Clinical Oncology Unit, Careggi University Hospital, 50134 Florence, Italy.
Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Int J Mol Sci. 2023 Mar 2;24(5):4877. doi: 10.3390/ijms24054877.
Resectable gastric or gastroesophageal (G/GEJ) cancer is a heterogeneous disease with no defined molecularly based treatment strategy. Unfortunately, nearly half of patients experience disease recurrence despite standard treatments (neoadjuvant and/or adjuvant chemotherapy/chemoradiotherapy and surgery). In this review, we summarize the evidence of potential tailored approaches in perioperative treatment of G/GEJ cancer, with a special focus on patients with human epidermal growth factor receptor-2(HER2)-positive and microsatellite instability-high (MSI-H) tumors. In patients with resectable MSI-H G/GEJ adenocarcinoma, the ongoing INFINITY trial introduces the concept of non-operative management for patients with complete clinical-pathological-molecular response, and this could be a novel and potential practice changing strategy. Other pathways involving vascular endothelial growth factor receptor (VEGFR), fibroblast growth factor receptor (FGFR), claudin18 isoform 2 (CLDN18.2), and DNA damage repair proteins are also described, with limited evidence until now. Although tailored therapy appears to be a promising strategy for resectable G/GEJ cancer, there are several methodological issues to address: inadequate sample size for pivotal trials, underestimation of subgroup effects, and choice of primary endpoint (tumor-centered vs. patient-centered endpoints). A better optimization of G/GEJ cancer treatment allows maximizing patient outcomes. In the perioperative phase, although caution is mandatory, times are changing and tailored strategies could introduce new treatment concepts. Overall, MSI-H G/GEJ cancer patients possess the characteristics to be the subgroup that could receive the most benefit from a tailored approach.
可切除的胃或胃食管交界处(G/GEJ)癌症是一种异质性疾病,目前没有基于分子的标准治疗策略。不幸的是,尽管采用了标准治疗(新辅助和/或辅助化疗/放化疗和手术),近一半的患者仍会出现疾病复发。在这篇综述中,我们总结了 G/GEJ 癌症围手术期治疗中潜在的个体化方法的证据,特别关注人表皮生长因子受体 2(HER2)阳性和微卫星不稳定高(MSI-H)肿瘤患者。对于可切除的 MSI-H G/GEJ 腺癌患者,正在进行的 INFINITY 试验提出了对完全临床-病理-分子反应患者非手术管理的概念,这可能是一种新颖且有潜力改变实践的策略。其他涉及血管内皮生长因子受体(VEGFR)、成纤维细胞生长因子受体(FGFR)、claudin18 同工型 2(CLDN18.2)和 DNA 损伤修复蛋白的途径也有描述,但迄今为止证据有限。尽管个体化治疗似乎是可切除 G/GEJ 癌症的有前途的策略,但仍存在几个方法学问题需要解决:关键试验的样本量不足、亚组效应低估以及选择主要终点(肿瘤中心与患者中心终点)。更好地优化 G/GEJ 癌症治疗可以最大限度地提高患者的治疗效果。在围手术期,尽管必须谨慎,但时代正在发生变化,个体化策略可能会引入新的治疗概念。总体而言,MSI-H G/GEJ 癌症患者具有接受个体化方法最获益的亚组特征。