Evidence map›Paper›PMID 42034501›Full record

ReviewBlood reviews2026

Immunotherapy in acute myeloid leukemia: The antibodies, TriKEs, and CARs on the arduous road to cure.

B Adhikari, M R Litzow, A L Dias

Abstract readReview
In one paragraph

Review in Blood reviews, 2026. 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
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.

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

3 authors.

B AdhikariDivision of Hematology, National Heart, Lung and Blood Institute, Bethesda, MD, USA.
M R LitzowDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
A L DiasImmune Deficiency-Cellular Therapy Program, National Cancer Institute, Bethesda, MD, USA. Electronic address: ajoydias@gmail.com.

Funding

Intramural NIH HHS Z99 HL999999
6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a complex, heterogeneous and aggressive hematopoietic clonal disorder with limited curative options beyond allogeneic stem cell transplantation. The disease presents significant challenges due to high relapse rates resistance to chemotherapy, and the immunosuppressive tumor microenvironment. The immune system plays an important role in leukemia survival and resistance. Various immunotherapeutic approaches, ranging from the use of monoclonal antibodies, antibody-drug conjugates (ADCs), bispecific T-cell engagers (BiTE's), chimeric antigen receptor T (CAR-T) cells, vaccines and therapeutic infusions of NK cells, are currently being tested with promising, yet conflicting results. We review the various types of immunotherapies in pre-clinical and clinical development and discuss how best to use them in clinical practice from the point of view of a clinical hematologist.

Indexed as

ImmunotherapyLeukemia, Myeloid, AcuteAnimalsAntibodies, BispecificAntineoplastic Agents, ImmunologicalHumansImmunotherapy, AdoptiveReceptors, Chimeric AntigenTreatment OutcomeAntibodies, BispecificAntineoplastic Agents, ImmunologicalReceptors, Chimeric AntigenAcute myeloid leukemia (AML)bispecific antibodieschimeric antigen receptor therapy (CAR-T therapy)immunotherapymonoclonal antibodiesT-cell receptorsvaccines

Identifiers

PMID42034501
PMCPMC13359886

What OpenQuestion holds

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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.