Ibrutinib in Chronic Lymphocytic Leukemia
A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Cancer Therapy".
Deadline for manuscript submissions: 30 September 2024 | Viewed by 427
Special Issue Editor
Interests: chronic lymphocytic leukemia; tumor microenvironment; targeted therapy; immunomodulation
Special Issue Information
Dear Colleagues,
Introduction of Bruton Tyrosine kinase (BTK) inhibitors in the clinical practice has deeply altered the treatment paradigm of Chronic Lymphocytic Leukemia (CLL) patients. In particular, ibrutinib is the first BTK inhibitor used in the treatment of CLL that is able to bind covalently to cysteine residue (C481) in the ATP-binding domain of the BTK kinase leading to inhibition of its enzymatic activity. Inhibition of BTK prevents downstream activation of the BCR pathway affecting cell growth, proliferation, homing and survival of the leukemic B cells.
CLL is the most common adult leukemia in Western countries and is an example of hematological disease where cooperation between genetic defects and tumor microenvironmental interaction is involved in pathogenesis. In this scenario, CLL is a disease considered as “addicted to the host”; indeed, the crosstalk between leukemic cells and the tumor microenvironment is essential for leukemic clone maintenance supporting CLL cells’ survival, proliferation, and protection from drug-induced apoptosis.
Although ibrutinib has shown excellent effects on CLL cell component inducing mobilization of lymphocytes from tissue into the blood with the consequent cell death, recently different studies have demonstrated the on-target effects on off-tumor cells related to tumor microenvironment.
This Special Issue aims to summarize the current knowledge and cutting-edge research on BTK inhibitors in CLL.
In this Special Issue, original research articles and reviews are welcome.
Dr. Stefania Fiorcari
Guest Editor
Manuscript Submission Information
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Keywords
- BTK inhibitors
- ibrutinib
- chronic lymphocytic leukemia
- targeted therapy
- BTK
- tumor microenvironment
- drug combination
- immunomodulation
- drug resisitance
