| Literature DB >> 30231398 |
Ramon Andrade De Mello1, Luis Castelo-Branco1, Pedro Castelo-Branco1, Daniel Humberto Pozza1, Louis Vermeulen1, Sofia Palacio1, Matthew Salzberg1, A Craig Lockhart1.
Abstract
Esophageal cancer and gastric cancer are aggressive diseases for which treatment approaches are facing a new era. Some molecular pathways, such as VEGF, EGFR, fibroblast growth factor receptor, PIK3CA, and PARP-1, have been studied, and novel targeted drugs are presumed to be developed in the near future. From The Cancer Genome Atlas report, 80% of Epstein-Barr virus tumors and 42% of tumors with microsatellite instability have PIK3CA mutations, suggesting that this pathway could be reevaluated as a possible target for new systemic treatment of gastric cancer. Notably, higher PARP-1 expression can be found in gastric cancer, which might be related to more advanced disease and worse prognosis. In addition, PD-L1 expression, high microsatellite instability, and mismatch repair deficiency can be found in gastric cancer, thus suggesting that immunotherapy may also play a role in those patients. We discuss trends related to the potential of novel therapies for patients with esophageal and gastric cancers in the near future.Entities:
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Year: 2018 PMID: 30231398 DOI: 10.1200/EDBK_198805
Source DB: PubMed Journal: Am Soc Clin Oncol Educ Book ISSN: 1548-8748