Evidence map›Paper›PMID 36230677›Full record

ReviewCancers2022

Updates on the Management of Acute Myeloid Leukemia.

Sofía Huerga-Domínguez, Sara Villar, Felipe Prósper, Ana Alfonso-Piérola

Abstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. A Review of FLT3 Kinase Inhibitors in AML.Journal of clinical medicine · 2023
    Review
  6. Article
  7. Article
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

4 authors.

Sofía Huerga-DomínguezHematology and Hemotherapy Department, Clínica Universidad de Navarra, 31008 Pamplona, Spain.
Sara VillarHematology and Hemotherapy Department, Clínica Universidad de Navarra, 31008 Pamplona, Spain.
Felipe PrósperHematology and Hemotherapy Department, Clínica Universidad de Navarra, 31008 Pamplona, Spain.ORCID 0000-0001-6115-8790
Ana Alfonso-PiérolaHematology and Hemotherapy Department, Clínica Universidad de Navarra, 31008 Pamplona, Spain.

Funding

Instituto de Salud Carlos III JR19/00011
6 · The paper itself

Abstract

Acute myeloid leukemia is a heterogeneous disease defined by a large spectrum of genetic aberrations that are potential therapeutic targets. New targeted therapies have changed the landscape for a disease with poor outcomes. They are more effective than standard chemotherapy with a good safety profile. For "fit patients" in first-line, the combination of gemtuzumab ozogamicin or midostaurin with intensive chemotherapy or Vyxeos is now considered the "standard of care" for selected patients. On the other hand, for "unfit patients", azacitidine-venetoclax has been consolidated as a frontline treatment, while other combinations with magrolimab or ivosidenib are in development. Nevertheless, global survival results, especially in relapsed or refractory patients, remain unfavorable. New immunotherapies or targeted therapies, such as Menin inhibitors or sabatolimab, represent an opportunity in this situation. Future directions will probably come from combinations of different targeted therapies ("triplets") and maintenance strategies guided by measurable residual disease.

Indexed as

acute myeloblastic leukemiaCC-486gemtuzumab ozogamicinivosidenibmagrolimabmidostaurinquizartinibtarget-therapyvenetoclaxvyxeos

Identifiers

PMID36230677
PMCPMC9563665

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.