Evidence map›Paper›PMID 38351683›Full record

ArticleCancer research and treatment2024

CD19-Specific CAR-T Cell Treatment of 115 Children and Young Adults with Acute B Lymphoblastic Leukemia: Long-term Follow-up.

Yu Wang, Yu-Juan Xue, Ying-Xi Zuo, Yue-Ping Jia, Ai-Dong Lu, Hui-Min Zeng, Le-Ping Zhang

Open access · diamondAbstract read
In one paragraph

Article in Cancer research and treatment, 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
2.8field-weighted citation impact, top 8% 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.

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, 10 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. Article
  5. Review
  6. Article
  7. 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

7 authors at 2 institutions in 1 country.

Yu WangDepartment of Pediatrics, Peking University People's Hospital, Peking University, Beijing, China.
Yu-Juan XueDepartment of Pediatrics, Peking University People's Hospital, Peking University, Beijing, China.
Ying-Xi ZuoDepartment of Pediatrics, Peking University People's Hospital, Peking University, Beijing, China.
Yue-Ping JiaDepartment of Pediatrics, Peking University People's Hospital, Peking University, Beijing, China.
Ai-Dong LuDepartment of Pediatrics, Peking University People's Hospital, Peking University, Beijing, China.
Hui-Min ZengDepartment of Pediatrics, Peking University People's Hospital, Peking University, Beijing, China.
Le-Ping ZhangDepartment of Pediatrics, Peking University People's Hospital, Peking University, Beijing, China.
Peking University People's Hospital · CNPeking University · CN

Funding

Foundation of 2018 Beijing Key Clinical Specialty Construction Project-Pediatrics 2199000726National Natural Science Foundation of China 82000151Peking University People's Hospital
6 · The paper itself

Abstract

purposeChemotherapy has been the primary treatment for patients with B-cell acute lymphoblastic leukemia (B-ALL). However, there are still patients who are not sensitive to chemotherapy, including those with refractory/relapse (R/R) disease and those experiencing minimal residual disease (MRD) re-emergence. Chimeric antigen receptor-T lymphocytes (CAR-T) therapy may provide a new treatment option for these patients. MATERIALS AND

methodsOur institution conducted a single-arm prospective clinical trial (ChiCTR-OPN-17013507) using CAR-T-19 to treat R/R B-ALL and MRD re-emergent patients. One hundred and fifteen patients, aged 1-25 years (median age, 8 years), were enrolled, including 67 R/R and 48 MRD re-emergent CD19-positive B-ALL patients.

resultsAll patients achieved morphologic complete remission (CR), and within 1 month after infusion, 111 out of 115 (96.5%) patients achieved MRD-negative CR. With a median follow-up time of 48.4 months, the estimated 4-year leukemia-free survival (LFS) rate and overall survival (OS) rate were 68.7%±4.5% and 70.7%±4.3%, respectively. There were no significant differences in long-term efficacy observed among patients with different disease statuses before infusion (4-year OS: MRD re-emergence vs. R/R B-ALL, 70.6%±6.6% vs. 66.5%±6.1%, p=0.755; 4-year LFS: MRD re-emergence vs. R/R B-ALL, 67.3%±7.0% vs. 63.8%±6.2%, p=0.704). R/R B-ALL patients bridging to transplantation after CAR-T treatment had a superior OS and LFS compared to those who did not. However, for MRD re-emergent patients, there was no significant difference in OS and LFS, regardless of whether they underwent hematopoietic stem cell transplantation or not.

conclusionCD19 CAR-T therapy effectively and safely cures both R/R B-ALL and MRD re-emergent patients.

Indexed as

Antigens, CD19Immunotherapy, AdoptivePrecursor B-Cell Lymphoblastic Leukemia-LymphomaAdolescentAdultChildChild, PreschoolFemaleFollow-Up StudiesHumansInfantMaleNeoplasm, ResidualProspective StudiesReceptors, Chimeric AntigenTreatment OutcomeAntigens, CD19Receptors, Chimeric AntigenCD19 CAR-T therapyMRD re-emergencePrognosisR/R B-ALL

Identifiers

PMID38351683
PMCPMC11261203
OpenAlexW4391782158

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Registered trials

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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.