Evidence map›Paper›PMID 35768164›Full record

ArticleJournal for immunotherapy of cancer2022

NY-ESO-1-specific redirected T cells with endogenous TCR knockdown mediate tumor response and cytokine release syndrome.

Mikiya Ishihara, Shigehisa Kitano, Shinichi Kageyama, Yoshihiro Miyahara, Noboru Yamamoto, Hidefumi Kato, Hideyuki Mishima, Hiroyoshi Hattori, Takeru Funakoshi, Takashi Kojima and 16 more

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

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02366546 (Multi-center, Investigator Initiated Phase 1 Study of NY-ESO-1 Specific TCR Gene Transferred T Lymphocytes With Solid Tumors), which is not on this map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
5.9field-weighted citation impact, top 3% 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.

NCT02366546 phase1unknown statusnot on this map

Multi-center, Investigator Initiated Phase 1 Study of NY-ESO-1 Specific TCR Gene Transferred T Lymphocytes With Solid Tumors

TypeinterventionalSponsorMie UniversityRan2015Enrolled9ConditionsSolid TumorsArmsTBI-1301, Cyclophosphamide, Fludarabine
3 · Its place in the literature

Who cites it

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Advances in immunotherapies in ovarian cancer.Journal for immunotherapy of cancer · 2026
    Review
  9. Article
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  11. Article
  12. Article
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  15. Article
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  17. Converting TCR-based chimeric antigen receptor STAR into dual-specific targeting receptor for cancer immunotherapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  18. Review
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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

26 authors at 12 institutions in 1 country.

Mikiya IshiharaCancer Center, Mie University Hospital, Tsu, Japan.ORCID 0000-0002-7581-2615
Shigehisa KitanoDivision of Cancer Immunotherapy Development, Advanced Medical Development Center, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID 0000-0002-4041-8298
Shinichi KageyamaDepartments of Immuno-Gene Therapy and Personalized Cancer Immunotherapy, Mie University Graduate School of Medicine, Tsu, Japan kageyama@med.mie-u.ac.jp.ORCID 0000-0002-7682-3295
Yoshihiro MiyaharaDepartments of Immuno-Gene Therapy and Personalized Cancer Immunotherapy, Mie University Graduate School of Medicine, Tsu, Japan.
Noboru YamamotoDepartment of Experimental Therapeutics, National Cancer Institue Hospital, Tokyo, Japan.
Hidefumi KatoDepartment of Transfusion Medicine, Aichi Medical University, Nagakute, Japan.
Hideyuki MishimaCancer Center, Aichi Medical University, Nagakute, Japan.
Hiroyoshi HattoriLaboratory of Advanced Therapy, Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Takeru FunakoshiDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.
Takashi KojimaDepartment of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Tetsuro SasadaDivision of Cancer Immunotherapy, Kanagawa Cancer Center Research Institute, Yokohama, Japan.ORCID 0000-0002-2313-8833
Eiichi SatoInstitute of Medical Science, Tokyo Medical University, Tokyo, Japan.
Sachiko OkamotoTakara Bio Inc, Kusatsu, Japan.
Daisuke TomuraTakara Bio Inc, Kusatsu, Japan.
Ikuei NukayaTakara Bio Inc, Kusatsu, Japan.
Hideto ChonoTakara Bio Inc, Kusatsu, Japan.
Junichi MinenoTakara Bio Inc, Kusatsu, Japan.
Muhammad Faris KairiImmunoScape Pte. Ltd, Singapore.
Phuong Diem Hoang NguyenImmunoScape Pte. Ltd, Singapore.
Yannick SimoniImmunoScape Pte. Ltd, Singapore.
Alessandra NardinImmunoScape Pte. Ltd, Singapore.
Evan NewellImmunoScape Pte. Ltd, Singapore.
Michael FehlingsImmunoScape Pte. Ltd, Singapore.
Hiroaki IkedaDepartment of Oncology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Takashi WatanabeDepartments of Immuno-Gene Therapy and Personalized Cancer Immunotherapy, Mie University Graduate School of Medicine, Tsu, Japan.
Hiroshi ShikuDepartments of Immuno-Gene Therapy and Personalized Cancer Immunotherapy, Mie University Graduate School of Medicine, Tsu, Japan.
Takara (Japan) · JPMie University · JPAichi Medical University · JPKanagawa Prefectural Hospital Organization · JPKeio University · JPMie University Hospital · JPNagasaki University · JPNational Cancer Center Hospital East · JPNational Hospital Organization · JPThe Cancer Institute Hospital · JPTokyo Medical University · JPTokyo National Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBecause of the shortage of ideal cell surface antigens, the development of T-cell receptor (TCR)-engineered T cells (TCR-T) that target intracellular antigens such as NY-ESO-1 is a promising approach for treating patients with solid tumors. However, endogenous TCRs in vector-transduced T cells have been suggested to impair cell-surface expression of transduced TCR while generating mispaired TCRs that can become self-reactive.

methodsWe conducted a first-in-human phase I clinical trial with the TCR-transduced T-cell product (TBI-1301) in patients with NY-ESO-1-expressing solid tumors. In manufacturing TCR-T cells, we used a novel affinity-enhanced NY-ESO-1-specific TCR that was transduced by a retroviral vector that enables siRNA (small interfering RNA)-mediated silencing of endogenous TCR. The patients were divided into two cohorts. Cohort 1 was given a dose of 5×10

resultsIn vitro study showed that both the CD8

conclusionsThe trial showed that endogenous TCR-silenced and affinity-enhanced NY-ESO-1 TCR-T cells were safely administered except for grade 3 lung injury. The TCR-T cell infusion exhibited significant tumor response and early-onset CRS in patients with tumors that express NY-ESO-1 at high levels. The differentiation properties of the manufactured T cells may be prognostic for TCR-T-related CRS. TRIAL REGISTRATION NUMBER: NCT02366546.

Indexed as

Cytokine Release SyndromeImmunotherapyNeoplasmsReceptors, Antigen, T-CellT-LymphocytesAntigens, NeoplasmCyclophosphamideCytokinesHumansMembrane ProteinsAntigens, NeoplasmCTAG1B protein, humanCyclophosphamideCytokinesMembrane ProteinsReceptors, Antigen, T-Cellcell engineeringclinical trials as topiccytokinesimmunotherapy, adoptive

Identifiers

PMID35768164
PMCPMC9244667
OpenAlexW4283740261

What OpenQuestion holds

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LicenceCC BY-NC
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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.