Vijoice Granted First Approval for Treatment of PROS
Real-world data show 27 percent of patients with PIK3CA-related overgrowth spectrum treated with Vijoice had radiological response at 24 weeks
MONDAY, April 18, 2022 (HealthDay News) -- Vijoice (alpelisib) has been granted accelerated approval for severe PIK3CA-related overgrowth spectrum (PROS), the U.S. Food and Drug Administration announced April 6.
Vijoice, the first treatment to be FDA-approved for PROS, is indicated for patients aged 2 years or older with severe manifestations of PROS at a dose of 50 mg and 250 mg taken orally once daily with food for those aged 2 to 18 years old and those aged 18 years or older, respectively. For pediatric patients, the dose can be increased to 125 mg after 24 weeks if clinically indicated.
The approval was based on real-world efficacy data from the single-arm EPIK-P1 clinical study. The 37 patients included in the efficacy population of EPIK-P1 were aged 2 years or older and had clinical manifestations of PROS that treating physicians assessed as severe or life-threatening and required systemic treatment. The patients received Vijoice as part of an expanded access program for compassionate use. They had at least one target lesion identified on imaging within 24 weeks before receipt of the first dose.
Twenty-seven percent of the patients had a radiological response at week 24, determined by a blinded independent central radiology review. Radiological response was defined as at least a 20 percent reduction from baseline in the sum of measurable target lesion volume in up to three lesions and confirmed by at least one subsequent imaging assessment. Of the responding patients, 60 percent had a response that lasted a year or longer.
Seventy-four percent of patients showed reduction in target lesion volume, with a mean reduction of 13.7 percent. Researchers also reported improvements in pain, fatigue, vascular malformation, limb asymmetry, and disseminated intravascular coagulation in subsets of patients.
The most commonly reported adverse reactions included diarrhea, stomatitis, and hyperglycemia.
Approval was granted to Novartis Pharmaceuticals.