Evidence map›Paper›PMID 30103457›Full record

ReviewVaccines2018

Early Investigations and Recent Advances in Intraperitoneal Immunotherapy for Peritoneal Metastasis.

Anusha Thadi, Marian Khalili, William F Morano, Scott D Richard, Steven C Katz, Wilbur B Bowne

Erratum issuedOpen access · goldAbstract readReview
In one paragraph

Review in Vaccines, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.2field-weighted citation impact, top 17% 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

25 citing papers in PubMed, 43 citations in OpenAlex.

  1. Trial
  2. Review
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  6. Advances in the treatment of malignant ascites in China.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2024
    Review
  7. Article
  8. Review
  9. Challenges and interventions of chimeric antigen receptor-T cell therapy in solid tumors.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2023
    Article
  10. Review
  11. Review
  12. Article
  13. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Anusha ThadiDepartment of Surgery, Drexel University College of Medicine, Philadelphia, PA 19102, USA. anusha.thadi@gmail.com.ORCID 0000-0002-1271-0398
Marian KhaliliDepartment of Surgery, Drexel University College of Medicine, Philadelphia, PA 19102, USA. mariankhalili@gmail.com.
William F MoranoDepartment of Surgery, Drexel University College of Medicine, Philadelphia, PA 19102, USA. morano.william@gmail.com.ORCID 0000-0002-6977-5221
Scott D RichardDepartment of Obstetrics and Gynecology, Thomas Jefferson University Hospital, Philadelphia, PA 19107, USA. scott.richard@jefferson.edu.
Steven C KatzDepartment of Surgery, Boston University School of Medicine, Boston, MA 02118, USA. skatz@chartercare.org.
Wilbur B BowneDepartment of Surgery, Drexel University College of Medicine, Philadelphia, PA 19102, USA. wbb28@drexel.edu.
Drexel University · USBoston University · USThomas Jefferson University Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peritoneal metastasis (PM) is an advanced stage malignancy largely refractory to modern therapy. Intraperitoneal (IP) immunotherapy offers a novel approach for the control of regional disease of the peritoneal cavity by breaking immune tolerance. These strategies include heightening T-cell response and vaccine induction of anti-cancer memory against tumor-associated antigens. Early investigations with chimeric antigen receptor T cells (CAR-T cells), vaccine-based therapies, dendritic cells (DCs) in combination with pro-inflammatory cytokines and natural killer cells (NKs), adoptive cell transfer, and immune checkpoint inhibitors represent significant advances in the treatment of PM. IP delivery of CAR-T cells has shown demonstrable suppression of tumors expressing carcinoembryonic antigen. This response was enhanced when IP injected CAR-T cells were combined with anti-PD-L1 or anti-Gr1. Similarly, CAR-T cells against folate receptor α expressing tumors improved T-cell tumor localization and survival when combined with CD137 co-stimulatory signaling. Moreover, IP immunotherapy with catumaxomab, a trifunctional antibody approved in Europe, targets epithelial cell adhesion molecule (EpCAM) and has shown considerable promise with control of malignant ascites. Herein, we discuss immunologic approaches under investigation for treatment of PM.

Indexed as

ascitescarcinoembryonic antigenCAR-T cellsdendritic cellsfolate receptor αintraperitoneal immunotherapymetastasisperitonealvaccines

Identifiers

PMID30103457
PMCPMC6160982
OpenAlexW2885741312

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.