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How I treat CML blast crisis

Journal

BLOOD
Volume 120, Issue 4, Pages 737-747

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2012-03-380147

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Funding

  1. German CML Study Group
  2. Deutsche Krebshilfe [106642]
  3. Novartis Germany
  4. Kompetenznetz fur Akute and Chronische Leukamien [BMBF 01GI0270]
  5. Jose-Carreras Leukamiestiftung (DJCLS) [H09/01f, H06/04v, H03/01]
  6. European Commission [LSHC-CT-2004-503216]
  7. Roche and Essex

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Blast crisis (BC) remains the major challenge in the management of chronic myeloid leukemia (CML). It is now generally accepted that BC is the consequence of continued BCR-ABL activity leading to genetic instability, DNA damage, and impaired DNA repair. Most patients with BC carry multiple mutations, and up to 80% show additional chromosomal aberrations in a nonrandom pattern. Treatment with tyrosine kinase inhibitors has improved survival in BC modestly, but most long-term survivors are those who have been transplanted. Patients in BC should be treated with a tyrosine kinase inhibitor according to mutation profile, with or without chemotherapy, with the goal of achieving a second chronic phase and proceeding to allogeneic stem cell transplantation as quickly as possible. Although long-term remissions are rare, allogeneic stem cell transplantation provides the best chance of a cure in BC. Investigational agents are not likely to provide an alternative in the near future. In view of these limited options, prevention of BC by a rigorous and early elimination of BCR-ABL is recommended. Early response indicators should be used to select patients for alternative therapies and early transplantation. Every attempt should be made to reduce or eliminate BCR-ABL consistent with good patient care as far as possible. (Blood. 2012; 120(4):737-747)

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