Ignite Creation Date:
2025-12-25 @ 2:39 AM
Ignite Modification Date:
2025-12-30 @ 7:40 PM
Study NCT ID:
NCT06805734
Status:
RECRUITING
Last Update Posted:
2025-02-03
First Post:
2024-12-10
Is Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Natural History With Focus on Oncological Risk Evaluation in Pediatric Patients With PTEN Pathogenic Variants - Observational Study
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D006223', 'term': 'Hamartoma Syndrome, Multiple'}], 'ancestors': [{'id': 'D006222', 'term': 'Hamartoma'}, {'id': 'D009369', 'term': 'Neoplasms'}, {'id': 'D009378', 'term': 'Neoplasms, Multiple Primary'}, {'id': 'D009386', 'term': 'Neoplastic Syndromes, Hereditary'}, {'id': 'D030342', 'term': 'Genetic Diseases, Inborn'}, {'id': 'D009358', 'term': 'Congenital, Hereditary, and Neonatal Diseases and Abnormalities'}]}}, 'protocolSection': {'designModule': {'studyType': 'OBSERVATIONAL', 'designInfo': {'timePerspective': 'PROSPECTIVE', 'observationalModel': 'CASE_ONLY'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 50}, 'patientRegistry': False}, 'statusModule': {'overallStatus': 'RECRUITING', 'startDateStruct': {'date': '2024-08-01', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2024-12', 'completionDateStruct': {'date': '2029-07', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2025-01-28', 'studyFirstSubmitDate': '2024-12-10', 'studyFirstSubmitQcDate': '2025-01-28', 'lastUpdatePostDateStruct': {'date': '2025-02-03', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2025-02-03', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2029-07', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Rate of tumor onset in the pediatric subjects with PTEN pathogenic variants', 'timeFrame': '5 years', 'description': 'In the 5 years follow-up the subjects must complete annually the provided follow-up. Most of the exams are performed in order to exclude the onset of PTEN-related tumors, in particular:\n\n* blood tests: thyroid function, renal function, hepatic function, blood count cell exam: screening for thyroid, kidney, liver and intestinal tumors\n* fecal occult blood (FOB): screening for colorectal cancer and polyps\n* dermatological evaluation (at the diagnosis, further evaluations if clinically needed)\n* thyroid US: screening for thyroid tumors\n* abdominal US: screening for kidney, liver and intestinal tumors\n* clinical follow-up (performed either by a geneticist, a pediatrician or a pediatric neurologist): exams evaluation and global monitoring.\n\nThe oncological risk of the patients would be estimated basing on the number of patients who will develop a tumor, benign or malignant, in the 5-years follow-up.'}, {'measure': 'Rate of tumor onset in the adult relatives of the pediatric subjects also carrying the PTEN pathogenic variant', 'timeFrame': '5 years', 'description': 'We would compare the oncological risk of the tumor onset of the pediatric cohort with that of the relatives carrying the pathogenic variants.\n\nThe pediatric patients will carry on the annual follow-up during the 5 years of the study. In the same time frame, also the adult relatives of the index case carrying the same PTEN variant will be monitored in order to compare adult and pediatric oncological risk and evaluate the phenotypic differences in different life moments.'}], 'secondaryOutcomes': [{'measure': 'Rate of major malformations', 'timeFrame': '5 years', 'description': 'Children will be evaluated in order to exclude the presence of major malformations, including:\n\n* heart malformations: a heart US would be also performed at diagnosis\n* skin anomalies and global examination: a subcutaneous US will be performed if signs of possible peripheral vascular anomalies are present\n* kidney and liver anomalies: those would be also assessed in the abdominal US already planned yearly\n* limbs anomalies: in particular number of fingers/toes and limbs asymmetry'}, {'measure': 'Rate of incidence of brain MRI anomalies', 'timeFrame': '5 years', 'description': 'All children will undergo a brain MRI to evaluate the presence or absence of cerebral anomalies'}, {'measure': 'Rate of incidence of neurological comorbidities', 'timeFrame': '5 years', 'description': 'The presence or absence of possible neurological comorbidities will be investigated at diagnosis and at every clinical follow-up and data will be recorded in order to estimate the prevalence of the problem in the PTEN cohort.\n\nSpecifically, data about the following issues will be collected:\n\n* epilepsy\n* clinical neurological signs\n* sleep disorder\n* other neurological comorbidities.'}, {'measure': 'Rate of incidence of neurodevelopmental disorders', 'timeFrame': '5 years', 'description': 'The presence or absence of neurodevelopmental diagnosis will be investigated at diagnosis, if not already assessed, and at every clinical follow-up and data will be recorded in order to estimate the prevalence of the problem in the PTEN cohort.\n\nGlobal development and/or Intelligence Quotient level will be evaluated with standardized assessment tools, optimized for age and development. Griffiths Mental Development Scale - GMDS, Wechsler Preschool and Primary Scale of Intelligence - WPPSI, Wechsler Intelligence Scale for Children - WISC, and Leiter scales.\n\nThe presence of signs and symptoms of Autism Spectrum Disorder and other possible behavioral problems would also be assessed with standardized tools, both scales (Autism Diagnostic Observation Schedule - ADOS) and questionnaires (Child Behavior Checklist - CBCL, Social Responsiveness Scale - SRS, Adaptive Behavior Assessment System - ABAS).'}, {'measure': 'To analyze Head Circumferences and development of growth HC curves in PTEN patients (data of affected parents will be also recorded)', 'timeFrame': '5 years', 'description': 'The HC measures will be monitored at diagnosis at at every follow-up visit in order to follow the head growth of the patients; data about the affected parents will also be recorded. To record data, WHO growth charts will be used as standardized charts.\n\nData will be used to develop a PTEN-specific head circumference growth chart.'}]}, 'oversightModule': {'isUsExport': False, 'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['PTEN', 'PTHS'], 'conditions': ['PTEN Hamartoma Syndrome']}, 'referencesModule': {'references': [{'pmid': '6046409', 'type': 'BACKGROUND', 'citation': 'Compton-Smith RN, Fawcett JW. Systemic lupus erythematosus associated with procainamide. Br J Clin Pract. 1967 May;21(5):248-51. No abstract available.'}, {'pmid': '30038596', 'type': 'BACKGROUND', 'citation': 'Chen CY, Chen J, He L, Stiles BL. PTEN: Tumor Suppressor and Metabolic Regulator. Front Endocrinol (Lausanne). 2018 Jul 9;9:338. doi: 10.3389/fendo.2018.00338. eCollection 2018.'}, {'pmid': '31427284', 'type': 'BACKGROUND', 'citation': 'Rademacher S, Eickholt BJ. PTEN in Autism and Neurodevelopmental Disorders. Cold Spring Harb Perspect Med. 2019 Nov 1;9(11):a036780. doi: 10.1101/cshperspect.a036780.'}]}, 'descriptionModule': {'briefSummary': 'This is an observational study in pediatric patientis carryng PTEN pathogenic variants aimed to define oncological risk in children and provide a deeper insight of the clinical course, establishing an updated follow-up protocol.', 'detailedDescription': 'PTEN is a tumor suppressor gene that was first linked to cancer predisposition syndromes but, in the following years, its phenotypic spectrum has been in continuous evolution and expansion, and nowadays we know that pathogenic variants n this gene may also be found in children presenting with Autism Spectrum Disorder (ASD), and/or DD and macrocephaly, or also with macrocephaly alone. Thus, the term PTEN Hamartoma Tumor Syndrome (PTHS) is now used when referring to PTEN-related conditions.\n\nNowadays, there is no recognized standard protocol for pediatric follow-up. The screening in mostly single-Centre-based and generally not performed in infancy, with large variability in protocols and timing.\n\nThe penetrance, which was previously believed to follow an age-related pattern, nowadays seems rather to be age-specific, as children mainly present macrocephaly and neuropsychiatric problems (DD/ASD), while adults are diagnosed mostly because of gastrointestinal malignancies, breast cancer, thyroid carcinoma or other tumors. However, it is not always true that adult symptoms never occur in PTHS children and, conversely, pediatric signs may also persist through adulthood.\n\nThe present study aims to collect PTEN mutated patients and their relatives diagnosed in Italy and followed in different Centers, offering a large pediatric cohort with a full clinical description and trying to provide a deeper insight of the clinical course and oncological manifestations of PTEN-related syndrome; we would like to establish an updated follow-up protocol in order to address all the possible clinical needs of these children.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD'], 'maximumAge': '17 Years', 'samplingMethod': 'NON_PROBABILITY_SAMPLE', 'studyPopulation': 'Pediatric patients (\\<18 years of age at enrollment) with pathogenic variants of PTEN genes (gene sequence variant, intragenic deletion/duplication, whole gene deletion) Carrier parents data would also be collected', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* PTEN pathogenic variants (class 4/5 SNV, gene deletion, intragenic duplication/deletion)\n* Pediatric patients (\\<18 years old) and their affected relatives, male/female, all ethnicities\n* The legal representative must agree to follow the screening protocol\n* Informed consent signed by the legal representative\n\nExclusion Criteria:\n\n* Refuse to undergo the exams of the protocol assessment at the diagnosis\n* PTEN non-pathogenic variants (VOUS or benign/likely benign vatiants)\n* No signed informed consent'}, 'identificationModule': {'nctId': 'NCT06805734', 'acronym': 'PTEN_Ped', 'briefTitle': 'Natural History With Focus on Oncological Risk Evaluation in Pediatric Patients With PTEN Pathogenic Variants - Observational Study', 'organization': {'class': 'OTHER', 'fullName': 'Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta'}, 'officialTitle': 'Natural History With Focus on Oncological Risk Evaluation in Pediatric Patients With PTEN Pathogenic Variants - Observational Study', 'orgStudyIdInfo': {'id': 'PTEN_Ped'}}, 'contactsLocationsModule': {'locations': [{'zip': '20133', 'city': 'Milan', 'status': 'RECRUITING', 'country': 'Italy', 'contacts': [{'name': "Stefano D'Arrigo, MD", 'role': 'CONTACT', 'email': 'stefano.darrigo@istituto-besta.it', 'phone': '02.2394.2210'}, {'name': 'Claudia Ciaccio, MD', 'role': 'CONTACT'}, {'name': 'Claudia Ciaccio, MD', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'Fondazione IRCCS Istituto Neurologico Carlo Besta', 'geoPoint': {'lat': 42.78235, 'lon': 12.59836}}]}, 'ipdSharingStatementModule': {'infoTypes': ['STUDY_PROTOCOL', 'ICF'], 'timeFrame': '10 years, from August 1st 2024 to July 31st 2034', 'ipdSharing': 'YES', 'description': 'The participant centers in Italy will share data with the PI Institution. Study protocols and consent forms will be shared with the Institutions collaborating in the study in order to have omogeneous data record.\n\nClinicians from the collaborative Centers will return anonymized data to the PI Institution.', 'accessCriteria': 'Data would be collected and recorded in encrypted Excel sheets with no name/surname/tax code shown; we ensure at each site the accuracy, completeness and timeliness of the files.\n\nOnly the clinical personnel (medical doctors and neuropsychologists) involved in the study will have access to data, that could be accessed anytime but only from the Institutional Organizations participating in the study.\n\nData will be stored at Carlo Besta Institute (SSD Sindromi Genetiche con Disabilità Intellettiva e Disturbi dello Spettro Autistico) for 10 years.'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta', 'class': 'OTHER'}, 'collaborators': [{'name': "Azienda Ospedaliera Sant'Anna", 'class': 'OTHER'}, {'name': 'Fondazione Policlinico Universitario Agostino Gemelli IRCCS', 'class': 'OTHER'}], 'responsibleParty': {'type': 'SPONSOR'}}}}