A favorable inductive remission rate for decitabine combined with chemotherapy as a first course in <60-year-old acute myeloid leukemia patients with myelodysplasia syndrome features.


Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
Sep 2019
Historique:
received: 29 11 2018
revised: 01 06 2019
accepted: 29 06 2019
pubmed: 20 7 2019
medline: 4 9 2020
entrez: 20 7 2019
Statut: ppublish

Résumé

In acute myeloid leukemia (AML), myelodysplasia-related changes contribute to a poor prognosis. This retrospective, propensity score-matched study analyzed 108 newly diagnosed AML patients with features of myelodysplasia syndrome (MDS) (aged 14-60 years) from 2014 to 2018, who received either idarubicin and cytarabine (IA) or decitabine, idarubicin and cytarabine (DAC+IA), and compared efficacy and toxicity between the two regimens. After propensity score matching, there were 54 patients in each group. The rate of complete remission (CR) was higher in the DAC+IA group than in the IA group (85.2% vs 68.5%, P = .040) after the first course, and toxicities were comparable in both groups. Multivariate analysis indicated that the combination with DAC was independent factor for CR rate after the first induction therapy (OR = 2.978, 95% CI:1.090-8.137, P = .033). Subgroup analysis showed a CR advantage for DAC+IA (vs IA) for patients of intermediate-high risk status according to National Comprehensive Cancer Network prognostic stratification. In conclusion, DAC+IA is therefore offered as a new induction choice for newly diagnosed AML patients with features of MDS, aged <60 years old, especially in intermediate-high risk status.

Identifiants

pubmed: 31322840
doi: 10.1002/cam4.2418
pmc: PMC6718585
doi:

Substances chimiques

Biomarkers 0
Decitabine 776B62CQ27

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5108-5115

Subventions

Organisme : Natural Science Foundation of Guangdong
ID : 2016A030313197
Organisme : Clinical Medical Research 5010 Program of Sun Yat-sen University
ID : 2017005
Organisme : Science and Technology Planning Project of Guangdong Province
ID : 2017A020215105

Informations de copyright

© 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

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Auteurs

Fengqi Liu (F)

Department of Hematology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Hehua Wang (H)

Department of Hematology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Junru Liu (J)

Department of Hematology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Zhenhai Zhou (Z)

Department of Hematology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Dong Zheng (D)

Department of Hematology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Beihui Huang (B)

Department of Hematology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Chang Su (C)

Department of Hematology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Waiyi Zou (W)

Department of Hematology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Duorong Xu (D)

Department of Hematology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Xiuzhen Tong (X)

Department of Hematology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Juan Li (J)

Department of Hematology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

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