Evidence map›Paper›PMID 39192970›Full record

ReviewFrontiers in immunology2024

Acute T-cell lymphoblastic leukemia: chimeric antigen receptor technology may offer a new hope.

Jiajie Jing, Yuan Ma, Ziwen Xie, Bingyan Wang, Yueming Chen, Enjie Chi, Jiadong Wang, Kejin Zhang, Zhujun Wang, Sisi Li

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2024. 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. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Precision sniper for solid tumors: CAR-NK cell therapy.Cancer immunology, immunotherapy : CII · 2025
    Review
  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

10 authors.

Jiajie JingDepartment of Clinical Medicine, Hangzhou City University School of Medicine, Hangzhou, China.
Yuan MaDepartment of Clinical Medicine, Hangzhou City University School of Medicine, Hangzhou, China.
Ziwen XieDepartment of Clinical Medicine, Hangzhou City University School of Medicine, Hangzhou, China.
Bingyan WangDepartment of Clinical Medicine, Hangzhou City University School of Medicine, Hangzhou, China.
Yueming ChenDepartment of Clinical Medicine, Hangzhou City University School of Medicine, Hangzhou, China.
Enjie ChiDepartment of Clinical Medicine, Hangzhou City University School of Medicine, Hangzhou, China.
Jiadong WangDepartment of Clinical Medicine, Hangzhou City University School of Medicine, Hangzhou, China.
Kejin ZhangDepartment of Clinical Medicine, Hangzhou City University School of Medicine, Hangzhou, China.
Zhujun WangDepartment of Pediatrics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Sisi LiDepartment of Clinical Medicine, Hangzhou City University School of Medicine, Hangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute lymphoblastic leukemia (ALL) is a prevalent malignancy affecting the hematopoietic system, encompassing both B-cell ALL (B-ALL) and T-cell ALL (T-ALL). T-ALL, characterized by the proliferation of T-cell progenitors in the bone marrow, presents significant treatment challenges, with patients often experiencing high relapse rates and poor long-term survival despite advances in chemotherapy and hematopoietic stem cell transplantation (HSCT). This review explores the pathogenesis and traditional treatment strategies of T-ALL, emphasizing the promising potential of chimeric antigen receptor (CAR) technology in overcoming current therapeutic limitations. CAR therapy, leveraging genetically modified immune cells to target leukemia-specific antigens, offers a novel and precise approach to T-ALL treatment. The review critically analyzes recent developments in CAR-T and CAR-NK cell therapies, their common targets, optimization strategies, clinical outcomes, and the associated challenges, providing a comprehensive overview of their clinical prospects in T-ALL treatment.

Indexed as

Immunotherapy, AdoptivePrecursor T-Cell Lymphoblastic Leukemia-LymphomaReceptors, Chimeric AntigenAnimalsHumansKiller Cells, NaturalReceptors, Antigen, T-CellT-LymphocytesReceptors, Antigen, T-CellReceptors, Chimeric AntigenCAR-NKCAR-Tchimeric antigen receptorpathogenesisT-ALL

Identifiers

PMID39192970
PMCPMC11347323

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.