Real-life Outcomes on Acute Promyelocytic Leukemia in Brazil - Early Deaths Are Still a Problem.


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:
02 2019
Historique:
received: 30 08 2018
revised: 10 10 2018
accepted: 02 11 2018
pubmed: 5 12 2018
medline: 14 4 2020
entrez: 5 12 2018
Statut: ppublish

Résumé

Although a considerable improvement in survival of patients with acute promyelocytic leukemia (APL) has been seen over the past decades, real-life outcomes seem to be worse than those reported by prospective studies. We aim to describe clinical characteristics and outcomes of adult patients diagnosed with APL in an academic hospital from the University of Sao Paulo. We retrospectively reviewed the medical charts of 61 patients with APL diagnosed between January 2007 and May 2017. Baseline clinical features and follow-up data were collected, focusing on early toxicity variables such as infection, bleeding, and thrombosis in the first 30 days from diagnosis. Among the 61 patients with APL, 54 received any chemotherapy. All patients also received all-trans retinoic acid (ATRA). Bleeding events were the main cause of death before receiving chemotherapy. Most patients belonged to the intermediate (43%) and high-risk (41%) groups, according to Sanz score. The '7 + 3 + ATRA' regimen was the most used regimen (n = 38). An early death rate of 20% was found, predominantly owing to sepsis. After a median follow-up of 5 years, only 1 relapse was diagnosed. The overall survival at 5 years was 59%. In comparison with prospective trials with ATRA-based regimens, we found an inferior overall survival, mostly on account of a high early-death rate. Our results are in line with other real-life retrospective reports published in the past decades. Results of real-life studies differ from those found by prospective trials. Accordingly, early actions and supportive care are still needed, aiming to decrease toxicity, especially in developing countries.

Identifiants

pubmed: 30509780
pii: S2152-2650(18)31311-9
doi: 10.1016/j.clml.2018.11.004
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e116-e122

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Wellington F da Silva (WFD)

Institute of Cancer of São Paulo, University of São Paulo, São Paulo, Brazil. Electronic address: wellington.fernandes@hc.fm.usp.br.

Lidiane Inês da Rosa (LID)

Institute of Cancer of São Paulo, University of São Paulo, São Paulo, Brazil.

Gabriel Lacerda Marquez (GL)

Institute of Cancer of São Paulo, University of São Paulo, São Paulo, Brazil.

Lucas Bassolli (L)

Hospital das Clinicas, University of São Paulo, São Paulo, Brazil.

Luciana Tucunduva (L)

Hospital das Clinicas, University of São Paulo, São Paulo, Brazil.

Douglas Rafaele Almeida Silveira (DRA)

Hospital das Clinicas, University of São Paulo, São Paulo, Brazil.

Valeria Buccheri (V)

Institute of Cancer of São Paulo, University of São Paulo, São Paulo, Brazil; Hospital das Clinicas, University of São Paulo, São Paulo, Brazil.

Israel Bendit (I)

Hospital das Clinicas, University of São Paulo, São Paulo, Brazil.

Eduardo Magalhães Rego (EM)

Institute of Cancer of São Paulo, University of São Paulo, São Paulo, Brazil; Hospital das Clinicas, University of São Paulo, São Paulo, Brazil.

Vanderson Rocha (V)

Institute of Cancer of São Paulo, University of São Paulo, São Paulo, Brazil; Hospital das Clinicas, University of São Paulo, São Paulo, Brazil.

Elvira D R P Velloso (EDRP)

Institute of Cancer of São Paulo, University of São Paulo, São Paulo, Brazil; Hospital das Clinicas, University of São Paulo, São Paulo, Brazil.

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Classifications MeSH