Imatinib mesylate in the treatment of chronic myeloid leukemia: a local experience

This study was done to assess the overall response rate of imatinib mesylate in local patients with chronic myeloid leukaemia. A total of 69 patients were recruited with male/female ratio of 7:3. Of the 69 patients; 35% were in the chronic phase, 41% were in the accelerated phase, 17% were in blast...

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Main Authors: Bee, P.C., Gan, G.G., Teh, A., Haris, A.R.
Format: Article
Published: Malaysian Medical Association 2006
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Online Access:http://eprints.um.edu.my/12019/
http://www.e-mjm.org/2006/v61n5/Chronic_Myeloid_Leukemia.pdf
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spelling my.um.eprints.120192015-01-14T01:13:44Z http://eprints.um.edu.my/12019/ Imatinib mesylate in the treatment of chronic myeloid leukemia: a local experience Bee, P.C. Gan, G.G. Teh, A. Haris, A.R. R Medicine This study was done to assess the overall response rate of imatinib mesylate in local patients with chronic myeloid leukaemia. A total of 69 patients were recruited with male/female ratio of 7:3. Of the 69 patients; 35% were in the chronic phase, 41% were in the accelerated phase, 17% were in blast crisis and the remaining 7% were after stem cell transplantation. Complete haematological response rates of patients in chronic phase, accelerated phase and blast crisis were 95.8%, 96.4% and 41.7% respectively. Thirty-eight percent of patients achieved complete cytogenetic response and 10% achieved partial cytogenetic response. The cytogenetic response rates were 80%, 41.7% and 18.2% in chronic, accelerated and blast crisis phase respectively (p < 0.005). Twenty-six percent of patients developed anaemia, 13% had neutropenia and 12% had thrombocytopenia after starting on treatment. In addition, 14% of patients developed peripheral oedema, 13% complained of musculoskeletal pain, 12% had gastrointestinal side effects which include nausea, vomiting and diarrhoea, 9% had grade 1 hepatotoxicity, 7% developed skin rashes and one patient had an abnormal renal function test. Patients taking 600mg or higher dosage of imatinib had more gastrointestinal side effects. Patients who weighed less than 60kg had a much higher risk of developing anaemia. Anaemia was a negative predictor of cytogenetic response. Presenting high white blood cell counts and absence of cytogenetic response were also negative predictors of survival. Overall survival was 87%. This was affected by the different phases of disease (chronic phase was better than accelerated and blast crisis) (p < 0.001). In conclusion, our local CML patients did well on treatment with imatinib. Malaysian Medical Association 2006 Article PeerReviewed Bee, P.C. and Gan, G.G. and Teh, A. and Haris, A.R. (2006) Imatinib mesylate in the treatment of chronic myeloid leukemia: a local experience. Medical Journal of Malaysia, 61 (5). pp. 547-552. ISSN 0300-5283 http://www.e-mjm.org/2006/v61n5/Chronic_Myeloid_Leukemia.pdf
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic R Medicine
spellingShingle R Medicine
Bee, P.C.
Gan, G.G.
Teh, A.
Haris, A.R.
Imatinib mesylate in the treatment of chronic myeloid leukemia: a local experience
description This study was done to assess the overall response rate of imatinib mesylate in local patients with chronic myeloid leukaemia. A total of 69 patients were recruited with male/female ratio of 7:3. Of the 69 patients; 35% were in the chronic phase, 41% were in the accelerated phase, 17% were in blast crisis and the remaining 7% were after stem cell transplantation. Complete haematological response rates of patients in chronic phase, accelerated phase and blast crisis were 95.8%, 96.4% and 41.7% respectively. Thirty-eight percent of patients achieved complete cytogenetic response and 10% achieved partial cytogenetic response. The cytogenetic response rates were 80%, 41.7% and 18.2% in chronic, accelerated and blast crisis phase respectively (p < 0.005). Twenty-six percent of patients developed anaemia, 13% had neutropenia and 12% had thrombocytopenia after starting on treatment. In addition, 14% of patients developed peripheral oedema, 13% complained of musculoskeletal pain, 12% had gastrointestinal side effects which include nausea, vomiting and diarrhoea, 9% had grade 1 hepatotoxicity, 7% developed skin rashes and one patient had an abnormal renal function test. Patients taking 600mg or higher dosage of imatinib had more gastrointestinal side effects. Patients who weighed less than 60kg had a much higher risk of developing anaemia. Anaemia was a negative predictor of cytogenetic response. Presenting high white blood cell counts and absence of cytogenetic response were also negative predictors of survival. Overall survival was 87%. This was affected by the different phases of disease (chronic phase was better than accelerated and blast crisis) (p < 0.001). In conclusion, our local CML patients did well on treatment with imatinib.
format Article
author Bee, P.C.
Gan, G.G.
Teh, A.
Haris, A.R.
author_facet Bee, P.C.
Gan, G.G.
Teh, A.
Haris, A.R.
author_sort Bee, P.C.
title Imatinib mesylate in the treatment of chronic myeloid leukemia: a local experience
title_short Imatinib mesylate in the treatment of chronic myeloid leukemia: a local experience
title_full Imatinib mesylate in the treatment of chronic myeloid leukemia: a local experience
title_fullStr Imatinib mesylate in the treatment of chronic myeloid leukemia: a local experience
title_full_unstemmed Imatinib mesylate in the treatment of chronic myeloid leukemia: a local experience
title_sort imatinib mesylate in the treatment of chronic myeloid leukemia: a local experience
publisher Malaysian Medical Association
publishDate 2006
url http://eprints.um.edu.my/12019/
http://www.e-mjm.org/2006/v61n5/Chronic_Myeloid_Leukemia.pdf
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score 13.15806