Evidence map›Paper›PMID 38339430›Full record

ReviewCancers2024

Claudin 18.2 as a New Biomarker in Gastric Cancer-What Should We Know?

Maria Cecília Mathias-Machado, Victor Hugo Fonseca de Jesus, Alexandre Jácome, Mauro Daniel Donadio, Marcelo Porfirio Sunagua Aruquipa, João Fogacci, Renato Guerino Cunha, Leonard Medeiros da Silva, Renata D'Alpino Peixoto

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
10.1field-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.

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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
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  12. Efficacy of CLDN18.2-Targeted Radiotheranostics in Patient-Derived Models of Gastric Cancer.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
    Article
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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

9 authors at 1 institution in 1 country.

Maria Cecília Mathias-MachadoDivision of Gastrointestinal Medical Oncology, Oncoclínicas, São Paulo 04538-132, Brazil.
Victor Hugo Fonseca de JesusDivision of Gastrointestinal Medical Oncology, Oncoclínicas, Florianópolis 88015-020, Brazil.
Alexandre JácomeDivision of Gastrointestinal Medical Oncology, Oncoclínicas, Belo Horizonte 30360-680, Brazil.
Mauro Daniel DonadioDivision of Gastrointestinal Medical Oncology, Oncoclínicas, São Paulo 04538-132, Brazil.ORCID 0000-0002-4705-4802
Marcelo Porfirio Sunagua AruquipaDivision of Gastrointestinal Medical Oncology, Oncoclínicas, São Paulo 04538-132, Brazil.
João FogacciDivision of Gastrointestinal Medical Oncology, Oncoclínicas, Rio de Janeiro 22775-003, Brazil.
Renato Guerino CunhaCellular Therapy Program, Division of Hematology, Oncoclínicas, São Paulo 04538-132, Brazil.
Leonard Medeiros da SilvaOncoclinicas Prescision Medicine, Oncoclínicas, São Paulo 04513-020, Brazil.
Renata D'Alpino PeixotoDivision of Gastrointestinal Medical Oncology, Oncoclínicas, São Paulo 04538-132, Brazil.ORCID 0000-0003-0053-7951
Centro de Pesquisas Oncológicas · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric cancer (GC) remains a formidable global health challenge, ranking among the top-five causes of cancer-related deaths worldwide. The majority of patients face advanced stages at diagnosis, with a mere 6% five-year survival rate. First-line treatment for metastatic GC typically involves a fluoropyrimidine and platinum agent combination; yet, predictive molecular markers have proven elusive. This review navigates the evolving landscape of GC biomarkers, with a specific focus on Claudin 18.2 (CLDN18.2) as an emerging and promising target. Recent phase III trials have unveiled the efficacy of Zolbetuximab, a CLDN18.2-targeting antibody, in combination with oxaliplatin-based chemotherapy for CLDN18.2-positive metastatic GC. As this novel therapeutic avenue unfolds, understanding the nuanced decision making regarding the selection of anti-CLDN18.2 therapies over other targeted agents in metastatic GC becomes crucial. This manuscript reviews the evolving role of CLDN18.2 as a biomarker in GC and explores the current status of CLDN18.2-targeting agents in clinical development. The aim is to provide concise insights into the potential of CLDN18.2 as a therapeutic target and guide future clinical decisions in the management of metastatic GC.

Indexed as

biomarkerscancergastric cancertreatment

Identifiers

PMID38339430
PMCPMC10854563
OpenAlexW4391566678

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.