Evidence map›Paper›PMID 39080180›Full record

ReviewBioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy2024

Prospects of Synergy: Local Interventions and CAR T Cell Therapy in Solid Tumors.

Anne Holtermann, Mila Gislon, Martin Angele, Marion Subklewe, Michael von Bergwelt-Baildon, Kirsten Lauber, Sebastian Kobold

Abstract readReview
In one paragraph

Review in BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

7 authors.

Anne HoltermannDivision of Clinical Pharmacology, Department of Medicine IV, University Hospital, Ludwig Maximilian University (LMU) of Munich, Lindwurmstrasse 2a, 80336, Munich, Germany.ORCID http://orcid.org/0009-0006-7604-9910
Mila GislonDivision of Clinical Pharmacology, Department of Medicine IV, University Hospital, Ludwig Maximilian University (LMU) of Munich, Lindwurmstrasse 2a, 80336, Munich, Germany.
Martin AngeleDepartment of General, Visceral, and Transplant Surgery, Ludwig-Maximilians-University Munich, Munich, Germany.
Marion SubkleweDepartment of Medicine III, University Hospital, Ludwig Maximilian University (LMU) of Munich, Munich, Germany.
Michael von Bergwelt-BaildonDepartment of Medicine III, University Hospital, Ludwig Maximilian University (LMU) of Munich, Munich, Germany.
Kirsten LauberDepartment of Radiation Oncology, LMU University Hospital, LMU Munich, Munich, Germany.
Sebastian KoboldDivision of Clinical Pharmacology, Department of Medicine IV, University Hospital, Ludwig Maximilian University (LMU) of Munich, Lindwurmstrasse 2a, 80336, Munich, Germany. Sebastian.kobold@med.uni-muenchen.de.

Funding

Bayerische Forschungsstiftung BAYCELLATORBayerisches Staatsministerium für Wirtschaft, Infrastruktur, Verkehr und Technologie m4-AwardBayerisches Zentrum für Krebsforschung TANGOBruno and Helene Jöster Foundation 360° CARDeutsche Forschungsgemeinschaft KO5055-2-1Deutsche Forschungsgemeinschaft KO5055/3-1Deutsche Krebshilfe AvantCAR.deElitenetzwerk Bayern i-TargetElse Kröner-Fresenius-Stiftung IOLINEuropean Research Council 101100460European Research Council 101124203European Research Council 756017H2020 Marie Skłodowska-Curie Actions 955575Melanoma Research Alliance 409510SFB-TRR 338/1 2021-452881907
6 · The paper itself

Abstract

Chimeric antigen receptor T cell therapy has been established in the treatment of various B cell malignancies. However, translating this therapeutic effect to treat solid tumors has been challenging because of their inter-tumoral as well as intratumoral heterogeneity and immunosuppressive microenvironment. Local interventions, such as surgery, radiotherapy, local ablation, and locoregional drug delivery, can enhance chimeric antigen receptor T cell therapy in solid tumors by improving tumor infiltration and reducing systemic toxicities. Additionally, ablation and radiotherapy have proven to (re-)activate systemic immune responses via abscopal effects and reprogram the tumor microenvironment on a physical, cellular, and chemical level. This review highlights the potential synergy of the combined approaches to overcome barriers of chimeric antigen receptor T cell therapy and summarizes recent studies that may pave the way for new treatment regimens.

Indexed as

Immunotherapy, AdoptiveNeoplasmsReceptors, Chimeric AntigenTumor MicroenvironmentAnimalsCombined Modality TherapyHumansT-LymphocytesReceptors, Chimeric Antigen

Identifiers

PMID39080180
PMCPMC11358237

What OpenQuestion holds

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Registered trials

None linked

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.