Difference between revisions of "Sacituzumab govitecan (Trodelvy)"

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==Diseases for which it is used==
 
==Diseases for which it is used==
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*[[Bladder cancer]]
 
*[[Breast_cancer,_triple_negative|TNBC]]
 
*[[Breast_cancer,_triple_negative|TNBC]]
  
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[[Category:Topoisomerase inhibitors]]
 
[[Category:Topoisomerase inhibitors]]
  
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[[Category:Bladder cancer medications]]
 
[[Category:Breast cancer medications]]
 
[[Category:Breast cancer medications]]
  
 
[[Category:FDA approved in 2020]]
 
[[Category:FDA approved in 2020]]

Revision as of 01:41, 14 April 2021

Mechanism of action

From the NCI Drug Dictionary: An antibody-drug conjugate containing the humanized monoclonal antibody, hRS7, against tumor-associated calcium signal transducer 2 (TACSTD2 or TROP2) and linked to the active metabolite of irinotecan, 7-ethyl-10-hydroxycamptothecin (SN-38), with potential antineoplastic activity. The antibody moiety of sacituzumab govitecan selectively binds to TROP2. After internalization and proteolytic cleavage, SN-38 selectively stabilizes topoisomerase I-DNA covalent complexes, resulting in DNA breaks that inhibit DNA replication and trigger apoptosis.

Diseases for which it is used

History of changes in FDA indication

  • 4/22/2020: Granted accelerated approval for adult patients with metastatic triple-negative breast cancer who received at least two prior therapies for metastatic disease.
  • 4/7/2021: Granted regular approval for patients with unresectable locally advanced or metastatic triple-negative breast cancer (mTNBC) who have received two or more prior systemic therapies, at least one of them for metastatic disease.
  • 4/13/2021: Granted accelerated approval for patients with locally advanced or metastatic urothelial cancer (mUC) who previously received a platinum-containing chemotherapy and either a programmed death receptor-1 (PD-1) or a programmed death-ligand 1 (PD-L1) inhibitor.

Also known as

  • Code names: IMMU-132, RS7-SN38
  • Generic name: sacituzumab govitecan-hziy
  • Brand name: Trodelvy