[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT05978557":3,"trial-entities:NCT05978557":82,"trial-summary:NCT05978557":86},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":7,"overall_status":8,"completion_date":9,"status_verified_date":10,"last_update_date":11,"start_date":12,"sponsor_name":13,"lead_sponsor_class":14,"has_dmc":15,"brief_summary":16,"detailed_description":17,"conditions":18,"keywords":20,"study_type":23,"primary_purpose":17,"phases":24,"enrollment_info":25,"interventions":28,"primary_outcomes":32,"secondary_outcomes":37,"sex":41,"minimum_age":17,"maximum_age":17,"healthy_volunteers":42,"eligibility_criteria":43,"std_ages":47,"locations":51,"central_contacts":68,"overall_officials":74,"references":77,"see_also_links":78},"NCT05978557","LCCC2212","Brain Slice Explants to Predict Drug Response in Brain Tumors","A Feasibility Study to Determine if a Novel Patient-derived Explant Platform Can Produce Drug Sensitivity Scores Within a Clinically Relevant Time Frame in Patients With CNS Tumors","RECRUITING","2028-03-01","2025-08","2025-08-29","2023-07-27","UNC Lineberger Comprehensive Cancer Center","OTHER",true,"This biospecimen collection study will evaluate the feasibility of engrafting and testing resected Central nervous system (CNS) tumors tumor tissue ex vivo to estimate drug response, in pediatric and adult subjects. CNS tumors display remarkable heterogeneity and unfortunately there are no reliable precision oncology platforms that can identify the most effective therapy for each patient. Recent work has demonstrated the success of functional precision oncology platforms using patient-derived explant (PDE) at predicting drug response in various cancers. Since PDEs maintain important aspects of tumor heterogeneity they may prove effective as functional models for CNS tumors. The purpose of this study is to explore the feasibility of using a novel PDE platform to generate drug sensitivity scores from patients with central nervous system tumors in Pediatric and adult subjects having low- or high-grade CNS tumors resected. The secondary objective is to estimate the proportion of successfully scaled PDEs generated per given tumor size.",null,[19],"Central Nervous System Tumor",[21,22],"patient-derived explant","tissue","OBSERVATIONAL",[],{"count":26,"type":27},50,"ESTIMATED",[29],{"type":14,"name":30,"description":31},"Biospecimen collection","Biospecimen will be collected during surgery.",[33],{"measure":34,"description":35,"timeFrame":36},"Proportion of specimens yielding scores","The proportion of evaluable specimens yielding patient-derived explant (PDE) drug sensitivity scores. Specimens will be collected during surgery for tumor resection. Excised specimens will be processed to generate PDE-based functional drug screening models. A panel of therapeutics will be chosen for each specimen according to pre-set criteria determined.","Up to 28 days",[38],{"measure":39,"description":40,"timeFrame":36},"The scalability of evaluable specimens","The percentage of evaluable specimens amenable to proportionally scaled patient-derived explant (PDE) generation per specimen size will be studied.","ALL",false,{"inclusion":44,"exclusion":45,"raw_text":46},[],[],"In order to participate in this study a subject must meet all of the eligibility criteria outlined below.\n\nInclusion Criteria:\n\n1. Written informed consent obtained to participate in the study and HIPAA authorization for the release of personal health information or written assent and parental consent for pediatric subjects or surrogate consent provided by the subject's legally authorized guardians.\n2. A diagnosis of a tumor residing in the central nervous system with surgery plan to have surgical resection.\n3. The subject is willing and able to comply with study procedures based on the judgment of the investigator or protocol designer.\n\nExclusion Criteria:\n\n1. All subjects must not meet any of the following exclusion criteria prior to enrollment to participate in this study:\n\n   Any serious medical or psychiatric disorder that would interfere with the subject's ability to give informed consent.\n2. Incarcerated individuals.",[48,49,50],"CHILD","ADULT","OLDER_ADULT",[52],{"facility":13,"status":8,"city":53,"state":54,"zip":55,"country":56,"contacts":57,"geoPoint":65},"Chapel Hill","North Carolina","27516","United States",[58,62],{"name":59,"role":60,"email":61},"Andrew B Satterlee, PhD","CONTACT","satterle@email.unc.edu",{"name":63,"role":60,"email":64},"Devin McCarthy","devin_mccarthy@med.unc.edu",{"lat":66,"lon":67},35.9132,-79.05584,[69,71],{"name":63,"role":60,"phone":70,"email":64},"919-966-7654",{"name":72,"role":60,"email":73},"Luz Cuaboy","luz_cuaboy@med.unc.edu",[75],{"name":59,"affiliation":13,"role":76},"PRINCIPAL_INVESTIGATOR",[],[79],{"label":80,"url":81},"University of North Carolina Lineberger Comprehensive Cancer Center Clinical Trials","http:\u002F\u002Funclineberger.org\u002Fpatientcare\u002Fclinical-trials\u002Fclinical-trials",{"nct_id":4,"conditions":83,"biomarkers":85},[84],"Central Nervous System Neoplasm",[],{"nct_id":4,"found":15,"summary":87,"prompt_version":96},{"design":88,"status":89,"heading":6,"summary":90,"follow_up":91,"word_count":92,"commitments":93,"compensation":94,"drugs_mentioned":95},"This is an observational study with a planned enrollment of 50 participants. It is not a drug trial but focuses on collecting and testing biospecimens.","completed","This observational study is looking at whether using brain tissue collected during surgery can help predict how well different treatments might work for central nervous system (CNS) tumors. Researchers will take a small piece of your tumor tissue after it's removed and test it in the lab to see how it responds to various drugs. This approach, called patient-derived explant (PDE), aims to find the most effective therapy for each patient, as CNS tumors can be very different from person to person. The study plans to enroll 50 participants, both children and adults. The main goal is to see how many of these tissue samples can be successfully tested within 28 days.","The primary endpoint is measured up to 28 days after the biospecimen is collected.",112,"You would provide a biospecimen (tumor tissue) during your surgery. The trial record does not specify any other visits, procedures, or tests for participants.","Not stated in the trial record.",[],"v2"]