Summary

for people ages up to 25 years (full criteria)
at Oakland, California and other locations
study started

Description

Summary

This research trial studies the Project: Every Child for younger patients with cancer. Gathering health information over time from younger patients with cancer may help doctors find better methods of treatment and on-going care.

Official Title

The Project: EveryChild Protocol: A Registry, Eligibility Screening, Biology and Outcome Study

Details

PRIMARY OBJECTIVES:

  1. To maintain a Childhood Cancer Registry for infants, children, adolescents, and young adults with cancer.

II. To utilize clinical and biological data to help determine eligibility or stratification, based on childhood cancer disease classification schemas, for potential enrollment of research subjects onto Children's Oncology Group (COG) therapeutic clinical trials.

III. To develop a well annotated childhood cancer biobank for current and future research through the collection of biospecimens (at diagnosis, time of progression, time of recurrence and/or post-mortem), including tumor, host and when feasible parental germline deoxyribonucleic acid (DNA); and key clinical data, including presentation, diagnostic, staging, summary treatment, and outcome information, from every child diagnosed with cancer at COG institutions.

IV. To allow use of registry data for permission to be contacted in the future to consider participating in non-therapeutic and prevention research studies involving the child or their parents.

OUTLINE:

Patients undergo medical data review to create a Childhood Cancer Registry. Patients also undergo collection of bio-specimen samples (e.g., tissue, blood, bone marrow, plasma, serum, buccal cells, saliva, cerebrospinal fluid, or urine).

Keywords

Central Nervous System Neoplasm Childhood Immature Teratoma Childhood Langerhans Cell Histiocytosis Childhood Malignant Neoplasm Childhood Mature Teratoma Congenital Mesoblastic Nephroma Desmoid-Type Fibromatosis Lymphoproliferative Disorder Myeloproliferative Neoplasm Stromal Neoplasm Neoplasms Myeloproliferative Disorders Teratoma Lymphoproliferative Disorders Histiocytosis Histiocytosis, Langerhans-Cell Nervous System Neoplasms Central Nervous System Neoplasms Fibroma Dermoid Cyst Nephroma, Mesoblastic Fibromatosis, Aggressive Cytology Specimen Collection Procedure Medical Chart Review

Eligibility

For people ages up to 25 years

Inclusion Criteria:

  • Enrollment must occur within 6 months of initial disease presentation OR within 6 months of refractory disease, disease progression, disease recurrence, second or secondary malignancy, or post-mortem
  • Patients previously enrolled on ACCRN07 are eligible to enroll on Tracking Outcome,Registry and Future Contact components of APEC14B1 any time after they reach age of majority
  • Patients with a known or suspected neoplasm that occurs in the pediatric, adolescent or young adult populations are eligible for enrollment as follows:
  • 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)
  • All neoplastic lesions of the central nervous system regardless of behavior,i.e., benign, borderline or malignant
  • The following other benign/borderline conditions:
  • Mesoblastic nephroma
  • Teratomas (mature and immature types)
  • Myeloproliferative diseases including transient myeloproliferative disease
  • Langerhans cell histiocytosis
  • Lymphoproliferative diseases
  • Desmoid tumors
  • Gonadal stromal cell tumors
  • 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 which there is a higher upper age limit
  • All patients or their parents or legally authorized representatives must sign a written informed consent and agree to participate in at least one component of the study; parents will be asked to sign a separate consent for their own biospecimen submission
  • If patients or their parents or legally authorized representatives have not signed the Part A subject consent form at the time of a diagnostic bone marrow procedure, it is recommended that they initially provide consent for drawing extra bone marrow using the Consent for Collection of Additional Bone Marrow;consent using the Part A subject consent form must be provided prior to any other procedures for eligibility screening or banking under APEC14B1

Locations

  • Children's Hospital and Research Center at Oakland accepting new patients
    Oakland California 94609-1809 United States
  • UCSF Medical Center-Mission Bay accepting new patients
    San Francisco California 94158 United States

Details

Status
accepting new patients
Start Date
Sponsor
Children's Oncology Group
ID
NCT02402244
Study Type
Observational
Last Updated