Evidence map›Paper›PMID 35409248›Full record

ReviewInternational journal of molecular sciences2022

New Perspectives in Treating Acute Myeloid Leukemia: Driving towards a Patient-Tailored Strategy.

Fabio Andreozzi, Fulvio Massaro, Sebastian Wittnebel, Chloé Spilleboudt, Philippe Lewalle, Adriano Salaroli

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The Prognostic Value of the CD8Hematology reports · 2026
    Article
  5. Review
  6. Article
  7. Article
  8. A Leukemic Target with a Thousand Faces: The Mitochondria.International journal of molecular sciences · 2023
    Review
  9. Review
  10. Divergent CD4Frontiers in immunology · 2023
    Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. 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

6 authors at 3 institutions in 2 countries.

Fabio AndreozziHematology Department, Institut Jules Bordet, Université Libre de Bruxelles, 1000 Bruxelles, Belgium.
Fulvio MassaroHematology Department, Institut Jules Bordet, Université Libre de Bruxelles, 1000 Bruxelles, Belgium.
Sebastian WittnebelHematology Department, Institut Jules Bordet, Université Libre de Bruxelles, 1000 Bruxelles, Belgium.
Chloé SpilleboudtHematology Department, Institut Jules Bordet, Université Libre de Bruxelles, 1000 Bruxelles, Belgium.
Philippe LewalleHematology Department, Institut Jules Bordet, Université Libre de Bruxelles, 1000 Bruxelles, Belgium.
Adriano SalaroliHematology Department, Institut Jules Bordet, Université Libre de Bruxelles, 1000 Bruxelles, Belgium.
Institut Jules Bordet · BEUniversité Libre de Bruxelles · BEUniversity of Modena and Reggio Emilia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For decades, intensive chemotherapy (IC) has been considered the best therapeutic option for treating acute myeloid leukemia (AML), with no curative option available for patients who are not eligible for IC or who have had failed IC. Over the last few years, several new drugs have enriched the therapeutic arsenal of AML treatment for both fit and unfit patients, raising new opportunities but also new challenges. These include the already approved venetoclax, the IDH1/2 inhibitors enasidenib and ivosidenib, gemtuzumab ozogamicin, the liposomal daunorubicin/cytarabine formulation CPX-351, and oral azacitidine. Venetoclax, an anti BCL2-inhibitor, in combination with hypomethylating agents (HMAs), has markedly improved the management of unfit and elderly patients from the perspective of improved quality of life and better survival. Venetoclax is currently under investigation in combination with other old and new drugs in early phase trials. Recently developed drugs with different mechanisms of action and new technologies that have already been investigated in other settings (BiTE and CAR-T cells) are currently being explored in AML, and ongoing trials should determine promising agents, more synergic combinations, and better treatment strategies. Access to new drugs and inclusion in clinical trials should be strongly encouraged to provide scientific evidence and to define the future standard of treatment in AML.

Indexed as

Antineoplastic AgentsLeukemia, Myeloid, AcuteAgedAntineoplastic Combined Chemotherapy ProtocolsGemtuzumabHumansQuality of LifeAntineoplastic AgentsGemtuzumabacute myeloid leukemiaimmunotherapytarget therapyvenetoclax

Identifiers

PMID35409248
PMCPMC8999556
OpenAlexW4221138161

What Socratic 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 Socratic graph.