Project: Every Child for Younger Patients With Cancer

About

Brief Summary

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.

Study Type

Observational

Phase

N/A

Eligibility

Gender

All

Healthy Volunteers

Minimum Age

N/A

Maximum Age

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 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
- 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
  - Neuroendocrine tumors including pheochromocytoma
  - Melanocytic tumors, except clearly benign nevi
  - Ganglioneuromas
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

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