Xeloda () vs Fruzaqla (fruquintinib)

Xeloda () vs Fruzaqla (fruquintinib)

Xeloda (capecitabine) is an orally-administered chemotherapeutic agent commonly used to treat various types of cancer, including colorectal and breast cancers, by interfering with DNA synthesis and slowing the growth of cancer cells. Fruquintinib is a newer, orally-administered small molecule drug that targets vascular endothelial growth factor receptors (VEGFR), which are involved in the angiogenesis (formation of new blood vessels) that tumors need to grow; it is primarily used in the treatment of metastatic colorectal cancer after failure of standard chemotherapy. When deciding between Xeloda and Fruquintinib, a patient should consider factors such as the specific type and stage of cancer, previous treatments, potential side effects, and the mechanism of action of each drug, in consultation with their healthcare provider.

Difference between Xeloda and Fruzaqla

Metric Xeloda () Fruzaqla (fruquintinib)
Generic name Capecitabine Fruquintinib
Indications Colorectal cancer, metastatic breast cancer Metastatic colorectal cancer
Mechanism of action Antimetabolite, thymidine phosphorylase activation VEGFR inhibitor
Brand names Xeloda Fruzaqla
Administrative route Oral Oral
Side effects Hand-foot syndrome, diarrhea, nausea Hypertension, fatigue, hand-foot syndrome
Contraindications Severe renal impairment, DPD deficiency Not provided
Drug class Antimetabolite Tyrosine kinase inhibitor
Manufacturer Roche Hutchison MediPharma

Efficacy

Xeloda (Capecitabine) in Colorectal Cancer Treatment

Xeloda, the brand name for capecitabine, is an orally-administered chemotherapeutic agent that is commonly used in the treatment of colorectal cancer. It is a prodrug that is enzymatically converted to 5-fluorouracil (5-FU) in the body, which then inhibits DNA synthesis and slows the growth of tumor cells. Clinical trials have demonstrated that Xeloda is effective as a first-line treatment for metastatic colorectal cancer, and it is often used in combination with other drugs to enhance its efficacy. Xeloda has been shown to be comparable in effectiveness to intravenous 5-FU when used in combination with other agents such as oxaliplatin or irinotecan.

Fruquintinib (Elunate) and Its Role in Colorectal Cancer

Fruquintinib, marketed under the brand name Elunate, is a relatively new oral kinase inhibitor that targets vascular endothelial growth factor receptors (VEGFR), which play a key role in angiogenesis, the formation of new blood vessels that supply nutrients to tumors. In colorectal cancer, fruquintinib has been studied in the metastatic setting for patients who have progressed on standard therapies. The efficacy of fruquintinib was evaluated in a Phase III clinical trial, which demonstrated a significant improvement in overall survival and progression-free survival in patients with metastatic colorectal cancer compared to placebo.

Comparative Efficacy in Treatment Regimens

When considering the efficacy of Xeloda and fruquintinib, it is important to note that they are often used at different stages of colorectal cancer treatment. Xeloda is frequently used as a first-line treatment, while fruquintinib is typically reserved for patients who have failed previous treatments. Both medications have shown efficacy in improving patient outcomes, but their mechanisms of action and points of intervention in the disease process differ. As a result, they may be used sequentially rather than interchangeably in the treatment of colorectal cancer.

Conclusion

In conclusion, both Xeloda and fruquintinib have demonstrated efficacy in the treatment of colorectal cancer, albeit at different stages of the disease. Xeloda's role as an alternative to intravenous 5-FU and its oral administration make it a convenient option for patients. Fruquintinib's targeted approach against VEGFRs offers a valuable option for patients with metastatic disease who have limited treatment options. The selection of either drug should be based on the individual patient's disease characteristics, prior treatment history, and overall health status, with the guidance of a healthcare professional.

Regulatory Agency Approvals

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

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If Xeloda or Fruzaqla 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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