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Article — CML: the good, the better, and the difficult choices, by Dr. Jorge Cortes

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#1 ChrisC


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Posted 21 November 2012 - 12:30 PM


CML: the good, the better, and the difficult choices

Jorge Cortes

doi: 10.1182/blood-2012-09-452789

Blood November 8, 2012 vol. 120 no. 19 3866-3867

In this issue of Blood, Radich and colleagues from 4 cooperative groups report on the results of a randomized study of dasatinib versus imatinib as initial treatment for patients with chronic phase chronic myeloid leukemia (CML).1

This study is the sequel to a trial where they first compared imatinib standard-dose to imatinib high-dose. The results of the second portion of the study presented here show an improved outcome for patients receiving therapy with dasatinib compared with standard-dose imatinib. The rate of complete cytogenetic response was 84% with dasatinib and 69% with imatinib, and the rate of 3-log reduction of transcripts at 1 year was 59% versus 44%, respectively. With a median follow-up of 3 years, no differences in progression-free survival or relapse-free survival were identified, perhaps due to the small number of events in either arm.

These results confirm previous observations using second-generation tyrosine kinase inhibitors (TKIs; dasatinib, nilotinib or bosutinib) as initial therapy for chromic myeloid leukemia (CML).2?-4 The study by Radich et al has the merit of providing an independent confirmation of data obtained mostly through industry-sponsored studies. The results have been very reproducible: second-generation TKIs provide a higher rate of responses and responses occur earlier, with a trend toward a decreased rate of transformation to accelerated or blast phase. Other unfortunate conclusions are also shared. One of great concern is the high rate of early treatment discontinuation reported in all of these studies. The present study reports that 20% of patients treated with imatinib and 28% with dasatinib discontinued therapy within 12 months.1 Rates reported at approximately the same follow-up time from other trials are 19% to 21% for imatinib, 16% to 18% for nilotinib,2 16% for dasatinib,3 and 28% for bosutinib.4 With longer follow-up (2 years), rates have increased to 23% for dasatinib5 and 22% to 26% for nilotinib.6 These rates are surprising considering the improved efficacy and generally favorable toxicity profile of the new agents compared with imatinib. It is possible that the availability of a greater menu of treatment options is leading to a trend toward changing therapy too soon without full evaluation of efficacy or management of mild to moderate adverse events through therapeutic interventions and/or dose adjustments. It will be important, as these drugs are being used more frequently as initial therapy, that we use the agent of choice to its full potential and avoid quick transition from one drug to another for questionable indications.

A frequent question now is whether results such as the ones reported here mean that all patients should be treated with a second-generation TKI. Taken at face value, we should always aim in cancer treatment to use our best agent first to have the best chance of rendering our patient free of disease for the longest time, and cured if possible. Our first shot is always our best shot. Nonetheless, one cannot disregard some important facts: (1) most patients do well with imatinib, (2) most patients with resistance to imatinib are still in chronic phase and in generally good condition, and (3) many patients with resistance to imatinib respond to second-generation TKIs. If one adjusts for the sequential use of effective therapy, the current event-free survival is 88% at 7 years compared with the unadjusted rate of 81%.7 However, only 40% to 50% of patients with resistance to imatinib achieve a complete cytogenetic response with second-generation TKIs.8?-10 With growing awareness of the relevance of early responses, an argument can be made for using imatinib first and switch patients who are lagging behind early on. This is an attractive approach, but one without data that confirms that patients who fall behind on their response can catch up (in long-term outcome) after such intervention. Then there is the argument of what would we use if we start with a second-generation TKI and the patient develops resistance to it. This argument reminds me of a family anecdote when my father wanted to buy all the balloons from a balloon vendor for my infant brother many years ago. The balloon vendor would not sell them to my father because he would not have anything else to sell if he did. In cancer, using our best therapy first gives us the best long-term outcome, even if the patients who do not have an adequate response might be more difficult to treat. Despite all these arguments for and against, we have to be realistic that circumstances will exist that will mandate the use of one agent or the other, because of our medical expertise and interpretation of the data, or because of peripheral factors such as economics. Based on results such as the ones presented by Radich et al, second-generation TKI might give us the best outcome overall and would be preferred whenever possible. For patients for whom these options are not available or preferred, proper monitoring, suitable management of adverse events, and adequate dose optimization are of increasing relevance to offer each patient the opportunity for the best long-term outcome. With optimal management, our goal today ought to be that no patient should die of CML. And we should aim higher, to cure all patients with CML. If we are to accomplish this, continued research is needed and all patients should be included in clinical trials that help us understand the biology and optimal management of CML.


  • Conflict-of-interest disclosure: The author has received research support from and is a consultant for Novartis, Bristol-Myers Squibb, Pfizer, and Ariad.
  • © 2012 by The American Society of Hematology


1. Radich JP, Kopecky KJ, Appelbaum FR, et al. A randomized trial of dasatinib 100 mg versus imatinib 400 mg in newly diagnosed chronic-phase chromic myeloid leukemia. Blood 2012;120(19):3898-3905. Abstract/FREE Full Text

2. Saglio G, Kim DW, Issaragrisil S, et al. Nilotinib versus imatinib for newly diagnosed chronic myeloid leukemia. N Engl J Med 2010;362(24):2251-2259. CrossRefMedline

3. Kantarjian H, Shah NP, Hochhaus A, et al. Dasatinib versus imatinib in newly diagnosed chronic-phase chronic myeloid leukemia. N Engl J Med 2010;362(24):2260-2270. CrossRefMedline

4. Cortes J, Kim D, Kantarjian H, et al. Bosutinib versus imatinib in newly diagnosed chronic-phase chronic myeloid leukemia: results from the BELA Trial. J Clin Oncol 2012;30(28):3486-3492. Abstract/FREE Full Text

5. Kantarjian HM, Shah NP, Cortes JE, et al. Dasatinib or imatinib in newly diagnosed chronic-phase chronic myeloid leukemia: 2-year follow-up from a randomized phase 3 trial (DASISION). Blood 2012;119(5):1123-1129. Abstract/FREE Full Text

6. Kantarjian HM, Hochhaus A, Saglio G, et al. Nilotinib versus imatinib for the treatment of patients with newly diagnosed chronic phase, Philadelphia chromosome-positive, chronic myeloid leukaemia: 24-month minimum follow-up of the phase 3 randomised ENESTnd trial. Lancet Oncol 2011;12(9):841-851. CrossRefMedline

7. Al-Kali A, Kantarjian H, Shan J, et al. Current event-free survival after sequential tyrosine kinase inhibitor therapy for chronic myeloid leukemia. Cancer 2011;117(2):327-335. CrossRefMedline

8. Cortes JE, Kantarjian HM, Brummendorf TH, et al. Safety and efficacy of bosutinib (SKI-606) in chronic phase Philadelphia chromosome-positive chronic myeloid leukemia patients with resistance or intolerance to imatinib. Blood 2011;118(17):4567-4576. Abstract/FREE Full Text

9. Shah NP, Kim DW, Kantarjian H, et al. Potent, transient inhibition of BCR-ABL with dasatinib 100 mg daily achieves rapid and durable cytogenetic responses and high transformation-free survival rates in chronic phase chronic myeloid leukemia patients with resistance, suboptimal response or intolerance to imatinib. Haematologica 2010;95(2):232-240. Abstract/FREE Full Text

10. Kantarjian HM, Giles FJ, Bhalla KN, et al. Nilotinib is effective in patients with chronic myeloid leukemia in chronic phase after imatinib resistance or intolerance: 24-month follow-up results. Blood 2011;117(4):1141-1145. Abstract/FREE Full Text

Be alert, but not overly concerned.


• Dx Oct. 22, 2008, WBC 459k, in ICU for 2 days + in hospital 1 week

• Leukapheresis for 1 week, to reduce WBC (wasn't given Hydroxyurea)

• Oct. 28, 2008: CML confirmed, start Gleevec 400mg

• Oct. 31, 2008: sent home when WBC reached 121k

• On/off, reduced dose Gleevec for 7 months

• April 2009: Started Sprycel 100mg

• Sept. 2009: PCRU 0.000

• Sept. 2011: after 2 years steady PCRU & taking Sprycel 100mg before bed, quit Sprycel (with permission)

• Currently: still steady PCRU, testing every 6 months 🤗

— Fatigue, hearing loss continue, alas, but I prefer to think it is all getting better!



#2 Trey


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Posted 21 November 2012 - 09:27 PM

I think this article and others show that the issue regarding whether to start with Gleevec or Sprycel (or Tasigna or Bosulif, although not addressed here) comes down to 2 issues:

1) Sprycel works faster for most people than Gleevec

2) Sprycel has double the rates of toxicity as Gleevec when measured by dose interruptions (drug holidays)

Still no clear answer as to which is best as the initial CML drug.  The Gleevec vs Sprycel, Tasigna, or Bosulif will be a debate for a long time.  As Gleevec goes off patent in 2015 and prices drop there will be another reason to start with Gleevec, and then countries with centralized health care will almost certainly require Gleevec or its generic as the starting drug.  Overall, if there are any high risk factors then Sprycel should be used.  Otherwise it is not so clear.

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