The Hidden Pathogenesis of CML: Is BCR-ABL1 the First Event?

Naranie Shanmuganathan, Susan Branford

Research output: Contribution to journalReview articlepeer-review

1 Citation (Scopus)


Purpose of Review: Identification of the BCR-ABL1 fusion oncogene in patients diagnosed with chronic myeloid leukemia (CML) led to the development of targeted therapy responsible for the dramatic survival benefits observed in the past two decades. However, despite these revolutionary findings, there remains marked disparity in patient outcomes. Why do some patients present de novo while others evolve to the more aggressive stages of CML? Why can select patients successfully discontinue therapy as part of a treatment-free remission attempt whereas others fail to meet specific molecular milestones? Recent Findings: BCR-ABL1 kinase mutations are only identified in approximately 50% of patients with poor responses and disease progression, suggesting the presence of alternative resistance mechanisms. Numerous institutions have identified the presence of additional genomic events in addition to BCR-ABL1 with the increasing availability of next-generation sequencing. Summary: We explore the potential pathways and events that may cooperate with BCR-ABL1 to answer these questions but also challenge the fundamental tenet that BCR-ABL1 is always the sole event initiating CML.

Original languageEnglish
Pages (from-to)501-506
Number of pages6
JournalCurrent Hematologic Malignancy Reports
Issue number6
Publication statusPublished - Dec 2019


  • Disease progression
  • Mutations
  • Next-generation sequencing
  • Resistance

ASJC Scopus subject areas

  • Hematology
  • Oncology
  • Cancer Research

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