Evidence map›Paper›PMID 39038917›Full record

ArticleJournal for immunotherapy of cancer2024

First-in-human dose escalation trial to evaluate the clinical safety and efficacy of an anti-MAGEA1 autologous TCR-transgenic T cell therapy in relapsed and refractory solid tumors.

Martin Wermke, Tobias A W Holderried, Jason John Luke, Van K Morris, Winfried H Alsdorf, Katrin Wetzko, Borje S Andersson, Ignacio I Wistuba, Edwin R Parra, Mohammad B Hossain and 22 more

2 registry-linked trialsAbstract readClinical Trial, Phase I
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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.

NCT04639245 phase1 / phase2terminatednot on this map

ATTAMAGE-A1.: Phase I/II Study of Autologous CD8+ and CD4+ Transgenic T Cells Expressing High Affinity MAGE-A1-Specific T-Cell Receptor (TCR) Combined With Atezolizumab in Patients With Metastatic MAGE-A1 Expressing Cancer

TypeinterventionalSponsorFred Hutchinson Cancer CenterRan2021 to 2022Enrolled1ConditionsAnatomic Stage IV Breast Cancer AJCC v8, Metastatic Lung Non-Small Cell Carcinoma, Metastatic Malignant Solid Neoplasm, Metastatic Triple-Negative Breast CarcinomaArmsAtezolizumab, Cyclophosphamide, Fludarabine, MAGE-A1-specific T Cell Receptor-transduced Autologous T-cells, PD1 Inhibitor
NCT05430555 phase1 / phase2terminatednot on this map

A Phase 1/2, First-in-Human, Open-Label, Accelerated-Titration, Two-Part Clinical Trial of TK-8001 (MAGE-A1-Directed TCR-Transduced Autologous CD8+ T-cells) in Patients With HLA-A*02:01 Genotype and Advanced-Stage/Metastatic, MAGE-A1+ Solid Tumors That Either Have No Further Approved Therapeutic Alternative(s) or Are Not Eligible for Them or Are in a Non- Curable State and Have Received a Minimum of Two Lines of Systemic Therapy

TypeinterventionalSponsorT-knife GmbHRan2022 to 2024Enrolled23ConditionsAdvanced Solid TumorsArmsAutologous CD8+ T-cells, transduced with MAGE-A1 directed TCR
3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. Trial
  2. Cardiotoxicity of T cell immunotherapies.Nature reviews. Cardiology · 2026
    Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Targeting tumor metabolism to augment CD8Journal of pharmaceutical analysis · 2025
    Review
  13. Review
  14. Article
  15. Review
  16. Engaging T cells for cleanup.Frontiers in immunology · 2025
    Review
  17. Current and future immunotherapy for breast cancer.Journal of hematology & oncology · 2024
    Review
  18. 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

32 authors.

Martin WermkeDepartment of Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany Martin.Wermke@uniklinikum-dresden.de.
Tobias A W HolderriedDepartment of Hematology, Oncology, Immunooncology, Stem Cell Transplantation, and Rheumatology, University Hospital Bonn, Bonn, Germany.
Jason John LukeCancer Immunotherapeutics Center, UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, USA.ORCID http://orcid.org/0000-0002-1182-4908
Van K MorrisDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center Division of Cancer Medicine, Houston, Texas, USA.
Winfried H AlsdorfDepartment of Oncology, Hematology, and Bone Marrow Transplantation with Section Pneumology, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
Katrin WetzkoDepartment of Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany.
Borje S AnderssonThe University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Ignacio I WistubaDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Edwin R ParraDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Mohammad B HossainImmatics US, Inc, Houston, Texas, USA.
Sandra Grund-GröschkeImmatics Biotechnologies GmbH, Tuebingen, Germany.
Katrin AslanImmatics Biotechnologies GmbH, Tuebingen, Germany.
Arun SatelliImmatics US, Inc, Houston, Texas, USA.
Anantha MarisettyImmatics US, Inc, Houston, Texas, USA.
Swapna SatamImmatics Biotechnologies GmbH, Tuebingen, Germany.
Mamta KalraImmatics US, Inc, Houston, Texas, USA.
Jens HukelmannImmatics Biotechnologies GmbH, Tuebingen, Germany.
M Alper KursunelImmatics Biotechnologies GmbH, Tuebingen, Germany.
Karine PozoImmatics US, Inc, Houston, Texas, USA.
Andreas AcsImmatics Biotechnologies GmbH, Tuebingen, Germany.ORCID http://orcid.org/0009-0008-3391-2539
Linus BackertImmatics Biotechnologies GmbH, Tuebingen, Germany.
Melissa BaumeisterImmatics Biotechnologies GmbH, Tuebingen, Germany.
Sebastian BunkImmatics Biotechnologies GmbH, Tuebingen, Germany.
Claudia WagnerImmatics Biotechnologies GmbH, Tuebingen, Germany.
Oliver SchoorImmatics Biotechnologies GmbH, Tuebingen, Germany.
Ali S MohamedImmatics US, Inc, Houston, Texas, USA.
Andrea Mayer-MoklerImmatics Biotechnologies GmbH, Tuebingen, Germany.
Norbert HilfImmatics Biotechnologies GmbH, Tuebingen, Germany.
Delfi KrishnaImmatics US, Inc, Houston, Texas, USA.
Steffen WalterImmatics US, Inc, Houston, Texas, USA.
Apostolia M Tsimberidou *Department of Investigational Cancer Therapeutics, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID http://orcid.org/0000-0003-2713-233X
Cedrik M Britten *Immatics Biotechnologies GmbH, Tuebingen, Germany.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

rationale of the trialAlthough the use of engineered T cells in cancer immunotherapy has greatly advanced the treatment of hematological malignancies, reaching meaningful clinical responses in the treatment of solid tumors is still challenging. We investigated the safety and tolerability of IMA202 in a first-in-human, dose escalation basket trial in human leucocyte antigen A*02:01 positive patients with melanoma-associated antigen A1 (MAGEA1)-positive advanced solid tumors. TRIAL

designThe 2+2 trial design was an algorithmic design based on a maximally acceptable dose-limiting toxicity (DLT) rate of 25% and the sample size was driven by the algorithmic design with a maximum of 16 patients. IMA202 consists of autologous genetically modified cytotoxic CD8

conclusionIn conclusion, IMA202 had a manageable safety profile, and it was associated with biological and potential clinical activity of MAGEA1-targeting genetically engineered TCR-T cells in a poor prognosis, multi-indication solid tumor cohort. TRIAL REGISTRATION NUMBERS: NCT04639245, NCT05430555.

Indexed as

Antigens, NeoplasmImmunotherapy, AdoptiveNeoplasmsAdultAgedFemaleHumansMaleMiddle AgedNeoplasm ProteinsReceptors, Antigen, T-CellAntigens, NeoplasmNeoplasm ProteinsReceptors, Antigen, T-CellAdoptive cell therapy - ACTSolid tumorT cell Receptor - TCR

Identifiers

PMID39038917
PMCPMC11268062

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.