Abstract

Most patients with advanced NSCLC do not harbor genomic alterations associated with approved first-line targeted therapies. The standard of care for these patients is a programmed death (ligand)-1 (PD-[L]1) inhibitor alone, if the tumor highly expresses PD-L1, or in combination with platinum doublet chemotherapy, independent of PD-L1 expression. However, most patients do not respond to these therapies or achieve only a transient response, highlighting an unmet need. Sacituzumab govitecan (SG) is an antibody-drug conjugate composed of an anti-Trop-2 antibody coupled to the cytotoxic SN-38 payload via a proprietary, hydrolyzable linker.

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