Treatment of Chronic Myeloid Leukemia in Chronic Phase with Imatinib
Main Article Content
Abstract
Objective: Imatinib (Gleevec®) is accepted to be the first line therapy for chronic myeloid leukemia-chronic phase (CML-CP) with positive Philadelphia chromosome (Ph’). This study is aimed to describe the complete hematologic response (CHR) among the patients with CML-CP with positive Ph’ chromosome that are treated with imatinib 100-400 mg/day Patients and Methods: The CML-CP patients with positive Ph’ who were treated with imatinib 100-400 mg/day at Maharat Nakohn Ratchasima Hospital during the year 2009-2013, were retrospectively reviewed. The CHR and side effects were evaluated at the third, sixth and twelfth months of treatment. Results: In 5-year duration, 43 patients, 28 males and 15 females, were treated with imatinib of 100-400 mg/day. Ages ranged from 3 to 77 years. At the 3rd, 6th and 12th months of treatment, the CHRs were 97.7%, 95.3% and 83.7%, respectively. The side effects included neutropenia, seven cases with grade 1, three with grade 2 and two cases with minimal nausea. There were five cases emerging blast crisis and three cases dying of various causes unrelated to therapy. Conclusion: Forty-three CML-CP patients are treated with imatinib of 100-400 mg/day. In one year, CHR is 83.7%. The side effect is neutropenia, 7 cases with grade 1, 3 with grade 2. Five cases develop blast crisis and three cases die of various causes unrelated to therapy.
Article Details
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
References
Van Etten RA. Clinical manifestations and diagnosis of chronic myeloid leukemia.In: UpToDate,
Basow DS (Ed), UpToDate, Waltham, MA. (Accessed on November 25, 2013.)
Baccarani M, Pileri S, Steegmann J-L, et al. Chronic myeloid leukemia: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol 2012; 23 (suppl 7): vii72-7.
Goldman JM, Marin D.Is imatinib still an acceptable firstline treatment for CML in chronic phase? Oncology (Williston Park) 2012; 26: 901-7.
O’Brien SG, Guilhot F, Larson RA, et al. Imatinib compared with interferon and low-dose cytarabine for newly diagnosed chronic-phase chronic myeloid leukemia. N Engl J Med 2003; 348: 994-1004.
Roshni Paul T, Uppin SG, Uppin MS, et al. Evaluation of cytopeniasoccurring in imatinibtreated chronic myeloid leukemia (CML) patients. Indian J Hematol Blood Transfus2010; 26: 56-61.
Medhi K, Raina V, Kumar L, et al.Response assessment of patients with chronic myeloid leukemia receiving imatinibmesylate (Glivec) therapy: experience from a single center in a developing country.Leuk Lymphoma 2010;51: 1850-4.
Kantarjian H, Sawyers C, Hochhaus A, et al. Hematologic and cytogenetic responses to imatinibmesylate in chronic myelogenousleukemia. N Engl J Med 2002; 346:645-52.
Millot F, Baruchel A, Guilhot J, et al. Imatinibis effective in children with previously untreated chronic myelogenou-sleukemia in early chronic phase:Results of the French national phase IV trial. J ClinOncol 2011; 29: 2827-32.
Mughal TI, Schrieber A. Principal long-term adverse effects of imatinib in patients with chronic myeloid leuke-mia in chronic phase Biologics 2010; 4: 315-23.
De Lavallade H, Apperley JF, Khorashad JS, et al. Imatinib for newly diagnosed patients with chronic myeloid leukemia: incidence of sustained responses in an intention-to-treat analysis. J ClinOncol 2008; 26: 3358-63.
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 randomisedENESTnd trial.Lancet Oncol 2011;12:841-51.
Jootar S. CML treatment in Asia-Pacific region. Hematol 2012; suppl1: S72-4.
Kerkela R, Grazette L, Yacobi R, et al. Cardiotoxicity of the cancer therapeutic agent imatinibmesylate. Nat Med 2006; 12: 908-16.
Kong JH, Yoo SH, Lee KE, et al. Early imatinibmesylateinduced hepatotoxicity in chronic myeloid leukemia. Acta Haematol 2007; 118: 205-8.