Improved survival in chronic myeloid leukemia since the introduction of imatinib therapy: a single-institution historical experience

Author:

Kantarjian Hagop1,O'Brien Susan1,Jabbour Elias1,Garcia-Manero Guillermo1,Quintas-Cardama Alfonso1,Shan Jenny1,Rios Mary Beth1,Ravandi Farhad1,Faderl Stefan1,Kadia Tapan1,Borthakur Gautam1,Huang Xuelin1,Champlin Richard2,Talpaz Moshe3,Cortes Jorge1

Affiliation:

1. Departments of Leukemia, and

2. Stem Cell Transplant and Cellular Therapy, MD Anderson Cancer Center, Houston, TX; and

3. Cancer Center and Geriatric Center, University of Michigan, Ann Arbor, MI

Abstract

Abstract A total of 1569 patients with chronic myeloid leukemia (CML) referred to our institution within 1 month of diagnosis since 1965 were reviewed: 1148 chronic phase (CP), 175 accelerated phase (AP), and 246 blastic phase (BP). The median survival was 8.9 years in CP, 4.8 years in AP, and 6 months in BP. In CP, the 8-year survival was ≤ 15% before 1983, 42%-65% from 1983-2000, and 87% since 2001. Survival was worse in older patients (P = .004), but this was less significant since 2001 (P = .07). Survival by Sokal risk was significantly different before 2001 (P < .001), but not since 2001 (P = .4). In AP, survival improved over time (P < .001); the 8-year survival in patients treated since 2001 was 75%. Survival by age was not different in years < 2001 (P = .09), but was better since 2001 in patients ≤ 70 years of age (P = .004). In BP, the median survival improved over time (P < .001), although it has been only 7 months since 2001. In summary, survival in CML has significantly improved since 2001, particularly so in CP-AML and AP-CML. Imatinib therapy minimized the impact of known prognostic factors and Sokal risk in CP-CML and accentuated the impact of age in AP- and BP-CML.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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