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New applications of sacituzumab govitecan for breast cancer

Marina Virko
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A large-scale study has shown that a drug approved for treatment of triple-negative breast cancer is also effective in metastasizing hormone-positive tumors.

About the drug

The medicine called sacituzumab govitecan (the brand name is Trodelvi) combines two active components: a monoclonal antibody (sacituzumab) and the cytotoxic substance govitecan.

Sacituzumab govitecan structural composition

The first component is directed against the surface antigen of trophoblast 2 (Trop-2) cells. This is a glycoprotein (two-component protein) that is expressed by more than 90% of breast and bladder cancer cells and is involved in carcinogenesis and tumor progression. The second component is a cytostatic agent (a DNA topoisomerase inhibitor), its action is to stop DNA replication of tumor cells.

Sacituzumab govitecan was first approved in the USA, and in November 2021 in the European Union as well, as a monotherapy for the treatment of unresectable or metastatic triple-negative breast cancer in cases when 2 or more attempts of systemic therapy for advanced disease have already been made.

A recent study has expanded the scope of Trodelvie® use

At the 43rd Annual Congress of the German Society for Senology (DGS) in Dresden in June 2024, the results of the TROPiCS-02 study (a prospective, randomized trial involving 543 female patients with locally recurrent or metastasizing inoperable HR+/Her2- breast cancer) were released. All of them had previously received at least one line of therapy with an antihormonal drug, taxane, and a cyclin-dependent kinases 4 and 6 inhibitor (2 to 4 lines in total).

In TROPiCS-02, participants received sacituzumab govitecan or some other drug of the physician's choice.

The results for both parameters (progression-free survival and overall survival) were better with the two-component drug.

In the group of patients who had previously undergone 2 lines of therapy, the clinical benefit rate reached 41% compared to 25% in the control group. In the case of 3 lines of prior therapy it was 29 % compared to 20 %.

The incidence of grade 3/4 treatment-related adverse events was also independent of the number of prior lines of therapy.

Based on the results of the study, the researchers concluded: sacituzumab govitecan is effective for the treatment of metastatic breast cancer in hormone receptor-positive and HER2-negative patients regardless of the number of prior courses of therapy. It reduces the risk of recurrence by 39%.

References

  1. https://www.aerzteblatt.de/nachrichten/152790/Sacituzumab-Govitecan-verbessert-Prognose-beim-metastasierten-Brustkrebs?rt=33b3f3a8193547fd222fecc0138a4241
  2. https://www.aerzteblatt.de/nachrichten/134855/Brustkrebs-Sacituzumab-Govitecan-ist-moegliche-neue-Option-bei-inoperablen-intensiv-vorbehandelten-HR-Her2-Tumoren
  3. Hope S Rugo, MD  †, Aditya Bardia, MD †, Frederik Marmé, MD,Javier Cortés, MD, Peter Schmid, MD, Delphine Loirat, MD et al.
  4. Overall survival with sacituzumab govitecan in hormone receptor-positive and human epidermal growth factor receptor 2-negative metastatic breast cancer (TROPiCS-02): a randomised, open-label, multicentre, phase 3 trial. The Lancet. Open AccessPublished:August 23, 2023DOI:https://doi.org/10.1016/S0140-6736(23)01245-X

 

 

 

 

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