Conticchio Maria, Uldry Emilie, Hübner Martin, Digklia Antonia, Fraga Montserrat, Sempoux Christine, Raisaro Jean Louis, Fuks David
Faculty of Biology and Medicine, University of Lausanne, 1005 Lausanne, Switzerland.
Department of Visceral Surgery, Centre Hospitalier Universitaire Vaudois (CHUV), 1005 Lausanne, Switzerland.
Cancers (Basel). 2025 Jul 31;17(15):2539. doi: 10.3390/cancers17152539.
: Colorectal liver metastasis (CRLM) represents a major clinical challenge in oncology, affecting 25-50% of colorectal cancer patients and significantly impacting survival. While multimodal therapies-including surgical resection, systemic chemotherapy, and local ablative techniques-have improved outcomes, prognosis remains heterogeneous due to variations in tumor biology, patient factors, and institutional practices. : This review synthesizes current evidence on prognostic factors influencing CRLM management, encompassing clinical (e.g., tumor burden, anatomic distribution, timing of metastases), biological (e.g., CEA levels, inflammatory markers), and molecular (e.g., RAS/BRAF mutations, MSI status, HER2 alterations) determinants. : Key findings highlight the critical role of molecular profiling in guiding therapeutic decisions, with RAS/BRAF mutations predicting resistance to anti-EGFR therapies and MSI-H status indicating potential responsiveness to immunotherapy. Emerging tools like circulating tumor DNA (ctDNA) and radiomics offer promise for dynamic risk stratification and early recurrence detection, while the gut microbiome is increasingly recognized as a modulator of treatment response. : Despite advancements, challenges persist in standardizing resectability criteria and integrating multidisciplinary approaches. Current guidelines (NCCN, ESMO, ASCO) emphasize personalized strategies but lack granularity in terms of incorporating novel biomarkers. This exhaustive review underscores the imperative for the development of a unified, biomarker-integrated framework to refine CRLM management and improve long-term outcomes.
结直肠癌肝转移(CRLM)是肿瘤学中的一项重大临床挑战,影响25%-50%的结直肠癌患者,并对生存率产生重大影响。虽然包括手术切除、全身化疗和局部消融技术在内的多模式疗法已改善了治疗结果,但由于肿瘤生物学、患者因素和机构实践的差异,预后仍然存在异质性。
本综述综合了当前关于影响CRLM管理的预后因素的证据,包括临床(如肿瘤负荷、解剖分布、转移时间)、生物学(如癌胚抗原水平、炎症标志物)和分子(如RAS/BRAF突变、微卫星不稳定性状态、人表皮生长因子受体2改变)决定因素。
主要发现强调了分子谱分析在指导治疗决策中的关键作用,RAS/BRAF突变预示着对抗表皮生长因子受体疗法的耐药性,而微卫星高度不稳定状态表明对免疫疗法可能有反应。循环肿瘤DNA(ctDNA)和放射组学等新兴工具为动态风险分层和早期复发检测带来了希望,同时肠道微生物群越来越被认为是治疗反应的调节因子。
尽管取得了进展,但在标准化可切除性标准和整合多学科方法方面仍存在挑战。当前的指南(美国国立综合癌症网络、欧洲肿瘤内科学会、美国临床肿瘤学会)强调个性化策略,但在纳入新型生物标志物方面缺乏详细说明。这项详尽的综述强调了开发一个统一的、整合生物标志物的框架以优化CRLM管理并改善长期结果的必要性。