Skip to main content

Fruzaqla FDA Approved for Refractory Metastatic Colorectal Cancer

Web Exclusives - FDA Approvals

On November 8, 2023, the FDA approved fruquintinib (Fruzaqla; Takeda Pharmaceuticals), a tyrosine kinase inhibitor, for the treatment of metastatic colorectal cancer (mCRC) in adults who received previous fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy, an anti–vascular endothelial growth factor (VEGF) therapy, and, if RAS wild-type and medically appropriate, an anti–epidermal growth factor receptor therapy. Fruquintinib is an oral inhibitor of VEGF receptor–1, –2, and –3 . The FDA granted fruquintinib priority review for this indication.

The approval of fruquintinib was based on the efficacy results of 2 phase 3 trials, FRESCO (NCT02314819) and FRESCO-2 (NCT04322539). The multicenter, placebo-controlled FRESCO trial was conducted in China and enrolled 416 patients with mCRC who had disease progression during or after receiving fluoropyrimidine-, oxaliplatin-, or irinotecan-based chemotherapy. In the international, multicenter, randomized, double-blind, placebo-controlled FRESCO-2 trial, 691 patients with mCRC were required to have disease progression during or after receiving trifluridine plus tipiracil, or regorafenib. They were also required to have received fluoropyrimidine-, oxaliplatin-, or irinotecan-based chemotherapy; an anti-VEGF biologic therapy; or, if RAS wild-type, an anti-VEGF therapy.

In both trials, patients were randomized to receive fruquintinib 5 mg orally once daily or placebo for the first 21 days of each 28-day cycle plus best supportive care. The patients received therapy until disease progression or until unacceptable adverse events.

The primary efficacy end point in both trials was overall survival (OS). In FRESCO-2, the median OS was 7.4 months (95% confidence interval [CI], 6.7-8.2) for patients receiving fruquintinib and 4.8 months (95% CI, 4.0-5.8) for patients receiving placebo (hazard ratio [HR], 0.66; 95% CI, 0.55-0.80; P<.001). In the FRESCO study, the median OS was 9.3 months (95% CI, 8.2-10.5) and 6.6 months (95% CI, 5.9-8.1) in the 2 treatment arms, respectively (HR, 0.65; 95% CI, 0.51-0.83; P<.001).

“Patients with metastatic [CRC] are often fragile and fatigued—due to both their condition as well as the therapies they have been exposed to. An oral chemotherapy-free option that offers a survival benefit despite treatment with prior therapies is a critical need for treating metastatic colorectal cancer,” stated Cathy Eng, MD, FACP, Vanderbilt University Medical Center, in a press release. “Colorectal cancer is a highly heterogeneous disease, making it difficult to bring advancements to patients whose cancer has metastasized. I look forward to being able to offer a new solution to appropriate patients,” she added.

The most common (≥20%) adverse events with fruquintinib were hypertension, palmar-plantar erythrodysesthesia, proteinuria, dysphonia, abdominal pain, diarrhea, and asthenia.

The recommended dosage of fruquintinib is 5 mg orally once daily with or without food for the first 21 days of each 28-day cycle until disease progression or unacceptable adverse events.

Related Items
Directory of FDA Approvals, August Through December 2023
December 2023 Vol 16, Payers' Guide to FDA Updates published on January 26, 2024 in FDA Approvals
Iwilfin FDA Approved for Adults and Pediatric Patients with High-Risk Neuroblastoma
Web Exclusives published on January 16, 2024 in FDA Approvals
Welireg Now FDA Approved for Patients with Advanced Renal Cell Carcinoma
Web Exclusives published on January 16, 2024 in FDA Approvals
Ogsiveo First Treatment FDA Approved for Desmoid Tumors
Web Exclusives published on January 2, 2024 in FDA Approvals
Keytruda Plus Chemotherapy Receives New FDA Approvals for Advanced Biliary Tract Cancer and 2 Forms of Advanced Gastroesophageal Junction Adenocarcinoma
Web Exclusives published on December 18, 2023 in FDA Approvals
Last modified: December 12, 2023