Fotivda (tivozanib) vs Inlyta (axitinib)

Fotivda (tivozanib) vs Inlyta (axitinib)

Fotivda (tivozanib) and Inlyta (axitinib) are both oral medications used to treat advanced renal cell carcinoma (RCC), a type of kidney cancer. Fotivda is a once-daily tyrosine kinase inhibitor that targets vascular endothelial growth factor receptors, which can help to slow tumor growth and reduce the supply of blood to the tumor, and is typically used as a third-line treatment option. Inlyta, taken twice daily, also targets similar pathways but may be used in different lines of therapy and has a different side effect profile, which may influence the choice of treatment based on individual patient health, prior treatments, and physician recommendation.

Difference between Fotivda and Inlyta

Metric Fotivda (tivozanib) Inlyta (axitinib)
Generic name Tivozanib Axitinib
Indications Advanced renal cell carcinoma Advanced renal cell carcinoma
Mechanism of action VEGF receptor tyrosine kinase inhibitor VEGF receptor tyrosine kinase inhibitor
Brand names Fotivda Inlyta
Administrative route Oral Oral
Side effects Hypertension, diarrhea, fatigue, dysphonia, etc. Diarrhea, hypertension, fatigue, nausea, dysphonia, etc.
Contraindications Hypersensitivity to tivozanib or any component of the formulation Hypersensitivity to axitinib or any component of the formulation
Drug class Tyrosine kinase inhibitor Tyrosine kinase inhibitor
Manufacturer Aveo Pharmaceuticals Pfizer

Efficacy

Fotivda (Tivozanib) Efficacy in Kidney Cancer

Fotivda (tivozanib) is an oral, once-daily, vascular endothelial growth factor (VEGF) tyrosine kinase inhibitor (TKI) specifically indicated for the treatment of adult patients with relapsed or refractory advanced renal cell carcinoma (RCC). The efficacy of Fotivda in kidney cancer was demonstrated in a phase 3 clinical trial known as TIVO-3. This trial compared tivozanib to sorafenib, another TKI, in patients with advanced RCC who had undergone two or more prior systemic treatments. The results showed that tivozanib significantly improved progression-free survival (PFS) compared to sorafenib, with a median PFS of 5.6 months versus 3.9 months, respectively. Additionally, a higher response rate was observed in the tivozanib group.

Inlyta (Axitinib) Efficacy in Kidney Cancer

Inlyta (axitinib) is another oral, potent, and selective inhibitor of VEGF receptors 1, 2, and 3, which are implicated in the growth and progression of renal cell carcinoma. Inlyta is approved for the treatment of advanced RCC after failure of one prior systemic therapy. The AXIS trial, a pivotal phase 3 study, established the efficacy of axitinib in this setting. In this study, axitinib demonstrated a median PFS of 6.7 months compared to 4.7 months for sorafenib, the active comparator. Axitinib's efficacy has been shown to be consistent across various patient subgroups, including those with different risk factors and prior treatments.

Comparative Efficacy and Considerations

When comparing Fotivda and Inlyta, both have shown to be effective in improving PFS in patients with advanced RCC. However, direct comparisons between the two drugs are challenging due to differences in trial designs, patient populations, and comparator agents. It is important for healthcare providers to consider individual patient characteristics, prior treatments, and potential side effects when choosing between these medications. The choice of treatment should be personalized to achieve the best possible outcome for each patient.

Conclusion

In conclusion, both Fotivda (tivozanib) and Inlyta (axitinib) have demonstrated efficacy in the treatment of advanced renal cell carcinoma, offering valuable options for patients who have experienced disease progression after prior treatments. Their roles in the management of RCC continue to evolve as ongoing research and clinical experience further define their optimal use in various treatment sequences and combinations. Healthcare professionals should remain abreast of the latest evidence to inform their clinical decisions in the management of kidney cancer.

Regulatory Agency Approvals

Fotivda
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Inlyta
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

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If Fotivda or Inlyta 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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