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This study aims to examine tumor samples through gene panel sequencing in patients with high-risk neuroblastoma. It includes patients aged 1 to 30 with recurrent, refractory or persistent high-risk neuroblastoma who agree to undergo a clinically indicated biopsy. It is a non-phase study and is currently active but not recruiting participants.
The summary above is a plain-language rendering of the official record. The original English title is shown for reference.
Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.
Inclusion Criteria: * Patients must be ≥ 1 year and ≤ 30 years of age at study registration * Patients must have had a diagnosis of neuroblastoma either by histological verification of neuroblastoma and/or demonstration of tumor cells in the bone marrow with increased urinary catecholamines. * Patients must have a history of high-risk neuroblastoma according to * COG risk classification at the time of study registration. Patients must have at least one of the following: Recurrent/progressive disease, Refractory disease, Persistent disease * Patient must be willing to undergo a clinically indicated biopsy and meet at least one of the following requirements: Bone biopsy, Soft tissue biopsy, Bone marrow biopsy and aspirate * Patients must not be receiving any other anti-cancer agents or radiotherapy during the interval Exclusion Criteria: * Patients with disease of any major organ system that would compromise their ability to withstand biopsy procedures of soft tissue, bone and/or bone marrow. * Patients who enroll and successfully receive a NANT Precision Report may not re-enroll at a future time. * Patient declines participation in NANT 2004-05, the NANT Biology Study.