Evidence map›Paper›PMID 40536724›Full record

ReviewAnnals of hematology2025

Latest updates on pathogenesis mechanisms and management strategies for cytokine release syndrome, neurotoxicity, and hemophagocytic lymphohistiocytosis related to CAR-T cell therapies.

Xin Wang, Xiaoyuan He, Tao Zhang, Jile Liu, Mingfeng Zhao

Abstract readReview
In one paragraph

Review in Annals of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. CAR-T Cell Therapy for Autoimmune Kidney Diseases: Where Do We Stand Now?International journal of molecular sciences · 2025
    Review
  14. Article
  15. Predictive Power of Baseline [Diagnostics (Basel, Switzerland) · 2025
    Article
  16. 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

5 authors.

Xin WangFirst Center Clinical College, Tianjin Medical University, Tianjin, 300070, China.
Xiaoyuan HeDepartment of Hematology, Tianjin Thrombosis and Hemostasis Institute, Tianjin First Central Hospital, No.2 Baoshan West Road, Xiqing District, Tianjin, 300192, China.
Tao ZhangNankai University School of Medicine, Nankai University, Tianjin, 300071, China.
Jile LiuFirst Center Clinical College, Tianjin Medical University, Tianjin, 300070, China.
Mingfeng ZhaoDepartment of Hematology, Tianjin Thrombosis and Hemostasis Institute, Tianjin First Central Hospital, No.2 Baoshan West Road, Xiqing District, Tianjin, 300192, China. mingfengzhao@sina.com.

Funding

The major special project on public health science and technology in Tianjin 24ZXGZSY00120the Science and Technology Project of Tianjin Municipal Health Committee TJWJ2022XK018, TJWJ2022QN030Tianjin Health Research Project Grant No. TJWJ2024QN040Tianjin Key Medical Discipline (Specialty) Construction Project TJYXZDXK-056B
6 · The paper itself

Abstract

Nowadays, chimeric antigen receptor (CAR) -T cell therapy has shown significant efficacy in treating hematological tumors, with an obvious increase in patient survival rates. However, with the widespread application of CAR-T, the incidence of CAR-T related adverse events has gradually increased, including cytokine release syndrome (CRS), immune effector cell associated neurotoxicity syndrome (ICANS), and hemophagocytic lymphohistiocytosis (HLH). These complications may be life-threatening, so early diagnosis and intervention treatment are crucial for the prognosis of patients. In this review, we first comprehensively summarize the latest insights into the pathogenesis and clinical manifestations of CRS, ICANS, and HLH after CAR-T, with a focus on elaborating on the specific mechanisms and related pathways of the inflammatory storm caused by a large number of cytokines after CAR-T. We also discussed the established prevention and management strategies for the three complications mentioned above, and demonstrated the effectiveness of the treatment by introducing the therapeutic effects of various treatment methods in current clinical or preclinical trials. In addition, we provide a prospective perspective on the measures and modifications currently being studied to mitigate the toxicity associated with CAR-T cell therapy.

Indexed as

Cytokine Release SyndromeImmunotherapy, AdoptiveLymphohistiocytosis, HemophagocyticNeurotoxicity SyndromesCytokinesHumansReceptors, Chimeric AntigenCytokinesReceptors, Chimeric AntigenChimeric antigen receptor (CAR)-T cell therapiesCytokine release syndromeHemophagocytic lymphohistiocytosisImmune effector cell-associated neurotoxicity syndrome

Identifiers

PMID40536724
PMCPMC12283850

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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.