Keytruda (pembrolizumab) vs Nerlynx (neratinib)

Keytruda (pembrolizumab) vs Nerlynx (neratinib)

Keytruda (pembrolizumab) is an immune checkpoint inhibitor used primarily for various types of cancer, including melanoma, lung cancer, head and neck cancer, and others, by enhancing the body's immune response against cancer cells. Nerlynx (neratinib) is a tyrosine kinase inhibitor specifically indicated for the extended adjuvant treatment of HER2-positive breast cancer, aiming to reduce the risk of cancer recurrence after initial treatment. When deciding between these medications, it is essential to consider the specific type of cancer being treated, as Keytruda is used for a broader range of cancers, while Nerlynx is tailored for a specific subtype of breast cancer, and the decision should be made in consultation with an oncologist who can evaluate the patient's individual condition and treatment history.

Difference between Keytruda and Nerlynx

Metric Keytruda (pembrolizumab) Nerlynx (neratinib)
Generic name Pembrolizumab Neratinib
Indications Various types of cancers including melanoma, lung cancer, head and neck cancer, Hodgkin lymphoma, and stomach cancer Extended adjuvant treatment of HER2-positive breast cancer
Mechanism of action Programmed death receptor-1 (PD-1) blocking antibody Tyrosine kinase inhibitor
Brand names Keytruda Nerlynx
Administrative route Intravenous injection Oral
Side effects Fatigue, musculoskeletal pain, decreased appetite, pruritus, diarrhea, nausea, rash, pyrexia, cough, dyspnea, constipation, pain in extremity, and headache Diarrhea, nausea, abdominal pain, fatigue, vomiting, rash, stomatitis, decreased appetite, muscle spasms, dyspepsia, AST or ALT increased, nail disorder, dry skin, abdominal distention, weight decreased, and urinary tract infection
Contraindications Individuals with hypersensitivity to pembrolizumab or any of its excipients Individuals with hypersensitivity to neratinib or any of its excipients
Drug class Anti-PD-1 monoclonal antibody Tyrosine kinase inhibitor
Manufacturer Merck & Co. Puma Biotechnology

Efficacy

Keytruda (Pembrolizumab) Efficacy in Breast Cancer

Keytruda, also known by its generic name pembrolizumab, is an immunotherapy drug that has shown efficacy in the treatment of certain types of breast cancer. Specifically, pembrolizumab is a PD-1 (Programmed Death receptor-1) inhibitor that helps to activate the immune system to recognize and fight cancer cells. Its use in breast cancer is generally focused on PD-L1 positive, metastatic triple-negative breast cancer (TNBC), which is a more aggressive and difficult-to-treat form of the disease. Clinical trials have demonstrated that when combined with chemotherapy, Keytruda can improve progression-free survival in patients with advanced TNBC who express PD-L1, compared to chemotherapy alone.

However, the efficacy of Keytruda can vary based on the expression of PD-L1 and the stage of breast cancer. The KEYNOTE-355 trial, for instance, showed that patients with a PD-L1 combined positive score (CPS) of 10 or more experienced a significant improvement in progression-free survival when treated with Keytruda in combination with chemotherapy. This highlights the importance of biomarker testing in personalizing treatment for breast cancer patients.

Nerlynx (Neratinib) Efficacy in Breast Cancer

Nerlynx, or neratinib, is an oral tyrosine kinase inhibitor that targets the HER2 protein, which can promote the growth of cancer cells. In breast cancer, Nerlynx is used for the extended adjuvant treatment of HER2-positive early-stage breast cancer in patients who have previously been treated with trastuzumab-based therapy. The ExteNET study, a pivotal phase III clinical trial, demonstrated that Nerlynx significantly reduced the risk of invasive disease recurrence or death by 27% compared to placebo in this patient population.

Moreover, the efficacy of Nerlynx is particularly notable in patients who initiate treatment within one year of completing trastuzumab therapy, underscoring the importance of timely treatment. The benefit of Nerlynx has been shown to persist over time, with a sustained reduction in the risk of recurrence. However, the effectiveness of Nerlynx can be accompanied by side effects, such as diarrhea, which can be managed with prophylactic and symptomatic treatments. Patients considering Nerlynx should discuss the potential benefits and risks with their healthcare provider.

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

Access Keytruda or Nerlynx today

If Keytruda or Nerlynx 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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