Evidence map›Paper›PMID 35338773›Full record

Trial reportBlood2022

Efficacy and safety of CD19-specific CAR T cell-based therapy in B-cell acute lymphoblastic leukemia patients with CNSL.

Yuekun Qi, Mingfeng Zhao, Yongxian Hu, Ying Wang, Ping Li, Jiang Cao, Ming Shi, Jiaqi Tan, Meng Zhang, Xia Xiao and 14 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Blood, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02782351 (Humanized CAR-T Therapy for Treatment of Recurrent or Refractory B Cell Malignancy by Targeting CD19), which is not on this map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
9.0field-weighted citation impact, top 1% of its field
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.

NCT02782351 phase1 / phase2unknown statusnot on this map

Humanized CAR-T Therapy for Treatment of Recurrent or Refractory B Cell Malignancy by Targeting CD19

TypeinterventionalSponsorKai Lin Xu; Jun Nian ZhengRan2016 to 2018Enrolled50ConditionsLeukemia, Lymphocytic, Chronic, B-CellArmsCAR-T
3 · Its place in the literature

Who cites it

67 citing papers in PubMed, 93 citations in OpenAlex.

  1. Trial
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  14. A Novel MICB-Targeting CAR-NK Cells for the Treatment of Pancreatic Cancer.International journal of molecular sciences · 2026
    Article
  15. Review
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7 more citing papers are in PubMed but not listed here.

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

24 authors at 5 institutions in 1 country.

Yuekun QiBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.ORCID 0000-0003-4431-3060
Mingfeng ZhaoDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Yongxian HuBone Marrow Transplantation Center, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Ying WangBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Ping LiDepartment of Hematology, Tongji Hospital of Tongji University, Shanghai, China.
Jiang CaoBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.ORCID 0000-0003-3767-9283
Ming ShiCancer Institute, Xuzhou Medical University, Xuzhou, China.
Jiaqi TanDepartment of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Meng ZhangDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Xia XiaoDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Jieyun XiaBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Sha MaBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Jianlin QiaoBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.ORCID 0000-0002-0456-0940
Zhiling YanBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Hujun LiBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Bin PanBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Wei SangBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.ORCID 0000-0002-1170-7074
Depeng LiBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Zhenyu LiBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Jianfeng ZhouDepartment of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
He HuangBone Marrow Transplantation Center, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Aibin LiangDepartment of Hematology, Tongji Hospital of Tongji University, Shanghai, China.
Junnian ZhengCancer Institute, Xuzhou Medical University, Xuzhou, China.
Kailin XuBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.ORCID 0000-0003-1375-1084
Xuzhou Medical College · CNTianjin First Center Hospital · CNFirst Affiliated Hospital Zhejiang University · CNTongji Hospital · CNTongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Few studies have described chimeric antigen receptor (CAR) T-cell therapy for patients with B-cell acute lymphoblastic leukemia (B-ALL) with central nervous system leukemia (CNSL) because of concerns regarding poor response and treatment-related neurotoxicity. Our study included 48 patients with relapsed/refractory B-ALL with CNSL to evaluate the efficacy and safety of CD19-specific CAR T cell-based therapy. The infusion resulted in an overall response rate of 87.5% (95% confidence interval [CI], 75.3-94.1) in bone marrow (BM) disease and remission rate of 85.4% (95% CI, 72.8-92.8) in CNSL. With a median follow-up of 11.5 months (range, 1.3-33.3), the median event-free survival was 8.7 months (95% CI, 3.7-18.8), and the median overall survival was 16.0 months (95% CI, 13.5-20.1). The cumulative incidences of relapse in BM and CNS diseases were 31.1% and 11.3%, respectively, at 12 months (P = .040). The treatment was generally well tolerated, with 9 patients (18.8%) experiencing grade ≥3 cytokine release syndrome. Grade 3 to 4 neurotoxic events, which developed in 11 patients (22.9%), were associated with a higher preinfusion disease burden in CNS and were effectively controlled under intensive management. Our results suggest that CD19-specific CAR T cell-based therapy can induce similar high response rates in both BM and CNS diseases. The duration of remission in CNSL was longer than that in BM disease. CD19 CAR T-cell therapy may provide a potential treatment option for previously excluded patients with CNSL, with manageable neurotoxicity. The clinical trials were registered at www.clinicaltrials.gov as #NCT02782351 and www.chictr.org.cn as #ChiCTR-OPN-16008526.

Indexed as

Burkitt LymphomaCentral Nervous System NeoplasmsPrecursor Cell Lymphoblastic Leukemia-LymphomaReceptors, Chimeric AntigenAcute DiseaseAntigens, CD19Cytokine Release SyndromeHumansImmunotherapy, AdoptiveT-LymphocytesAntigens, CD19Receptors, Chimeric Antigen

Identifiers

PMID35338773
PMCPMC11022988
OpenAlexW4220685620

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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 Socratic graph.