Low serum albumin level deteriorates prognosis in azacitidine-treated myelodysplastic syndromes patients - results of the PALG study 'PolAZA'.


Journal

Hematology (Amsterdam, Netherlands)
ISSN: 1607-8454
Titre abrégé: Hematology
Pays: England
ID NLM: 9708388

Informations de publication

Date de publication:
Dec 2021
Historique:
entrez: 13 8 2021
pubmed: 14 8 2021
medline: 31 8 2021
Statut: ppublish

Résumé

Azacitidine (AZA) is the standard of care for higher-risk myelodysplastic syndrome (HR-MDS) patients ineligible for intensive therapy. Clinical outcome discrepancies reported in clinical trials and real-life settings stimulate the search for new prognostic factors. We retrospectively evaluated 315 MDS, 20-30% blast acute myeloid leukemia (AML) and chronic myelomonocytic leukemia (CMML) patients treated with azacitidine in 12 centers cooperating within the Polish Adult Leukemia Group (PALG). The median number of AZA cycles was 7 (1-69) and 24% patients received fewer than 4 cycles (early failure, EF). Serum albumin level was an independent predictor of EF occurrence. Complete remission (CR) was obtained in 20% and partial remission (PR) in 12% of patients. Hematologic improvement - erythroid (HI-E), neutrophil (HI-N), or platelet (HI-P) was achieved in 51%, 36%, and 48% of patients, respectively. No factors significantly predicted CR or PR in the multivariate analysis. For HI-E and HI-P, lower LDH level predicted response. Median survival was 15 (13-19) months. Lower serum albumin level, serious infection and receiving <4 AZA cycles independently predicted a worse overall survival (OS) ( Serum albumin assessment before azacitidine treatment can help to identify patients with higher risk of early failure and worse clinical outcome.

Sections du résumé

BACKGROUND BACKGROUND
Azacitidine (AZA) is the standard of care for higher-risk myelodysplastic syndrome (HR-MDS) patients ineligible for intensive therapy. Clinical outcome discrepancies reported in clinical trials and real-life settings stimulate the search for new prognostic factors.
METHODS METHODS
We retrospectively evaluated 315 MDS, 20-30% blast acute myeloid leukemia (AML) and chronic myelomonocytic leukemia (CMML) patients treated with azacitidine in 12 centers cooperating within the Polish Adult Leukemia Group (PALG).
RESULTS RESULTS
The median number of AZA cycles was 7 (1-69) and 24% patients received fewer than 4 cycles (early failure, EF). Serum albumin level was an independent predictor of EF occurrence. Complete remission (CR) was obtained in 20% and partial remission (PR) in 12% of patients. Hematologic improvement - erythroid (HI-E), neutrophil (HI-N), or platelet (HI-P) was achieved in 51%, 36%, and 48% of patients, respectively. No factors significantly predicted CR or PR in the multivariate analysis. For HI-E and HI-P, lower LDH level predicted response. Median survival was 15 (13-19) months. Lower serum albumin level, serious infection and receiving <4 AZA cycles independently predicted a worse overall survival (OS) (
CONCLUSION CONCLUSIONS
Serum albumin assessment before azacitidine treatment can help to identify patients with higher risk of early failure and worse clinical outcome.

Identifiants

pubmed: 34384334
doi: 10.1080/16078454.2021.1956182
doi:

Substances chimiques

Antimetabolites, Antineoplastic 0
Azacitidine M801H13NRU
Serum Albumin, Human ZIF514RVZR

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

556-564

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.

Andrzej Tukiendorf (A)

Department of Public Health, Wrocław Medical University, Wrocław, Poland.

Paweł Szwedyk (P)

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

Katarzyna Kapelko-Słowik (K)

Department of Hematology, Blood Neoplasms and Bone Marrow Transplantation, University Hospital, Wrocław, Poland.

Edyta Subocz (E)

Department of Hematology, Warmian-Masurian Cancer Center of the Ministry of the Interior and Administration's Hospital, Olsztyn, Poland.

Aleksandra Gołos (A)

Department of Hematology, Institute of Hematology and Blood Transfusion, Warsaw, Poland.

Wioletta Makowska (W)

Department of Hematology, Institute of Hematology and Blood Transfusion, Warsaw, Poland.

Anna Masternak (A)

Department of Hematology and Hematooncology, District Specialist Hospital, Opole, Poland.

Anna Kopińska (A)

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

Magdalena Czemerska (M)

Department of Hematology, Medical University of Łódź, Łódź, Poland.

Sara Zawadzka-Leska (S)

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

Patrycja Rusicka (P)

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

Joanna Drozd-Sokołowska (J)

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

Elżbieta Wiater (E)

Department of Hematology, District Hospital in Toruń, Toruń, Poland.

Jadwiga Hołojda (J)

Department of Hematology, District Specialist Hospital in Legnica, Legnica, Poland.

Bartłomiej Pogłódek (B)

Department of Hematooncology, Specialist Hospital, Brzozów, Poland.

Piotr Centkowski (P)

Department of Hematology, District Specialist Hospital in Biała Podlaska, Biała Podlaska, Poland.

Anna Waszczuk-Gajda (A)

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

Rafał Machowicz (R)

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

Janusz Hałka (J)

Department of Hematology, Warmian-Masurian Cancer Center of the Ministry of the Interior and Administration's Hospital, Olsztyn, Poland.

Tomasz Czerw (T)

Department of Bone Marrow Transplantation and Oncohematology, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Warszawa, Poland.

Grzegorz Basak (G)

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

Jadwiga Dwilewicz-Trojaczek (J)

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

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Classifications MeSH