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Trifluridine and tipiracil with bevacizumab is approved by FDA for previously treated metastatic colorectal cancer

Sai SreeWritten by Sai SreeMedically ReviewedUpdated August 14, 20234 min read
Trifluridine and tipiracil with bevacizumab is approved by FDA for previously treated metastatic colorectal cancer
In this article
  1. FDA Approval of Lonsurf with Bevacizumab for Metastatic Colorectal Cancer
  2. SUNLIGHT Trial Results: Survival and Efficacy Outcomes
  3. Adverse Reactions and Recommended Dosage Guidelines
  4. How CancerFax Helps

FDA Approval of Lonsurf with Bevacizumab for Metastatic Colorectal Cancer

August 2023: For metastatic colorectal cancer (mCRC) that has already been treated with fluoropyrimidine, oxaliplatin, and irinotecan-based chemotherapy, an anti-VEGF biological therapy, and if RAS wild-type, an anti-EGFR therapy, the Food and Drug Administration has approved trifluridine and tipiracil (LONSURF, Taiho Oncology, Inc.). LONSURF, a single-agent medication, has already received FDA approval for this use in September 2015.

SUNLIGHT Trial Results: Survival and Efficacy Outcomes

In SUNLIGHT (NCT04737187), a randomised, open-label, multicenter, international trial comparing LONSURF with bevacizumab to single-agent LONSURF in 492 patients with metastatic colorectal cancer who had received a maximum of two prior chemotherapy regimens and showed progression of their disease or intolerance to the last regimen, safety and efficacy were assessed.

Overall survival (OS) and progression-free survival (PFS) were the key effectiveness outcome metrics. Patients assigned to the LONSURF plus bevacizumab arm of the trial showed a statistically significant OS improvement when compared to patients assigned to the LONSURF arm (Hazard ratio 0.61; 95% CI: 0.49, 0.77; 1-sided p0.001). The median OS for the LONSURF plus bevacizumab arm was 10.8 months (95% CI: 9.4, 11.8) and for the LONSURF arm was 7.5 months (95% CI: 6.3, 8.6). In the LONSURF plus bevacizumab arm, the median PFS was 5.6 months (95% CI: 4.5, 5.9), while in the LONSURF arm, it was 2.4 months (95% CI: 2.1, 3.2) (Hazard ratio: 0.44; 95% CI: 0.36, 0.54; 1-sided p0.001).

Adverse Reactions and Recommended Dosage Guidelines

Neutropenia, anaemia, thrombocytopenia, fatigue, nausea, increased AST, increased ALT, increased alkaline phosphatase, decreased sodium, diarrhoea, stomach discomfort, and decreased appetite are the most frequent side events or laboratory abnormalities for LONSURF with bevacizumab (20%).

On days 1 through 5 and days 8 through 12 of each 28-day cycle, the recommended dose of LONSURF is 35 mg/m2 taken orally twice daily with food. For details about bevacizumab dosage, consult the prescribing information.

View full prescribing information for LONSURF.

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Sai Sree

About Sai Sree

✓ Reviewed for medical accuracy by the CancerFax review panel.

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This article is for educational purposes only and should not replace medical advice, diagnosis, or treatment from a qualified oncology specialist. Every patient's case is different. Treatment decisions should always be made after a review of complete medical records by the treating medical team.

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