Trodelvy (sacituzumab govitecan-hziy) vs Padcev (enfortumab vedotin-ejfv)

Trodelvy (sacituzumab govitecan-hziy) vs Padcev (enfortumab vedotin-ejfv)

Trodelvy (sacituzumab govitecan-hziy) is an antibody-drug conjugate specifically approved for the treatment of metastatic triple-negative breast cancer and has been shown to be effective in patients who have received two or more prior therapies for metastatic disease. Padcev (enfortumab vedotin-ejfv), on the other hand, is an antibody-drug conjugate that targets Nectin-4 and is used for the treatment of advanced urothelial cancer in patients who have previously received a PD-1 or PD-L1 inhibitor and a platinum-containing chemotherapy. When deciding between Trodelvy and Padcev, the choice would largely depend on the type of cancer being treated, as each medication is targeted for different cancer indications and their use would be guided by the patient's specific cancer type and treatment history.

Difference between Trodelvy and Padcev

Metric Trodelvy (sacituzumab govitecan-hziy) Padcev (enfortumab vedotin-ejfv)
Generic name Sacituzumab govitecan-hziy Enfortumab vedotin-ejfv
Indications Previously treated metastatic triple-negative breast cancer Locally advanced or metastatic urothelial cancer
Mechanism of action Antibody-drug conjugate targeting TROP-2 Antibody-drug conjugate targeting Nectin-4
Brand names Trodelvy Padcev
Administrative route Intravenous Intravenous
Side effects Neutropenia, diarrhea, nausea, fatigue, anemia, vomiting Rash, peripheral neuropathy, fatigue, decreased appetite, alopecia
Contraindications Severe hypersensitivity to sacituzumab govitecan-hziy Severe hypersensitivity to enfortumab vedotin-ejfv
Drug class Antibody-drug conjugate Antibody-drug conjugate
Manufacturer Gilead Sciences, Inc. Astellas Pharma Inc. and Seagen Inc.

Efficacy

Trodelvy (Sacituzumab Govitecan-hziy) and Its Efficacy in Urothelial Carcinoma

Trodelvy (sacituzumab govitecan-hziy) is an antibody-drug conjugate that has shown promise in the treatment of multiple types of cancer, including urothelial carcinoma. While initially approved for the treatment of metastatic triple-negative breast cancer, its efficacy in urothelial carcinoma has been evaluated in clinical trials. Trodelvy targets the Trop-2 antigen, which is highly expressed in many epithelial cancers, including urothelial carcinoma. The drug conjugate delivers a potent chemotherapy agent directly to the cancer cells, thereby limiting the exposure of the rest of the body to the cytotoxic agent.

Studies have demonstrated that Trodelvy can lead to significant antitumor activity in patients with metastatic urothelial cancer who have previously received platinum-based chemotherapy and PD-1/PD-L1 inhibitors. The results have shown a meaningful objective response rate, indicating that a proportion of patients experienced a reduction in tumor size. The data also suggest an improvement in progression-free survival, which is the length of time during and after medication treatment that a patient lives with the disease without it getting worse.

Padcev (Enfortumab Vedotin-ejfv) and Its Efficacy in Urothelial Carcinoma

Padcev (enfortumab vedotin-ejfv) is another antibody-drug conjugate specifically approved for the treatment of advanced urothelial carcinoma. It targets Nectin-4, a protein that is highly expressed on urothelial cancer cells. By binding to Nectin-4, Padcev delivers a cytotoxic agent directly to the cancer cells, which can lead to cell death. This targeted approach allows for the delivery of high concentrations of chemotherapy to the cancer cells while sparing normal, healthy cells, potentially reducing the side effects associated with traditional chemotherapy.

Clinical trials have demonstrated that Padcev is effective in patients with locally advanced or metastatic urothelial carcinoma who have previously been treated with a PD-1 or PD-L1 inhibitor and a platinum-containing chemotherapy. The drug has shown a significant objective response rate, with a portion of patients achieving complete response, meaning no detectable signs of cancer. Additionally, Padcev has been associated with an extension in overall survival, providing a potential new treatment option for patients with few alternatives.

Regulatory Agency Approvals

Trodelvy
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Padcev
  • Food and Drug Administration (FDA), USA

Access Trodelvy or Padcev today

If Trodelvy or Padcev are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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