Opdivo (Nivolumab) vs Trodelvy (sacituzumab govitecan-hziy)

Opdivo (Nivolumab) vs Trodelvy (sacituzumab govitecan-hziy)

Opdivo (nivolumab) is an immune checkpoint inhibitor that works by blocking the PD-1 pathway, which can help the immune system detect and fight cancer cells, and it is commonly used in various types of cancers including melanoma, lung cancer, and kidney cancer. Trodelvy (sacituzumab govitecan-hziy), on the other hand, is an antibody-drug conjugate that targets the Trop-2 receptor on cancer cells to deliver a cytotoxic drug directly to the tumor, and is primarily used for the treatment of triple-negative breast cancer. When deciding between these two medications, it is essential to consider the specific type of cancer being treated, as their effectiveness and indications are based on the cancer's unique properties and the patient's overall health condition.

Difference between Opdivo and Trodelvy

Metric Opdivo (Nivolumab) Trodelvy (sacituzumab govitecan-hziy)
Generic name Nivolumab Sacituzumab govitecan-hziy
Indications Various types of cancers, including melanoma, lung cancer, and renal cell carcinoma Metastatic triple-negative breast cancer, urothelial cancer
Mechanism of action PD-1 inhibitor that enhances T-cell function against cancer cells Antibody-drug conjugate targeting TROP-2 for delivering cytotoxic agent to cancer cells
Brand names Opdivo Trodelvy
Administrative route Injection (IV) Injection (IV)
Side effects Fatigue, rash, musculoskeletal pain, pruritus, diarrhea, nausea Neutropenia, diarrhea, nausea, fatigue, anemia, vomiting, alopecia, constipation, decreased appetite, rash
Contraindications Severe hypersensitivity to nivolumab or any of its excipients Severe hypersensitivity to sacituzumab govitecan-hziy or any of its excipients
Drug class Monoclonal antibody, Immune checkpoint inhibitor Antibody-drug conjugate
Manufacturer Bristol Myers Squibb Gilead Sciences, Inc.

Efficacy

Efficacy of Opdivo (Nivolumab) in Urothelial Carcinoma

Opdivo (nivolumab) is a programmed death receptor-1 (PD-1) blocking antibody used in the treatment of various cancers, including urothelial carcinoma. In urothelial carcinoma, the efficacy of Opdivo has been demonstrated in several clinical trials. For instance, the CheckMate 275 trial, a phase II study, evaluated nivolumab in patients with metastatic or surgically unresectable urothelial carcinoma who had progressed on or after platinum-based chemotherapy. The study reported an objective response rate (ORR) of approximately 20%, with a small percentage of patients achieving a complete response. The median overall survival (OS) was noted to be around 8.7 months, indicating a potential survival benefit for this patient population.

Long-term Efficacy and Survival Benefits

Further analysis of long-term data from the CheckMate 275 trial has shown sustained responses and survival benefits in a subset of patients treated with Opdivo. Some patients experienced durable responses lasting more than two years, which is significant given the aggressive nature of metastatic urothelial carcinoma. The long-term follow-up suggests that while not all patients will respond to Opdivo, those who do may achieve prolonged survival.

Efficacy of Trodelvy (Sacituzumab Govitecan-hziy) in Urothelial Carcinoma

Trodelvy (sacituzumab govitecan-hziy) is an antibody-drug conjugate directed against Trop-2, a protein overexpressed in many epithelial cancers, including urothelial carcinoma. Trodelvy has shown promise in the treatment of urothelial carcinoma, particularly in the TROPHY-U-01 trial, a phase II study. This study evaluated Trodelvy in patients with metastatic urothelial cancer who had previously received platinum-based chemotherapy and PD-1 or PD-L1 inhibitors. The trial reported an ORR of 27%, with a median duration of response of 7.2 months, suggesting that Trodelvy can induce meaningful tumor shrinkage in a significant proportion of patients.

Considerations for Treatment Selection

When considering the efficacy of Opdivo and Trodelvy for the treatment of urothelial carcinoma, it is important to take into account individual patient factors such as prior treatment history, PD-L1 expression status, and overall health. Both agents have demonstrated efficacy in this setting, but their use may be influenced by the specific clinical scenario. As with all cancer treatments, the potential benefits must be weighed against the possible side effects, and treatment decisions should be made in collaboration with a healthcare professional specialized in oncology.

Regulatory Agency Approvals

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

Access Opdivo or Trodelvy today

If Opdivo 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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