Xeloda () vs Nerlynx (neratinib)

Xeloda () vs Nerlynx (neratinib)

Xeloda (capecitabine) is an oral chemotherapy drug that is commonly used to treat certain types of breast and colorectal cancer by interfering with the growth of cancer cells. Nerlynx (neratinib), on the other hand, is an oral tyrosine kinase inhibitor specifically designed to treat a certain kind of early-stage breast cancer that has a high chance of coming back and is HER2-positive, by blocking specific enzymes that promote cell growth. The choice between Xeloda and Nerlynx would depend on the specific characteristics and stage of the cancer, the presence of HER2 receptors, and the overall treatment plan determined by the healthcare provider.

Difference between Xeloda and Nerlynx

Metric Xeloda () Nerlynx (neratinib)
Generic name Capecitabine Neratinib
Indications Colorectal cancer, metastatic breast cancer Early-stage breast cancer, extended adjuvant treatment of HER2-positive breast cancer
Mechanism of action Antimetabolite, thymidylate synthase inhibitor Tyrosine kinase inhibitor
Brand names Xeloda Nerlynx
Administrative route Oral Oral
Side effects Hand-foot syndrome, diarrhea, nausea, vomiting, abdominal pain Diarrhea, nausea, abdominal pain, fatigue, rash
Contraindications Dihydropyrimidine dehydrogenase (DPD) deficiency Liver impairment, severe renal impairment
Drug class Antimetabolite, Fluoropyrimidine Tyrosine kinase inhibitor
Manufacturer Roche Puma Biotechnology

Efficacy

Xeloda (Capecitabine) in Breast Cancer Treatment

Xeloda, also known by its generic name capecitabine, is an oral chemotherapy medication that is used in the treatment of breast cancer. It is a prodrug that is converted to 5-fluorouracil (5-FU) in the body, which is a cytotoxic agent that inhibits DNA synthesis and function, leading to cell death. The efficacy of Xeloda has been demonstrated in several clinical trials, particularly in patients with metastatic breast cancer. When used either as monotherapy or in combination with other drugs, Xeloda has shown to be effective in improving overall survival rates, delaying disease progression, and achieving partial or complete tumor responses in a significant number of patients.

Nerlynx (Neratinib) in Breast Cancer Management

Nerlynx, with the active ingredient neratinib, is an oral tyrosine kinase inhibitor that targets HER2-positive breast cancer, a subtype in which cancer cells have higher levels of the HER2 protein. The efficacy of Nerlynx has been primarily evaluated in the extended adjuvant treatment of HER2-positive early breast cancer. In clinical trials, Nerlynx has been shown to significantly reduce the risk of cancer recurrence when used following adjuvant trastuzumab therapy. This benefit is particularly notable in patients who have completed one year of trastuzumab, a standard treatment for HER2-positive breast cancer.

Comparative Efficacy in Different Settings

While both Xeloda and Nerlynx are used in the treatment of breast cancer, their application and efficacy differ based on the cancer's characteristics and the treatment setting. Xeloda is often used in metastatic settings and can be effective in HER2-negative breast cancer, while Nerlynx is specifically indicated for early-stage HER2-positive breast cancer in the extended adjuvant setting. The choice between these medications, or their use in combination with other treatments, depends on factors such as the stage of cancer, HER2 status, and previous treatments the patient has undergone.

Conclusion on Efficacy

In conclusion, both Xeloda and Nerlynx have shown efficacy in the treatment of breast cancer, albeit in different contexts and patient populations. Xeloda's role in metastatic breast cancer and its ability to improve survival and response rates make it a valuable option for patients with advanced disease. On the other hand, Nerlynx serves as an important treatment for reducing the risk of recurrence in early-stage HER2-positive breast cancer following initial therapy with trastuzumab. The use of these medications should be tailored to the individual patient's needs and should be guided by the oncologist's expertise in the light of the latest clinical evidence.

Regulatory Agency Approvals

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

Access Xeloda or Nerlynx today

If Xeloda 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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