Evidence map›Paper›PMID 38273140›Full record

ArticleAnnals of hematology2024

Hypomethylating agent monotherapy in core binding factor acute myeloid leukemia: a French multicentric retrospective study.

Ludovic Gabellier, Pierre Peterlin, Sylvain Thepot, Yosr Hicheri, Franciane Paul, Maria Pilar Gallego-Hernanz, Sarah Bertoli, Pascal Turlure, Arnaud Pigneux, Romain Guieze and 9 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Annals of hematology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 99% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 13 institutions in 1 country.

Ludovic GabellierDépartement d'Hématologie Clinique, CHU Montpellier, Université Montpellier-Nîmes, 80, Avenue Augustin Fliche, 34090, Montpellier, France. l-gabellier@chu-montpellier.fr.ORCID http://orcid.org/0000-0003-0663-8083
Pierre PeterlinDépartement d'Hématologie Clinique, CHU Nantes, Université de Nantes, Nantes, France.
Sylvain ThepotDépartement d'Hématologie Clinique, CHU Angers, Université d'Angers, Angers, France.
Yosr HicheriDépartement d'Hématologie Clinique, Institut Paoli-Calmettes, Marseille, France.
Franciane PaulDépartement d'Hématologie Clinique, CHU Montpellier, Université Montpellier-Nîmes, 80, Avenue Augustin Fliche, 34090, Montpellier, France.
Maria Pilar Gallego-HernanzDépartement d'Hématologie Clinique, CHU Poitiers, Université de Poitiers, Poitiers, France.
Sarah BertoliService d'Hématologie Clinique, CHU Toulouse, Institut Universitaire du Cancer de Toulouse - Oncopôle, Université Toulouse III - Paul Sabatier, Toulouse, France.
Pascal TurlureDépartement d'Hématologie Clinique, CHU Limoges, Université de Limoges, Limoges, France.
Arnaud PigneuxDépartement d'Hématologie Clinique, CHU Bordeaux, Université de Bordeaux, Bordeaux, France.
Romain GuiezeDépartement d'Hématologie Clinique, CHU Clermont-Ferrand, Université de Clermont-Ferrand, Clermont-Ferrand, France.
Marlène OchmannDépartement d'Hématologie Clinique, Orléans, Orléans, CH, France.
Jean-Valère MalfusonDépartement d'Hématologie Clinique, Hôpital d'instruction Des Armées, Percy, France.
Thomas CluzeauDépartement d'Hématologie Clinique, CHU Nice, Université de Nice, Nice, France.
Xavier ThomasDépartement d'Hématologie Clinique, Hospices Civils de Lyon, CHU Lyon, Université de Lyon, Lyon, France.
Emmanuelle TavernierDépartement d'Hématologie Clinique, Institut de Cancérologie Lucien Neuwirth, Université de Saint-Etienne, Saint-Etienne, France.
Eric JourdanDépartement d'Hématologie Clinique, CHU Nîmes, Université de Montpellier-Nîmes, Nîmes, France.
Sarah BonnetDépartement d'Hématologie Clinique, CHU Montpellier, Université Montpellier-Nîmes, 80, Avenue Augustin Fliche, 34090, Montpellier, France.
Jean-Jacques TudesqDépartement d'Hématologie Clinique, CHU Montpellier, Université Montpellier-Nîmes, 80, Avenue Augustin Fliche, 34090, Montpellier, France.
Emmanuel RaffouxDépartement d'Hématologie Clinique Adultes, Hôpital Saint-Louis, APHP, Université Paris Diderot, Paris, France.
Université de Montpellier · FRCentre Hospitalier Universitaire d'Angers · FRCentre hospitalier universitaire d'Orléans · FRDélégation Paris 7 · FRHôpital d'instruction des Armées Percy · FRInstitute Cancer De La Loire Lucien Neuwirth · FRInstitut Paoli-Calmettes · FRNantes Université · FRUniversité Claude Bernard Lyon 1 · FRUniversité de Bordeaux · FRUniversité de Limoges · FRUniversité de Poitiers · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Very few data are available about hypomethylating agent (HMA) efficiency in core binding factor acute myeloid leukemias (CBF-AML). Our main objective was to evaluate the efficacy and safety of HMA in the specific subset of CBF-AML. Here, we report the results of a multicenter retrospective French study about efficacy of HMA monotherapy, used frontline or for R/R CBF-AML. Forty-nine patients were included, and received a median of 5 courses of azacitidine (n = 46) or decitabine (n = 3). ORR was 49% for the whole cohort with a median time to response of 112 days. After a median follow-up of 72.3 months, median OS for the total cohort was 10.6 months. In multivariate analysis, hematological relapse of CBF-AML at HMA initiation was significantly associated with a poorer OS (HR: 2.13; 95%CI: 1.04-4.36; p = 0.038). Responders had a significantly improved OS (1-year OS: 75%) compared to non-responders (1-year OS: 15.3%; p < 0.0001). Hematological improvement occurred for respectively 28%, 33% and 48% for patients who were red blood cell or platelet transfusion-dependent, or who experienced grade 3/4 neutropenia at HMA initiation. Adverse events were consistent with the known safety profile of HMA. Our study highlights that HMA is a well-tolerated therapeutic option with moderate clinical activity for R/R CBF-AML and for patients who cannot handle intensive chemotherapy.

Indexed as

AzacitidineLeukemia, Myeloid, AcuteAntineoplastic Combined Chemotherapy ProtocolsCore Binding FactorsDecitabineHumansRetrospective StudiesTreatment OutcomeAzacitidineCore Binding FactorsDecitabineAcute myeloid leukemiaAzacitidineCore binding factorDecitabineHypomethylating agents

Identifiers

PMID38273140
PMCPMC10867066
OpenAlexW4391239567

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.