Abstract

An early molecular response is spectacularly predictive of outcome in chronic myeloid leukemia (CML) and early response landmarks may identify the high-risk patients likely to be benefit from an early therapy switch. In this study, we evaluated the most relevant cutoffs for early molecular response markers (BCR-ABL1 values at 3 months, log reduction and halving time between diagnosis and 3 months) in 476 first-line imatinib-treated Chinese patients with chronic phase CML. All outcomes were significantly superior for the 324 patients with 3-month BCR-ABL1 ≤10%, so did for the 270 patients with BCR-ABL1 >0.61 log reduction. BCR-ABL1 halving time ≤22 days was identified for patients with the most favorable outcome. Moreover, the prognosis was significantly poorest for patients with both halving time >44 days and BCR-ABL1 >10%. Importantly, multivariate regression analysis demonstrated that a BCR-ABL1 log reduction calculated at 3 months of 0.61 was the only variable that significantly predicted for OS. Our results highlight the importance of rapid initial decline of BCR-ABL1 in predicting satisfactory outcome. Our data support the evidence that monitoring BCR-ABL1 values at an early time point could contribute to accurately assess response and ultimately guide clinical decisions regarding the timing of therapeutic intervention.

Highlights

  • Prognosis of patients with chronic myeloid leukemia (CML) has been dramatically improved with the introduction of imatinib as the first tyrosine kinase inhibitor (TKI)[1]

  • The mean daily doses (MDDs) of imatinib led to differences in the percentage of patients with ≤10% BCR-ABL1 at 3 months

  • No MDDs cutoff could be identified that allowed a discrimination concerning overall survival (OS), progression-free survival (PFS), event-free survival (EFS), or PFS, as well as no statistical difference in outcome was found among the dose groups (Table 2)

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Summary

Introduction

Prognosis of patients with chronic myeloid leukemia (CML) has been dramatically improved with the introduction of imatinib as the first tyrosine kinase inhibitor (TKI)[1]. BCR-ABL1 transcript level ≤10% on the international reporting scale (IS) at 3 months is consistently associated with significantly superior overall survival (OS), progression-free survival (PFS), event-free survival (EFS), failure-free survival (FFS), as well as cytogenetic and molecular responses[6,7]. This molecular milestone value was incorporated into the National Comprehensive Cancer Network (NCCN) and European Leukemia Net (ELN) recommendations for the management of CML8.

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