Efficacy and Safety of Sirolimus in Children and Adolescents With Juvenile Nasopharyngeal Angiofibroma (JNA)

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexMale
Age7-18
SponsorFederal Research Institute of Pediatric Hematology, Oncology and Immunology

About this trial

Juvenile nasopharyngeal angiofibroma (JNA) is a pathologically benign yet locally aggressive and destructive tumor that develops in the choana and nasopharynx. Historical treatment of JNA has included embolization, surgical resection, and radiation. mTOR signaling way demonstrated to be involved in regulation of growth and angiogenesis of JNA. Sirolimus, as mTOR inhibitor, is a potential target JNA therapy.

The main purpose of the study is to evaluate the efficacy and safety of sirolimus in children and adolescents with primary or recurrent JNA. Efficacy will be estimated based on dynamics of the JNA progression. Historical control group will be used for comparison as standard therapy.

Due to limited experience of sirolimus in JNA in routine practice, study should be conducted in 2 phases: pilot and extended. Decision regarding extended phase will be based on the results of pilot phase.

Eligibility criteria

Qualifiers

Confirmed diagnosis of JNA.

Male gender.

Age 7-18 years.

Signed informed consent of the parents or the official representative for patients under 14 years of age, the patient and the patient's parents for persons from 14 to 18 years of age.

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Sirolimus

Treatment groups

117 Participants
are divided into 1 treatment group