Kisqali (ribociclib) vs Xeloda ()

Kisqali (ribociclib) vs Xeloda ()

Kisqali (ribociclib) is a targeted therapy known as a CDK4/6 inhibitor used primarily in combination with hormone therapy for the treatment of HR-positive, HER2-negative advanced or metastatic breast cancer. Xeloda (capecitabine) is an oral chemotherapy drug that is metabolized into 5-fluorouracil (5-FU) in the body and is used to treat various types of cancer, including breast, colorectal, and gastric cancers. The choice between Kisqali and Xeloda would depend on the specific type of cancer, its molecular characteristics, the stage of the disease, and the patient's overall health status, as these medications have different mechanisms of action and are used in different clinical scenarios.

Difference between Kisqali and Xeloda

Metric Kisqali (ribociclib) Xeloda (capecitabine)
Generic name Ribociclib Capecitabine
Indications Advanced or metastatic breast cancer (HR-positive, HER2-negative) Colorectal cancer, metastatic breast cancer
Mechanism of action CDK4/6 inhibitor, halts cell cycle progression Prodrug, converted to 5-fluorouracil, inhibits DNA synthesis
Brand names Kisqali Xeloda
Administrative route Oral Oral
Side effects Neutropenia, nausea, infections, fatigue, diarrhea Hand-foot syndrome, diarrhea, nausea, vomiting, fatigue
Contraindications QT prolongation, liver disease, pregnancy Dihydropyrimidine dehydrogenase (DPD) deficiency, severe renal impairment
Drug class CDK4/6 inhibitor Antimetabolite, fluoropyrimidine
Manufacturer Novartis Roche

Efficacy

Kisqali (Ribociclib) Efficacy in Breast Cancer Treatment

Kisqali (ribociclib) is a targeted therapy drug used in the treatment of certain types of breast cancer. Specifically, it is approved for use in combination with an aromatase inhibitor for the treatment of pre/perimenopausal or postmenopausal women with hormone receptor-positive, human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced or metastatic breast cancer. Ribociclib is a cyclin-dependent kinase inhibitor that works by interfering with the progression of the cell cycle, thereby inhibiting the proliferation of cancer cells.

Clinical trials have demonstrated the efficacy of Kisqali in improving progression-free survival in patients with advanced breast cancer. In the MONALEESA-2, MONALEESA-7, and MONALEESA-3 clinical trials, patients treated with ribociclib in combination with endocrine therapy had a significant delay in disease progression compared to those who received endocrine therapy alone. The MONALEESA trials showed that the addition of ribociclib resulted in a substantial increase in median progression-free survival, highlighting its benefit in the treatment regimen for eligible breast cancer patients.

Xeloda (Capecitabine) Efficacy in Breast Cancer Treatment

Xeloda (capecitabine) is an oral chemotherapy medication that is used to treat breast cancer among other types of cancer. It is a prodrug that is converted to 5-fluorouracil (5-FU) in the body, which is a cytotoxic agent that interferes with DNA synthesis and cell division. Xeloda is indicated for the treatment of patients with metastatic breast cancer, and it is often used when standard chemotherapy options have not been successful or in combination with other drugs for enhanced efficacy.

The efficacy of Xeloda in breast cancer treatment has been established through several clinical studies. In metastatic settings, Xeloda has been shown to be effective as a single agent and also in combination with other chemotherapeutic agents. Studies have indicated that Xeloda can improve response rates and may also contribute to an increase in overall survival in certain patient populations. Its oral administration is a significant advantage, providing a more convenient option for patients compared to intravenous chemotherapy regimens.

Regulatory Agency Approvals

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

Access Kisqali or Xeloda today

If Kisqali or Xeloda 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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