Evidence map›Paper›PMID 38712978›Full record

ReviewJournal of cellular and molecular medicine2024

Recent advances in CAR-T cell therapy for acute myeloid leukaemia.

Chi Gao, Xin Li, Yao Xu, Tongcun Zhang, Haichuan Zhu, Di Yao

Abstract readReview
In one paragraph

Review in Journal of cellular and molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Recent advances in CAR-T cell therapy for acute myeloid leukaemia.Journal of cellular and molecular medicine · 2024
    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.

Chi GaoCollege of Life Science and Health, Wuhan University of Science and Technology, Wuhan, China.ORCID 0009-0008-0251-8723
Xin LiCollege of Biotechnology, Tianjin University of Science and Technology, Tianjin, China.
Yao XuCollege of Life Science and Health, Wuhan University of Science and Technology, Wuhan, China.ORCID 0000-0001-7926-3791
Tongcun ZhangCollege of Life Science and Health, Wuhan University of Science and Technology, Wuhan, China.
Haichuan ZhuCollege of Life Science and Health, Wuhan University of Science and Technology, Wuhan, China.
Di YaoCollege of Life Science and Health, Wuhan University of Science and Technology, Wuhan, China.ORCID 0009-0005-1957-1772

Funding

Hubei Province Supporting Enterprise Technology Innovation Development Project 2021BAB12Wuhan East Lake High-tech Zone "JieBangGuaShuai" Project 2022KJB113Wuhan Science and Technology Plan Project 2019030703011533
6 · The paper itself

Abstract

Acute myeloid leukaemia (AML) is a fatal and refractory haematologic cancer that primarily affects adults. It interferes with bone marrow cell proliferation. Patients have a 5 years survival rate of less than 30% despite the availability of several treatments, including chemotherapy, allogeneic haematopoietic stem cell transplantation (Allo-HSCT), and receptor antagonist drugs. Allo-HSCT is the mainstay of acute myeloid leukaemia treatment. Although it does work, there are severe side effects, such as graft-versus-host disease (GVHD). In recent years, chimeric antigen receptor (CAR)-T cell therapies have made significant progress in the treatment of cancer. These engineered T cells can locate and recognize tumour cells in vivo and release a large number of effectors through immune action to effectively kill tumour cells. CAR-T cells are among the most effective cancer treatments because of this property. CAR-T cells have demonstrated positive therapeutic results in the treatment of acute myeloid leukaemia, according to numerous clinical investigations. This review highlights recent progress in new targets for AML immunotherapy, and the limitations, and difficulties of CAR-T therapy for AML.

Indexed as

Immunotherapy, AdoptiveLeukemia, Myeloid, AcuteReceptors, Chimeric AntigenAnimalsHumansT-LymphocytesReceptors, Chimeric Antigenacute myeloid leukaemiachimeric antigen receptor T cellsscFvtarget antigen

Identifiers

PMID38712978
PMCPMC11075639

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.