Rapidly Evolving Treatment Landscape for Metastatic Esophagogastric Carcinoma: Review of Recent Data

被引:2
作者
Fonkoua, Lionel Aurelien Kankeu [1 ,2 ]
Yoon, Harry H. [1 ]
机构
[1] Mayo Clin, Dept Oncol, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Hematol, Rochester, MN 55905 USA
来源
ONCOTARGETS AND THERAPY | 2021年 / 14卷
关键词
esophagogastric cancer; gastric cancer; esophageal cancer; targeted therapy; immunotherapy; precision medicine; ADVANCED GASTRIC-CANCER; RANDOMIZED PHASE-III; NIVOLUMAB PLUS CHEMOTHERAPY; SQUAMOUS-CELL CARCINOMA; RECEPTOR; EXPRESSION; OPEN-LABEL; GASTROESOPHAGEAL JUNCTION; 1ST-LINE THERAPY; DOUBLE-BLIND; SINGLE-ARM;
D O I
10.2147/OTT.S216047
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Esophagogastric cancer (EGC) is a heterogeneous group of malignancies that collectively represent the 2nd leading cause of cancer deaths worldwide. While surgery in combination with chemotherapy and/or radiation therapy represents the primary curative treatment for early stage disease, survival outcomes for the majority of patients with later-stage disease remain poor. Cytotoxic chemotherapy with platinum doublets such as 5-FU/leucovorin/oxaliplatin is the mainstay of treatment with incremental benefits provided by targeted therapy (trastuzumab, trastuzumab deruxtecan, ramucirumab) and immunotherapy (pembrolizumab, nivolumab). In this article, we provide an updated review and perspectives on the management of advanced EGC. We examine the distinct epidemiological, etiological and molecular features of each disease entity comprising EGC. After reviewing the critical studies that established conventional systemic cytotoxic and targeted therapeutics, we elaborate on recent promising and complex data with immune checkpoint inhibition focusing on implications of tumor histology and PD-L1 expression in the tumor microenvironment. We also highlight novel diagnostic and therapeutic strategies to build on these recent advances.
引用
收藏
页码:4361 / 4381
页数:21
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