Evidence map›Paper›PMID 40144774›Full record

ReviewTherapeutic advances in hematology2025

Recent advances of CAR-T cells in acute myeloid leukemia.

Huan Deng, Qi Wang, Xiaodong Tong, Zhiwei Cui, Yang Yang, Ying Xiang

Abstract readReview
In one paragraph

Review in Therapeutic advances in hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Molecularly targeted therapy and immunotherapy in leukemias.Journal of hematology & oncology · 2026
    Review
  3. Review
  4. Targets for CAR Therapy in Multiple Myeloma.International journal of molecular sciences · 2025
    Review
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.

Huan DengDepartment of Medical Laboratory, The People's Hospital of Leshan, No. 238, Baita Street, Shizhong District, Leshan, Sichuan 614000, China.ORCID https://orcid.org/0009-0008-2209-3654
Qi WangDepartment of Medical Records and Statistics Room, The People's Hospital of Leshan, Leshan, Sichuan, China.
Xiaodong TongDepartment of Medical Laboratory, The People's Hospital of Leshan, Leshan, Sichuan, China.
Zhiwei CuiDepartment of Medical Laboratory, The People's Hospital of Leshan, Leshan, Sichuan, China.
Yang YangDepartment of Medical Laboratory, The People's Hospital of Leshan, Leshan, Sichuan, China.
Ying XiangDepartment of Medical Laboratory, The People's Hospital of Leshan, Leshan, Sichuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML), the most common type of leukemia in adults, is a highly heterogeneous and aggressive hematologic malignancy. Since the 20th century, the combination of cytosine arabinoside and anthracyclines has been the most common chemotherapy drug used to treat patients with AML. Although, new targeted medicines have emerged, such as midostaurin and gilteritinib targeting FMS-like tyrosine kinase 3 (FLT3), ivosidenib (isocitrate dehydrogenase 1 (IDH1) inhibitor) and enasidenib (IDH2 inhibitor) targeting IDH, and gemtuzumab ozogamicin targeting CD33, which have changed the treatment strategies of AML. But, until now, hematopoietic stem cell transplantation remains the best treatment option in most cases. However, treatment resistance and relapse are still the major consequences of disease progression in AML, highlighting the urgent need for novel therapeutic approaches. As an alternative, chimeric antigen receptor (CAR)-T cells are engineered T-cells developed as a breakthrough in cancer therapy in recent years, and explored and used in various tumor types. In particular, it has achieved remarkable efficacy in the field of relapsed and refractory B lymphocyte tumors. This review mainly summarizes and discusses the research progress and the clinical application of CAR-T cell immunotherapy in AML in recent years.

Indexed as

acute myeloid leukemiachimeric antigen receptor T cellsimmunotherapytarget antigen

Identifiers

PMID40144774
PMCPMC11938459

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.