Yeung Cecilia C S, Egan Daniel, Radich Jerald
Clinical Research Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave North, G7-910, Seattle, WA, 98109, USA.
Curr Hematol Malig Rep. 2016 Apr;11(2):94-101. doi: 10.1007/s11899-016-0303-8.
In chronic myeloid leukemia (CML), the BCR-ABL fusion gene is both the therapeutic target of tyrosine kinase inhibitors and the indisputable direct marker of disease burden. Thus, sensitive assays for BCR-ABL now drive therapeutic options and are good surrogates for short- and long-term outcomes. Because CML is such an ideal model, new methods are arising that should make testing in CML faster, more reliable, and reach a greater sensitivity. These methods should be able to be transferred to other hematological malignancies that have mutation markers.
在慢性粒细胞白血病(CML)中,BCR-ABL融合基因既是酪氨酸激酶抑制剂的治疗靶点,也是无可争议的疾病负担直接标志物。因此,目前针对BCR-ABL的灵敏检测方法决定了治疗方案的选择,并且是短期和长期治疗结果的良好替代指标。由于CML是一个如此理想的模型,新的检测方法不断涌现,有望使CML检测更快、更可靠,且灵敏度更高。这些方法应能够应用于其他具有突变标志物的血液系统恶性肿瘤。