: The overall prognosis of acute myeloid leukemia (AML) patients with mixed-lineage leukemia (MLL) gene-positivity is unfavorable. In this study, we evaluated the expression levels of the MLL gene in AML patients. MATERIAL/METHODS: We enrolled 68 MLL gene-positive patients out of 433 newly...

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Autores principales: Huang, Sai, Yang, Hua, Li, Yan, Feng, Cong, Gao, Li, Chen, Guo-feng, Gao, Hong-hao, Huang, Zhi, Li, Yong-hui, Yu, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5012461/
https://www.ncbi.nlm.nih.gov/pubmed/27561414
http://dx.doi.org/10.12659/MSM.900429
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author Huang, Sai
Yang, Hua
Li, Yan
Feng, Cong
Gao, Li
Chen, Guo-feng
Gao, Hong-hao
Huang, Zhi
Li, Yong-hui
Yu, Li
author_facet Huang, Sai
Yang, Hua
Li, Yan
Feng, Cong
Gao, Li
Chen, Guo-feng
Gao, Hong-hao
Huang, Zhi
Li, Yong-hui
Yu, Li
author_sort Huang, Sai
collection PubMed
description BACKGROUND: The overall prognosis of acute myeloid leukemia (AML) patients with mixed-lineage leukemia (MLL) gene-positivity is unfavorable. In this study, we evaluated the expression levels of the MLL gene in AML patients. MATERIAL/METHODS: We enrolled 68 MLL gene-positive patients out of 433 newly diagnosed AML patients, and 216 bone marrow samples were collected. Real-time fluorescence quantitative PCR (RQ-PCR) was used to precisely detect the expression levels of the MLL gene. RESULTS: We divided 41 patients into 2 groups according to the variation of MRD (minimal residual disease) level of the MLL gene. Group 1 (n=22) had a rapid reduction of MRD level to ≤10(−4) in all samples collected in the first 3 chemotherapy cycles, while group 2 (n=19) had MRD levels constantly >10(−4) in all samples collected in the first 3 chemotherapy cycles. Group 1 had a significantly better overall survival (p=0.001) and event-free survival (p=0.001) compared to group 2. Moreover, the patients with >10(−4) MRD level before the start of HSCT (hematopoietic stem cell transplantation) had worse prognosis and higher risk of relapse compared to patients with ≤10(−4) before the start of HSCT. CONCLUSIONS: We found that a rapid reduction of MRD level to ≤10(−4) appears to be a prerequisite for better overall survival and event-free survival during the treatment of AML. The MRD levels detected by RQ-PCR were basically in line with the clinical outcome and may be of great importance in guiding early allogeneic HSCT (allo-HSCT) treatment.
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spelling pubmed-50124612016-09-16 Prognostic Significance of Mixed-Lineage Leukemia (MLL) Gene Detected by Real-Time Fluorescence Quantitative PCR Assay in Acute Myeloid Leukemia Huang, Sai Yang, Hua Li, Yan Feng, Cong Gao, Li Chen, Guo-feng Gao, Hong-hao Huang, Zhi Li, Yong-hui Yu, Li Med Sci Monit Clinical Research BACKGROUND: The overall prognosis of acute myeloid leukemia (AML) patients with mixed-lineage leukemia (MLL) gene-positivity is unfavorable. In this study, we evaluated the expression levels of the MLL gene in AML patients. MATERIAL/METHODS: We enrolled 68 MLL gene-positive patients out of 433 newly diagnosed AML patients, and 216 bone marrow samples were collected. Real-time fluorescence quantitative PCR (RQ-PCR) was used to precisely detect the expression levels of the MLL gene. RESULTS: We divided 41 patients into 2 groups according to the variation of MRD (minimal residual disease) level of the MLL gene. Group 1 (n=22) had a rapid reduction of MRD level to ≤10(−4) in all samples collected in the first 3 chemotherapy cycles, while group 2 (n=19) had MRD levels constantly >10(−4) in all samples collected in the first 3 chemotherapy cycles. Group 1 had a significantly better overall survival (p=0.001) and event-free survival (p=0.001) compared to group 2. Moreover, the patients with >10(−4) MRD level before the start of HSCT (hematopoietic stem cell transplantation) had worse prognosis and higher risk of relapse compared to patients with ≤10(−4) before the start of HSCT. CONCLUSIONS: We found that a rapid reduction of MRD level to ≤10(−4) appears to be a prerequisite for better overall survival and event-free survival during the treatment of AML. The MRD levels detected by RQ-PCR were basically in line with the clinical outcome and may be of great importance in guiding early allogeneic HSCT (allo-HSCT) treatment. International Scientific Literature, Inc. 2016-08-26 /pmc/articles/PMC5012461/ /pubmed/27561414 http://dx.doi.org/10.12659/MSM.900429 Text en © Med Sci Monit, 2016 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
spellingShingle Clinical Research
Huang, Sai
Yang, Hua
Li, Yan
Feng, Cong
Gao, Li
Chen, Guo-feng
Gao, Hong-hao
Huang, Zhi
Li, Yong-hui
Yu, Li
Prognostic Significance of Mixed-Lineage Leukemia (MLL) Gene Detected by Real-Time Fluorescence Quantitative PCR Assay in Acute Myeloid Leukemia
title Prognostic Significance of Mixed-Lineage Leukemia (MLL) Gene Detected by Real-Time Fluorescence Quantitative PCR Assay in Acute Myeloid Leukemia
title_full Prognostic Significance of Mixed-Lineage Leukemia (MLL) Gene Detected by Real-Time Fluorescence Quantitative PCR Assay in Acute Myeloid Leukemia
title_fullStr Prognostic Significance of Mixed-Lineage Leukemia (MLL) Gene Detected by Real-Time Fluorescence Quantitative PCR Assay in Acute Myeloid Leukemia
title_full_unstemmed Prognostic Significance of Mixed-Lineage Leukemia (MLL) Gene Detected by Real-Time Fluorescence Quantitative PCR Assay in Acute Myeloid Leukemia
title_short Prognostic Significance of Mixed-Lineage Leukemia (MLL) Gene Detected by Real-Time Fluorescence Quantitative PCR Assay in Acute Myeloid Leukemia
title_sort prognostic significance of mixed-lineage leukemia (mll) gene detected by real-time fluorescence quantitative pcr assay in acute myeloid leukemia
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5012461/
https://www.ncbi.nlm.nih.gov/pubmed/27561414
http://dx.doi.org/10.12659/MSM.900429
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