Abstract
The development of targeted treatment of chronic lymphocytic leukaemia (CLL) is changing the prognostic outlook for CLL patients. The B-cell antigen receptor pathway is identified as pivotal for CLL pathogenesis and CLL cell proliferation. Inhibition of this pathway by ibrutinib (Bruton's tyrosin kinase inhibition) and idelalisib (phosphatidylinositol 3-kinase inhibition) has recently shown impressive clinical results, also for CLL patients with relapsed/refractory disease and unfavourable prognostic markers. Apoptosis induction by inhibition of BCL2 with ABT-199 is reported with likewise promising clinical results.
MeSH terms
-
Adenine / analogs & derivatives
-
Aminopyridines
-
Antineoplastic Agents / therapeutic use*
-
Bridged Bicyclo Compounds, Heterocyclic / therapeutic use
-
Humans
-
Leukemia, Lymphocytic, Chronic, B-Cell / drug therapy*
-
Leukemia, Lymphocytic, Chronic, B-Cell / immunology
-
Leukemia, Lymphocytic, Chronic, B-Cell / metabolism
-
Morpholines
-
Oxazines / therapeutic use
-
Piperidines
-
Purines / therapeutic use
-
Pyrazoles / therapeutic use
-
Pyridines / therapeutic use
-
Pyrimidines / therapeutic use
-
Quinazolinones / therapeutic use
-
Receptors, Antigen, B-Cell / antagonists & inhibitors*
-
Receptors, Antigen, B-Cell / drug effects
-
Receptors, Antigen, B-Cell / immunology
-
Receptors, Antigen, B-Cell / metabolism
-
Signal Transduction / drug effects
-
Signal Transduction / physiology
-
Sulfonamides / therapeutic use
Substances
-
Aminopyridines
-
Antineoplastic Agents
-
Bridged Bicyclo Compounds, Heterocyclic
-
Morpholines
-
Oxazines
-
Piperidines
-
Purines
-
Pyrazoles
-
Pyridines
-
Pyrimidines
-
Quinazolinones
-
Receptors, Antigen, B-Cell
-
Sulfonamides
-
ibrutinib
-
Adenine
-
venetoclax
-
fostamatinib
-
idelalisib