©2022 Stanford Medicine
Enrollment on the Childhood Cancer Research Network (CCRN) of the Children s Oncology Group
Not Recruiting
Trial ID: NCT01117168,7,21,33,37,35550
Purpose
Background:
- The Children s Oncology Group has established a research network, the Childhood Cancer
Research Network (CCRN), to collect information about children with cancer and other
conditions that are benign but involve abnormal cell growth in order to help doctors and
scientists better understand childhood cancer. The CCRN's goal is to collect clinical
information about every child diagnosed with cancer and similar conditions in the United
States and Canada, to allow researchers to study patterns, characteristics, and causes of
childhood cancer. The information can also help researchers study the causes of childhood
cancer. To expand the CCRN, parents of children who have been diagnosed with cancer will be
asked to provide information about themselves and their child for research purposes.
Objectives:
- To obtain informed consent from parents (and the child, when appropriate) of infants,
children, adolescents, and young adults newly diagnosed with cancer to enter their names
and certain information concerning their child into the Childhood Cancer Research
Network.
- To obtain informed consent from parents (and the child, when appropriate) of infants,
children, adolescents, and young adults newly diagnosed with cancer for permission to be
contacted in the future to consider participating in non-therapeutic and prevention
research studies involving the parents and/or the child.
Eligibility:
- Parents of children who have been seen at or treated by a hospital that is a member of the
Children s Oncology Group.
Design:
- Parents will provide permission to have personal information sent from their child s
hospital to the CCRN, including the child and parents' names; child's gender, birth
date, race, and ethnicity; information about the disease; and the treating institution.
- Parents will also give permission for CCRN to contact the diagnostic laboratory to
obtain specific information about the tumor or cancer cells.
- Parents will be asked if they are willing to be contacted in the future to consider
participating in CCRN research studies, and will provide contact information (name, home
address, and telephone number) to be entered in the CCRN.
- Parents or patients who change their minds about having information available in the
CCRN can ask the treatment institution to restrict access to the identifying
information. Parents or patients who refuse to have information included in the CCRN or
be contacted in the future will still be able to enter clinical cancer research studies.
Official Title
Protocol for the Enrollment on the Official COG Registry, The Childhood Cancer Research Network (CCRN) Children s Oncology Group
Stanford Investigator(s)
Eligibility
- INCLUSION CRITERIA:
- Pre-CCRN Entry
- All new patients seen in COG member institutions with any of the following diagnoses
are eligible:
- All cancer cases with an ICD-O histologic behavior code of two 2 (carcinoma in
situ)or three 3 (malignant).
- All lesions of the central nervous system regardless of behavior, i.e., benign,
borderline or malignant.
- The benign/borderline conditions which will be reportable by agreement shall
include: Mesoblastic nephroma, all teratomas, regardless of locations, Theca cell
- granulosa cell tumor, lymphoproliferative disease, ganglioneuroma,
myeloproliferative disease, Langerhan s Cell histiocytosis
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
CCTO
650-498-7061