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TEST:
MRDx BCR-ABL Test

Company:
Icon plc
Type:
FDA Approved
Evidence Level:
Sensitive: B - Late Trials

[BCR-ABL1 fusion-Chronic Myeloid Leukemia-nilotinib]

Title:
Durable treatment-free remission in patients with chronic myeloid leukemia in chronic phase following frontline nilotinib: 96-week update of the ENESTfreedom study
Excerpt:
Patients consistently in MR4.5 during consolidation had higher TFR rates (50.6%) than patients with ≥ 1 assessment without MR4.5 during consolidation (35.0%). In a landmark analysis, 96-week TFR rates for patients with MR4.5, MR4 (BCR-ABL1IS ≤ 0.01%) but not MR4.5, and MMR but not MR4 at TFR week 12 were 82.6, 23.1, and 0%, respectively. There were no reports of disease progression or death due to CML; overall adverse event frequency decreased following TFR. Within the follow-up period, TFR did not adversely affect disease outcomes.
DOI:
10.1007/s00432-018-2604-x
Trial ID: