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Nicolini FE et al. – The BCR–ABL T315I mutation represents a major mechanism of resistance to tyrosine kinase inhibitors (TKIs). The objectives of this retrospective observational study were to estimate overall (OS) and progression–free survival (PFS) for CML in chronic (CP), accelerated (AP), or blastic (BP) phase, and Ph+ ALL patients with T315I mutation. The results confirm that survival of patients harboring a T315I mutation is dependent on disease phase at the time of mutation detection.


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