Evidence map›Paper›PMID 33919570›Full record

ReviewCancers2021

Recent Advances and Future Prospects in Immune Checkpoint (ICI)-Based Combination Therapy for Advanced HCC.

Yawen Dong, Jeffrey Sum Lung Wong, Ryohichi Sugimura, Ka-On Lam, Bryan Li, Gerry Gin Wai Kwok, Roland Leung, Joanne Wing Yan Chiu, Tan To Cheung, Thomas Yau

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 2 pooled it
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

31 citing papers in PubMed, 2 syntheses or guidelines pooled it, 61 citations in OpenAlex.

  1. Pooled it
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  9. The Interplay of Autoimmune Disease, Cancer, and Immunity: Current Understanding and Therapeutic Prospects.International journal of hematology-oncology and stem cell research · 2025
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  20. Systemic treatment for unresectable hepatocellular carcinoma.World journal of gastroenterology · 2023
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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

10 authors at 2 institutions in 3 countries.

Yawen DongDepartment of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China.
Jeffrey Sum Lung WongDepartment of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China.
Ryohichi SugimuraSchool of Biomedical Science, The University of Hong Kong, Hong Kong, China.ORCID 0000-0001-5701-3628
Ka-On LamDepartment of Clinical Oncology, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China.
Bryan LiDepartment of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China.
Gerry Gin Wai KwokDepartment of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China.
Roland LeungDepartment of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China.
Joanne Wing Yan ChiuDepartment of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China.
Tan To CheungDepartment of Surgery, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China.
Thomas YauDepartment of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China.
Queen Mary Hospital · CNUniversity of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advanced, unresectable hepatocellular carcinoma has a dismal outcome. Multiple immune checkpoint inhibitors (ICIs) targeting the programmed-cell death 1 pathway (PD-1/L1) have been approved for the treatment of advanced HCC. However, outcomes remain undesirable and unpredictable on a patient-to-patient basis. The combination of anti-PD-1/L1 with alternative agents, chiefly cytotoxic T-lymphocyte antigen-4 (CTLA-4) ICIs or agents targeting other oncogenic pathways such as the vascular endothelial growth factor (VEGF) pathway and the c-MET pathway, has, in addition to the benefit of directly targeting alterative oncogenic pathways, in vitro evidence of synergism through altering the genomic and function signatures of T cells and expression of immune checkpoints. Several trials have been completed or are underway evaluating such combinations. Finally, studies utilizing transcriptomics and organoids are underway to establish biomarkers to predict ICI response. This review aims to discuss the biological rationale and clinical advances in ICI-based combinations in HCCs, as well as the progress and prospects of the search for the aforementioned biomarkers in ICI treatment of HCC.

Indexed as

biomarkercheckpoint inhibitorscombination therapyhepatocellular carcinomaICI responseprecision medicinetargeted therapytranscriptomics

Identifiers

PMID33919570
PMCPMC8072916
OpenAlexW3156902516

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.