Evidence map›Paper›PMID 35454930›Full record

ArticleCancers2022

Azacitidine Plus Venetoclax for the Treatment of Relapsed and Newly Diagnosed Acute Myeloid Leukemia Patients.

Sylvain Garciaz, Marie-Anne Hospital, Anne-Sophie Alary, Colombe Saillard, Yosr Hicheri, Bilal Mohty, Jérôme Rey, Evelyne D'Incan, Aude Charbonnier, Ferdinand Villetard and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 4 pooled it
8.7field-weighted citation impact, top 1% 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

39 citing papers in PubMed, 4 syntheses or guidelines pooled it, 58 citations in OpenAlex.

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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

16 authors at 2 institutions in 1 country.

Sylvain GarciazINSERM, CNRS, Department of Hematology, Institut Paoli-Calmettes, Aix-Marseille University, 13009 Marseille, France.
Marie-Anne HospitalDeparment of Hematology, Institut Paoli-Calmettes, 13009 Marseille, France.
Anne-Sophie AlaryDepartment of Molecular Biology, Institut Paoli-Calmettes, 13009 Marseille, France.
Colombe SaillardDeparment of Hematology, Institut Paoli-Calmettes, 13009 Marseille, France.
Yosr HicheriDeparment of Hematology, Institut Paoli-Calmettes, 13009 Marseille, France.
Bilal MohtyDeparment of Hematology, Institut Paoli-Calmettes, 13009 Marseille, France.
Jérôme ReyDeparment of Hematology, Institut Paoli-Calmettes, 13009 Marseille, France.
Evelyne D'IncanDeparment of Hematology, Institut Paoli-Calmettes, 13009 Marseille, France.
Aude CharbonnierDeparment of Hematology, Institut Paoli-Calmettes, 13009 Marseille, France.
Ferdinand VilletardDeparment of Hematology, Institut Paoli-Calmettes, 13009 Marseille, France.
Valerio MaisanoDeparment of Hematology, Institut Paoli-Calmettes, 13009 Marseille, France.
Laura LombardiDeparment of Hematology, Institut Paoli-Calmettes, 13009 Marseille, France.
Antoine IttelDepartment of Biopathology, Institut Paoli-Calmettes, 13009 Marseille, France.
Marie-Joelle MozziconacciDepartment of Biopathology, Institut Paoli-Calmettes, 13009 Marseille, France.
Véronique Gelsi-BoyerDepartment of Biopathology, Institut Paoli-Calmettes, 13009 Marseille, France.
Norbert VeyINSERM, CNRS, Department of Hematology, Institut Paoli-Calmettes, Aix-Marseille University, 13009 Marseille, France.ORCID 0000-0001-7027-040X
Institut Paoli-Calmettes · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Venetoclax (VEN) belongs the BH3-mimetic class that selectively targets BCL-2, activating apoptosis. The combination of VEN and azacitidine (AZA) has changed the paradigm of treatment of newly diagnosed (ND) acute myeloid leukemia (AML) patients ineligible for intensive chemotherapy. There is scarce evidence for the use of VEN-AZA for relapsed or refractory (R/R) AML. We compared the outcome of 39 R/R AML and 38 ND AML patients treated between 01/20 and 12/21. The median age was 69 (22-86) and 73 (61-81) in the R/R and ND groups, respectively. Adverse cytogenetics were found in 36% of patients in the R/R group and 59% of patients in the ND group. Overall response rate was 37% in R/R AML, including 13% CR, 8% CRi, 3% PR and 13% MLFS, and 58% in the ND AML, including 32% CR, 13% CRi and 13% MLFS. Adverse cytogenetics was associated with treatment failure in the R/R group (Relative Risk = 0.13,

Indexed as

acute myeloid leukemiavenetoclax

Identifiers

PMID35454930
PMCPMC9028084
OpenAlexW4224097560

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.