TY - JOUR
T1 - Early responses predict better outcomes in patients with newly diagnosed chronic myeloid leukemia
T2 - Results with four tyrosine kinase inhibitor modalities
AU - Jain, Preetesh
AU - Kantarjian, Hagop
AU - Nazha, Aziz
AU - O’Brien, Susan
AU - Jabbour, Elias
AU - Romo, Carlos Guillermo
AU - Pierce, Sherry
AU - Cardenas-Turanzas, Marylou
AU - Verstovsek, Srdan
AU - Borthakur, Gautam
AU - Ravandi, Farhad
AU - Quintás-Cardama, Alfonso
AU - Cortes, Jorge
N1 - Funding Information:
This study was supported in part by the MD Anderson Cancer Center Support Grant CA016672 and award number P01 CA049639 from the National Cancer Institute.
Funding Information:
This study was supported in part by the MD Anderson Cancer Center Support Grant CA016672 and award number P01 CA049639 from the National Cancer Institute. Conflict-of-interest disclosure: J.C. is a consultant for Pfizer, Ariad, and Teva and received research support from Pfizer, Ariad, Chemgenex, Bristol Myers Squibb (BMS), and Novartis. F.R. received research funding from BMS and honoraria from BMS, Novartis, and Pfizer. The remaining authors declare no competing financial interests.
Publisher Copyright:
© 2013 by The American Society of Hematology.
PY - 2013/6/13
Y1 - 2013/6/13
N2 - Early responses to tyrosine kinase inhibitors (TKIs) in chronic myeloid leukemia (CML)-chronic phase (CP) are associated with improved outcome. We analyzed the impact of such a response on outcomes among patients treated with 4 TKI modalities as frontline therapy in CML-CP. A total of 483 patients who received 400 or 800 mg imatinib, nilotinib, or dasatinib were analyzed. The median follow-up was 72 mo. Landmark analysis at 3 mo by molecular response showed that the cumulative proportions of 3-y event-free survival (EFS) for 3-mo BCR-ABL levels was 95% for those with £1%, 98% for >1% to 10%, and 61% for those with >10% (P 5 .001). The corresponding values by cytogenetic responses were 97% if Ph1 5 0%, 89% if Ph1 5 1% to 35%, and 81% if Ph1 >35% (P 5 .001). Cytogenetic response at 3 mo significantly discriminated for 3-y overall survival (OS): 98%, 96%, and 92%, respectively (P 5 .01). In multivariate analysis, young patients, high Sokal index, and treatment with imatinib 400 significantly predicted for poor (>35%) cytogenetic response at 3 mo. Early responses are predictive for EFS and failure-free survival and to a lesser extent OS, regardless of the treatment modality, although therapies other than standard-dose imatinib result in higher rates of deep early responses. This trial was registered at www.clinicaltrials.gov as ID01-151 NCT00038649, ID01-015 NCT00048672, DM00-163 NCT00333840, ID02-534 NCT00050531, 2005-0422 NCT00254423, and 2005-0048 NCT00129740.
AB - Early responses to tyrosine kinase inhibitors (TKIs) in chronic myeloid leukemia (CML)-chronic phase (CP) are associated with improved outcome. We analyzed the impact of such a response on outcomes among patients treated with 4 TKI modalities as frontline therapy in CML-CP. A total of 483 patients who received 400 or 800 mg imatinib, nilotinib, or dasatinib were analyzed. The median follow-up was 72 mo. Landmark analysis at 3 mo by molecular response showed that the cumulative proportions of 3-y event-free survival (EFS) for 3-mo BCR-ABL levels was 95% for those with £1%, 98% for >1% to 10%, and 61% for those with >10% (P 5 .001). The corresponding values by cytogenetic responses were 97% if Ph1 5 0%, 89% if Ph1 5 1% to 35%, and 81% if Ph1 >35% (P 5 .001). Cytogenetic response at 3 mo significantly discriminated for 3-y overall survival (OS): 98%, 96%, and 92%, respectively (P 5 .01). In multivariate analysis, young patients, high Sokal index, and treatment with imatinib 400 significantly predicted for poor (>35%) cytogenetic response at 3 mo. Early responses are predictive for EFS and failure-free survival and to a lesser extent OS, regardless of the treatment modality, although therapies other than standard-dose imatinib result in higher rates of deep early responses. This trial was registered at www.clinicaltrials.gov as ID01-151 NCT00038649, ID01-015 NCT00048672, DM00-163 NCT00333840, ID02-534 NCT00050531, 2005-0422 NCT00254423, and 2005-0048 NCT00129740.
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UR - http://www.scopus.com/inward/citedby.url?scp=84881289808&partnerID=8YFLogxK
U2 - 10.1182/blood-2013-03-490128
DO - 10.1182/blood-2013-03-490128
M3 - Article
C2 - 23620574
AN - SCOPUS:84881289808
SN - 0006-4971
VL - 121
SP - 4867
EP - 4874
JO - Blood
JF - Blood
IS - 24
ER -