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MLL基因重排成人急性髓系白血病的特征和预后分析

OBJECTIVE: To analyze the clinical and laboratory characteristics, and prognosis of adult acute myeloid leukemia (AML) patients with MLL gene rearrangements. METHODS: The medical records of 92 adult AML patients with MLL gene rearrangements from January 2010 to December 2016 were retrospectively ana...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2018
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343107/
https://www.ncbi.nlm.nih.gov/pubmed/29551026
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2018.01.003
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collection PubMed
description OBJECTIVE: To analyze the clinical and laboratory characteristics, and prognosis of adult acute myeloid leukemia (AML) patients with MLL gene rearrangements. METHODS: The medical records of 92 adult AML patients with MLL gene rearrangements from January 2010 to December 2016 were retrospectively analyzed. RESULTS: 92 cases (6.5%) with MLL gene rearrangements were identified in 1 417 adult AML (Non-M(3)) patients, the median age of the patients was 35.5 years (15 to 64 years old) with an equal sex ratio, the median WBC were 21.00(0.42–404.76)×10(9)/L, and 78 patients (84.8%) were acute monoblastic leukemia according to FAB classification. Eleven common partner genes were detected in 32 patients, 9 cases (28.1%) were MLL/AF9(+), 5 cases (15.6%) were MLL/AF6(+), 5 cases (15.6%) were MLL/ELL(+), 2 cases (6.3%) were MLL/AF10(+), 1 case (3.1%) was MLL/SETP6(+), and the remaining 10 patients' partner genes weren't identified. Of 92 patients, 83 cases with a median follow-up of 10.3 (0.3–74.0) months were included for the prognosis analysis, the complete remission (CR) rate was 85.5% (71/83), the median overall survival (OS) and relapse free survival (RFS) were 15.4 and 13.1 months, respectively. Two-year OS and RFS were 36.6% and 29.5%, respectively. Of 31 patients underwent allogeneic hematopoietic stem-cell transplantation (allo-HSCT), two-year OS and RFS for patients received and non-received allo-HSCT were 57.9% and 21.4%, 52.7% and 14.9%, respectively (P<0.001). Among patients with partner genes tested, 9 of 32 cases (28.1%) were MLL/AF9(+), the median follow-up was 6.0(4.1–20.7) months. 3 patients with MLL/AF9 underwent allo-HSCT. 23 cases (71.9%) were non-MLL/AF9(+), the median follow-up was 7.8 (0.3–26.6) months. 14 patients (60.1%) with non-MLL/AF9 underwent allo-HSCT. One-year OS for patients with MLL/AF9 and non-MLL/AF9 were 38.1% and 55.5%, respectively (P=0.688). Multivariate analysis revealed that high WBC (RR=1.825, 95% CI 1.022–3.259, P=0.042), one cycle to achieve CR (RR=0.130, 95% CI 0.063–0.267, P<0.001), post-remission treatment with allo-HSCT (RR=0.169, 95% CI 0.079–0.362, P<0.001) were independent prognostic factors affecting OS. CONCLUSION: AML with MLL gene rearrangements was closely associated with monocytic differentiation, and MLL/AF9 was the most frequent partner gene. Conventional chemotherapy produced a high response rate, but likely to relapse, allo-HSCT may have the potential to further improve the prognosis of this group of patients.
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spelling pubmed-73431072020-07-16 MLL基因重排成人急性髓系白血病的特征和预后分析 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To analyze the clinical and laboratory characteristics, and prognosis of adult acute myeloid leukemia (AML) patients with MLL gene rearrangements. METHODS: The medical records of 92 adult AML patients with MLL gene rearrangements from January 2010 to December 2016 were retrospectively analyzed. RESULTS: 92 cases (6.5%) with MLL gene rearrangements were identified in 1 417 adult AML (Non-M(3)) patients, the median age of the patients was 35.5 years (15 to 64 years old) with an equal sex ratio, the median WBC were 21.00(0.42–404.76)×10(9)/L, and 78 patients (84.8%) were acute monoblastic leukemia according to FAB classification. Eleven common partner genes were detected in 32 patients, 9 cases (28.1%) were MLL/AF9(+), 5 cases (15.6%) were MLL/AF6(+), 5 cases (15.6%) were MLL/ELL(+), 2 cases (6.3%) were MLL/AF10(+), 1 case (3.1%) was MLL/SETP6(+), and the remaining 10 patients' partner genes weren't identified. Of 92 patients, 83 cases with a median follow-up of 10.3 (0.3–74.0) months were included for the prognosis analysis, the complete remission (CR) rate was 85.5% (71/83), the median overall survival (OS) and relapse free survival (RFS) were 15.4 and 13.1 months, respectively. Two-year OS and RFS were 36.6% and 29.5%, respectively. Of 31 patients underwent allogeneic hematopoietic stem-cell transplantation (allo-HSCT), two-year OS and RFS for patients received and non-received allo-HSCT were 57.9% and 21.4%, 52.7% and 14.9%, respectively (P<0.001). Among patients with partner genes tested, 9 of 32 cases (28.1%) were MLL/AF9(+), the median follow-up was 6.0(4.1–20.7) months. 3 patients with MLL/AF9 underwent allo-HSCT. 23 cases (71.9%) were non-MLL/AF9(+), the median follow-up was 7.8 (0.3–26.6) months. 14 patients (60.1%) with non-MLL/AF9 underwent allo-HSCT. One-year OS for patients with MLL/AF9 and non-MLL/AF9 were 38.1% and 55.5%, respectively (P=0.688). Multivariate analysis revealed that high WBC (RR=1.825, 95% CI 1.022–3.259, P=0.042), one cycle to achieve CR (RR=0.130, 95% CI 0.063–0.267, P<0.001), post-remission treatment with allo-HSCT (RR=0.169, 95% CI 0.079–0.362, P<0.001) were independent prognostic factors affecting OS. CONCLUSION: AML with MLL gene rearrangements was closely associated with monocytic differentiation, and MLL/AF9 was the most frequent partner gene. Conventional chemotherapy produced a high response rate, but likely to relapse, allo-HSCT may have the potential to further improve the prognosis of this group of patients. Editorial office of Chinese Journal of Hematology 2018-01 /pmc/articles/PMC7343107/ /pubmed/29551026 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2018.01.003 Text en 2018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
MLL基因重排成人急性髓系白血病的特征和预后分析
title MLL基因重排成人急性髓系白血病的特征和预后分析
title_full MLL基因重排成人急性髓系白血病的特征和预后分析
title_fullStr MLL基因重排成人急性髓系白血病的特征和预后分析
title_full_unstemmed MLL基因重排成人急性髓系白血病的特征和预后分析
title_short MLL基因重排成人急性髓系白血病的特征和预后分析
title_sort mll基因重排成人急性髓系白血病的特征和预后分析
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343107/
https://www.ncbi.nlm.nih.gov/pubmed/29551026
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2018.01.003
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