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1.
J Gastrointest Oncol ; 12(6): 3123-3132, 2021 Dec.
Article in English | MEDLINE | ID: mdl-35070435

ABSTRACT

Hepatoid adenocarcinoma of the stomach is an uncommon subtype of gastric cancer remarkably similar to hepatocellular carcinoma in histopathological analysis. It is also commonly associated with high serum alfa-fetoprotein and a poorer prognosis, despite the emergence of new therapeutic options. In recent years, next generation sequencing (NGS) technology has made it possible to identify and describe the genes and molecular alterations common to gastric cancer thereby contributing to the advancement of targeted therapies. A 62-year-old patient, with no prior risk factor for hepatocellular carcinoma (HCC), presented to the emergency room with dysphagia for solids, abdominal pain and weight loss of about 3 kilograms over 3 months. Histopathological analysis presented with disparities regarding HER2 and programmed death-ligand 1 (PD-L1) status in the primary and metastatic sites. We describe a case of a de novo metastatic, human epidermal growth factor receptor 2 (HER2) positive esophagogastric junction hepatoid adenocarcinoma. Although this is a rare subgroup of gastric cancer, treatment strategies were based in recent studies in immunotherapy and guided therapy, taking into consideration the molecular findings from the patient's tumor NGS analysis. Data about HER2 and PDL1 heterogeneity were also reviewed. Despite the aggressiveness and rarity of this histology, the patient had a good response to treatment.

2.
Future Oncol ; 12(6): 839-54, 2016 03.
Article in English | MEDLINE | ID: mdl-26838766

ABSTRACT

In this article, we review the literature on the current advances in targeted therapies for metastatic gastric cancer aimed at improving patient care. We conclude that the key to guiding targeted therapy is individual biomarkers, which are not completely elucidated. HER2 overexpression is the only predictive biomarker currently in use. Furthermore, it is necessary to understand that gastric tumors are heterogeneous; therefore, is impossible to evaluate a novel biological compound without evaluating personal biomarkers. The selection of patients who are able to receive each treatment is paramount for improving advanced gastric cancer survival and reducing unnecessary costs.


Subject(s)
Antineoplastic Agents/therapeutic use , Molecular Targeted Therapy , Stomach Neoplasms/drug therapy , Stomach Neoplasms/pathology , Angiogenesis Inhibitors/pharmacology , Angiogenesis Inhibitors/therapeutic use , Antineoplastic Agents/pharmacology , Clinical Trials as Topic , Drug Discovery , ErbB Receptors/antagonists & inhibitors , Humans , Neoplasm Metastasis , Patient Care , Protein Kinase Inhibitors/pharmacology , Protein Kinase Inhibitors/therapeutic use , Quality Improvement , Receptor, ErbB-2/antagonists & inhibitors , Stomach Neoplasms/metabolism , Stomach Neoplasms/mortality , Treatment Outcome
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