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Updated: Mar 16, 2026

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
Charlson comorbidity index predicts poor outcome in CML patients treated with tyrosine kinase inhibitor
Makiko Uemura1, Osamu Imataki2,3, Yasunori Kawachi4,5
1Division of Hematology, Rheumatology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Kagawa University, Miki-town, Japan.
Insights
Comorbidity at diagnosis significantly impacts treatment outcomes for chronic myeloid leukemia (CML) patients receiving tyrosine kinase inhibitors (TKIs). Higher comorbidity scores predict poorer survival in CML.
Area of Science:
- Hematology
- Oncology
- Clinical Medicine
Background:
- Sokal and Hasford scoring systems are established prognostic models for chronic myeloid leukemia (CML).
- The predictive accuracy of these models in elderly CML patients with comorbidities remains unclear.
- Comorbidities can influence treatment response and survival in various cancers.
Purpose of the Study:
- To evaluate the association between comorbidity at diagnosis and treatment outcomes in chronic phase CML patients.
- To assess the impact of comorbidities on survival in CML patients treated with tyrosine kinase inhibitors (TKIs).
Main Methods:
- A cohort of 79 chronic phase CML patients diagnosed between 2001 and 2012 and treated with TKIs was studied.
- The Charlson Comorbidity Index (CCI) was used to quantify comorbidity burden at diagnosis.
- Treatment outcomes, including major molecular response and complete cytogenetic response, and overall survival were analyzed.
Main Results:
- A significant proportion of patients (27/79) had a CCI score greater than 3.
- Patients with a CCI score >3 exhibited significantly poorer survival compared to those with lower scores.
- CCI scores were inversely associated with overall survival, indicating higher comorbidity predicts worse outcomes.
- Major molecular response was achieved in 46 patients, and complete cytogenetic response in 73.4% at 12 months.
Conclusions:
- Concomitant comorbidity at diagnosis is a significant negative prognostic factor in CML patients treated with TKIs.
- The Charlson Comorbidity Index is a valuable tool for predicting outcomes in this patient population.
- Comorbidity assessment should be integrated into prognostic models for CML, especially in older adults.
Abstract:
Although the Sokal and Hasford scoring systems are well-known prognostic models specific to chronic myeloid leukemia (CML), whether they can effectively predict outcomes in elderly CML patients with comorbidities has not been fully elucidated. We evaluated the association between comorbidity at diagnosis with treatment outcome and survival in chronic phase CML patients. A questionnaire was administered to patients diagnosed with CML between 2001 and 2012 and treated with tyrosine kinase inhibitors (TKIs). The Charlson comorbidity index (CCI) was used to determine concomitant diseases. In total, 79 patients (33 females; median age, 57 years) were enrolled. CCI scores at diagnosis were between 2 and 11. At the last follow-up, 46 patients showed a major molecular response. Complete cytogenetic response was achieved in 73.4 % of the cases 12 months after TKI administration. We observed only five deaths during the 55.5-month median follow-up period. The risk categories (low/intermediate/high) associated with Sokal and Hasford scores were 33/27/7 and 21/43/3, respectively. The 27 cases with a CCI score >3 had significantly poorer survival after diagnosis (52 cases had a CCI score <2). CCI scores were inversely associated to overall survival. Concomitant comorbidity at diagnosis is associated with poor outcome in CML patients treated with TKIs.
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