Evidence map›Paper›PMID 39358720›Full record

ArticleJournal of translational medicine2024

Efficacy and safety of CAR-T therapy targeting CLL1 in patients with extramedullary diseases of acute myeloid leukemia.

Yifan Zhao, Xue Bai, Shujing Guo, Xiaomei Zhang, Jile Liu, Mohan Zhao, Tianle Xie, Haotian Meng, Yu Zhang, Xiaoyuan He and 1 more

Registry-linked trialAbstract read
In one paragraph

Article in Journal of translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07432100 (Clinical Study on the Safety, Efficacy and Pharmacokinetics of Universal CLL1 Chimeric Antigen Receptor T-Cell in Relapsed/Refractory Acute Myeloid Leukemia), which is not on this map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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.

NCT07432100 phase1not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Clinical Study on the Safety, Efficacy and Pharmacokinetics of Universal CLL1 Chimeric Antigen Receptor T-Cell in Relapsed/Refractory Acute Myeloid Leukemia

TypeinterventionalSponsorMingfeng ZhaoRan2026 to 2028Enrolled20ConditionsAcute Myeloid Leukemia, Chimeric Antigen Receptor T-cell, Universal CLL1 CAR-TArmsuniversal CLL1 CAR-T cells
3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

  1. Review
  2. Review
  3. Pediatric AML CAR T cell therapy.Molecular therapy. Oncology · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Strategic innovations: Tackling challenges of immunotherapy in acute myeloid leukemia.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2025
    Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Is There (Still) a Place for Sequential Conditioning?Current oncology (Toronto, Ont.) · 2025
    Review
  19. Article
  20. 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

11 authors.

Yifan Zhao *The First Central Clinical College of Tianjin Medical University, Tianjin, 300380, China.
Xue Bai *The First Central Clinical College of Tianjin Medical University, Tianjin, 300380, China.
Shujing Guo *The First Central Clinical College of Tianjin Medical University, Tianjin, 300380, China.
Xiaomei ZhangNankai University School of Medicine, Tianjin, 300380, China.
Jile LiuThe First Central Clinical College of Tianjin Medical University, Tianjin, 300380, China.
Mohan ZhaoThe First Central Clinical College of Tianjin Medical University, Tianjin, 300380, China.
Tianle XieNankai University School of Medicine, Tianjin, 300380, China.
Haotian MengNankai University School of Medicine, Tianjin, 300380, China.
Yu ZhangDepartment of Hematology, Tianjin First Central Hospital, No.2 Baoshanxi Rd, Xiqing District, Tianjin, 300380, China.
Xiaoyuan HeDepartment of Hematology, Tianjin First Central Hospital, No.2 Baoshanxi Rd, Xiqing District, Tianjin, 300380, China.
Mingfeng ZhaoDepartment of Hematology, Tianjin First Central Hospital, No.2 Baoshanxi Rd, Xiqing District, Tianjin, 300380, China. mingfengzhao@sina.com.

Funding

Key projects of Tianjin Applied Basic Research and Multi-Investment Fund 21JCZDJC01240the Key Science and Technology Support Project of Tianjin Science and Technology Bureau 20YFZCSY00800the Science and Technology Project of Tianjin Municipal Health Committee TJWJ2022QN030Tianjin Key Medical Discipline (Specialty) Construction Project TJYXZDXK-056BTianjin Municipal Science and Technology Committee TJWJ2022XK018
6 · The paper itself

Abstract

backgroundsThe incidence of extramedullary diseases (EMDs) in patients diagnosed with acute myeloid leukemia (AML) is approximately 10-20%. These patients exhibit a significantly distinct etiology, therapeutic response, and prognosis compared to patients without EMDs. CLL1 CAR-T therapy has been demonstrated satisfactory efficacy and safety in the treatment of refractory and relapsed AML patients. However, concerns have been raised regarding the potential impact of extramedullary niduses on the effectiveness of CLL1 CAR-T therapy.

methodsA total of 47 patients were enrolled in this study, including 27 patients with isolated AML tumor bone marrow infiltration and 20 patients with both extramedullary and bone marrow infiltration of AML. CLL1 CAR-T cells were manufactured and subjected to rigorous quality control in the hematology laboratory of Tianjin First Central Hospital. The efficacy and adverse reactions were assessed following CAR-T cell infusion, while expansion of CAR-T cells, levels of cytokines releasing, and other indicators were closely monitored.

resultsAmong the 20 patients with EMDs and the 27 individuals without EMDs, complete remission in bone marrow was achieved by 65.00% and 81.48% of patients, respectively. Meanwhile, among the patients with EMDs, 55.00% achieved complete remission while 10.00% achieved partial remission when assessing the efficacy of CLL1 CAR-T cells against extramedullary niduses. Although the overall survival, progression-free survival, and duration of remission period appeared to be shorter for patients with EMDs compared to those without EMDs, this difference did not reach statistical significance. The incidence rates of complications were comparable between both groups. Meanwhile, there were no significant differences observed in the levels of CAR-T cell expansion and accompanying cytokines release between patients with and without EMDs.

conclusionsOur study findings have demonstrated the efficacy of CLL1 CAR-T therapy in the treatment of AML patients with EMDs, while also indicating manageable occurrence rates of complications within a tolerable range. The CLL1 CAR-T therapy, serving as an ideal strategy for AML patients irrespective of the presence of EMDs, effectively ameliorates the conditions of AML patients and provides them with an opportunity to undergo curative hematopoietic stem cell transplantation while significantly enhancing their prognosis.

Indexed as

Immunotherapy, AdoptiveLeukemia, Myeloid, AcuteAdolescentAdultAgedBone MarrowFemaleHumansMaleMiddle AgedReceptors, Chimeric AntigenTreatment OutcomeYoung AdultReceptors, Chimeric AntigenCAR-TCLL1, acute myeloid leukemiaExtramedullary diseases

Identifiers

PMID39358720
PMCPMC11446059

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Registered trials

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.