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Updated: May 22, 2026

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
Tyrosine kinase inhibitors as potential drugs for B-cell lymphoid malignancies and autoimmune disorders
1Medical University of Lodz, Department of Hematology, Lodz, Poland. robaktad@csk.umed.lodz.pl
Introduction:
In the last few years, several tyrosine kinase inhibitors (TKIs) have been synthesized and become available for preclinical studies and clinical trials. This article summarizes recent achievements in the mechanism of action, pharmacological properties, and clinical activity and toxicity, as well as the emerging role of TKIs in lymphoid malignancies, allergic diseases, and autoimmune disorders.
Areas Covered:
A literature review was conducted of the MEDLINE database PubMed for articles in English. Publications from 2000 through January 2012 were scrutinized. The search terms used were Bruton's tyrosine kinase (Btk) inhibitors, PCI-32765, GDC-0834, LFM-A13, AVL-101, AVL-292, spleen tyrosine kinase (Syk) inhibitors, R343, R406, R112, R788, fostamatinib, BAY-61-3606, C-61, piceatannol, Lyn, imatinib, nilotinib, bafetinib, dasatinib, GDC-0834, PP2, SU6656 in conjunction with lymphoid malignancy, NHL, CLL, autoimmune disease, allergic disease, asthma, and rheumatoid arthritis. Conference proceedings from the previous 5 years of the American Society of Hematology, European Hematology Association, American Society of Clinical Oncology, and ACR/ARHP Annual Scientific Meetings were searched manually. Additional relevant publications were obtained by reviewing the references from the chosen articles.
Expert Opinion:
The use of TKIs, especially inhibitors of Btk, Syk, and Lyn, is a promising new strategy for targeted treatment of B-cell lymphoid malignancies, autoimmune disorders and allergic diseases. However, definitive data from ongoing and future clinical trials will aid in better defining the status of TKIs in the treatment of these disorders.
Insights
Tyrosine kinase inhibitors (TKIs) show promise for treating B-cell lymphoid malignancies, autoimmune, and allergic diseases by targeting Bruton's tyrosine kinase (Btk), spleen tyrosine kinase (Syk), and Lyn. Further clinical trials are needed to confirm their efficacy.
Area of Science:
- Pharmacology
- Oncology
- Immunology
Background:
- Numerous tyrosine kinase inhibitors (TKIs) have emerged for research and clinical trials.
- TKIs are being investigated for their potential in treating lymphoid malignancies, allergic diseases, and autoimmune disorders.
Purpose of the Study:
- To summarize recent advancements in the mechanism of action, pharmacology, and clinical activity of TKIs.
- To review the emerging role of TKIs in lymphoid malignancies, allergic diseases, and autoimmune disorders.
Main Methods:
- A comprehensive literature review of the MEDLINE database (PubMed) was performed for English articles published between 2000 and January 2012.
- Searches included specific tyrosine kinase inhibitors (e.g., Btk, Syk, Lyn inhibitors) combined with relevant disease terms.
- Manual searches of conference proceedings and reference lists of selected articles were also conducted.
Main Results:
- TKIs, particularly those inhibiting Bruton's tyrosine kinase (Btk), spleen tyrosine kinase (Syk), and Lyn, represent a novel targeted therapy approach.
- These inhibitors demonstrate potential in managing B-cell lymphoid malignancies, autoimmune conditions, and allergic diseases.
Conclusions:
- Targeted inhibition of Btk, Syk, and Lyn with TKIs offers a promising therapeutic strategy for B-cell lymphoid malignancies, autoimmune disorders, and allergic diseases.
- Ongoing and future clinical trials are essential to fully establish the role of TKIs in treating these conditions.
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