Predictive Model for Infection Risk in Myelodysplastic Syndromes, Acute Myeloid Leukemia, and Chronic Myelomonocytic Leukemia Patients Treated With Azacitidine; Azacitidine Infection Risk Model: The Polish Adult Leukemia Group Study.


Journal

Clinical lymphoma, myeloma & leukemia
ISSN: 2152-2669
Titre abrégé: Clin Lymphoma Myeloma Leuk
Pays: United States
ID NLM: 101525386

Informations de publication

Date de publication:
05 2019
Historique:
received: 22 10 2018
revised: 04 01 2019
accepted: 10 01 2019
pubmed: 23 3 2019
medline: 7 7 2020
entrez: 23 3 2019
Statut: ppublish

Résumé

Myelodysplastic syndromes (MDS), chronic myelomonocytic leukemia (CMML), and acute myeloid leukemia (AML) patients, including those treated with azacitidine, are at increased risk for serious infections. The aim of our study was to identify patients with higher infectious risk at the beginning of azacitidine treatment. We performed a retrospective evaluation of 298 MDS/CMML/AML patients and included in the analysis 232 patients who completed the first 3 cycles of azacitidine therapy or developed Grade III/IV infection before completing the third cycle. Overall, 143 patients (62%) experienced serious infection, and in 94 patients (41%) infection occurred within the first 3 cycles. The following variables were found to have the most significant effect on the infectious risk in multivariate analysis: red blood cell transfusion dependency (odds ratio [OR], 2.38; 97.5% confidence interval [CI], 1.21-4.79), neutropenia <0.8 × 10 We selected a subset with high early risk for serious infection and worse clinical outcome among patients treated with azacitidine.

Sections du résumé

BACKGROUND
Myelodysplastic syndromes (MDS), chronic myelomonocytic leukemia (CMML), and acute myeloid leukemia (AML) patients, including those treated with azacitidine, are at increased risk for serious infections. The aim of our study was to identify patients with higher infectious risk at the beginning of azacitidine treatment.
PATIENTS AND METHODS
We performed a retrospective evaluation of 298 MDS/CMML/AML patients and included in the analysis 232 patients who completed the first 3 cycles of azacitidine therapy or developed Grade III/IV infection before completing the third cycle.
RESULTS
Overall, 143 patients (62%) experienced serious infection, and in 94 patients (41%) infection occurred within the first 3 cycles. The following variables were found to have the most significant effect on the infectious risk in multivariate analysis: red blood cell transfusion dependency (odds ratio [OR], 2.38; 97.5% confidence interval [CI], 1.21-4.79), neutropenia <0.8 × 10
CONCLUSION
We selected a subset with high early risk for serious infection and worse clinical outcome among patients treated with azacitidine.

Identifiants

pubmed: 30898482
pii: S2152-2650(18)31510-6
doi: 10.1016/j.clml.2019.01.002
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Antifungal Agents 0
Antimetabolites, Antineoplastic 0
Azacitidine M801H13NRU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

264-274.e4

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Krzysztof Mądry (K)

Department of Hematology, Oncology and Internal Diseases, Medical University, Warsaw, Poland.

Karol Lis (K)

Department of Hematology, Oncology and Internal Diseases, Medical University, Warsaw, Poland. Electronic address: k.lis@linux.pl.

Przemysław Biecek (P)

Faculty of Mathematics and Information Science, Warsaw University of Technology, Warsaw, Poland.

Magda Młynarczyk (M)

Faculty of Mathematics and Information Science, Warsaw University of Technology, Warsaw, Poland.

Jagoda Rytel (J)

Department of Hematology, Oncology and Internal Diseases, Medical University, Warsaw, Poland.

Michał Górka (M)

Department of Hematology, Oncology and Internal Diseases, Medical University, Warsaw, Poland.

Piotr Kacprzyk (P)

Department of Hematology, Oncology and Internal Diseases, Medical University, Warsaw, Poland.

Magdalena Dutka (M)

Department of Hematology and Bone Marrow Transplantation, Medical University, Gdańsk, Poland.

Marek Rodzaj (M)

Department of Hematology, Voivodal Specialistic Hospital, Kraków, Poland.

Łukasz Bołkun (Ł)

Department of Hematology, Medical University, Białystok, Poland.

Dorota Krochmalczyk (D)

Department of Hematology, Jagiellonian University, Kraków, Poland.

Ewa Łątka (E)

Department of Hematology, Jagiellonian University, Kraków, Poland.

Joanna Drozd-Sokołowska (J)

Department of Hematology, Oncology and Internal Diseases, Medical University, Warsaw, Poland.

Anna Waszczuk-Gajda (A)

Department of Hematology, Oncology and Internal Diseases, Medical University, Warsaw, Poland.

Wanda Knopińska-Posłuszny (W)

Department of Hematology, SP ZOZ WMCO Oncology Center, Olsztyn, Poland.

Anna Kopińska (A)

Department of Hematology and Bone Marrow Transplantation, Medical University of Silesia, Katowice, Poland.

Edyta Subocz (E)

Department of Hematology and Internal Diseases, Military Institute of Medicine, Warsaw, Poland.

Anna Masternak (A)

Department of Hematology, Specialist Hospital, Opole, Poland.

Renata Guzicka-Kazimierczak (R)

Department of Hematology, Pomeranian Medical University, Szczecin, Poland.

Lidia Gil (L)

Department of Hematology, Medical University, Poznań, Poland.

Rafał Machowicz (R)

Department of Hematology, Oncology and Internal Diseases, Medical University, Warsaw, Poland.

Jarosław Biliński (J)

Department of Hematology, Oncology and Internal Diseases, Medical University, Warsaw, Poland.

Sebastian Giebel (S)

Department of Bone Marrow Transplantation and Hematology-Oncology, Cancer Center and Institute of Oncology, Gliwice, Poland.

Tomasz Czerw (T)

Department of Bone Marrow Transplantation and Hematology-Oncology, Cancer Center and Institute of Oncology, Gliwice, Poland.

Jadwiga Dwilewicz-Trojaczek (J)

Department of Hematology, Oncology and Internal Diseases, Medical University, Warsaw, Poland.

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Classifications MeSH