Zolbetuximab: a potential breakthrough in the treatment landscape of gastric cancer.

Future Oncol

International Department, Gustave Roussy Cancer Campus, Villejuif, 94800, France.

Published: January 2024

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http://dx.doi.org/10.2217/fon-2023-0523DOI Listing

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Article Synopsis
  • Zolbetuximab is a chimeric monoclonal antibody designed to target the Claudin 18.2 protein, which is overexpressed in certain gastrointestinal cancers, notably gastric and gastroesophageal junction adenocarcinomas.
  • This drug initiates an immune response to attack cancer cells when combined with standard chemotherapy regimens, and it has been approved as a first-line treatment for advanced, unresectable cancers in specific patient populations.
  • Clinical trials show that zolbetuximab significantly improves progression-free survival and overall survival rates compared to chemotherapy alone, while maintaining a relatively safe profile for patients.
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The immunohistochemical expression of various members of the claudin family has already been studied in pathological affections of the vulva whether to differentiate precancerous lesions from vulvar squamous cell carcinoma or in inflammatory conditions such as lichen sclerosus. From an oncological perspective, however, immunohistochemical analysis of claudin 18.2 protein expression has become increasingly clinically relevant nowadays since the impressive therapeutic benefits of the claudin 18.

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Emerging targets in gastric and pancreatic cancer: Focus on claudin 18.2.

Cancer Lett

December 2024

Department of Medicine, Division of Hematology & Oncology, University of Pittsburgh Medical Center (UPMC), Pittsburgh, PA, 15213, USA; UPMC Hillman Cancer Center, Pittsburgh, PA, 15213, USA. Electronic address:

Recently, the molecular landscape of gastric and pancreatic cancers has advanced with Claudin 18.2 (CLDN18.2) emerging as a promising therapeutic target.

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Article Synopsis
  • * A cost-effectiveness analysis using a 10-year Markov model found that in the U.S., the combination treatment resulted in an incremental cost-effectiveness ratio (ICER) of $821,515.65 per quality-adjusted life-year (QALY) gained, while in China the ICER was $273,568.01/QALY gained.
  • * The treatment was determined not to be cost-effective according to common willingness-to-pay thresholds, suggesting that the
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Expression of claudin 18.2 in poorly cohesive carcinoma and its association with clinicopathologic parameters in East Asian patients.

Pathol Res Pract

November 2024

Department of Oncology/Hematology, Kyungpook National University Chilgok Hospital, School of Medicine, Kyungpook National University, Kyungpook National University Cancer Research Institute, Daegu, Republic of Korea. Electronic address:

Background: Poorly cohesive carcinoma (PCC) is a distinct subtype of gastric cancer with limited therapeutic options. This study investigated claudin (CLDN) 18.2 expression status in PCCs using a 43-13 A clone.

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