Evidence map›Paper›PMID 40425233›Full record

ArticleJournal for immunotherapy of cancer2025

B7-H3 and CSPG4 co-targeting as Pan-CAR-T cell treatment of triple-negative breast cancer.

Simone Stucchi, Roberto Borea, Susana Garcia-Recio, Manuela Zingarelli, Patrick D Rädler, Elena Camerini, Caroline Marnata Pellegry, Siobhan O'Connor, H Shelton Earp, Lisa A Carey and 3 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Cellular immunotherapy in melanoma: the next frontier in cancer treatment.Journal of experimental & clinical cancer research : CR · 2026
    Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Platelet-engineered CAR-T cells as adjuvant therapy after cancer surgery.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. Review
  12. Article
  13. 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

13 authors.

Simone StucchiLineberger Cancer Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Roberto BoreaLineberger Cancer Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Susana Garcia-RecioDepartment of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Manuela ZingarelliLineberger Cancer Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Patrick D RädlerDepartment of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Elena CameriniLineberger Cancer Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Caroline Marnata PellegryLineberger Cancer Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Siobhan O'ConnorPathology & Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
H Shelton EarpLineberger Cancer Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Lisa A CareyDivision of Oncology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Charles M PerouDepartment of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Barbara SavoldoLineberger Cancer Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Gianpietro DottiLineberger Cancer Center, University of North Carolina, Chapel Hill, North Carolina, USA gdotti@med.unc.edu.ORCID http://orcid.org/0000-0002-2639-8526

Funding

Tissue Procurement & PathologyP50CA058223 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BENJAMIN CARLISLE CALHOUN · 1992 to 2026
$59.3M
NCI NIH HHS P50 CA058223
6 · The paper itself

Abstract

purposeChimeric antigen receptor T (CAR-T) cell therapy is under clinical investigation in patients with metastatic triple-negative breast cancer (TNBC). However, the identification of targetable antigens remains a high priority to avoid toxicity and prevent tumor escape. EXPERIMENTAL

designHere we analyzed the gene expression of B7-H3 (

resultsWe observed that

conclusionsThese data highlight the clinical potential of the proposed approach that could be applicable to the great majority of patients with TNBC as well as most of patients with breast cancer in general.

Indexed as

B7 AntigensChondroitin Sulfate ProteoglycansImmunotherapy, AdoptiveMembrane ProteinsReceptors, Chimeric AntigenTriple Negative Breast NeoplasmsAnimalsCell Line, TumorChondroitin Sulfate Proteoglycan 4FemaleHumansMiceXenograft Model Antitumor AssaysB7 AntigensCD276 protein, humanChondroitin Sulfate Proteoglycan 4Chondroitin Sulfate ProteoglycansCSPG4 protein, humanMembrane ProteinsReceptors, Chimeric AntigenAdoptive cell therapy - ACTBreast CancerChimeric antigen receptor - CAR

Identifiers

PMID40425233
PMCPMC12107568

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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 Socratic graph.