Evidence map›Paper›PMID 39717765›Full record

ArticleFrontiers in immunology2024

Case report: A novel third-generation anti-CD19/CD22 CAR T-cells combined with auto-HSCT for relapsed Burkitt lymphoma.

Xiaodan Luo, Ao Chen, Le Qin, Robert Weinkove, Rong Zhao, Ting Ye, Sihui Chen, Jianli Tang, Jianbo Liu, Jiayu Huang and 7 more

Abstract readCase Reports
In one paragraph

Article 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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

17 authors.

Xiaodan Luo *The Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Ao Chen *The Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Le QinChina-New Zealand Joint Laboratory on Biomedicine and Health, Key Laboratory of Immune Response and Immunotherapy, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, GIBH-HKU Guangdong- Hong Kong Stem Cell and Regenerative Medicine Research Centre, GIBH-CUHK Joint Research Laboratory on Stem Cell and Regenerative Medicine, Institute of Drug Discovery, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.
Robert WeinkoveCancer Immunotherapy Program, Malaghan Institute of Medical Research, Wellington, New Zealand.
Rong ZhaoThe Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Ting YeThe Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Sihui ChenThe Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Jianli TangThe Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Jianbo LiuThe Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Jiayu HuangThe Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Boyun ShiThe Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Danyun YuanThe Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Huo TanThe Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Dajiang QinThe Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Zhaoyang TangDepartment of Automation, Tsinghua University, Beijing, China.
Peng LiChina-New Zealand Joint Laboratory on Biomedicine and Health, Key Laboratory of Immune Response and Immunotherapy, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, GIBH-HKU Guangdong- Hong Kong Stem Cell and Regenerative Medicine Research Centre, GIBH-CUHK Joint Research Laboratory on Stem Cell and Regenerative Medicine, Institute of Drug Discovery, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.
Runhui ZhengThe Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study explores a novel therapeutic strategy for relapsed/refractory (R/R) Burkitt lymphoma (BL) by integrating autologous hematopoietic stem cell transplantation (ASCT) with tandem anti-CD19/CD22 chimeric antigen receptor (CAR) T cell therapy. A 20-year-old Asian male with refractory BL, whose lymphoma had not responded to multiple chemoimmunotherapy regimens, received myeloablative ASCT followed three days later by infusion of a novel third-generation CAR T cells engineered with CD28 and CD3ζ signaling domains, along with a TLR2 costimulatory domain. This resulted in sustained complete remission at the 306-day follow-up, without experiencing any severe complications. This case suggests that combining myeloablative ASCT with tandem anti-CD19/CD22 CAR T cell therapy could be an effective approach for R/R BL, warranting further clinical validation.

Indexed as

Antigens, CD19Burkitt LymphomaHematopoietic Stem Cell TransplantationImmunotherapy, AdoptiveReceptors, Chimeric AntigenSialic Acid Binding Ig-like Lectin 2Combined Modality TherapyHumansMaleNeoplasm Recurrence, LocalT-LymphocytesTransplantation, AutologousTreatment OutcomeYoung AdultAntigens, CD19CD19 molecule, humanCD22 protein, humanReceptors, Chimeric AntigenSialic Acid Binding Ig-like Lectin 2autologous hematopoietic stem cell transplantationCAR T-cell therapyCD19/CD22 dual targetimmunotherapyrelapsed/refractory Burkitt lymphoma

Identifiers

PMID39717765
PMCPMC11663888

What OpenQuestion holds

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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.