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FDA Approves Selumetinib for Neurofibromatosis Type 1

It is approved for patients who have symptomatic, inoperable plexiform neurofibromas
20 Apr 2020
Anticancer agents & Biologic therapy;  Cancer in Special Situations / Population;  Central nervous system malignancies

On 10 April 2020, the US Food and Drug Administration (FDA) approved selumetinib (KOSELUGO, AstraZeneca) for paediatric patients, 2 years of age and older, with neurofibromatosis type 1 (NF1) who have symptomatic, inoperable plexiform neurofibromas (PN).

Selumetinib, a kinase inhibitor, is the first therapy approved for paediatric patients who have this debilitating, and often disfiguring, rare disease. 

Efficacy of selumetinib was investigated in SPRINT (NCT01362803), a National Cancer Institute (NCI) sponsored, open-label, multicentre, single-arm trial in paediatric patients with NF1 and a measurable target PN that could not be surgically removed without risk of substantial morbidity.

Patients in the efficacy population (N=50) were also required to have at least one significant morbidity related to the target PN. Morbidities present in ≥20% of patients included disfigurement, motor dysfunction, pain, airway dysfunction, visual impairment, and bladder/bowel dysfunction.

Patients received selumetinib 25 mg/m2 orally twice a day until disease progression or unacceptable toxicity.

The primary efficacy outcome measure was overall response rate (ORR) as assessed by NCI and defined as the percentage of patients who experienced ≥20% reduction in tumour volume on Magnetic Resonance Imaging (MRI) confirmed on a subsequent MRI within 3-6 months.

The ORR was 66% (n=33; 95% confidence interval [CI] 51,79). All patients had a partial response, and 82% of responders had sustained responses lasting at least 12 months. An independent central review of ORR was performed using the same response criteria and demonstrated an ORR of 44% (95% CI 30,59).

The primary safety data were from 74 paediatric patients with NF1 and PN who received selumetinib during SPRINT. The most common adverse reactions (≥40% of patients) were vomiting, rash, abdominal pain, diarrhoea, nausea, dry skin, fatigue, musculoskeletal pain, fever, acne, stomatitis, headache, paronychia, and pruritus.

Selumetinib can also cause cardiomyopathy, ocular toxicity including retinal vein occlusion, retinal pigment epithelial detachment and impaired vision, and increased creatinine phosphokinase. Selumetinib should be withheld, dosage reduced, or permanently discontinued based on the severity of adverse reactions.

The recommended selumetinib dose is 25 mg/m2 orally twice a day on an empty stomach until disease progression or unacceptable toxicity.

Full prescribing information for KOSELUGO are available here.

FDA granted this application priority review and Breakthrough Therapy designation. Selumetinib also received fast track and orphan drug designations.

Healthcare professionals should report all serious adverse events suspected to be associated with the use of any medicine and device to FDA’s MedWatch Reporting System.

For assistance with single-patient INDs for investigational oncology products, healthcare professionals may contact FDA’s Oncology Center of Excellence Project Facilitate. 

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