The Project: EveryChild Protocol: A Registry, Eligibility Screening, Biology and Outcome Study
The Project: EveryChild Protocol: A Registry, Eligibility Screening, Biology and Outcome Study
This study gathers health information for 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.
PRIMARY OBJECTIVES:
I. 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 biorepository 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 permission to be contacted in the future to consider participating in non-therapeutic and prevention research studies involving the patient or their parents (if applicable).
V. For patients enrolled through adult cooperative groups, to develop a well annotated adolescent and young adult (AYA) cancer biorepository and to screen for eligibility for current and future research through the collection of biospecimens (at diagnosis, time of progression and time of recurrence), including tumor and host DNA; and key clinical data, including presentation, diagnostic, staging, and summary treatment information.
OUTLINE: This is an observational study. Patients are assigned to 1 of 2 protocols.
PROJECT: EVERY CHILD PROTOCOL: Patients undergo medical data review to create a Childhood Cancer Registry. Patients also undergo collection of biospecimen samples (e.g., tissue, blood, bone marrow, plasma, serum, buccal swab, saliva, cerebrospinal fluid, or urine).
PROJECT AYA PROTOCOL: Patients undergo collection of biospecimen samples (e.g., tissue, blood, bone marrow, plasma, serum, buccal swab, saliva, cerebrospinal fluid, or urine).
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 one "1" (borderline), 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
All neoplastic lesions of the kidney regardless of behavior, i.e., benign, borderline or malignant
The following other benign/borderline conditions:
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
Birmingham, Alabama 35233, United States
oncologyresearch@peds.uab.edu205-638-9285
Long Beach, California 90806, United States
Palo Alto, California 94304, United States
Sacramento, California 95817, United States
Torrance, California 90502, United States
Denver, Colorado 80218, United States
Washington D.C., District of Columbia 20007, United States
Washington D.C., District of Columbia 20010, United States
Hollywood, Florida 33021, United States
Miami, Florida 33136, United States
Atlanta, Georgia 30329, United States
Baltimore, Maryland 21287, United States
Worcester, Massachusetts 01655, United States
Detroit, Michigan 48201, United States
Grand Rapids, Michigan 49503, United States
Grand Rapids, Michigan 49503, United States
Norton Shores, Michigan 49444, United States
Saint Joseph, Michigan 49085, United States
Saint Joseph, Michigan 49085, United States
Minneapolis, Minnesota 55404, United States
Las Vegas, Nevada 89135, United States
Las Vegas, Nevada 89144, United States
Lebanon, New Hampshire 03756, United States
New Brunswick, New Jersey 08903, United States
New Hyde Park, New York 11040, United States
New York, New York 10016, United States
New York, New York 10032, United States
Syracuse, New York 13210, United States
Chapel Hill, North Carolina 27599, United States
Charlotte, North Carolina 28203, United States
Toledo, Ohio 43606, United States
Sioux Falls, South Dakota 57117-5134, United States
Houston, Texas 77030, United States
San Antonio, Texas 78229, United States
Burlington, Vermont 05405, United States
Spokane, Washington 99204, United States
Charleston, West Virginia 25304, United States
Madison, Wisconsin 53792, United States
Hunter Regional Mail Centre, New South Wales 2310, Australia
(02) 4985 5180
Saint Hobart, Tasmania 7000, Australia
Perth, Western Australia 6008, Australia
Sherbrooke, Quebec J1H 5N4, Canada
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207-973-4274
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410-601-9083
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301-319-2100
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855-776-0015
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