Division of Hematology/Oncology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina
Department of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas
J Natl Compr Canc Netw. 2017 Mar;15(3):411-419. doi: 10.6004/jnccn.2017.0038.
Although clinical management of colon cancer generally has not accounted for the primary tumor site, left-sided and right-sided colon cancers harbor different clinical and biologic characteristics. Right-sided colon cancers are more likely to have genome-wide hypermethylation via the CpG island methylator phenotype (CIMP), hypermutated state via microsatellite instability, and mutation. There are also differential exposures to potential carcinogenic toxins and microbiota in the right and left colon. Gene expression analyses further shed light on distinct biologic subtypes of colorectal cancers (CRCs), with 4 consensus molecular subtypes (CMSs) identified. Importantly, these subtypes are differentially distributed between right- and left-sided CRCs, with greater proportions of the "microsatellite unstable/immune" CMS1 and the "metabolic" CMS3 subtypes found in right-sided colon cancers. This review summarizes important biologic distinctions between right- and left-sided CRCs that likely impact prognosis and may predict for differential responses to biologic therapy. Given the inferior prognosis of stage III-IV right-sided CRCs and emerging data suggesting that anti-epidermal growth factor receptor antibody therapy is associated with worse survival in right-sided stage IV CRCs compared with left-sided cancers, these biologic differences between right- and left-sided CRCs provide critical context and may provide opportunities to personalize therapy.
虽然结肠癌的临床治疗一般不考虑原发肿瘤部位,但左、右半结肠癌具有不同的临床和生物学特征。右半结肠癌更有可能通过 CpG 岛甲基化表型(CIMP)发生全基因组超甲基化、通过微卫星不稳定发生高突变状态和突变。右半结肠和左半结肠也存在潜在致癌毒素和微生物群的差异暴露。基因表达分析进一步揭示了结直肠癌(CRC)的不同生物学亚型,确定了 4 种共识分子亚型(CMS)。重要的是,这些亚型在右半和左半 CRC 之间存在差异分布,在右半结肠癌中发现更多的“微卫星不稳定/免疫”CMS1 和“代谢”CMS3 亚型。这篇综述总结了右半和左半 CRC 之间重要的生物学差异,这些差异可能影响预后,并可能预测对生物治疗的不同反应。鉴于 III-IV 期右半结肠癌的预后较差,以及新兴数据表明,与左半结肠癌相比,抗表皮生长因子受体抗体治疗与右半结肠癌 IV 期的生存预后更差,这些右半和左半 CRC 之间的生物学差异提供了重要的背景,并可能为个体化治疗提供机会。