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.
| Original language | English |
|---|---|
| Pages (from-to) | 249-261 |
| Number of pages | 13 |
| Journal | American Society of Clinical Oncology educational book / ASCO. American Society of Clinical Oncology. Meeting |
| Issue number | 38 |
| DOIs | |
| Publication status | Published - 2018 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Biomarkers
- Biomarkers, Tumor
- Esophageal Neoplasms/diagnosis
- Humans
- Microsatellite Instability
- Microsatellite Repeats
- Mutation
- Stomach Neoplasms/diagnosis
- Treatment Outcome
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