Key result
Ibrutinib carries ~40% 1-year discontinuation rates in community-based CLL practice, driven by toxicities.
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Ibrutinib is a transformative therapy for high-risk and relapsed refractory chronic lymphocytic leukemia (CLL) patients. In clinical trials in relatively healthy younger patients, ibrutinib has been well tolerated. As its use has become more widespread in the community, however, its full adverse event profile has emerged and proven more challenging than was initially anticipated. Reports of community-based use have estimated discontinuation rates as high as 40% in the first year of therapy. This article therefore reviews my approach to the evaluation and management of a CLL patient starting on ibrutinib, with the goal of minimizing and managing toxicity to maintain patients on ibrutinib. Key topics discussed include bleeding risk; cardiac complications, particularly atrial fibrillation; drug interactions; and infections.
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Jennifer R. Brown (2017) conducted a review in Chronic lymphocytic leukemia (CLL). Ibrutinib was evaluated. Ibrutinib therapy in CLL has estimated community-based discontinuation rates up to 40% in year 1, requiring management of bleeding, atrial fibrillation, drug interactions, and infections.
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