TY - JOUR
T1 - What Will We Expect From Novel Therapies to Esophageal and Gastric Malignancies?
AU - De Mello, Ramon Andrade
AU - Castelo-Branco, Luis
AU - Castelo-Branco, Pedro
AU - Pozza, Daniel Humberto
AU - Vermeulen, Louis
AU - Palacio, Sofia
AU - Salzberg, Matthew
AU - Lockhart, A Craig
PY - 2018
Y1 - 2018
N2 - 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.
AB - 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.
KW - Biomarkers
KW - Biomarkers, Tumor
KW - Esophageal Neoplasms/diagnosis
KW - Humans
KW - Microsatellite Instability
KW - Microsatellite Repeats
KW - Mutation
KW - Stomach Neoplasms/diagnosis
KW - Treatment Outcome
U2 - https://doi.org/10.1200/EDBK_198805
DO - https://doi.org/10.1200/EDBK_198805
M3 - Review article
C2 - 30231398
SN - 1548-8756
SP - 249
EP - 261
JO - American Society of Clinical Oncology educational book / ASCO. American Society of Clinical Oncology. Meeting
JF - American Society of Clinical Oncology educational book / ASCO. American Society of Clinical Oncology. Meeting
IS - 38
ER -