ALPINE: zanubrutinib versus ibrutinib in relapsed/refractory chronic lymphocytic leukemia/small lymphocytic lymphoma
Treatment standards for chronic lymphocytic leukemia (CLL) have been transformed with the
advent of effective inhibitors of B-cell receptor signaling such as ibrutinib–a first-in-class …
advent of effective inhibitors of B-cell receptor signaling such as ibrutinib–a first-in-class …
[HTML][HTML] BTK inhibitors in chronic lymphocytic leukemia: biological activity and immune effects
M Palma, TA Mulder, A Österborg - Frontiers in immunology, 2021 - frontiersin.org
Bruton´ s tyrosine kinase (BTK) inhibitor (BTKi) s block the B-cell receptor (BCR) signaling
cascade by binding to the BTK enzyme preventing the proliferation and survival of malignant …
cascade by binding to the BTK enzyme preventing the proliferation and survival of malignant …
Chronic lymphocytic leukemia treatment algorithm 2018
SA Parikh - Blood cancer journal, 2018 - nature.com
The treatment landscape for patients with chronic lymphocytic leukemia (CLL) has changed
considerably with the introduction of very effective oral targeted therapies (such as ibrutinib …
considerably with the introduction of very effective oral targeted therapies (such as ibrutinib …
Apoptosis and cancer
A Letai - Annual Review of Cancer Biology, 2017 - annualreviews.org
Cancer is a disease involving the abnormal accumulation of cells resulting from an
imbalance of proliferation and programmed cell death. This review focuses on the …
imbalance of proliferation and programmed cell death. This review focuses on the …
Small molecule inhibitors targeting the cancers
Compared with traditional therapies, targeted therapy has merits in selectivity, efficacy, and
tolerability. Small molecule inhibitors are one of the primary targeted therapies for cancer …
tolerability. Small molecule inhibitors are one of the primary targeted therapies for cancer …
BRD4 profiling identifies critical chronic lymphocytic leukemia oncogenic circuits and reveals sensitivity to PLX51107, a novel structurally distinct BET inhibitor
Bromodomain and extra-terminal (BET) family proteins are key regulators of gene
expression in cancer. Herein, we utilize BRD4 profiling to identify critical pathways involved …
expression in cancer. Herein, we utilize BRD4 profiling to identify critical pathways involved …
Control of mitochondrial physiology and cell death by the Bcl-2 family proteins Bax and Bok
Neuronal cell death is often triggered by events that involve intracellular increases in Ca 2+.
Under resting conditions, the intracellular Ca 2+ concentration is tightly controlled by a …
Under resting conditions, the intracellular Ca 2+ concentration is tightly controlled by a …
Bendamustine followed by obinutuzumab and venetoclax in chronic lymphocytic leukaemia (CLL2-BAG): primary endpoint analysis of a multicentre, open-label …
P Cramer, J von Tresckow, J Bahlo, S Robrecht… - The Lancet …, 2018 - thelancet.com
Background Targeted agents such as the type II anti-CD20 antibody obinutuzumab and the
B-cell lymphoma-2 antagonist venetoclax have shown impressive therapeutic activity in …
B-cell lymphoma-2 antagonist venetoclax have shown impressive therapeutic activity in …
High-risk chronic lymphocytic leukemia in the era of pathway inhibitors: integrating molecular and cellular therapies
P Dreger, P Ghia, J Schetelig… - Blood, The Journal …, 2018 - ashpublications.org
High-risk chronic lymphocytic leukemia (CLL) has been defined by clinical and/or genetic
resistance (TP53 abnormalities) to treatment with chemoimmunotherapy (CIT). With the …
resistance (TP53 abnormalities) to treatment with chemoimmunotherapy (CIT). With the …
Targeting BCL2 with BH3 mimetics: basic science and clinical application of venetoclax in chronic lymphocytic leukemia and related B cell malignancies
AW Roberts, DCS Huang - Clinical Pharmacology & …, 2017 - Wiley Online Library
The intracellular protein B‐cell‐lymphoma‐2 (BCL2) has been considered an attractive
target for cancer therapy since the discovery of its function as a major promoter of cell …
target for cancer therapy since the discovery of its function as a major promoter of cell …