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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

33 Downloads (Pure)

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

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    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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