Evidence map›Paper›PMID 28186088›Full record

ReviewCancer gene therapy2017

Current status of immunotherapy for gastrointestinal stromal tumor.

Y Tan, J C Trent, B A Wilky, D A Kerr, A E Rosenberg

Abstract readReview
PubMed Publisher
In one paragraph

Review in Cancer gene therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
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  11. Immune Cell Infiltration and the Expression of PD-1 and PD-L1 in Primary PDGFRA-Mutant Gastrointestinal Stromal Tumors.Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract · 2021
    Article
  12. Review
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  16. Review
  17. Article
  18. Low Distribution of TIM-3Journal of immunology research · 2021
    Article
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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

5 authors at 2 institutions in 1 country.

Y TanDepartment of Pathology, University of Miami, Miller School of Medicine, Jackson Memorial Hospital, and University of Miami Hospital, Miami, Florida, USA.
J C TrentDepartment of Hematology/Oncology, University of Miami, Miller School of Medicine, Jackson Memorial Hospital, and University of Miami Hospital, Miami, Florida, USA.
B A WilkyDepartment of Hematology/Oncology, University of Miami, Miller School of Medicine, Jackson Memorial Hospital, and University of Miami Hospital, Miami, Florida, USA.
D A KerrDepartment of Pathology, University of Miami, Miller School of Medicine, Jackson Memorial Hospital, and University of Miami Hospital, Miami, Florida, USA.
A E RosenbergDepartment of Pathology, University of Miami, Miller School of Medicine, Jackson Memorial Hospital, and University of Miami Hospital, Miami, Florida, USA.
University of Miami Hospital · USSylvester Comprehensive Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastrointestinal stromal tumors (GIST) contain tumor-infiltrating immune cells and their presence provides an opportunity and rationale for developing effective forms of immunotherapy. The types of tumor-infiltrating inflammatory cells and relevant immune checkpoint inhibitors are the focus of active investigation. The most numerous tumor-infiltrating inflammatory cells are tumor-associated macrophages (TAMs) and CD3+ T cells. Studies have shown that patients with GISTs that harbor increased numbers of CD3+ T cells have better outcomes. However, the clinical behavior of GIST has not been shown to correlate with the number of TAMs. The biological significance of other less frequent tumor-infiltrating immune cells including tumor-infiltrating neurtrophils (TINs), natural killer cells (NKs), B cells, dendritic cells (DCs) remains unclear. The immune checkpoint inhibitors CTLA-4, PD1/PDL1 and TIM3/galectin-9 are molecules that can be targeted by synthesized antibodies. Clinical and pre-clinical trials using this approach against immune checkpoint inhibitors, anti-KIT antibody and the generation of chimeric antigen receptor (CAR) T-cells have shown promising results. The treatment of GIST with immunotherapy is complex and evolving; this article reviews its current status for patients with GISTs.

Indexed as

ImmunotherapyAnimalsAntineoplastic Agents, ImmunologicalBiomarkers, TumorCancer VaccinesCell- and Tissue-Based TherapyCombined Modality TherapyCytokinesGastrointestinal Stromal TumorsHumansImmune SystemImmunomodulationLymphocytes, Tumor-InfiltratingMolecular Targeted TherapyTumor MicroenvironmentAntineoplastic Agents, ImmunologicalBiomarkers, TumorCancer VaccinesCytokines

Identifiers

PMID28186088
OpenAlexW2586281401

What OpenQuestion holds

Textmetadata
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.