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Chronic granulocytic leukaemia. A study of 160 cases
L Kumar1, T G Sagar, V Maitreyan
1Department of Medical Oncology, Cancer Institute (WIA), Madras.
Insights
Chronic granulocytic leukaemia (CGL), India's most common adult leukaemia, showed a median survival of 33 months. Most patients presented with splenomegaly and weakness, with 72% of deaths due to blast crisis.
Area of Science:
- Hematology
- Oncology
- Epidemiology
Background:
- Chronic granulocytic leukaemia (CGL) is the most prevalent leukaemia in adult Indian populations.
- Understanding CGL epidemiology and outcomes in India is crucial for public health initiatives.
Purpose of the Study:
- To analyze the clinical characteristics, treatment, and survival outcomes of CGL patients in India.
- To identify key factors influencing CGL prognosis in the Indian context.
Main Methods:
- Retrospective review of 183 CGL patient records diagnosed between 1975 and 1985.
- Analysis of patient demographics, presenting symptoms, physical examination findings, treatment modalities, and survival data.
- Busulphan therapy with total leucocyte count monitoring was the primary treatment approach.
Main Results:
- The median age at diagnosis was 40.5 years.
- Common presenting symptoms included weakness, left upper abdominal fullness, and fever.
- Splenomegaly (90%) and hepatomegaly (48%) were frequent findings.
- The median survival was 33 months from diagnosis, with 87 deaths recorded.
- Blast crisis accounted for 72% of fatalities.
Conclusions:
- CGL in India presents with specific demographic and clinical features.
- Busulphan therapy demonstrated a median survival of 33 months, highlighting the significant impact of blast crisis.
- Further research into improved CGL management strategies in India is warranted.
Abstract:
Chronic granulocytic leukaemia (CGL) is the commonest leukaemia among adults in India. Case records of 183 CGL patients diagnosed between 1975 and 1985 were reviewed. The median age at diagnosis was 40.5 years. Most patients presented with weakness, fullness in the left upper abdomen and fever. Splenomegaly and hepatomegaly were present in 90% and 48% respectively. Patients were treated with oral, intermittent busulphan with monitoring of total leucocyte count. Overall, 87 patients expired, including 63 (72%) due to blast crisis. The median survival was 33 months from diagnosis and 44 months from the onset of symptoms.
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