Opinion|Videos|November 19, 2024
Integrating HER3-DXd: Clinical Considerations for Future Approval and Implementation in Practice
This episode explores management strategies for hematologic toxicities arising within the first 3 weeks of treatment with HER3-DXd, discusses the potential integration of HER3-DXd into clinical practice upon approval, and identifies unmet needs and suitable patient populations for future clinical trials evaluating HER3-DXd based on insights from the HERTHENA-Lung01 trial results.
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Video content above is prompted by the following:
- Please discuss your management approach to hematologic toxicities, which might occur within the first 3 weeks of treatment with HER3-DXd.
- If HER3-DXd is approved, where would you integrate HER3-DXd, and in what setting?
- What are your thoughts on the unmet needs for HER3-DXd? Which patient populations may be the most appropriate for future clinical trials evaluating HER3-DXd, based on the HERTHENA-Lung01 results?
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