Evidence map›Paper›PMID 35776199›Full record

ArticleJournal of cancer research and clinical oncology2023

A novel antibody-TCR (AbTCR) T-cell therapy is safe and effective against CD19-positive relapsed/refractory B-cell lymphoma.

Pengcheng He, Haibo Liu, Bryan Zimdahl, Jie Wang, Minna Luo, Qi Chang, Fangzhou Tian, Fan Ni, Duo Yu, Huasheng Liu and 5 more

Registry-linked trialOpen access · greenAbstract readClinical Trial, Phase I
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03642496 (The Clinical Study of Structurally Optimized ET019002-T Cell Therapy for Refractory/Relapsed B-Cell Malignancies), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 15% 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.

NCT03642496 early_phase1unknown statusnot on this map

The Clinical Study of Structurally Optimized ET019002-T Cell Therapy for Refractory/Relapsed B-Cell Malignancies

TypeinterventionalSponsorFirst Affiliated Hospital Xi'an Jiaotong UniversityRan2018 to 2020Enrolled18ConditionsB-Cell MalignanciesArmsLow dose ET019002- T Cells, Middle dose ET019002- T Cells, High dose ET019002- T Cells
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
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  5. Concept CARs are picking up speed.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
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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

15 authors at 3 institutions in 2 countries.

Pengcheng He *Department of Hematology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Haibo Liu *Department of Hematology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Bryan Zimdahl *Eureka Therapeutics, Inc., Emeryville, CA, USA.
Jie WangDepartment of Hematology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Minna LuoDepartment of Hematology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Qi ChangEureka Therapeutics, Inc., Emeryville, CA, USA.
Fangzhou TianEureka Therapeutics, Inc., Emeryville, CA, USA.
Fan NiEureka Therapeutics, Inc., Emeryville, CA, USA.
Duo YuEureka Therapeutics, Inc., Emeryville, CA, USA.
Huasheng LiuDepartment of Hematology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Limei ChenDepartment of Hematology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Huaiyu WangDepartment of Hematology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Mei ZhangDepartment of Hematology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Stephan A GruppDepartment of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Cheng LiuEureka Therapeutics, Inc., Emeryville, CA, USA. cheng.liu@eurekainc.com.ORCID http://orcid.org/0000-0002-7419-8529
First Affiliated Hospital of Xi'an Jiaotong University · CNEureka Therapeutics (United States) · USChildren's Hospital of Philadelphia · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeA barrier to widespread adoption of chimeric antigen receptor (CAR) T-cell therapy is toxicity. To address this, we recently developed a novel antibody-T-cell receptor (AbTCR) platform (trademarked as ARTEMIS

methodsWe generated ET019003 T cells, which are autologous CD19-directed AbTCR T cells. We then conducted an early phase I study to evaluate the safety and preliminary efficacy of ET019003 T cells for the treatment of CD19-positive relapsed/refractory (r/r) B-cell lymphoma.

resultsSixteen patients enrolled in this study and 12 patients were treated. Of the 12 patients treated, 6 patients (50%) achieved a complete response (CR), and 4 (33%) achieved a partial response (PR) (best objective response rate [ORR] of 83%). CRs were durable, including 2 patients with ongoing CRs for 22.7 months and 23.2 months. ET019003 was well-tolerated with an attractive safety profile. No patients experienced severe (grade ≥ 3) cytokine release syndrome (CRS) and only 1 patient experienced immune effector cell-associated neurotoxicity syndrome (ICANS) of any grade. Significant elevations of cytokine levels were not seen, even in patients with marked expansion of ET019003 T cells.

conclusionThis study provides initial clinical validation of the AbTCR platform as a novel cancer treatment with the potential to provide durable clinical benefit with low toxicity.

trial registrationNCT03642496; Date of registration: August 22, 2018.

Indexed as

Lymphoma, B-CellNeurotoxicity SyndromesAntibodiesAntigens, CD19Cell- and Tissue-Based TherapyHumansImmunotherapy, AdoptiveReceptors, Antigen, T-CellAntibodiesAntigens, CD19cell-associated neurotoxicityReceptors, Antigen, T-CellAntibody-T-cell receptor therapyB-cell lymphomaCD19-directed therapyImmunotherapyT-cell therapy

Identifiers

PMID35776199
PMCPMC11797221
OpenAlexW4283749230

What OpenQuestion holds

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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.