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胃癌的当前治疗方法和最新进展。

Current treatment and recent progress in gastric cancer.

机构信息

Gastrointestinal Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

出版信息

CA Cancer J Clin. 2021 May;71(3):264-279. doi: 10.3322/caac.21657. Epub 2021 Feb 16.

Abstract

Gastric cancer is not a top-10 malignancy in the United States but represents one of the most common causes of cancer death worldwide. Biological differences between tumors from Eastern and Western countries add to the complexity of identifying standard-of-care therapy based on international trials. Systemic chemotherapy, radiotherapy, surgery, immunotherapy, and targeted therapy all have proven efficacy in gastric adenocarcinoma; therefore, multidisciplinary treatment is paramount to treatment selection. Triplet chemotherapy for resectable gastric cancer is now accepted and could represent a plateau of standard cytotoxic chemotherapy for localized disease. Classification of gastric cancer based on molecular subtypes is providing an opportunity for personalized therapy. Biomarkers, in particular microsatellite instability (MSI), programmed cell death ligand 1 (PD-L1), human epidermal growth factor receptor 2 (HER2), tumor mutation burden, and Epstein-Barr virus, are increasingly driving systemic therapy approaches and allowing for the identification of populations most likely to benefit from immunotherapy and targeted therapy. Significant research opportunities remain for the less differentiated histologic subtypes of gastric adenocarcinoma and those without markers of immunotherapy activity.

摘要

在美国,胃癌不是十大恶性肿瘤之一,但它是全球癌症死亡的最常见原因之一。来自东方和西方国家的肿瘤的生物学差异增加了根据国际试验确定标准治疗的复杂性。全身化疗、放疗、手术、免疫疗法和靶向疗法都已被证明对胃腺癌有效;因此,多学科治疗对于治疗选择至关重要。可切除胃癌的三联化疗现在被接受,并且可能代表局部疾病标准细胞毒性化疗的一个平台。基于分子亚型的胃癌分类为个性化治疗提供了机会。生物标志物,特别是微卫星不稳定性(MSI)、程序性细胞死亡配体 1(PD-L1)、人表皮生长因子受体 2(HER2)、肿瘤突变负担和 Epstein-Barr 病毒,正在越来越多地推动系统治疗方法,并确定最有可能从免疫疗法和靶向疗法中获益的人群。对于胃腺癌的分化程度较低的组织学亚型和那些没有免疫疗法活性标志物的亚型,仍有很大的研究机会。

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