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Review
. 2024 Jan;48(1):102245.
doi: 10.1016/j.clinre.2023.102245. Epub 2023 Nov 11.

New developments and standard of care in the management of advanced gastric cancer

Affiliations
Review

New developments and standard of care in the management of advanced gastric cancer

Léonard Depotte et al. Clin Res Hepatol Gastroenterol. 2024 Jan.

Abstract

Advanced gastric adenocarcinoma is a common disease with a poor prognosis whose treatment has for decades been based on cytotoxic chemotherapy, including platinum salts in first-line, and taxane or irinotecan in second or later line. Recent years have seen the emergence of new drugs that have improved patient survival, such as trastuzumab in first-line for HER2-positive tumors, ramucirumab alone or in combination with paclitaxel in second-line, and trifluridine-tipiracil beyond the second-line treatment. More recently, two monoclonal antibodies have demonstrated their efficacy in combination with oxaliplatin-based first-line chemotherapy, nivolumab (anti-PD1) for PD-L1 CPS ≥5 tumors, and zolbetuximab for tumors overexpressing Claudin 18.2. In addition, regorafenib has been also showed effective in phase 3 trial for heavily pretreated patients. Based on phase 2 studies, trastuzumab-deruxtecan was approved in 2022 by the EMA for HER2-positive pretreated patients. This agent is currently evaluated in phase 3 study (DESTINY-Gastric04 trial), as are several other anti-HER2 (zanidatamab, margetuximab, tucatinib), immune checkpoint inhibitors, or targeted therapies (anti-FGFR2b).

Keywords: Drug combination; Immunotherapy; Molecular targeted therapy; Ramucirumab; Stomach neoplasms; Trastuzumab Deruxtecan; Trifluridine tipiracil.

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Conflict of interest statement

Declaration of Competing Interest Léonard Depotte certifies that all conflicts of interest, including specific financial interests and relationships and affiliations relevant to the subject matter or materials discussed in the manuscript (eg, employment/affiliation, grants or funding, consultancies, honoraria, stock ownership or options, expert testimony, royalties, or patents filed, received, or pending), are the following: none.

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