El Rami Fadi E, Barsoumian Hampartsoum B, Khneizer Gebran W
Department of Radiology, Stanford University School of Medicine, Stanford, CA, USA.
Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Ther Adv Med Oncol. 2020 Oct 31;12:1758835920967238. doi: 10.1177/1758835920967238. eCollection 2020.
Hereditary diffuse gastric cancer (HDGC) is a rare malignancy characterized by autosomal dominant inheritance of pathological variants of the gene encoding E-cadherin, which is involved in cell-cell adhesion, maintenance of epithelial architecture, tumor suppression, and regulation of intracellular signaling pathways. Late-stage recognition of HDGC is typically associated with a poor clinical outcome due to its metastatic potential and risk of lobular breast cancer (LBC) development. The American College of Gastroenterology issued guidelines to evaluate HDGC, test for genetic variants, and recommend prophylactic gastrectomy for carriers of mutations. If surgery is not pursued, endoscopy is a surveillance alternative, although it carries a limited ability to detect malignant foci. As part of clinical research efforts, novel endoscopy advances are currently studied, and a center of excellence for HDGC was created for a comprehensive multidisciplinary team approach. Within this review, we cover current conventional treatment modalities such as gastrectomy and chemotherapy, as the mainstay treatments, in addition to Pembrolizumab, an immune checkpoint inhibitor, as the last therapeutic resort. We also shed light on novel and promising approaches with emphasis on immunotherapy to treat HDGC. We further break down the therapeutic paradigms to utilize molecular tools, antibodies against checkpoint inhibitors, TGF-β and tyrosine kinase inhibitors, cell-based adoptive therapies, and oncolytic viral therapies. We aim to expand the understanding on how to modulate the tumor microenvironment to tip the balance towards an anti-tumor phenotype, prevent metastasis of the primary disease, and potentially alter the therapeutic landscape for HDGC.
遗传性弥漫性胃癌(HDGC)是一种罕见的恶性肿瘤,其特征为编码E-钙黏蛋白的基因的病理变异呈常染色体显性遗传,E-钙黏蛋白参与细胞间黏附、上皮结构维持、肿瘤抑制及细胞内信号通路调节。HDGC晚期确诊通常因具有转移潜能及发生小叶性乳腺癌(LBC)的风险而导致临床预后不良。美国胃肠病学会发布了评估HDGC、检测基因变异以及为突变携带者推荐预防性胃切除术的指南。如果不进行手术,内镜检查是一种监测替代方法,尽管其检测恶性病灶的能力有限。作为临床研究工作的一部分,目前正在研究新型内镜技术进展,并且成立了HDGC卓越中心,采用全面的多学科团队方法。在本综述中,我们涵盖了目前的传统治疗方式,如胃切除术和化疗作为主要治疗手段,以及作为最后治疗手段的免疫检查点抑制剂派姆单抗。我们还重点介绍了治疗HDGC的新颖且有前景的方法,尤其是免疫疗法。我们进一步剖析治疗模式,以利用分子工具、针对检查点抑制剂、转化生长因子-β和酪氨酸激酶抑制剂的抗体、基于细胞的过继性疗法以及溶瘤病毒疗法。我们旨在拓展对如何调节肿瘤微环境以促使平衡向抗肿瘤表型倾斜、预防原发性疾病转移以及潜在改变HDGC治疗格局的理解。