Chronic lymphocytic leukaemia
- PMID: 39068951
- DOI: 10.1016/S0140-6736(24)00595-6
Chronic lymphocytic leukaemia
Abstract
The last decade has seen remarkable progress in our understanding of disease biology of chronic lymphocytic leukaemia (CLL) and the development of novel targeted therapies. Randomised clinical trials have reported improved progression-free survival and overall survival with targeted therapies compared with chemoimmunotherapy, and thereby the role of chemoimmunotherapy in todays' era for treatment of CLL is limited. Bruton tyrosine kinase (BTK) inhibitors, BCL2 inhibitors, and CD20 monoclonal antibodies have been established as appropriate therapy options for patients with CLL, both as the first-line treatment and in the treatment of relapsed or refractory CLL. Several ongoing phase 3 trials are exploring different combinations of targeted therapies, and the results of these trials might change the treatment framework in first-line treatment of CLL. Non-covalent BTK inhibitors, chimeric antigen receptor T-cell therapy, and other therapeutic strategies are being investigated in relapsed CLL. Some of the therapies used in relapsed CLL, such as non-covalent BTK inhibitors, are now being pursued in earlier lines of therapy, including first-line treatment of CLL.
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Conflict of interest statement
Declaration of interests NJ received funding (to institution) from Pharmacyclics, AbbVie, Genentech, AstraZeneca, Bristol Myers Squibb, Pfizer, ADC Therapeutics, Cellectis, Adaptive Biotechnologies, Precision Biosciences, Fate Therapeutics, Kite–Gilead, Mingsight, Takeda, Medisix, Loxo Oncology, Novalgen, Dialectic Therapeutics, Newave, Novartis, Carna Biosciences, Sana Biotechnology, and Kisoji Biotechnology; and consulting and honorarium fees from Pharmacyclics, Janssen, AbbVie, Genentech, AstraZeneca, Bristol Myers Squibb, Adaptive Biotechnologies, Kite–Gilead, Precision Biosciences, Beigene, Cellectis, MEI Pharma, Ipsen, CareDX, Eli Lilly, MingSight, and Novalgen. WGW received funding (to institution) from AstraZeneca–Acerta Pharma, Cyclacel, Genentech, Gilead Sciences, GlaxoSmithKline, Novartis, Janssen, Juno Therapeutics, KITE Pharma, Loxo Oncology, Miragen, Oncternal Therapeutics, Pharmacyclics, Sunesis, and Xencor; personal fees from Cylacel, Loxo, Novartis, and Xencor; and travel support from AbbVie, Acerta Pharma, Genentech, Gilead Sciences, Janssen Biotech, Juno Therapeutics, Kite Pharma, Oncternal Therapeutics, and Pharmacyclics. SO received funding (to institution) from Alliance, AstraZeneca, Caribou Biosciences, Gilead, Kite, Mustang Bio, Nurix Therapeutics, Pfizer, Pharmacyclics, Regeneron, and TG Therapeutics; and consulting and honorarium fees from AbbVie, AstraZeneca, Autolus, Beigene, BMS, Eli Lilly, GlaxoSmithKline, Janssen, Johnson & Johnson, Merck, Pfizer, Pharmacyclics, TG Therapeutics, and Vanian Group.
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