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Antibody-drug conjugates: the clinical development in gastric cancer. | LitMetric

Antibody-drug conjugates: the clinical development in gastric cancer.

Front Oncol

School of Clinical Medicine, Affiliated Hospital, North China University of Science and Technology, Tangshan, China.

Published: May 2023

AI Article Synopsis

  • Gastric cancer (GC) is a leading cause of cancer-related deaths globally, with limited success from traditional treatments, resulting in a median survival of about eight months for advanced cases.
  • Antibody-drug conjugates (ADCs) are being researched as a more effective treatment option, targeting specific cancer cell receptors to deliver potent drugs directly to tumors.
  • This review highlights the developments in ADC therapies for gastric cancer, detailing their mechanisms and ongoing clinical trials targeting various receptors like EGFR and HER-2.

Article Abstract

Gastric cancer (GC) is a prevalent malignant tumor of the digestive system worldwide, ranking among the top five in terms of incidence and mortality. However, the clinical efficacy of conventional treatments for gastric cancer remains limited, with a median overall survival of approximately eight months for advanced cases. In recent years, researchers have increasingly focused on antibody-drug conjugates (ADCs) as a promising approach. ADCs are potent chemical drugs that selectively target cancer cells by binding to specific cell surface receptors with antibodies. Notably, ADCs have demonstrated promising results in clinical studies and have made significant strides in the treatment of gastric cancer. Currently, several ADCs are under investigation in clinical trials for gastric cancer patients, targeting various receptors such as EGFR, HER-2, HER-3, CLDN18.2, Mucin 1, among others. This review offers a comprehensive exploration of ADC drug characteristics and provides an overview of the research progress in ADC-based therapies for gastric cancer.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10250015PMC
http://dx.doi.org/10.3389/fonc.2023.1211947DOI Listing

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