What Will We Expect From Novel Therapies to Esophageal and Gastric Malignancies?

Ramon Andrade De Mello, Luis Castelo-Branco, Pedro Castelo-Branco, Daniel Humberto Pozza, Louis Vermeulen, Sofia Palacio, Matthew Salzberg, A Craig Lockhart

Research output: Contribution to journalReview articleAcademicpeer-review

2 Citations (Scopus)

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 languageEnglish
Pages (from-to)249-261
Number of pages13
JournalAmerican Society of Clinical Oncology educational book / ASCO. American Society of Clinical Oncology. Meeting
Issue number38
DOIs
Publication statusPublished - 2018

Keywords

  • Biomarkers
  • Biomarkers, Tumor
  • Esophageal Neoplasms/diagnosis
  • Humans
  • Microsatellite Instability
  • Microsatellite Repeats
  • Mutation
  • Stomach Neoplasms/diagnosis
  • Treatment Outcome

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