Evidence map›Paper›PMID 37601739›Full record

ReviewTranslational gastroenterology and hepatology2023

Impact of immune tolerance mechanisms on the efficacy of immunotherapy in primary and secondary liver cancers.

Kamya Sankar, Ashley N Pearson, Tejaswi Worlikar, Matthew D Perricone, Erin A Holcomb, Mishal Mendiratta-Lala, Zhen Xu, Neil Bhowmick, Michael D Green

Abstract readReview
In one paragraph

Review in Translational gastroenterology and hepatology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Review
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  12. Article
  13. Review
  14. Frontiers in pharmacology · 2024
    Article
  15. Article
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.

Kamya SankarDivision of Medical Oncology, Department of Medicine, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Ashley N PearsonGraduate Program in Immunology, School of Medicine, University of Michigan, Ann Arbor, MI, USA.
Tejaswi WorlikarDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.
Matthew D PerriconeProgram in Biomedical Sciences, University of Michigan Medical School, Ann Arbor, MI, USA.
Erin A HolcombGraduate Program in Immunology, School of Medicine, University of Michigan, Ann Arbor, MI, USA.
Mishal Mendiratta-LalaDepartment of Radiology, University of Michigan, Ann Arbor, MI, USA.
Zhen XuDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.
Neil BhowmickDivision of Medical Oncology, Department of Medicine, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Michael D GreenGraduate Program in Immunology, School of Medicine, University of Michigan, Ann Arbor, MI, USA.

Funding

The paradoxical roles of beta hydroxy butyrate in the liver pro-metastatic nicheP01CA233452 · NCI · CEDARS-SINAI MEDICAL CENTER · PI POSADAS, EDWIN MELENCIO · 2020 to 2024
$9.5M
Targeting BUB 1 for radio- and immuno-sensitization of Triple Negative Breast Cancer (TNBC)R21CA252010 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GREEN, MICHAEL DANIEL, NYATI, SHYAM · 2021 to 2021
$401k
Enhancing Ferroptosis to Augment Responses to Immune Checkpoint BlockadeI01BX005267 · VA · VETERANS HEALTH ADMINISTRATION · PI GREEN, MICHAEL DANIEL · 2022 to 2025
–
BLRD VA I01 BX005267NCI NIH HHS P01 CA233452NCI NIH HHS R21 CA252010
6 · The paper itself

Abstract

The liver is a functionally unique organ with an immunosuppressive microenvironment. The liver is the sixth most common site of primary cancer in humans and is a frequent site of metastasis from other solid tumors. The development of effective therapies for primary and metastatic liver cancer has been challenging due to the complex metabolic and immune microenvironment of the liver. The liver tumor microenvironment (TME) in primary and secondary (metastatic) liver cancers is heterogenous and consists of unique immune and stromal cell populations. Crosstalk between these cell populations and tumor cells creates an immunosuppressive microenvironment within the liver which potentiates cancer progression. Immune checkpoint inhibitors (ICIs) are now clinically approved for the management of primary and secondary liver cancer and can partially overcome liver immune tolerance, but their efficacy is limited. In this review, we describe the liver microenvironment and the use of immunotherapy in primary and secondary liver cancer. We discuss emerging combination strategies utilizing locoregional and systemic therapy approaches which may enhance efficacy of immunotherapy in primary and secondary liver cancer. A deeper understanding of the immunosuppressive microenvironment of the liver will inform novel therapies and therapeutic combinations in order to improve outcomes of patients with primary and secondary liver cancer.

Indexed as

Hepatocellular carcinoma (HCC)immunotherapy in liver cancerliver metastasestumor immune microenvironment

Identifiers

PMID37601739
PMCPMC10432235

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.