Evidence map›Paper›PMID 39425148›Full record

ReviewBiomarker research2024

Deciphering LAG-3: unveiling molecular mechanisms and clinical advancements.

Alejandra Martínez-Pérez, Rocío Granda-Díaz, Candelaria Aguilar-García, Christian Sordo-Bahamonde, Segundo Gonzalez

Erratum issuedAbstract readReview
In one paragraph

Review in Biomarker research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Trial
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  9. Glycoscience in Advancing PD-1/PD-L1-Axis-Targeted Tumor Immunotherapy.International journal of molecular sciences · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Alejandra Martínez-Pérez *Department of Functional Biology, Immunology, Universidad de Oviedo, Oviedo, Spain.
Rocío Granda-Díaz *Department of Functional Biology, Immunology, Universidad de Oviedo, Oviedo, Spain.
Candelaria Aguilar-GarcíaDepartment of Functional Biology, Immunology, Universidad de Oviedo, Oviedo, Spain.
Christian Sordo-BahamondeDepartment of Functional Biology, Immunology, Universidad de Oviedo, Oviedo, Spain. sordochristian@uniovi.es.
Segundo GonzalezDepartment of Functional Biology, Immunology, Universidad de Oviedo, Oviedo, Spain. segundog@uniovi.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment based on immune checkpoint blockade has revolutionized cancer therapy. Despite the remarkable success achieved and the preclinical development of multiple checkpoint inhibitors targeting other checkpoints, only antibodies targeting the PD-1/PD-L1 axis and CTLA-4 have been approved for patient treatment, especially in solid tumors. Currently, with the approval of relatlimab, a LAG-3 blocking antibody, a third player, has been used in the fight against cancer. The endorsement of relatlimab marks a significant milestone in cancer immunotherapy, opening new avenues for combination therapies and enhancing treatment outcomes. However, the complex biology of LAG-3 may hinder its full development as a therapeutic alternative. In this review, we provide in-depth insight into the biology of LAG-3 and its current and future development in cancer treatment.

Indexed as

Checkpoint blockadeFavezelimabFianlimabImmunotherapyLAG-3Relatlimab

Identifiers

PMID39425148
PMCPMC11487938

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.