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Leveraging Trial Data to Guide Frontline TKI Use

An expert discusses how landmark trials such as ASC4FIRST, ENESTnd, and BFORE provide evidence for frontline tyrosine kinase inhibitor (TKI) selection, with asciminib showing superior tolerability and lower discontinuation rates (4.5%) compared with first-generation (11%) and second-generation TKIs (9.8%).

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The ASC4FIRST trial has provided compelling evidence supporting asciminib as frontline chronic myeloid leukemia (CML) therapy, demonstrating superior efficacy and improved tolerability compared with traditional TKI options. This pivotal study, alongside the BFORE trial for bosutinib and the ENESTnd trial for nilotinib, has established the clinical foundation for modern CML treatment selection. These landmark trials offer over 10 years of safety data for some agents, providing clinicians with comprehensive long-term safety profiles, including important considerations such as cardiac toxicity risks with certain TKIs.

Extended 96-week data from the ASC4FIRST trial reveal significantly lower discontinuation rates with asciminib (4.5%) compared with first-generation TKIs (11%) and second-generation TKIs (9.8%). These discontinuation rates serve as important indicators of treatment tolerability and effectiveness in real-world clinical practice. Lower discontinuation rates translate directly to improved patient outcomes, as consistent treatment adherence remains crucial for achieving optimal CML management and preventing disease progression.

Clinical trial data increasingly influence daily CML treatment decisions, with newer agents such as asciminib offering improved tolerability profiles that benefit patients struggling with traditional TKI adverse effects. The integration of trial findings into clinical practice has revolutionized treatment selection, allowing clinicians to choose therapies based on both efficacy and quality-of-life considerations. This evidence-based approach ensures that patients with CML receive optimal treatment regimens tailored to their individual needs while maintaining the highest standards of care supported by robust clinical trial data.

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