Abstract | INTRODUCTION:
Gastric cancer (GC) and gastroesophageal junction cancer (GOJC) patients have a poor prognosis with a 5-year relative survival rate of 6% in the metastatic setting. Despite the well-characterized molecular features, patients have been historically considered for treatment with universal and undistinguishing chemotherapies and targeted agents, except for the HER2-positive population and some immunological approaches. AREAS COVERED: In this review, we discuss the intrinsic characteristics of GC/GOJC from an epidemiological, molecular, and clinical perspective with an exhaustive evaluation of the reported and ongoing phase II/III clinical trials with targeted therapies. EXPERT OPINION: The absence of robust biomarkers, the difficulties in measuring it due to the well-recognized molecular heterogeneity, and in part nonoptimistic clinical trial designs have been a major cause of frequent failure. Current efforts should focus on proper recognition of the distinctive molecular and clinical features of each GC/GOJC patient. Sequencing both tumor tissue DNA and ctDNA could identify targetable alterations, including rare alterations, thus allowing GC/GOJC patients for a precision medicine benefit.
|
Authors | Maria Alsina, Marc Diez, Josep Tabernero |
Journal | Expert opinion on emerging drugs
(Expert Opin Emerg Drugs)
Vol. 26
Issue 4
Pg. 385-400
(12 2021)
ISSN: 1744-7623 [Electronic] England |
PMID | 34814781
(Publication Type: Journal Article, Review)
|
Chemical References |
|
Topics |
- Adenocarcinoma
(drug therapy)
- Biological Products
- Esophageal Neoplasms
(drug therapy)
- Esophagogastric Junction
- Humans
- Stomach Neoplasms
(drug therapy)
|