Evidence map›Paper›PMID 32715491›Full record

ReviewHepatology (Baltimore, Md.)2021

Improving the Efficacy of Liver Cancer Immunotherapy: The Power of Combined Preclinical and Clinical Studies.

Gen-Sheng Feng, Kaisa L Hanley, Yan Liang, Xiaoxue Lin

Open access · greenAbstract readReview
In one paragraph

Review in Hepatology (Baltimore, Md.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 70 citations in OpenAlex.

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  15. A decade of liver organoids: Advances in disease modeling.Clinical and molecular hepatology · 2023
    Review
  16. Article
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  19. Review
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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

4 authors at 2 institutions in 1 country.

Gen-Sheng FengDepartment of Pathology, School of Medicine; Molecular Biology Section, Division of Biological Sciences; and Moores Cancer Center, University of California at San Diego, La Jolla, CA.
Kaisa L HanleyDepartment of Pathology, School of Medicine; Molecular Biology Section, Division of Biological Sciences; and Moores Cancer Center, University of California at San Diego, La Jolla, CA.
Yan LiangDepartment of Pathology, School of Medicine; Molecular Biology Section, Division of Biological Sciences; and Moores Cancer Center, University of California at San Diego, La Jolla, CA.
Xiaoxue LinDepartment of Pathology, School of Medicine; Molecular Biology Section, Division of Biological Sciences; and Moores Cancer Center, University of California at San Diego, La Jolla, CA.
Moores Cancer CenterUniversity of California, San Diego · US

Funding

Tumor-promoting liver injuries and mechanismsR01CA239629 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FENG, GEN-SHENG · 2020 to 2024
$2.5M
Intra- and inter-cellular signals that drive hepato-oncogenesisR01CA236074 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FENG, GEN-SHENG · 2020 to 2024
$2.1M
A new mechanism of hepatocyte proliferation under stressR01DK128320 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FENG, GEN-SHENG · 2021 to 2024
$1.9M
Dissection of Pten-regulated signals in hepatopathogenesisR01CA188506 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FENG, GEN-SHENG · 2015 to 2019
$1.9M
NCI NIH HHS R01 CA188506NCI NIH HHS R01 CA236074NCI NIH HHS R01 CA239629NIDDK NIH HHS R01 DK128320
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a most deadly malignant disease worldwide, with no effective mechanism-based therapy available. Therefore, following the "miracle" outcomes seen in a few patients at the advanced stages of melanoma or lung cancer, the immune checkpoint inhibitors (ICIs) immediately entered clinical trials for advanced HCC patients without pre-clinical studies. Emerging data of clinical studies showed manageable toxicity and safety but limited therapeutic benefit to HCC patients, suggesting low response rate. Thus, one urgent issue is how to convert the liver tumors from cold to hot and responsive, which may rely on in-depth mechanistic studies in animal models and large scale data analysis in human patients. One ongoing approach is to design combinatorial treatment of different ICIs with other reagents and modalities. Indeed, a phase 3 clinical trial showed that combination of atezolizumab and bevacizumab achieved better overall and progression-free survival rates than sorafenib in unresectable HCC. This review highlights the value of animal models and the power of combining pre-clinical and clinical studies in efforts to improve HCC immunotherapy.

Indexed as

AnimalsBiliary Tract NeoplasmsCarcinoma, HepatocellularHumansImmune Checkpoint InhibitorsImmunotherapyLiver NeoplasmsImmune Checkpoint Inhibitors

Identifiers

PMID32715491
PMCPMC7854886
OpenAlexW3044406317

What OpenQuestion holds

Textmetadata
LicenceTDM
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.