Abstract

Chronic Myeloid Leukaemia (CML) responds well with the targeted therapy drugs, Tyrosine Kinase Inhibitors (TKI), that give potentially long-term disease control for the patients. The objective of this study was to determine the disease burden and factors influencing the health-related quality of life (HRQoL) and health status of CML patients in Klang Valley, Malaysia. CML patients were recruited from haematological outpatient clinics in health centres in Klang Valley, Malaysia. A semi-guided self-administered questionnaire was used. HRQoL was measured by EQ-5D utility value and health status was by visual analogue score (VAS). Logistic regression analysis was conducted to determine the factors influencing HRQoL and health status. A total of 221 respondents participated, where more than half were Malay (56.6%), male (53.4%), and an Imatinib user (68.8%). Majority were diagnosed at the chronic phase (89.5%). The mean age of diagnosis was 41 years old. Significant determinant associated with HRQoL was age of diagnosis. These factors had no significant effect on the HRQoL of these patients regardless of types of TKI used and initial phase of CML. The overall HRQoL of CML patients were comparable to, if not higher, than the general population. Any TKI that was good enough to eliminate disease symptoms and erase patient’s worries, can possibly make CML patients have a better quality of life than typical cancer patients and even the general population.

Highlights

  • Chronic myeloid leukaemia (CML) is a type of myeloproliferative neoplasm derived from myeloblast cells [1]

  • We found that Imatinib was the main Tyrosine Kinase Inhibitor (TKI) used to treat Chronic Myeloid Leukaemia (CML), with more than two thirds (68.8%) of the patients using it

  • This study has demonstrated an assessment of health-related quality of life (HRQoL) by EQ-5D and visual analogue score (VAS) among CML patients in Klang Valley, Malaysia

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Summary

Introduction

Chronic myeloid leukaemia (CML) is a type of myeloproliferative neoplasm derived from myeloblast cells [1]. It is characterised by the presence of Philadelphia chromosome and its fusion gene, BCR-ABL1. The gene codes for an oncoprotein that stimulates the proliferation of myeloid cells. CML is the most uncommon of all the leukaemia, accounting for only 14% of overall leukaemia [2]. It affects all age groups, with the incidence rate varying between countries, from 0.3 to 1.6 for every 100,000 population [3, 4].

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