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Clinical heterogeneity under induction with different dosages of cytarabine in core binding factor acute myeloid leukaemia
Repeated cycles of post-remission high-dose cytarabine (Ara-C) have been suggested to improve survival in core binding factor (CBF) acute myeloid leukaemia (AML). High-dose Ara-C used for induction regimens has also been reported to be associated with increased treatment-related mortality (TRM). Few...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971028/ https://www.ncbi.nlm.nih.gov/pubmed/31959790 http://dx.doi.org/10.1038/s41598-020-57414-y |
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author | Wang, Biao Zhang, Jihong Hua, Xiaoying Li, Haiqian Wang, Zhilin Yang, Bin |
author_facet | Wang, Biao Zhang, Jihong Hua, Xiaoying Li, Haiqian Wang, Zhilin Yang, Bin |
author_sort | Wang, Biao |
collection | PubMed |
description | Repeated cycles of post-remission high-dose cytarabine (Ara-C) have been suggested to improve survival in core binding factor (CBF) acute myeloid leukaemia (AML). High-dose Ara-C used for induction regimens has also been reported to be associated with increased treatment-related mortality (TRM). Few data are available about intermediate-dose Ara-C serving as induction therapy. The aim of our study was to compare the tolerance and outcomes of standard- and intermediate-dose levels of Ara-C as induction in CBF AML and to analyse the clinical heterogeneity of the two AML entities under these induction settings. We retrospectively investigated the outcomes in adults with CBF AML induced with regimens based on standard-dose Ara-C at 100 to 200 mg/m(2) or intermediate-dose Ara-C at 1,000 mg/m(2). In total, 152 patients with t(8; 21) and 54 patients with inv(16) AML were administered an induction regimen containing anthracyclines plus either standard- or intermediate-dose Ara-C. After a single course of induction, the complete remission (CR) rate in the inv(16) cohort was 52/52 (100%), higher than the 127/147 (86.4%) in the t(8; 21) cohort (P = 0.005). Intermediate-dose Ara-C (HR = 9.931 [2.135–46.188], P = 0.003) and negative KITmut (HR = 0.304 [0.106–0.874], P = 0.027) independently produced an increased CR rate in the t(8; 21) cohort. Positive CD19 expression (HR = 0.133 [0.045–0.387], P = 0.000) and sex (male) (HR = 0.238 [0.085–0.667], P = 0.006) were associated with superior leukaemia-free survival (LFS) in the t(8; 21) cohort independently of KITmut status or the induction regimen. We conclude that intermediate-dose Ara-C is superior to standard-dose Ara-C for induction of remission in t(8; 21) AML, and CD19 status and sex independently confer prognostic significance for LFS. The KITmut status alone does not have an independent effect on survival in t(8; 21) AML. More intensive induction therapy is unnecessary in inv(16) AML. |
format | Online Article Text |
id | pubmed-6971028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69710282020-01-27 Clinical heterogeneity under induction with different dosages of cytarabine in core binding factor acute myeloid leukaemia Wang, Biao Zhang, Jihong Hua, Xiaoying Li, Haiqian Wang, Zhilin Yang, Bin Sci Rep Article Repeated cycles of post-remission high-dose cytarabine (Ara-C) have been suggested to improve survival in core binding factor (CBF) acute myeloid leukaemia (AML). High-dose Ara-C used for induction regimens has also been reported to be associated with increased treatment-related mortality (TRM). Few data are available about intermediate-dose Ara-C serving as induction therapy. The aim of our study was to compare the tolerance and outcomes of standard- and intermediate-dose levels of Ara-C as induction in CBF AML and to analyse the clinical heterogeneity of the two AML entities under these induction settings. We retrospectively investigated the outcomes in adults with CBF AML induced with regimens based on standard-dose Ara-C at 100 to 200 mg/m(2) or intermediate-dose Ara-C at 1,000 mg/m(2). In total, 152 patients with t(8; 21) and 54 patients with inv(16) AML were administered an induction regimen containing anthracyclines plus either standard- or intermediate-dose Ara-C. After a single course of induction, the complete remission (CR) rate in the inv(16) cohort was 52/52 (100%), higher than the 127/147 (86.4%) in the t(8; 21) cohort (P = 0.005). Intermediate-dose Ara-C (HR = 9.931 [2.135–46.188], P = 0.003) and negative KITmut (HR = 0.304 [0.106–0.874], P = 0.027) independently produced an increased CR rate in the t(8; 21) cohort. Positive CD19 expression (HR = 0.133 [0.045–0.387], P = 0.000) and sex (male) (HR = 0.238 [0.085–0.667], P = 0.006) were associated with superior leukaemia-free survival (LFS) in the t(8; 21) cohort independently of KITmut status or the induction regimen. We conclude that intermediate-dose Ara-C is superior to standard-dose Ara-C for induction of remission in t(8; 21) AML, and CD19 status and sex independently confer prognostic significance for LFS. The KITmut status alone does not have an independent effect on survival in t(8; 21) AML. More intensive induction therapy is unnecessary in inv(16) AML. Nature Publishing Group UK 2020-01-20 /pmc/articles/PMC6971028/ /pubmed/31959790 http://dx.doi.org/10.1038/s41598-020-57414-y Text en © The Author(s) 2020 Open Access 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 http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Biao Zhang, Jihong Hua, Xiaoying Li, Haiqian Wang, Zhilin Yang, Bin Clinical heterogeneity under induction with different dosages of cytarabine in core binding factor acute myeloid leukaemia |
title | Clinical heterogeneity under induction with different dosages of cytarabine in core binding factor acute myeloid leukaemia |
title_full | Clinical heterogeneity under induction with different dosages of cytarabine in core binding factor acute myeloid leukaemia |
title_fullStr | Clinical heterogeneity under induction with different dosages of cytarabine in core binding factor acute myeloid leukaemia |
title_full_unstemmed | Clinical heterogeneity under induction with different dosages of cytarabine in core binding factor acute myeloid leukaemia |
title_short | Clinical heterogeneity under induction with different dosages of cytarabine in core binding factor acute myeloid leukaemia |
title_sort | clinical heterogeneity under induction with different dosages of cytarabine in core binding factor acute myeloid leukaemia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971028/ https://www.ncbi.nlm.nih.gov/pubmed/31959790 http://dx.doi.org/10.1038/s41598-020-57414-y |
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