Evolving therapies in advanced oesophago-gastric cancers and the increasing role of immunotherapy

被引:6
作者
Attia, Hossameldin [1 ]
Smyth, Elizabeth [1 ]
机构
[1] Cambridge Univ Hosp NHS Fdn Trust, Addenbrookes Hosp, Hills Rd, Cambridge CB2 0QQ, England
关键词
Gastroesophageal cancer; esophagogastric cancer; gastric cancer; esophageal cancer; immunotherapy; review; anti-PD-1; cytotoxic chemotherapy; novel agents; ADVANCED GASTRIC-CANCER; ADVANCED ESOPHAGEAL CANCER; MULTICENTER PHASE-II; OPEN-LABEL; 1ST-LINE THERAPY; PERIOPERATIVE CHEMOTHERAPY; COMBINATION CHEMOTHERAPY; PLUS CHEMOTHERAPY; 2ND-LINE THERAPY; ELDERLY-PATIENTS;
D O I
10.1080/14737140.2021.1866548
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Esophagogastric cancers remain a considerable health burden and among the top causes of global cancer-related deaths. Chemotherapy remains the cornerstone of treatment for patients with advanced disease. Doublet platinum/fluoropyrimidine therapy is established as first-line treatment with the option of adding a taxane in selected patients. Irinotecan, taxanes, and ramucirumab are approved as second-line treatments. Results from the trials KEYNOTE-059, ATTRACTION-2, and TAGS have established the use of immune checkpoint inhibitors and trifluridine/tipiracil as a third-line treatment. High PD-L1 expression, microsatellite instability, tumor mutational burden, and Epstein-Barr virus status may also be used to enrich for responses to immunotherapy. Areas covered: In this review, we discuss the outcome of recent trials in the later lines of therapy for esophagogastric cancer and place these in the context of current treatment paradigms. We also discuss the biology of esophagogastric cancers and how this might inform the development of new treatments. Finally, we comment on promising new drugs in development. Expert opinion: Recent advances in the treatment of chemo-refractory esophagogastric cancer add to the improving survival of patients with this disease. Further research is needed to improve patient selection to therapies and the earlier incorporation of these agents in the treatment journey.
引用
收藏
页码:535 / 546
页数:12
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