Xeloda () vs Phesgo (pertuzumab, trastuzumab, and hyaluronidase)

Xeloda () vs Phesgo (pertuzumab, trastuzumab, and hyaluronidase)

Xeloda (capecitabine) is an oral chemotherapy medication that is commonly used to treat breast and colorectal cancers by interfering with the DNA synthesis of cancer cells, causing them to die. Phesgo, on the other hand, is a subcutaneous injection combining two monoclonal antibodies, pertuzumab and trastuzumab, with hyaluronidase, and is specifically indicated for the treatment of HER2-positive breast cancer by targeting the HER2 protein on cancer cells. The choice between Xeloda and Phesgo would largely depend on the specific type of cancer a patient has, its molecular characteristics such as HER2 status, and the overall treatment plan determined by the healthcare provider.

Difference between Xeloda and Phesgo

Metric Xeloda () Phesgo (pertuzumab, trastuzumab, and hyaluronidase)
Generic name Capecitabine Pertuzumab, Trastuzumab, and Hyaluronidase-zzxf
Indications Colorectal cancer, metastatic breast cancer HER2-positive breast cancer
Mechanism of action Thymidine phosphorylase activation, interfering with DNA synthesis HER2 receptor inhibition, preventing cell growth and proliferation
Brand names Xeloda Phesgo
Administrative route Oral Subcutaneous injection
Side effects Hand-foot syndrome, diarrhea, nausea Infusion-related reactions, alopecia, fatigue
Contraindications Dihydropyrimidine dehydrogenase (DPD) deficiency History of severe allergic reactions to active substances
Drug class Antimetabolite, fluoropyrimidine Monoclonal antibodies, enzyme inhibitor
Manufacturer Roche Roche

Efficacy

Xeloda (Capecitabine) in Breast Cancer Treatment

Xeloda, also known by its generic name capecitabine, is an oral chemotherapy medication that is used to treat breast cancer. It is a prodrug that is converted into 5-fluorouracil (5-FU) in the body, which is a cytotoxic agent that interferes with DNA synthesis and hinders the growth of cancer cells. Xeloda is particularly effective in the treatment of metastatic breast cancer, especially after the failure of standard chemotherapy regimens. Clinical trials have demonstrated that Xeloda is effective in prolonging progression-free survival and overall survival in some patients with metastatic breast cancer. Additionally, it has been used in combination with other drugs to enhance its efficacy.

Phesgo (Pertuzumab, Trastuzumab, and Hyaluronidase) in Breast Cancer Treatment

Phesgo is a combination of two monoclonal antibodies, pertuzumab and trastuzumab, with hyaluronidase, an enzyme that helps increase the absorption of the drugs. This combination is used for the treatment of HER2-positive breast cancer, which is a subtype of breast cancer characterized by the overexpression of the HER2 protein. Pertuzumab and trastuzumab work synergistically to inhibit the signaling pathways that promote the growth and survival of HER2-positive cancer cells. Phesgo has been shown to be effective when used in combination with chemotherapy as a first-line treatment for metastatic breast cancer and as an adjuvant treatment for early HER2-positive breast cancer.

Comparative Efficacy in Clinical Settings

The efficacy of Xeloda and Phesgo in treating breast cancer varies based on the cancer's characteristics and the stage at which treatment is initiated. Xeloda's effectiveness is generally considered in the context of metastatic disease, often as a subsequent line of therapy. In contrast, Phesgo's efficacy has been established in both the metastatic setting and as an adjuvant therapy, providing a significant benefit in terms of disease-free survival and overall survival. The combination of pertuzumab and trastuzumab in Phesgo targets the HER2-positive breast cancer specifically, making it a targeted therapy with a distinct mechanism of action compared to Xeloda's broader cytotoxic effects.

Conclusion on Efficacy

Both Xeloda and Phesgo have demonstrated efficacy in the treatment of breast cancer, albeit in different settings and patient populations. Xeloda is a valuable option for patients with metastatic breast cancer, particularly when other treatments have failed. Phesgo, on the other hand, has expanded treatment options for patients with HER2-positive breast cancer, offering a convenient subcutaneous administration and the potential for improved outcomes when used early in the treatment regimen. The choice between these medications depends on the specific characteristics of the breast cancer and the overall treatment plan designed by healthcare professionals.

Regulatory Agency Approvals

Xeloda
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Phesgo
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

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If Xeloda or Phesgo 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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