Cotellic (cobimetinib) vs Zynyz (retifanlimab-dlwr)

Cotellic (cobimetinib) vs Zynyz (retifanlimab-dlwr)

Cotellic (cobimetinib) is a MEK inhibitor used in combination with vemurafenib, a BRAF inhibitor, for the treatment of patients with advanced melanoma that has a BRAF V600 mutation. Zynyz (retifanlimab-dlwr) is an anti-PD-1 monoclonal antibody indicated for the treatment of adult patients with locally advanced or metastatic squamous cell carcinoma of the anal canal (SCAC) who have progressed on or who are intolerant of platinum-based chemotherapy. When deciding between these two medications, it is crucial to consider the type of cancer being treated, as their indications and mechanisms of action are specific to different cancer types and genetic profiles.

Difference between Cotellic and Zynyz

Metric Cotellic (cobimetinib) Zynyz (retifanlimab-dlwr)
Generic name cobimetinib retifanlimab-dlwr
Indications Used in combination with vemurafenib for the treatment of patients with advanced melanoma with a BRAF V600 mutation Used for the treatment of adult patients with locally advanced or metastatic squamous cell carcinoma of the anal canal (SCAC) who have progressed on or who are intolerant of platinum-based chemotherapy
Mechanism of action MEK inhibitor, which works by inhibiting mitogen-activated protein kinase enzymes MEK1 and MEK2 PD-1 blocking antibody, which works by inhibiting the programmed death receptor-1 (PD-1) pathway
Brand names Cotellic Zynyz
Administrative route Oral Intravenous
Side effects Diarrhea, photosensitivity, nausea, fever, vomiting, etc. Infusion-related reactions, fatigue, musculoskeletal pain, gastrointestinal disorders, skin rash, etc.
Contraindications None known beyond hypersensitivity to cobimetinib or its excipients None known beyond hypersensitivity to retifanlimab or its excipients
Drug class Antineoplastic agent, MEK inhibitor Antineoplastic agent, immune checkpoint inhibitor
Manufacturer Genentech (a member of the Roche Group) Incysus Therapeutics, Inc.

Efficacy

Efficacy of Cotellic (Cobimetinib) in Skin Cancer

Cotellic (cobimetinib) is a medication that has been approved for use in combination with another drug called Zelboraf (vemurafenib) for the treatment of a specific type of skin cancer known as melanoma. Cobimetinib specifically targets melanoma that cannot be removed by surgery or that has metastasized, and it is only effective in patients whose tumors express a gene mutation called BRAF V600E or V600K. The combination of cobimetinib and vemurafenib has been shown to improve progression-free survival in patients with this type of advanced melanoma compared to vemurafenib alone. The efficacy of cobimetinib in treating skin cancer is largely attributed to its ability to inhibit the activity of MEK proteins, which are part of a signaling pathway that contributes to the growth and survival of cancer cells.

Clinical trials have demonstrated that patients treated with the combination of cobimetinib and vemurafenib experience a significant delay in the progression of their disease. The co-administration of these drugs has been associated with an increase in the overall response rate, meaning that a higher percentage of patients experience a reduction in tumor size. However, it is important to note that the response to cobimetinib can vary, and not all patients with BRAF V600E or V600K mutation-positive melanoma will respond to the treatment. Additionally, the development of resistance to this combination therapy is possible, and researchers continue to investigate strategies to overcome this challenge.

Efficacy of Zynyz (Retifanlimab-dlwr) in Skin Cancer

Zynyz (retifanlimab-dlwr) is an investigational drug whose efficacy in skin cancer is currently being evaluated in clinical trials. Retifanlimab is a type of immunotherapy known as a checkpoint inhibitor, which works by targeting a protein called PD-1 on the surface of T cells. By blocking PD-1, retifanlimab is designed to enhance the body's immune response against cancer cells. While the precise efficacy of retifanlimab in skin cancer is still under investigation, the mechanism of action suggests that it has the potential to be effective in treating certain types of skin cancers, particularly those that are known to be responsive to immune checkpoint blockade.

As of the knowledge cutoff date, retifanlimab has not been approved by regulatory agencies for the treatment of skin cancer, and its efficacy and safety profile are still being determined through ongoing clinical trials. The results of these trials will provide critical information regarding the potential benefits and risks of retifanlimab in patients with skin cancer. Until such data is available, the efficacy of Zynyz (retifanlimab-dlwr) in the treatment of skin cancer remains to be fully established, and its use in this context is considered experimental.

Regulatory Agency Approvals

Cotellic
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Therapeutic Goods Administration (TGA), Australia
Zynyz
  • Food and Drug Administration (FDA), USA

Access Cotellic or Zynyz today

If Cotellic or Zynyz 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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