FDA Approves Trifluridine and Tipiracil with Bevacizumab for Metastatic Colorectal Cancer (mCRC) with Specific Mutation

On August 2, 2023, the U.S. Food and Drug Administration approved trifluridine and tipiracil (LONSURF) with bevacizumab for the treatment of metastatic colorectal cancer (mCRC) in patients who have previously received a maximum of two chemotherapy agents and showed progression or intolerance to the last agent. Single-agent LONSURF was approved for the same indication in September 2015.

 

Study ID number: NCT04737187

 

Approval was based on the SUNLIGHT trial (NCT04737187), a randomized, open-label, multicenter, global study that included 492 patients with mCRC. These patients had previously received regimens based on fluoropyrimidine, oxaliplatin, and irinotecan; anti-VEGF biological therapy; and if the tumor showed RAS wild-type mutation, an anti-EGFR therapy. Patients were confirmed to have mCRC with the necessary mutations using an FDA-approved test.

 

Trifluridine and tipiracil with bevacizumab were administered orally at 35 mg/m2 twice daily with food on days 1 through 5 and days 8 through 12 of each 28-day cycle. Treatment continued until disease progression or unacceptable toxicity.

 

Efficacy was established based on the primary outcome measures of overall survival (OS) and progression-free survival (PFS). Overall survival was statistically significant in patients treated with LONSURF plus bevacizumab compared to those who received LONSURF alone, with a hazard ratio of 0.61 (95% CI: 0.49, 0.77; 1-sided p<0.001). The median OS was 10.8 months vs. 7.5 months in the LONSURF plus bevacizumab arm (95% CI: 9.4, 11.8) and the LONSURF arm (95% CI: 6.3, 8.6), respectively. The median PFS was 5.6 months in the LONSURF plus bevacizumab arm (95% CI: 4.5, 5.9) and 2.4 months in the LONSURF arm (95% CI: 2.1, 3.2) (Hazard ratio 0.44; 95% CI: 0.36, 0.54; 1-sided p<0.001).

 

The side effects in the experimental arm were neutropenia, anemia, thrombocytopenia, fatigue, nausea, transaminitis, decreased sodium, diarrhea, abdominal pain, and decreased appetite.

 

In conclusion, the FDA approval of trifluridine and tipiracil (LONSURF) with bevacizumab provides a new treatment option for patients with metastatic colorectal cancer, especially those with specific mutations and prior treatment history. The combination therapy showed significant improvements in overall survival and progression-free survival compared to single-agent LONSURF.

Staff Writer - The Cancer News

Recent Posts

FDA Approves Tovorafenib for Pediatric Low-Grade Glioma With BRAF Mutation

By: Dr. Anish Shah Bronx-Lebanon Hospital; Bronx, NY On April 23, 2024, the U.S. Food and Drug…

5 hours ago

FDA Approves Tisotumab Vedotin for Recurrent or Metastatic Cervical Cancer

By: Dr. Anish Shah Bronx-Lebanon Hospital; Bronx, NY On April 29, 2024, the U.S. Food and Drug…

5 hours ago

FDA Approves Lutetium Lu 177 Dotatate for SSTR-Positive Gastroenteropancreatic Neuroendocrine Tumors

By: Dr. Anish Shah Bronx-Lebanon Hospital; Bronx, NY On April 23, 2024, the U.S. Food and Drug…

6 hours ago

FDA Approves Alectinib for Adjuvant Treatment in Non-Small Cell Lung Cancer

By: Dr. Anish Shah Bronx-Lebanon Hospital; Bronx, NY On April 18, 2024, the U.S. Food and Drug…

6 hours ago

FDA grants approval to Nogapendekin alfa inbakicept-pmln for bladder cancer

By: Dr. Anish Shah Bronx-Lebanon Hospital; Bronx, NY On April 22, 2024, the U.S. Food and Drug…

8 hours ago

Leaders in Health Equity Honored by the Binaytara Foundation

Announcing the 2024 Award Recipients for Humanitarianism, Distinguished Faculty, and Volunteer of the Year  …

3 weeks ago