Imfinzi (durvalumab) vs Trodelvy (sacituzumab govitecan-hziy)

Imfinzi (durvalumab) vs Trodelvy (sacituzumab govitecan-hziy)

Imfinzi (durvalumab) is an immune checkpoint inhibitor that works by helping the immune system recognize and attack cancer cells, commonly used in the treatment of certain types of lung cancer and bladder cancer. Trodelvy (sacituzumab govitecan-hziy) is an antibody-drug conjugate that targets and delivers chemotherapy directly to cancer cells, and it is used for the treatment of triple-negative breast cancer and metastatic urothelial cancer. The choice between Imfinzi and Trodelvy would depend on the specific type and stage of cancer, as well as the patient's overall health, previous treatments, and the presence of specific biomarkers, so a healthcare provider would need to evaluate the patient's condition to recommend the appropriate therapy.

Difference between Imfinzi and Trodelvy

Metric Imfinzi (durvalumab) Trodelvy (sacituzumab govitecan-hziy)
Generic name Durvalumab Sacituzumab govitecan-hziy
Indications Urothelial carcinoma, non-small cell lung cancer, extensive-stage small cell lung cancer Metastatic triple-negative breast cancer, urothelial cancer
Mechanism of action PD-L1 inhibitor, immune checkpoint inhibitor Antibody-drug conjugate targeting TROP-2
Brand names Imfinzi Trodelvy
Administrative route Intravenous Intravenous
Side effects Fatigue, rash, muscle pain, constipation, decreased appetite, etc. Neutropenia, diarrhea, nausea, fatigue, anemia, etc.
Contraindications Hypersensitivity to durvalumab or any excipients Hypersensitivity to sacituzumab govitecan-hziy or any excipients
Drug class Monoclonal antibody, immune checkpoint inhibitor Antibody-drug conjugate
Manufacturer AstraZeneca Gilead Sciences, Inc.

Efficacy

Imfinzi (Durvalumab) Efficacy in Urothelial Carcinoma

Imfinzi (durvalumab) is an immune checkpoint inhibitor that targets the PD-L1 protein found on the surface of cancer cells. In the context of urothelial carcinoma, which is a type of bladder cancer, durvalumab has shown efficacy as a treatment option. The approval of durvalumab for urothelial carcinoma was based on the results of clinical trials that demonstrated an increase in overall survival and progression-free survival rates in patients with locally advanced or metastatic urothelial carcinoma. Patients who have disease progression during or following platinum-containing chemotherapy, or whose disease has progressed within 12 months of neoadjuvant or adjuvant chemotherapy, may benefit from treatment with durvalumab.

In a pivotal phase III trial known as the DANUBE study, durvalumab was evaluated as a first-line treatment for patients with metastatic urothelial carcinoma. However, the study did not meet its primary endpoints of improving overall survival in patients with high PD-L1 expression or in the overall patient population when compared to standard chemotherapy. Despite this, durvalumab has shown positive results in other studies, such as the phase I/II trial that led to its accelerated approval by regulatory agencies for patients with locally advanced or metastatic urothelial carcinoma who have progressed after platinum-containing chemotherapy.

Trodelvy (Sacituzumab Govitecan-hziy) Efficacy in Urothelial Carcinoma

Trodelvy (sacituzumab govitecan-hziy) is an antibody-drug conjugate that targets the Trop-2 antigen, which is commonly expressed in multiple types of epithelial cancers, including urothelial carcinoma. Sacituzumab govitecan-hziy has demonstrated efficacy in patients with metastatic urothelial cancer who have previously received platinum-based chemotherapy and a PD-1 or PD-L1 inhibitor. The approval of sacituzumab govitecan-hziy for urothelial carcinoma was supported by the results of a single-arm, phase II study (TROPHY-U-01) that showed a meaningful objective response rate and a median duration of response in a heavily pretreated population.

Patients treated with sacituzumab govitecan-hziy in the TROPHY-U-01 trial experienced a significant clinical benefit, with a manageable safety profile. The observed efficacy of sacituzumab govitecan-hziy in this setting provides an important treatment option for patients with metastatic urothelial carcinoma who have limited therapeutic alternatives after failing first-line standard therapies. Ongoing clinical trials are further investigating the efficacy and safety of sacituzumab govitecan-hziy in urothelial carcinoma, including its use in earlier lines of therapy and in combination with other therapeutic agents.

Regulatory Agency Approvals

Imfinzi
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)
Trodelvy
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Imfinzi or Trodelvy today

If Imfinzi or Trodelvy 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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