Evidence map›Paper›PMID 37894439›Full record

ReviewCancers2023

Combination Therapy of Immune Checkpoint Inhibitors with Locoregional Therapy for Hepatocellular Carcinoma.

Yasuyuki Tamai, Naoto Fujiwara, Takamitsu Tanaka, Shugo Mizuno, Hayato Nakagawa

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

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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 1 institution in 1 country.

Yasuyuki TamaiDepartment of Gastroenterology and Hepatology, Graduate School of Medicine, Mie University, Tsu 514-8507, Japan.ORCID 0000-0002-8012-8578
Naoto FujiwaraDepartment of Gastroenterology and Hepatology, Graduate School of Medicine, Mie University, Tsu 514-8507, Japan.ORCID 0000-0002-4109-3421
Takamitsu TanakaDepartment of Gastroenterology and Hepatology, Graduate School of Medicine, Mie University, Tsu 514-8507, Japan.
Shugo MizunoDepartment of Hepatobiliary Pancreatic and Transplant Surgery, Graduate School of Medicine, Mie University, Tsu 514-8507, Japan.ORCID 0000-0002-2253-544X
Hayato NakagawaDepartment of Gastroenterology and Hepatology, Graduate School of Medicine, Mie University, Tsu 514-8507, Japan.ORCID 0000-0002-6973-5094
Mie University · JP

Funding

Daiichi Sankyo Foundation of Life Science Daiichi Sankyo Foundation of Life ScienceJapan Agency for Medical Research and Development JP23fk0210090Japan Agency for Medical Research and Development JP23fk0210115Japan Agency for Medical Research and Development JP23fk0210130Japan Society for the Promotion of Science 21H02892Japan Society for the Promotion of Science 23K16770Princess Takamatsu Cancer Research Fund Princess Takamatsu Cancer Research FundTakeda Science Foundation Takeda Science Foundation
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is estimated to be the fourth leading cause of cancer-related deaths globally, and its overall prognosis is dismal because most cases are diagnosed at a late stage and are unamenable to curative treatment. The emergence of immune checkpoint inhibitors (ICIs) has dramatically improved the therapeutic efficacy for advanced hepatocellular carcinoma; however, their response rates remain unsatisfactory, partly because >50% of HCC exhibit an ICI-nonresponsive tumor microenvironment characterized by a paucity of cytotoxic T cells (immune-cold), as well as difficulty in their infiltration into tumor sites (immune excluded). To overcome this limitation, combination therapies with locoregional therapies, including ablation, transarterial embolization, and radiotherapy, which are usually used for early stage HCCs, have been actively explored to enhance ICI efficacy by promoting the release of tumor-associated antigens and cytokines, and eventually accelerating the so-called cancer-immunity cycle. Various combination therapies have been investigated in early- to late-phase clinical trials, and some have shown promising results. This comprehensive article provides an overview of the immune landscape for HCC to understand ICI efficacy and its limitations and, subsequently, reviews the status of combinatorial therapies of ICIs with locoregional therapy for HCC.

Indexed as

cancer–immunity cycleclinical trialhepatocellular carcinomaimmune checkpoint inhibitorlocoregional therapy

Identifiers

PMID37894439
PMCPMC10605879
OpenAlexW4387822065

What Socratic 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 Socratic graph.