Allison Kimberly H, Sledge George W
Oncology (Williston Park). 2014 Sep;28(9):772-8.
Cancer heterogeneity, long recognized as an important clinical determinant of patient outcomes, was poorly understood at a molecular level. Genomic studies have significantly improved our understanding of heterogeneity, and have pointed to ways in which heterogeneity might be understood and defeated for therapeutic effect. Recent studies have evaluated intratumoral heterogeneity within the primary tumor, as well as heterogeneity observed between primary and metastasis. The existence of clonal heterogeneity in the primary and metastasis also affects response to therapy, since the Darwinian pressures of systemic therapy result in clonal selection for initially rare variants. Novel technologies (such as measurements of circulating tumor cells and circulating tumor DNA) may allow physicians to monitor the emergence of clonal subtypes and intervene at an early point to improve patient prognosis.
癌症异质性长期以来一直被认为是患者预后的重要临床决定因素,但在分子水平上却知之甚少。基因组研究显著增进了我们对异质性的理解,并指出了理解和克服异质性以实现治疗效果的方法。最近的研究评估了原发性肿瘤内的肿瘤内异质性,以及原发性肿瘤与转移灶之间观察到的异质性。原发性肿瘤和转移灶中克隆异质性的存在也会影响对治疗的反应,因为全身治疗的达尔文选择压力会导致对最初罕见变体的克隆选择。新技术(如循环肿瘤细胞和循环肿瘤DNA的检测)可能使医生能够监测克隆亚型的出现,并在早期进行干预以改善患者预后。