2022
DOI: 10.1177/10781552221090869
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Real-world management of targeted therapies in chronic lymphocytic leukemia

Abstract: The advent of novel targeted therapies, including B-cell receptor (BCR) pathway and B-cell lymphoma 2 (BCL2) inhibitors, has substantially changed the treatment paradigm for chronic lymphocytic leukemia (CLL). Although targeted therapies have improved outcomes compared to traditional chemoimmunotherapy in the front-line and relapsed or refractory settings, they are associated with resistance mutations and suboptimal outcomes in certain high-risk patients. Additionally, targeted therapies are associated with dr… Show more

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Cited by 2 publications
(2 citation statements)
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“…The fact that BTK is a key mediator of innate immunity and inflammation ( Weber et al, 2017 ; Weber, 2021 ) strongly suggest that TBBPA has the potential to lead to a strong imbalance, which in turn could induce and/or aggravate damages to the BBB integrity ( Ní Chasaide and Lynch, 2020 ), and permeate TBBPA in the central nervous system with more direct effects. Of note, BTK inhibitor share a variety of clinical applications, ranging from treatment of B cell malignancies, to autoimmune diseases and COVID-19 ( Zhu et al, 2021 ; Malekinejad et al, 2022 ; Rezaei et al, 2022 ; Weis et al, 2022 ), which raise the question on whether TBBPA may interfere with these therapeutic actions. This will certainly require dedicated experimental exploration and validation.…”
Section: Discussionmentioning
confidence: 99%
“…The fact that BTK is a key mediator of innate immunity and inflammation ( Weber et al, 2017 ; Weber, 2021 ) strongly suggest that TBBPA has the potential to lead to a strong imbalance, which in turn could induce and/or aggravate damages to the BBB integrity ( Ní Chasaide and Lynch, 2020 ), and permeate TBBPA in the central nervous system with more direct effects. Of note, BTK inhibitor share a variety of clinical applications, ranging from treatment of B cell malignancies, to autoimmune diseases and COVID-19 ( Zhu et al, 2021 ; Malekinejad et al, 2022 ; Rezaei et al, 2022 ; Weis et al, 2022 ), which raise the question on whether TBBPA may interfere with these therapeutic actions. This will certainly require dedicated experimental exploration and validation.…”
Section: Discussionmentioning
confidence: 99%
“…With the introduction of molecularly targeted agents for specific druggable proteins that are overexpressed in leukemia, an additional safety margin is added. Newer clinical treatments for B-cell leukemia targeted to molecular checkpoints can be divided into three groups of compounds that inhibit the uncontrolled growth of B cells: (1) Bcl-2, a mitochondrial antiapoptotic protein, (2) Bruton’s tyrosine kinase (BTK) inhibitors (TKI’s), (3) monoclonal antibodies, several of which are targeted to CD20, a surface antigen on B cells [ 5 ]. As molecularly targeted agents, these three compounds reduce off-target toxicities compared to earlier drugs, making them a preferred treatment option for patients from a wide demographic range [ 6 ].…”
Section: Introductionmentioning
confidence: 99%