Keytruda (pembrolizumab) vs Kadcyla (trastuzumab emtansine)

Keytruda (pembrolizumab) vs Kadcyla (trastuzumab emtansine)

Keytruda (pembrolizumab) is an immune checkpoint inhibitor that works by blocking the PD-1 pathway, thereby enabling the immune system to recognize and attack cancer cells, and is commonly used in various cancers including melanoma, lung, and head and neck cancers. Kadcyla (trastuzumab emtansine) is an antibody-drug conjugate that combines the HER2-targeting properties of trastuzumab with the chemotherapy agent emtansine, specifically indicated for HER2-positive breast cancer. The choice between Keytruda and Kadcyla would depend on the specific type and characteristics of the cancer; Keytruda is chosen for cancers with PD-L1 expression or MSI-H/dMMR biomarkers, while Kadcyla is selected for cancers that overexpress HER2.

Difference between Keytruda and Kadcyla

Metric Keytruda (pembrolizumab) Kadcyla (trastuzumab emtansine)
Generic name Pembrolizumab Trastuzumab emtansine
Indications Various types of cancers including melanoma, lung cancer, head and neck cancer, Hodgkin lymphoma, and others HER2-positive breast cancer
Mechanism of action Programmed death receptor-1 (PD-1) blocking antibody Combines HER2-targeted antitumor properties of trastuzumab with the cytotoxic activity of the microtubule-inhibitory agent DM1
Brand names Keytruda Kadcyla
Administrative route Intravenous infusion Intravenous infusion
Side effects Fatigue, musculoskeletal pain, decreased appetite, pruritus, diarrhea, nausea, rash, pyrexia, cough, dyspnea, constipation, pain in extremity, and headache Fatigue, nausea, musculoskeletal pain, hemorrhage, thrombocytopenia, headache, increased liver enzymes, constipation, and peripheral neuropathy
Contraindications Patients with severe hypersensitivity to pembrolizumab or any of its excipients Patients with hypersensitivity to trastuzumab emtansine or any of its components, including trastuzumab or the microtubule inhibitor DM1
Drug class Anti-PD-1 monoclonal antibody Antibody-drug conjugate
Manufacturer Merck & Co. Genentech (a member of the Roche Group)

Efficacy

Keytruda (Pembrolizumab) in Breast Cancer Treatment

Keytruda, also known by its generic name pembrolizumab, is a type of immunotherapy drug that has shown efficacy in the treatment of certain types of breast cancer. Pembrolizumab is a monoclonal antibody that works by blocking the PD-1 pathway, which some cancer cells use to hide from the immune system. By inhibiting this pathway, Keytruda can help the immune system to detect and fight cancer cells. It has been particularly effective in treating triple-negative breast cancer (TNBC), which is a more aggressive and difficult-to-treat form of the disease. Studies have shown that when Keytruda is combined with chemotherapy, it can improve the overall survival and progression-free survival rates in patients with metastatic TNBC.

Kadcyla (Trastuzumab Emtansine) in Breast Cancer Treatment

Kadcyla, also known as trastuzumab emtansine or T-DM1, is a targeted therapy drug used in the treatment of HER2-positive breast cancer. Kadcyla is a combination of the monoclonal antibody trastuzumab and the chemotherapy drug emtansine. Trastuzumab binds to the HER2 receptor on the cancer cells, and emtansine enters the cells to deliver its cytotoxic effect. This dual mechanism allows for a targeted approach to destroy cancer cells while sparing healthy cells. Clinical trials have demonstrated that Kadcyla significantly extends progression-free survival and overall survival in patients with HER2-positive metastatic breast cancer who have previously received other treatments, including trastuzumab and a taxane.

Comparative Efficacy in Breast Cancer Management

When comparing the efficacy of Keytruda and Kadcyla, it is important to note that they are used to treat different subtypes of breast cancer. Keytruda is primarily used for PD-L1 positive, triple-negative breast cancer, while Kadcyla is utilized for HER2-positive breast cancer. Both drugs have been shown to improve outcomes in their respective indications, but they are not directly comparable due to the differing mechanisms of action and patient populations they serve. The choice of treatment depends on the specific characteristics of the breast cancer and the patient's overall health and treatment history.

Conclusion

Both Keytruda and Kadcyla have brought significant advancements in the treatment of breast cancer, offering hope for improved survival rates and better quality of life for patients with these specific subtypes of the disease. Their efficacy highlights the importance of personalized medicine and the need for continued research to develop targeted therapies that can effectively combat the various forms of breast cancer. As with any medication, the use of Keytruda and Kadcyla should be guided by a healthcare professional, taking into account the individual patient's condition and the most current clinical evidence.

Regulatory Agency Approvals

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

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