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Updated: Aug 11, 2026

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 19, 2013
STI571: a gene product-targeted therapy for leukemia
1Leukemia Program, Division of Hematology and Medical Oncology, Department of Medicine, Oregon Health Sciences University, OP28, 3181 SW Sam Jackson Park Road, Portland, OR 97201, USA. maurom@ohsu.edu
Chronic myelogenous leukemia (CML) is a blood stem cell disorder. A new drug, STI571, targets the bcr-abl tyrosine kinase, offering hope for CML patients.
Area of Science:
- Hematology
- Oncology
- Molecular Biology
Background:
- Chronic myelogenous leukemia (CML) is a clonal hematopoietic stem-cell disorder.
- It is characterized by the (9:22) translocation, leading to the production of the bcr-abl tyrosine kinase.
- CML typically presents with myeloid proliferation and can progress to acute leukemia.
Purpose of the Study:
- To introduce STI571, a novel bcr-abl tyrosine kinase inhibitor.
- To highlight STI571 as a paradigm for targeted cancer therapy.
- To discuss the potential of STI571 in expanding treatment options for CML patients.
Main Methods:
- Rational drug development approach.
- Development of a specific inhibitor targeting the bcr-abl tyrosine kinase.
Main Results:
- STI571 has emerged as a promising therapeutic agent.
- The drug represents a new hope for patients with CML.
Conclusions:
- STI571 offers a targeted therapy approach for CML.
- This development expands treatment possibilities for CML patients.
- Gene product-targeted therapy shows significant promise in oncology.
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