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Recent updates of therapeutic strategy of esophagogastric junction adenocarcinoma

作     者:Suguru Maruyama Yu Imamura Yasukazu Kanie Kei Sakamoto Daisuke Fujiwara Akihiko Okamura JunKanamori Masayuki Watanabe Suguru Maruyama;Yu Imamura;Yasukazu Kanie;Kei Sakamoto;Daisuke Fujiwara;Akihiko Okamura;Jun Kanamori;Masayuki Watanabe

作者机构:Department of Gastroenterological SurgeryCancer Institute Hospital of Japanese Foundation of Cancer ResearchTokyo 135-8550Japan. 

出 版 物:《Journal of Cancer Metastasis and Treatment》 (癌症转移与治疗(英文版))

年 卷 期:2021年第7卷第1期

页      面:727-736页

学科分类:1002[医学-临床医学] 100214[医学-肿瘤学] 10[医学] 

基  金:  (20K09046) 

主  题:Esophagogastric junction adenocarcinoma Barrett’s esophagus microsatellite instability molecular subtype 

摘      要:The incidence of esophagogastric junction(EGJ)adenocarcinoma has been increasing in Asian *** the recent advances in multidisciplinary treatments,EGJ adenocarcinoma remains aggressive with unfavorable *** surgical strategy,EGJ adenocarcinoma arises between the esophagus and the stomach,and thus tumor cells spread through the lymphatic system both upward to the mediastinum and downward to the ***,an optimal extent of lymphadenectomy remains *** drug therapy,the latest topic in gastric and EGJ adenocarcinoma is trastuzumab deruxtecan,which is an antibody-drug conjugate consisting of an anti-HER2 *** addition,many clinical trials have recently demonstrated the efficacy of immune checkpoint ***,recent advances in sequencing technology have revealed that gastroesophageal adenocarcinoma could be categorized into four molecular subtypes:epstein-Barr virus-associated,high-level microsatellite instability,genomically stable,and chromosomal instability ***,these subtypes show distinct clinical phenotypes and molecular *** review the current surgical strategy and drug treatment such as molecular-targeted agents,immune checkpoint inhibitors,and molecular-subtype-based therapeutic strategies in EGJ *** and molecular characteristics and response to immune checkpoint inhibitors differ among molecular *** strategies based on molecular subtypes may be clinically beneficial for patients with EGJ adenocarcinoma.

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