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iwCLL 2023 | Clinical relevance of intensive laboratory monitoring during venetoclax initiation in CLL

Mazyar Shadman, MD, Fred Hutchinson Cancer Research Center, Seattle, WA, discusses his point of view on whether the recommended period of intensive laboratory monitoring during the standard ramp-up at time of venetoclax initiation for chronic lymphocytic leukemia (CLL) is necessary. From the anecdotal evidence of Dr Shadman in his clinic, few follow-up visits and blood draws lead to interventions in low- and intermediate-risk patients. Dr Shadman believes that generating a hypothesis and prospective study regarding the necessity of laboratory monitoring in low-risk patients may lead to regulatory changes for these individuals and require them to attend fewer follow-up visits during treatment. This interview took place at the biennial International Workshop on Chronic Lymphocytic Leukemia (iwCLL) 2023 meeting, held in Boston, MA.

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Disclosures

MEI Pharma: Consultancy; Fate Therapeutics: Consultancy; Bristol Myers Squibb: Consultancy, Research Funding; TG Therapeutics: Consultancy, Research Funding; Innate Pharma: Consultancy; Epi Lilly: Consultancy; Adaptimmune: Consultancy; AstraZeneca: Consultancy, Research Funding; Epizyme: Consultancy; Mustang Bio: Consultancy, Research Funding; Beigene: Consultancy, Research Funding; Genentech: Consultancy, Research Funding; Regeneron: Consultancy; Merck: Consultancy; Adaptive Biotechnologies: Consultancy; Morphosys/Incyte: Consultancy, Research Funding; Pharmacyclics: Consultancy, Research Funding; Sound Biologics: Consultancy; Kite Pharma: Consultancy; Abbvie: Consultancy, Research Funding; Atara Biotherapeutic: Consultancy, Research Funding; Celgene, a BMS Company: Research Funding; Gilead: Research Funding; Sunesis: Research Funding; Genmab: Research Funding.