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Assessment of Resistance to Tyrosine Kinase Inhibitors by an Interrogation of Signal Transduction Pathways by Antibody Arrays
Published on: September 19, 2018
Tyrosine kinase inhibitors and interferon
Maria Dimou1, Panagiotis Panayiotidis1
11 Department of Propaedeutic Medicine, Division of Hematology, University of Athens, Greece.
Interferon-alpha (INF) combined with tyrosine kinase inhibitors (TKIs) offers potential for improved chronic myeloid leukemia (CML) treatment. This approach may lead to deeper molecular responses and enable treatment discontinuation for some CML patients.
Area of Science:
- Hematology
- Oncology
- Pharmacology
Background:
- Interferon-alpha (INF) was a breakthrough therapy for chronic myeloid leukemia (CML) in the 1980s, especially for patients ineligible for bone marrow transplantation.
- Imatinib, the first tyrosine kinase inhibitor (TKI), became the standard CML treatment based on the IRIS trial, supplanting INF.
- Combining INF with imatinib has been explored for enhanced therapeutic responses in CML patients.
Purpose of the Study:
- To investigate the combined use of second-generation TKIs with pegylated interferon (peg-IFN) in CML treatment.
- To minimize treatment failures in CML patients.
- To increase the number of CML patients achieving deep molecular responses, potentially allowing treatment cessation.
Main Methods:
- Review of existing literature on INF and TKI combinations in CML therapy.
- Analysis of clinical trial data regarding second-generation TKIs and peg-IFN.
- Evaluation of molecular response rates and treatment discontinuation in CML patients.
Main Results:
- Previous studies demonstrated efficacy of INF combined with imatinib.
- Current research focuses on optimizing combinations of newer TKIs with peg-IFN.
- The goal is to achieve deeper molecular remission and explore treatment-free remission in CML.
Conclusions:
- The combination of second-generation TKIs with peg-IFN represents a promising strategy for CML management.
- This approach aims to overcome TKI resistance and improve outcomes.
- Achieving deep molecular responses may facilitate treatment discontinuation for select CML patients.
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