Korpan Martin, Puhr Hannah Christina, Berger Julia M, Friedrich Alexander, Prager Gerald W, Preusser Matthias, Ilhan-Mutlu Aysegül
Division of Oncology, Department of Medicine I, Medical University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria.
Christian Doppler Laboratory for Personalized Immunotherapy, Department of Medicine I, Medical University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria.
Cancers (Basel). 2025 Jan 21;17(3):340. doi: 10.3390/cancers17030340.
The treatment of metastasized gastroesophageal adenocarcinoma largely depends on molecular profiling based on immunohistochemical procedures. Therefore, the examination of HER2, PD-L1, and dMMR/MSI is recommended by the majority of clinical practice guidelines, as positive expression leads to different treatment approaches. Data from large phase-III trials and consequent approvals in various countries enable physicians to offer their patients several therapy options including immunotherapy, targeted therapy, or both combined with chemotherapy. The introduction of novel therapeutic targets such as CLDN18.2 leads to a more complex decision-making process as a significant number of patients show positive results for the co-expression of other biomarkers besides CLDN18.2. The aim of this review is to summarize the current biomarker landscape of patients with metastatic gastroesophageal tumors, its direct clinical impact on daily decision-making, and to evaluate current findings on biomarker co-expression. Furthermore, possible treatment strategies with multiple biomarker expression are discussed.
转移性胃食管腺癌的治疗在很大程度上依赖于基于免疫组织化学方法的分子谱分析。因此,大多数临床实践指南都建议检测HER2、PD-L1和错配修复缺陷/微卫星高度不稳定(dMMR/MSI),因为阳性表达会导致不同的治疗方法。来自大型III期试验的数据以及随后在各个国家的获批,使医生能够为患者提供多种治疗选择,包括免疫治疗、靶向治疗或两者与化疗联合使用。新型治疗靶点如紧密连接蛋白18.2(CLDN18.2)的出现,导致决策过程更加复杂,因为大量患者除CLDN18.2外,其他生物标志物共表达也呈阳性。本综述的目的是总结转移性胃食管肿瘤患者目前的生物标志物情况、其对日常决策的直接临床影响,并评估生物标志物共表达的当前研究结果。此外,还讨论了具有多种生物标志物表达的可能治疗策略。