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

Author:

Mathias-Machado Maria Cecília1,de Jesus Victor Hugo Fonseca2,Jácome Alexandre3,Donadio Mauro Daniel1ORCID,Aruquipa Marcelo Porfirio Sunagua1,Fogacci João4,Cunha Renato Guerino5,da Silva Leonard Medeiros6,Peixoto Renata D’Alpino1ORCID

Affiliation:

1. Division of Gastrointestinal Medical Oncology, Oncoclínicas, São Paulo 04538-132, Brazil

2. Division of Gastrointestinal Medical Oncology, Oncoclínicas, Florianópolis 88015-020, Brazil

3. Division of Gastrointestinal Medical Oncology, Oncoclínicas, Belo Horizonte 30360-680, Brazil

4. Division of Gastrointestinal Medical Oncology, Oncoclínicas, Rio de Janeiro 22775-003, Brazil

5. Cellular Therapy Program, Division of Hematology, Oncoclínicas, São Paulo 04538-132, Brazil

6. Oncoclinicas Prescision Medicine, Oncoclínicas, São Paulo 04513-020, Brazil

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.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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