Evidence map›Paper›PMID 30603054›Full record

ReviewGenes & cancer2018

The promising immune checkpoint LAG-3: from tumor microenvironment to cancer immunotherapy.

Long Long, Xue Zhang, Fuchun Chen, Qi Pan, Pronnaphat Phiphatwatchara, Yuyang Zeng, Honglei Chen

Registry-linked trialOpen access · diamondAbstract readReview
In one paragraph

Review in Genes & cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06494943 (Neoadjuvant IBI110 and Sintilimab in Combination with Chemotherapy in Resectable Locally Advanced Head and Neck Squamous Cell Carcinoma), which is not on this map. Cited by 233 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
233citing papers in PubMed, 2 pooled it
15.5field-weighted citation impact, top 1% 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.

NCT06494943 phase1 / phase2recruitingnot on this mapstarted 2024, after this paper: background citation

Neoadjuvant IBI110 and Sintilimab in Combination with Chemotherapy in Resectable Locally Advanced Head and Neck Squamous Cell Carcinoma (HNSCC)- a Phase Ib Clinical Trial

TypeinterventionalSponsorFudan UniversityRan2024 to 2028Enrolled27ConditionsHead and Neck Cancer, Head and Neck Squamous Cell CarcinomaArmsSintilimab, IBI110, Paclitaxel, Cis Platinum, Surgery
3 · Its place in the literature

Who cites it

233 citing papers in PubMed, 2 syntheses or guidelines pooled it, 381 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. First-Line Nivolumab and Relatlimab Plus Chemotherapy for Gastric or Gastroesophageal Junction Adenocarcinoma: The Phase II RELATIVITY-060 Study.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Trial
  4. Depletion of LAG-3Clinical pharmacology and therapeutics · 2021
    Trial
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review

173 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 1 country.

Long LongDepartment of Pathology, School of Basic Medical Science, Wuhan University, Wuhan, P. R. China.
Xue ZhangDepartment of Pathology, School of Basic Medical Science, Wuhan University, Wuhan, P. R. China.
Fuchun ChenDepartment of Thoracosurgery, Traditional Chinese Medical Hospital of Wenling, Wenling, Zhejiang, China.
Qi PanDepartment of Thoracosurgery, Traditional Chinese Medical Hospital of Wenling, Wenling, Zhejiang, China.
Pronnaphat PhiphatwatcharaDepartment of Pathology, School of Basic Medical Science, Wuhan University, Wuhan, P. R. China.
Yuyang ZengDepartment of Pathology, School of Basic Medical Science, Wuhan University, Wuhan, P. R. China.
Honglei ChenDepartment of Pathology, School of Basic Medical Science, Wuhan University, Wuhan, P. R. China.
Wuhan University · CNWenzhou Hospital of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer immunotherapy and tumor microenvironment have been at the forefront of research over the past decades. Targeting immune checkpoints especially programmed death 1 (PD-1)/programmed death ligand 1 (PD-L1) has made a breakthrough in treating advanced malignancies. However, the low response rate brings a daunting challenge, changing the focus to dig deeply into the tumor microenvironment for alternative therapeutic targets. Strikingly, the inhibitory immune checkpoint lymphocyte activation gene-3 (LAG-3) holds considerable potential. LAG-3 suppresses T cells activation and cytokines secretion, thereby ensuring immune homeostasis. It exerts differential inhibitory impacts on various types of lymphocytes and shows a remarkable synergy with PD-1 to inhibit immune responses. Targeting LAG-3 immunotherapy is moving forward in active clinical trials, and combination immunotherapy of anti-LAG-3 and anti-PD-1 has shown exciting efficacy in fighting PD-1 resistance. Herein, we shed light on the significance of LAG-3 in the tumor microenvironment, highlight its role to regulate different lymphocytes, interplay with other immune checkpoints especially PD-1, and emphasize new advances in LAG-3-targeted immunotherapy.

Indexed as

cancer immunotherapyimmune checkpointlymphocyte activation gene-3tumor microenvironment

Identifiers

PMID30603054
PMCPMC6305110
OpenAlexW2982786601

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.