Serum ferritin and ECOG performance status predict the response and improve the prognostic value of IPSS or IPSS-R in patients with high-risk myelodysplastic syndromes and oligoblastic acute myeloid leukemia treated with 5-azacytidine: a retrospective analysis of the Hellenic national registry of myelodysplastic and hypoplastic syndromes.

acute myeloid leukemia outcome prognosis risk classification system survival

Journal

Therapeutic advances in hematology
ISSN: 2040-6207
Titre abrégé: Ther Adv Hematol
Pays: England
ID NLM: 101549589

Informations de publication

Date de publication:
2020
Historique:
received: 08 07 2020
accepted: 23 09 2020
entrez: 21 12 2020
pubmed: 22 12 2020
medline: 22 12 2020
Statut: epublish

Résumé

5-azacytidine (5-AZA) improves survival of patients with higher-risk myelodysplastic syndromes (MDSs) and oligoblastic acute myeloid leukemia (AML); however, predictive factors for response and outcome have not been consistently studied. This study of the Hellenic MDS Study Group included 687 consecutive patients with higher-risk MDS and oligoblastic AML treated with 5-AZA. The International Prognostic Scoring System (IPSS) revised version (IPSS-R), Eastern Cooperative Oncology Group Performance Status (ECOG PS) (0 or 1 ECOG PS and SF levels > 520 ng/ml independently predict response to 5-AZA, OS and LFS. Their incorporation in the IPSS and IPSS-R scores enhances these scores' predictive power in 5-AZA-treated higher-risk MDS and oligoblastic AML patients.

Sections du résumé

BACKGROUND BACKGROUND
5-azacytidine (5-AZA) improves survival of patients with higher-risk myelodysplastic syndromes (MDSs) and oligoblastic acute myeloid leukemia (AML); however, predictive factors for response and outcome have not been consistently studied.
METHODS METHODS
This study of the Hellenic MDS Study Group included 687 consecutive patients with higher-risk MDS and oligoblastic AML treated with 5-AZA.
RESULTS RESULTS
The International Prognostic Scoring System (IPSS) revised version (IPSS-R), Eastern Cooperative Oncology Group Performance Status (ECOG PS) (0 or 1
CONCLUSIONS CONCLUSIONS
ECOG PS and SF levels > 520 ng/ml independently predict response to 5-AZA, OS and LFS. Their incorporation in the IPSS and IPSS-R scores enhances these scores' predictive power in 5-AZA-treated higher-risk MDS and oligoblastic AML patients.

Identifiants

pubmed: 33343854
doi: 10.1177/2040620720966121
pii: 10.1177_2040620720966121
pmc: PMC7727043
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2040620720966121

Informations de copyright

© The Author(s), 2020.

Déclaration de conflit d'intérêts

Conflict of interest statement: The authors declare that there is no conflict of interest.

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Auteurs

Sotirios G Papageorgiou (SG)

Consultant of Hematology, Second Department of Internal Medicine and Research Unit, University General Hospital "Attikon", 1 Rimini St., Haidari, Athens, 12462, Greece.

Ioannis Kotsianidis (I)

Department of Hematology, Democritus University of Thrace Medical School, University Hospital of Alexandroupolis, Alexandroupolis, Greece.

Anthi Bouchla (A)

Second Department of Internal Medicine and Research Unit, University General Hospital "Attikon", Haidari, Athens, Greece.

Argyris Symeonidis (A)

The Hellenic (Greek) MDS Study Group, Greece.

Athanasios Galanopoulos (A)

The Hellenic (Greek) MDS Study Group, Greece.

Nora-Athina Viniou (NA)

The Hellenic (Greek) MDS Study Group, Greece.

Eleftheria Hatzimichael (E)

University Hospital of Ioannina, Ioannina, Greece.

Theodoros P Vassilakopoulos (TP)

Department of Hematology, National and Kapodistrian University of Athens, Laikon General Hospital, Athens, Greece.

Dimitrios Gogos (D)

General Hospital "Bostanio" Mytilini, Greece.

Aikaterini Megalakaki (A)

Department of Hematology, "Metaxa" Piraeus Cancer Hospital, Piraeus, Greece.

Panagiotis Zikos (P)

General Hospital of Patras "Agios Andreas", Patras, Greece.

Panagiotis Diamantopoulos (P)

Department of Internal Medicine, National and Kapodistrian University of Athens, Athens, Greece.

Alexandra Kourakli (A)

General University Hospital of Patras, Rio Patron, Patras, Greece.

Panagiota Giannoulia (P)

Department of Hematology, "Evangelismos" Hospital, Athens, Greece.

Menelaos Papoutselis (M)

Department of Hematology, Democritus University of Thrace Medical School, University Hospital of Alexandroupolis, Alexandroupolis, Greece.

Elias Poulakidas (E)

"401" Army General Hospital of Athens, Mesogeion and Kanellopoulou 1, Athens, Greece.

Maria Arapaki (M)

Department of Hematology, National and Kapodistrian University of Athens, Laikon General Hospital, Athens, Greece.

Anna Vardi (A)

Hematology Department, General Hospital of Thessaloniki "George Papanikolaou", Thessaloniki, Greece.

Achilles Anagnostopoulos (A)

Hematology Department, General Hospital of Thessaloniki "George Papanikolaou", Thessaloniki, Greece.

Despoina Mparmparousi (D)

Department of Clinical Therapeutics, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Maria Papaioannou (M)

Hematology Department, University General Hospital of Thessaloniki AHEPA, Thessaloniki, Greece.

Eleni Bouronikou (E)

University General Hospital of Larissa, Mezourlo, Larissa, Greece.

Maria Dimou (M)

First Propaedeutic Department of Internal Medicine, National and Kapodistrian University of Athens, Athens, Greece.

Helen Papadaki (H)

University General Hospital of Heraklion, Voutes, Heraklion, Greece.

Panayiotis Panayiotidis (P)

First Propaedeutic Department of Internal Medicine, National and Kapodistrian University of Athens, Athens, Greece.

Vasiliki Pappa (V)

Second Department of Internal Medicine and Research Unit, University General Hospital "Attikon", Haidari, Athens, Greece.

Classifications MeSH