Sacituzumab govitecan: past, present and future of a new antibody-drug conjugate and future horizon: drug evaluation
Sacituzumab govitecan (SG) is a new antibody-drug conjugate directed against the cell-surface antigen Trop-2. Characteristics of the linker connecting the payload SN-38 to the antibody allows SG to kill tumor cells expressing Trop-2 and also the adjacent tumor cells (bystander effect). SG showed eff...
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| Hauptverfasser: | , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
7 Sep 2022
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| In: |
Future oncology
Year: 2022, Jahrgang: 18, Heft: 28, Pages: 3199-3215 |
| ISSN: | 1744-8301 |
| DOI: | 10.2217/fon-2022-0407 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.2217/fon-2022-0407 Verlag, lizenzpflichtig, Volltext: http://www.futuremedicine.com/doi/10.2217/fon-2022-0407 |
| Verfasserangaben: | Jenny Furlanetto, Frederik Marmé and Sibylle Loibl |
MARC
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| 520 | |a Sacituzumab govitecan (SG) is a new antibody-drug conjugate directed against the cell-surface antigen Trop-2. Characteristics of the linker connecting the payload SN-38 to the antibody allows SG to kill tumor cells expressing Trop-2 and also the adjacent tumor cells (bystander effect). SG showed efficacy and safety in several epithelial tumors. The phase III ASCENT trial led to the approval of SG (10 mg/kg, d1,8 q3w) in patients with advanced or metastatic triple-negative breast cancer (TNBC) who have received ≥2 prior systemic therapies, including ≥1 for metastatic disease. The phase III TROPiCS-02 trial in heavily pretreated advanced hormone receptor (HR)-positive breast cancer has recently shown an improvement in progression-free survival for patients treated with SG compared to single-agent chemotherapy. The phase III post-neoadjuvant SASCIA study in early high-risk TNBC and HR-positive breast cancer is currently recruiting patients. | ||
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