Jones R P, Brudvik K W, Franklin J M, Poston G J
North Western Hepatobiliary Unit, Aintree University Hospital, Liverpool, UK; School of Cancer Studies, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
Department of Hepato-Pancreato-Biliary Surgery, Oslo University Hospital, Oslo, Norway.
Eur J Surg Oncol. 2017 May;43(5):875-883. doi: 10.1016/j.ejso.2017.02.014. Epub 2017 Mar 6.
Precision surgery involves improving patient selection to ensure that surgical intervention that is proven to benefit on a population level is the optimal treatment for each individual patient. For patients with colorectal liver metastases (CRLM), existing prognostic scoring systems rely on well-recognised histopathological features such as size and number of lesions. Advances in preoperative imaging algorithms mean that increasingly low volume disease can be detected, improving assessment of these factors. In addition, novel imaging modalities mean that underlying tumour biology and metabolic behaviour during therapy can be assessed. Molecular analysis of tumours can provide crucial prognostic information, with the critical role of RAS/RAF mutations in prognosis well recognised. The optimal source of tissue for this level of analysis is debated, with good concordance between primary and metastatic lesions for some recognised prognostic factors but marked discrepancies for a variety of other relevant mutations. As well as mutational heterogeneity between primary and metastatic lesions, heterogeneity within tumours and dynamic changes in tumour biology over time present a significant challenge in assessing tumour for prognostic biomarkers. Circulating tumour cells offer one potential method of longitudinal tumour analysis, but are limited by current technologies. This review article summarises some of the key advances in prognostication for patients with resectable colorectal liver metastases, as well as highlighting the potential limitations of such an approach.
精准手术包括优化患者选择,以确保在群体层面上被证明有益的手术干预是每个患者的最佳治疗方法。对于结直肠癌肝转移(CRLM)患者,现有的预后评分系统依赖于诸如病灶大小和数量等公认的组织病理学特征。术前成像算法的进步意味着越来越少的病灶能够被检测到,从而改善了对这些因素的评估。此外,新型成像方式意味着可以评估治疗期间潜在的肿瘤生物学和代谢行为。肿瘤的分子分析可以提供关键的预后信息,RAS/RAF突变在预后中的关键作用已得到充分认识。对于这种水平的分析,最佳的组织来源存在争议,一些公认的预后因素在原发灶和转移灶之间具有良好的一致性,但对于各种其他相关突变则存在明显差异。除了原发灶和转移灶之间的突变异质性外,肿瘤内部的异质性以及肿瘤生物学随时间的动态变化在评估肿瘤预后生物标志物时构成了重大挑战。循环肿瘤细胞提供了一种纵向肿瘤分析的潜在方法,但受当前技术限制。这篇综述文章总结了可切除结直肠癌肝转移患者预后评估的一些关键进展,并强调了这种方法的潜在局限性。