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Haematological cancer

The rule of three in AML induction—is cladribine the answer?

In a randomized phase III trial of induction therapy in adult acute myeloid leukaemia, the addition of cladribine, but not fludarabine, to daunorubicin and cytarabine seemed to improve complete response rates and overall survival. However, serious methodological problems make it difficult to estimate the actual clinical importance of the result.

Key Points

  • Patients who receive standard induction chemotherapy for adult acute myeloid leukaemia should have a bone marrow biopsy performed 7–10 days after completion of chemotherapy to document hypoplasia

  • If residual leukaemia is present, additional treatment is recommended

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References

  1. Appelbaum, F. R. in Clinical Oncology 4th edn Ch. 104 (eds Abeloff, M. D. et al.) 2215–2234 (Elsevier, Philadelphia, USA, 2008).

    Google Scholar 

  2. Burnett, A. K. et al. Identification of patients with acute myeloblastic leukemia who benefit from the addition of gemtuzumab ozogamicin: results of the MRC AML15 trial. J. Clin. Oncol. 29, 369–377 (2011).

    Article  CAS  Google Scholar 

  3. Holowiecki, J. et al. Cladribine, but not fludarabine, added to daunorubicin and cytarabine during induction prolongs survival of patients with acute myeloid leukemia: a multicenter, randomized phase III study. J. Clin. Oncol. http://dx.doi.org/10.1200/JCO.2011.37.1286.

  4. Holowiecki, J. et al. Addition of cladribine to daunorubicin and cytarabine increases complete remission rate after a single course of induction treatment in acute myeloid leukemia. Multicenter, phase III study. Leukemia 18, 989–997 (2004).

    Article  CAS  Google Scholar 

  5. Fernandez, H. F. et al. Anthracycline dose intensification in acute myeloid leukemia. N. Engl. J. Med. 361, 1249–1259 (2009).

    Article  CAS  Google Scholar 

  6. Petersdorf, S. et al. Preliminary results of Southwest Oncology Group Study S0106: an international intergroup phase 3 randomized trial comparing the addition of gemtuzumab ozogamicin to standard induction therapy versus standard induction therapy followed by a second randomization to post-consolidation gemtuzumab ozogamicin versus no additional therapy for previously untreated acute myeloid leukemia [abstract]. Blood 114, a790 (2009).

    Google Scholar 

  7. Ohtake, S. et al. Randomized study of induction therapy comparing standard-dose idarubicin with high-dose daunorubicin in adult patients with previously untreated acute myeloid leukemia: the JALSG AML201 study. Blood 117, 2358–2365 (2011).

    Article  CAS  Google Scholar 

  8. O'Donnell, M. R. et al. Acute myeloid leukemia. J. Natl Compr. Canc. Netw. 9, 280–317 (2011).

    Article  CAS  Google Scholar 

  9. Luger, S. M. Is a nadir bone marrow required and, if so, what to do with residual disease? Best Pract. Res. Clin. Haematol. 24, 527–532 (2011).

    Article  Google Scholar 

  10. Gandhi, V. et al. Chlorodeoxyadenosine and arabinosylcytosine in patients with acute myelogenous leukemia: pharmacokinetic, pharmocodynamic, and molecular interactions. Blood 87, 256–264 (1996).

    CAS  PubMed  Google Scholar 

Download references

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Appelbaum, F. The rule of three in AML induction—is cladribine the answer?. Nat Rev Clin Oncol 9, 376–377 (2012). https://doi.org/10.1038/nrclinonc.2012.98

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