TITRE |
Le projet : un protocole pour chaque enfant : Registre, Éligibilité et Étude de la Biologie et des Résultats. |
PROTOCOLE ID |
COG-APEC14B1 |
CLINICAL TRIAL.gov ID |
NCT02402244 |
TYPE(S) DE CANCER |
Pédiatrique divers |
PHASE |
|
TYPE D'ÉTUDE |
|
INSTITUTION |
CENTRE HOSPITALIER UNIVERSITAIRE SAINTE-JUSTINE
3175 Chemin de la Côte Sainte-Catherine
(514) 345-4931
|
VILLE |
Montréal
|
INVESTIGATEUR(RICE) PRINCIPAL(E) |
Yvan Samson
|
COORDONATEUR(RICE) |
Linda Hershon linda.hershon@recherche-ste-justine.qc.ca 514-345-4931 poste 5899
|
STATUT |
Actif en recrutement
|
CRITÈRES D'ÉLIGIBILITÉ |
(EN)
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Enrollment can occur at any time after disease presentation including at time of disease progression or recurrence; for patients who are to be enrolled on COG therapeutic studies, enrollment on APEC14B1 must occur prior to enrollment onto the therapeutic trial
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Patients with a known or suspected neoplasm that occurs in the pediatric, adolescent or young adult populations are eligible for enrollment as follows:
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All cancer cases with an International Classification of Diseases for Oncology (ICD-O) histologic behavior code of two "2" (carcinoma in situ) or three "3" (malignant)
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All neoplastic lesions of the central nervous system regardless of behavior, i.e., benign, borderline or malignant
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Other benign/borderline conditions including:
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Mesoblastic nephroma
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Teratomas
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Myeloproliferative diseases including transient myeloproliferative disease
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Langerhan cell histiocytosis
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Lymphoproliferative diseases
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Subjects must be =< 25 years of age at time of original diagnosis, except for patients who are being screened specifically for eligibility onto a COG (or COG participating National Clinical Trials Network (NCTN) ) therapeutic study, for whom there is a higher upper age limit
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All patients or their parents or legally authorized representatives must sign a written informed consent; parents will be asked to sign a separate consent for their own biospecimen submission
|
CRITÈRES D'EXCLUSION |
(EN) |