| Literature DB >> 26946301 |
Cecilia C S Yeung1, Daniel Egan2, Jerald Radich2.
Abstract
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.Entities:
Keywords: BCR-ABL1 transcript levels molecular diagnostics; Chronic myeloid leukemia; Monitoring
Mesh:
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Year: 2016 PMID: 26946301 DOI: 10.1007/s11899-016-0303-8
Source DB: PubMed Journal: Curr Hematol Malig Rep ISSN: 1558-8211 Impact factor: 3.952