
Breaking New Ground: Emerging Therapies for Treatment of EGFR-Positive NSCLC
A panelist discusses how emerging advancements in non–small cell lung cancer (NSCLC) treatment include the anticipated FDA approval of subcutaneous amivantamab, which would significantly reduce infusion-related reactions seen in the MARIPOSA trials while improving patient experience and reducing infusion center chair time, as well as promising antibody-drug conjugates like sacituzumab govitecan (Trodelvy) that may provide better first and second-line treatment options with potentially less toxicity than current standard regimens.
Episodes in this series

Emerging Advancements in EGFR-Positive NSCLC Treatment
Near-Future Developments
Subcutaneous Amivantamab
Anticipated FDA approval represents a significant advancement in delivery method
•	Clinical benefits:
o	Expected reduction in infusion-related reactions, which are currently reported at high rates in MARIPOSA and MARIPOSA-2 trials
o	Potential to improve patient experience and adherence
o	Reduced infusion center chair time, improving health care resource utilization
o	Particularly valuable for first-line treatment settings
TROP-2 Inhibitors
•	Antibody-drug conjugates showing promising results
•	Specific agent: Datopotamab deruxtecan (Dato-DXd, Trodelvy)
•	Potential applications:
o	Emerging second-line treatment option with improved efficacy data
o	Possible future role in first-line settings
o	May offer improved outcomes while reducing toxicity compared with current standard second-line therapies
These developments highlight the continued evolution of targeted therapy approaches in EGFR-positive NSCLC, with innovations focused on both improving efficacy and reducing treatment-associated burdens for patients.
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