Lonsurf (trifluridine/tipiracil) vs Xeloda ()
Lonsurf (trifluridine/tipiracil) vs Xeloda ()
Lonsurf (trifluridine/tipiracil) and Xeloda (capecitabine) are both oral chemotherapeutic agents used in the treatment of metastatic colorectal cancer, among other conditions. Lonsurf is typically considered when other treatments have failed and works by incorporating into DNA and inhibiting a protein involved in cancer cell growth, while Xeloda is a prodrug that converts into 5-fluorouracil in the body, interfering with DNA synthesis and slowing cancer growth. The choice between Lonsurf and Xeloda would depend on the individual's specific medical history, prior treatments, potential side effects, and the treating physician's assessment of the most appropriate therapy for their condition.
Difference between Lonsurf and Xeloda
Metric | Lonsurf (trifluridine/tipiracil) | Xeloda (capecitabine) |
---|---|---|
Generic name | Trifluridine/Tipiracil | Capecitabine |
Indications | Metastatic colorectal cancer, Gastric cancer | Metastatic colorectal cancer, Metastatic breast cancer |
Mechanism of action | Thymidine-based nucleoside analogue; inhibits cell proliferation | Prodrug of 5-fluorouracil; inhibits thymidylate synthase |
Brand names | Lonsurf | Xeloda |
Administrative route | Oral | Oral |
Side effects | Neutropenia, anemia, fatigue, nausea, decreased appetite | Hand-foot syndrome, diarrhea, nausea, vomiting, fatigue |
Contraindications | Severe bone marrow suppression, severe renal impairment | DPD (dihydropyrimidine dehydrogenase) deficiency |
Drug class | Antineoplastic combination | Antimetabolite |
Manufacturer | Taiho Oncology | Roche |
Efficacy
Efficacy of Lonsurf (trifluridine/tipiracil) in Colorectal Cancer
Lonsurf, containing the active ingredients trifluridine and tipiracil, is a medication approved for the treatment of patients with metastatic colorectal cancer who have been previously treated with chemotherapy and biological therapy. Clinical trials have demonstrated the efficacy of Lonsurf in prolonging survival in this patient population. In a pivotal phase III trial, known as the RECOURSE study, patients treated with Lonsurf showed a median overall survival of 7.1 months compared to 5.3 months for those receiving placebo. This indicates a statistically significant improvement in survival for patients with refractory metastatic colorectal cancer.
The RECOURSE trial also measured progression-free survival as a secondary endpoint. Results showed that Lonsurf extended progression-free survival to a median of 2 months compared to 1.7 months for the placebo group. While the improvement in progression-free survival was modest, the overall survival benefit and the safety profile of Lonsurf support its use as a valuable treatment option for patients with limited alternatives.
Efficacy of Xeloda (capecitabine) in Colorectal Cancer
Xeloda, the brand name for capecitabine, is an oral chemotherapeutic agent 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 exerts its anti-cancer effects. Xeloda has been shown to be effective as both monotherapy and in combination with other drugs in the treatment of metastatic colorectal cancer. In clinical studies, Xeloda has demonstrated comparable efficacy to the intravenous 5-FU/leucovorin regimen, which is a standard treatment for colorectal cancer, with the added benefit of oral administration.
One of the key trials establishing the efficacy of Xeloda in colorectal cancer is the X-ACT trial, which showed that adjuvant treatment with Xeloda significantly improved disease-free survival compared to 5-FU/leucovorin in patients with stage III colon cancer. Furthermore, Xeloda has been evaluated in combination with other chemotherapeutic agents, such as oxaliplatin, showing enhanced efficacy in terms of response rates and survival outcomes in metastatic settings. Xeloda's oral administration route offers a convenient alternative to intravenous chemotherapy, potentially improving the quality of life for patients undergoing treatment.
Regulatory Agency Approvals
Lonsurf
Xeloda
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