An update on imatinib mesylate therapy in chronic myeloid leukaemia patients in a teaching hospital in Malaysia

INTRODUCTION: The introduction of imatinib mesylate in 1998 has changed the management of chronic myeloid leukaemia. It is now the first-line therapy for newly diagnosed chronic myeloid leukaemia patients worldwide. However, its long-term survival benefit still needs to be established in clinical s...

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Main Authors: Bee, P.C., Gan, G.G., Tai, Y.T., Haris, A.R., Chin, E., Veera, S.N.
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Published: 2012
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Online Access:http://eprints.um.edu.my/2983/
http://www.ncbi.nlm.nih.gov/pubmed/22252185
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spelling my.um.eprints.29832014-12-21T08:03:59Z http://eprints.um.edu.my/2983/ An update on imatinib mesylate therapy in chronic myeloid leukaemia patients in a teaching hospital in Malaysia Bee, P.C. Gan, G.G. Tai, Y.T. Haris, A.R. Chin, E. Veera, S.N. R Medicine INTRODUCTION: The introduction of imatinib mesylate in 1998 has changed the management of chronic myeloid leukaemia. It is now the first-line therapy for newly diagnosed chronic myeloid leukaemia patients worldwide. However, its long-term survival benefit still needs to be established in clinical setting among Asian patients. METHODS: All chronic myeloid leukaemia patients in the chronic phase who were on imatinib mesylate therapy were retrospectively reviewed. Data was collected through a review of case notes, which was then processed, managed and analysed. RESULTS: A total of 44 patients were included in the study. The cumulative rates of complete haematological response, major cytogenetic response and major molecular response were 93.2%, 75.0% and 34.2%, respectively. The overall survival and event-free survival at five years were 86.0% and 84.9%, respectively. 31.8% of the patients developed anaemia, 29.5% neutropenia and 27.3% thrombocytopenia. A total of 43.2% of patients developed non-haematological side effects. Higher dosage (> 600 mg) and smaller body size (< 60 kg) were risk factors for haematological side effects. Patients with major cytogenetic response and absence of thrombocytopenia had better survival. CONCLUSION: The majority of our chronic myeloid leukaemia patients did well with imatinib therapy. The adverse effects in our patients were tolerable, and no patient had to stop treatment permanently. 2012-01 Article PeerReviewed Bee, P.C. and Gan, G.G. and Tai, Y.T. and Haris, A.R. and Chin, E. and Veera, S.N. (2012) An update on imatinib mesylate therapy in chronic myeloid leukaemia patients in a teaching hospital in Malaysia. Singapore Medical Journal, 53 (1). pp. 57-61. ISSN 0037-5675 http://www.ncbi.nlm.nih.gov/pubmed/22252185 PMID: 22252185
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.
Tai, Y.T.
Haris, A.R.
Chin, E.
Veera, S.N.
An update on imatinib mesylate therapy in chronic myeloid leukaemia patients in a teaching hospital in Malaysia
description INTRODUCTION: The introduction of imatinib mesylate in 1998 has changed the management of chronic myeloid leukaemia. It is now the first-line therapy for newly diagnosed chronic myeloid leukaemia patients worldwide. However, its long-term survival benefit still needs to be established in clinical setting among Asian patients. METHODS: All chronic myeloid leukaemia patients in the chronic phase who were on imatinib mesylate therapy were retrospectively reviewed. Data was collected through a review of case notes, which was then processed, managed and analysed. RESULTS: A total of 44 patients were included in the study. The cumulative rates of complete haematological response, major cytogenetic response and major molecular response were 93.2%, 75.0% and 34.2%, respectively. The overall survival and event-free survival at five years were 86.0% and 84.9%, respectively. 31.8% of the patients developed anaemia, 29.5% neutropenia and 27.3% thrombocytopenia. A total of 43.2% of patients developed non-haematological side effects. Higher dosage (> 600 mg) and smaller body size (< 60 kg) were risk factors for haematological side effects. Patients with major cytogenetic response and absence of thrombocytopenia had better survival. CONCLUSION: The majority of our chronic myeloid leukaemia patients did well with imatinib therapy. The adverse effects in our patients were tolerable, and no patient had to stop treatment permanently.
format Article
author Bee, P.C.
Gan, G.G.
Tai, Y.T.
Haris, A.R.
Chin, E.
Veera, S.N.
author_facet Bee, P.C.
Gan, G.G.
Tai, Y.T.
Haris, A.R.
Chin, E.
Veera, S.N.
author_sort Bee, P.C.
title An update on imatinib mesylate therapy in chronic myeloid leukaemia patients in a teaching hospital in Malaysia
title_short An update on imatinib mesylate therapy in chronic myeloid leukaemia patients in a teaching hospital in Malaysia
title_full An update on imatinib mesylate therapy in chronic myeloid leukaemia patients in a teaching hospital in Malaysia
title_fullStr An update on imatinib mesylate therapy in chronic myeloid leukaemia patients in a teaching hospital in Malaysia
title_full_unstemmed An update on imatinib mesylate therapy in chronic myeloid leukaemia patients in a teaching hospital in Malaysia
title_sort update on imatinib mesylate therapy in chronic myeloid leukaemia patients in a teaching hospital in malaysia
publishDate 2012
url http://eprints.um.edu.my/2983/
http://www.ncbi.nlm.nih.gov/pubmed/22252185
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