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早期评估NPM1突变阳性急性髓系白血病患者残留白血病水平的预后意义
OBJECTIVE: To explore prognostic significance of early assessment of minimal residual leukemia (MRD) in adult patients with de novo acute myeloid leukemia (AML) with mutated NPM1. METHODS: The response, NPM1 mutated transcript level after induction chemotherapy and the first 2 cycles of consolidatio...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
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Editorial office of Chinese Journal of Hematology
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7348393/ https://www.ncbi.nlm.nih.gov/pubmed/28219218 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2017.01.003 |
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collection | PubMed |
description | OBJECTIVE: To explore prognostic significance of early assessment of minimal residual leukemia (MRD) in adult patients with de novo acute myeloid leukemia (AML) with mutated NPM1. METHODS: The response, NPM1 mutated transcript level after induction chemotherapy and the first 2 cycles of consolidation chemotherapy, disease-free survival (DFS) and overall survival (OS) in 137 patients with AML with NPM1 mutations of A, B and D were retrospectively analyzed. RESULTS: Data of 137 patients were collected, 67 were male, the median age was 49 years (16–67 years), 107 (78.1%) had normal karyotype, 57 (41.6%) had positive FLT3-ITD mutation, the median NPM1 mutated transcript level at diagnosis was 84.1%. Among the 134 evaluable patients, 115 (85.8%) achieved a complete remission (CR). Multivariate analyses revealed that WBC<100×10(9)/L (OR=0.3, 95% CI 0.1–0.9, P=0.027) and first induction therapy with “IA10” protocol (OR=0.3, 95% CI 0.1–0.8, P=0.015) were factors associated with achieving a CR. With a median follow-up period of 24 months (range, 2 to 91 months) in 77 survived CR patients, the probabilities of DFS and OS at 3 years were 48.0% and 63.9%, respectively. Multivariate analyses showed that positive FLT3-ITD (HR=3.2, 95% CI 1.6–6.7, P=0.002), high MRD level after 2 cycles of consolidation chemotherapy (NPM1 mutation transcript level <3-log reduction from the individual baseline, HR=23.2, 95% CI 7.0–76.6, P<0.001) and chemotherapy or autologous hematopoietic stem cell transplantation (auto-HSCT) rather than allogeneic HSCT (allo-HSCT) (HR=2.6, 95% CI 1.0–6.6, P=0.045) were the unfavorable factors affecting DFS, high MRD level at the time of achieving the first CR (NPM1 mutation transcript level <2-log reduction from the individual baseline, OR=2.5, 95% CI 1.0–6.1, P=0.040) and after 2 cycles of consolidation chemotherapy (HR=4.5, 95% CI 2.0–10.3, P<0.001) were the unfavorable factors affecting OS. Furthermore, DFS and OS rates at 3 years in those receiving chemotherapy or auto-HSCT were 39.7% and 59.1%, respectively; positive FLT3-ITD and high MRD level after 2 cycles of consolidation chemotherapy were independent factors associated with both shorter DFS (HR=3.5, 95% CI 1.6–7.6, P=0.002 and HR=8.9, 95% CI 3.8–20.7, P<0.001) and OS (HR=2.7, 95% CI 1.1–6.9, P=0.036 and HR=3.1, 95% CI 1.2–8.0, P=0.021); meanwhile, high MRD level at the time of achieving the first CR associated with shorter OS (HR=3.1, 95% CI 1.2–8.0, P=0.022). CONCLUSION: Positive FLT3-ITD mutation and high MRD level after induction or consolidation chemotherapy associated with poor outcomes in AML patients with mutated NPM1. |
format | Online Article Text |
id | pubmed-7348393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Editorial office of Chinese Journal of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-73483932020-07-16 早期评估NPM1突变阳性急性髓系白血病患者残留白血病水平的预后意义 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To explore prognostic significance of early assessment of minimal residual leukemia (MRD) in adult patients with de novo acute myeloid leukemia (AML) with mutated NPM1. METHODS: The response, NPM1 mutated transcript level after induction chemotherapy and the first 2 cycles of consolidation chemotherapy, disease-free survival (DFS) and overall survival (OS) in 137 patients with AML with NPM1 mutations of A, B and D were retrospectively analyzed. RESULTS: Data of 137 patients were collected, 67 were male, the median age was 49 years (16–67 years), 107 (78.1%) had normal karyotype, 57 (41.6%) had positive FLT3-ITD mutation, the median NPM1 mutated transcript level at diagnosis was 84.1%. Among the 134 evaluable patients, 115 (85.8%) achieved a complete remission (CR). Multivariate analyses revealed that WBC<100×10(9)/L (OR=0.3, 95% CI 0.1–0.9, P=0.027) and first induction therapy with “IA10” protocol (OR=0.3, 95% CI 0.1–0.8, P=0.015) were factors associated with achieving a CR. With a median follow-up period of 24 months (range, 2 to 91 months) in 77 survived CR patients, the probabilities of DFS and OS at 3 years were 48.0% and 63.9%, respectively. Multivariate analyses showed that positive FLT3-ITD (HR=3.2, 95% CI 1.6–6.7, P=0.002), high MRD level after 2 cycles of consolidation chemotherapy (NPM1 mutation transcript level <3-log reduction from the individual baseline, HR=23.2, 95% CI 7.0–76.6, P<0.001) and chemotherapy or autologous hematopoietic stem cell transplantation (auto-HSCT) rather than allogeneic HSCT (allo-HSCT) (HR=2.6, 95% CI 1.0–6.6, P=0.045) were the unfavorable factors affecting DFS, high MRD level at the time of achieving the first CR (NPM1 mutation transcript level <2-log reduction from the individual baseline, OR=2.5, 95% CI 1.0–6.1, P=0.040) and after 2 cycles of consolidation chemotherapy (HR=4.5, 95% CI 2.0–10.3, P<0.001) were the unfavorable factors affecting OS. Furthermore, DFS and OS rates at 3 years in those receiving chemotherapy or auto-HSCT were 39.7% and 59.1%, respectively; positive FLT3-ITD and high MRD level after 2 cycles of consolidation chemotherapy were independent factors associated with both shorter DFS (HR=3.5, 95% CI 1.6–7.6, P=0.002 and HR=8.9, 95% CI 3.8–20.7, P<0.001) and OS (HR=2.7, 95% CI 1.1–6.9, P=0.036 and HR=3.1, 95% CI 1.2–8.0, P=0.021); meanwhile, high MRD level at the time of achieving the first CR associated with shorter OS (HR=3.1, 95% CI 1.2–8.0, P=0.022). CONCLUSION: Positive FLT3-ITD mutation and high MRD level after induction or consolidation chemotherapy associated with poor outcomes in AML patients with mutated NPM1. Editorial office of Chinese Journal of Hematology 2017-01 /pmc/articles/PMC7348393/ /pubmed/28219218 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2017.01.003 Text en 2017年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal. |
spellingShingle | 论著 早期评估NPM1突变阳性急性髓系白血病患者残留白血病水平的预后意义 |
title | 早期评估NPM1突变阳性急性髓系白血病患者残留白血病水平的预后意义 |
title_full | 早期评估NPM1突变阳性急性髓系白血病患者残留白血病水平的预后意义 |
title_fullStr | 早期评估NPM1突变阳性急性髓系白血病患者残留白血病水平的预后意义 |
title_full_unstemmed | 早期评估NPM1突变阳性急性髓系白血病患者残留白血病水平的预后意义 |
title_short | 早期评估NPM1突变阳性急性髓系白血病患者残留白血病水平的预后意义 |
title_sort | 早期评估npm1突变阳性急性髓系白血病患者残留白血病水平的预后意义 |
topic | 论著 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7348393/ https://www.ncbi.nlm.nih.gov/pubmed/28219218 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2017.01.003 |
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