Evidence map›Paper›PMID 27080226›Full record

ArticleCancer gene therapy2016

Regional CAR-T cell infusions for peritoneal carcinomatosis are superior to systemic delivery.

S C Katz, G R Point, M Cunetta, M Thorn, P Guha, N J Espat, C Boutros, N Hanna, R P Junghans

Open access · greenAbstract read
In one paragraph

Article in Cancer gene therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 114 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed, 1 pooled it
15.1field-weighted citation impact, top 1% 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.

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

114 citing papers in PubMed, 1 synthesis or guideline pooled it, 169 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Spatial Regulation of CAR Signaling Enables Logic-Gated Activity.bioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
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  15. Intraperitoneal infusion of NKG2D CAR-NK cells induces endogenous CD8Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review

54 more citing papers are in PubMed but not listed here.

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

9 authors at 5 institutions in 1 country.

S C KatzDepartment of Surgery, Roger Williams Medical Center, Providence, RI, USA.
G R PointDepartment of Surgery, Roger Williams Medical Center, Providence, RI, USA.
M CunettaDepartment of Surgery, Roger Williams Medical Center, Providence, RI, USA.
M ThornDepartment of Surgery, Roger Williams Medical Center, Providence, RI, USA.
P GuhaDepartment of Surgery, Roger Williams Medical Center, Providence, RI, USA.
N J EspatDepartment of Surgery, Roger Williams Medical Center, Providence, RI, USA.
C BoutrosDepartment of Surgery, University of Maryland School of Medicine, Baltimore, MD, USA.
N HannaDepartment of Surgery, University of Maryland School of Medicine, Baltimore, MD, USA.
R P JunghansDepartment of Medicine, Tufts Medical Center, Boston, MA, USA.
Providence College · USUniversity of Maryland, Baltimore · USBoston University · USRoger Williams Medical Center · USTufts Medical Center · US

Funding

Reversing genetically modified T cell suppression in a model of liver metastasesK08CA160662 · NCI · ROGER WILLIAMS MEDICAL CENTER · PI KATZ, STEVEN C · 2012 to 2016
$838k
NCI NIH HHS K08 CA160662
6 · The paper itself

Abstract

Metastatic spread of colorectal cancer (CRC) to the peritoneal cavity is common and difficult to treat, with many patients dying from malignant bowel obstruction. Chimeric antigen receptor T cell (CAR-T) immunotherapy has shown great promise, and we previously reported murine and phase I clinical studies on regional intrahepatic CAR-T infusion for CRC liver metastases. We are now studying intraperitoneal (IP) delivery of CAR-Ts for peritoneal carcinomatosis. Regional IP infusion of CAR-T resulted in superior protection against carcinoembryonic antigen (CEA+) peritoneal tumors, when compared with systemically infused CAR-Ts. IP CAR-Ts also provided prolonged protection against IP tumor re-challenges and demonstrated an increase in effector memory phenotype over time. IP CAR-Ts provided protection against tumor growth at distant subcutaneous (SC) sites in association with increases in serum IFNγ levels. Given the challenges posed by immunoinhibitory pathways in solid tumors, we combined IP CAR-T treatment with suppressor cell targeting. High frequencies of myeloid-derived suppressor cells (MDSC) and regulatory T cells (Treg) were found within the IP tumors, with MDSC expressing high levels of immunosuppressive PD-L1. Combinatorial IP CAR-T treatment with depleting antibodies against MDSC and Treg further improved efficacy against peritoneal metastases. Our data support further development of combinatorial IP CAR-T immunotherapy for peritoneal malignancies.

Indexed as

Recombinant Fusion ProteinsAnimalsAntigens, NeoplasmBiomarkersCell- and Tissue-Based TherapyCytotoxicity, ImmunologicDisease Models, AnimalHumansImmunomodulationImmunophenotypingImmunotherapy, AdoptiveMicePeritoneal NeoplasmsReceptors, Antigen, T-CellT-Lymphocyte SubsetsTreatment OutcomeAntigens, NeoplasmBiomarkersReceptors, Antigen, T-CellRecombinant Fusion Proteins

Identifiers

PMID27080226
PMCPMC5153580
OpenAlexW2340381526

What OpenQuestion holds

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Registered trials

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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.