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Childhood Cancer Survivor Study

RecruitingObservational studyHealthy volunteers welcome

Who can join

All ages · All sexes · Healthy volunteers welcome

Full eligibility criteria
Inclusion Criteria:

Initial Cohort:

* Five-year survival following diagnosis of leukemia, lymphoma, CNS tumor, bone tumor, Wilms tumor, neuroblastoma, or soft tissue sarcoma before age 21 years between January 1, 1970 and December 31, 1986 at one of participating centers.

Expanded cohort:

* Five-year survival following diagnosis of leukemia, lymphoma, CNS tumor, bone tumor, kidney tumor, neuroblastoma, or rhabdomyosarcoma before age 21 years between January 1, 1987 and December 31, 1999 at one of participating centers.
* English- or Spanish-speaking and living in the U.S. or Canada at the time of diagnosis.

Exclusion Criteria:

* Diagnosis of non-malignant tumors (i.e., Langerhans cell histiocytosis, meningioma, craniopharyngioma, etc.) treated with radiation and/or chemotherapy.
* Non-English speaking or residence outside the US or Canada.

Sibling Controls:

* For comparison purposes, a group of sibling controls will be identified to represent a stratified random sample based on the distribution of survivors with regard to cancer diagnosis, age, sex, race, and geographic location.

About the study

The Childhood Cancer Survivor Study (CCSS) will investigate the long-term effects of cancer and its associated therapies. A retrospective cohort study will be conducted through a multi-institutional collaboration, which will involve the identification and active follow-up of a cohort of approximately 50,000 survivors of cancer, diagnosed before 21 years of age, between 1970 and 1999 and 10,000 sibling controls. This project will study children and young adults exposed to specific therapeutic modalities, including radiation, chemotherapy, and/or surgery, who are at increased risk of late-occurring adverse health outcomes. A group of sibling controls will be identified and data collected for comparison purposes.

Sponsor: St. Jude Children's Research Hospital · Participants: 50,000 · Started: Jan 5, 1995

Contact the study team

Official record on ClinicalTrials.gov — NCT01120353

Locations in the U.S.

AlabamaUniversity of Alabama at Birmingham/Children's of Alabama, Birmingham
CaliforniaCity of Hope National Medical Center, Duarte
Children's Hospital Los Angeles, Los Angeles
University of California-Los Angeles, Los Angeles
Children's Hospital of Orange County, Orange
University of California-San Francisco, San Francisco
Stanford University School of Medicine, Stanford
ColoradoChildren's Hospital Colorado, Aurora
District of ColumbiaChildren's National Medical Center, Washington D.C.
GeorgiaEmory University/Children's Health Care of Atlanta, Atlanta
IllinoisAna & Robert H. Lurie Children's Hospital of Chicago, Chicago
University of Chicago, Chicago
IndianaIndiana University/Riley Hospital for Children, Indianapolis
MassachusettsDana-Farber Cancer Institute, Boston
MichiganUniversity of Michigan/Mott Children's Hospital, Ann Arbor
MinnesotaChildren's Hospitals & Clinics of Minnesota, Minneapolis
MissouriSt. Louis Children's Hospital/The Washington University, St Louis
New YorkRoswell Park Cancer Institute, Buffalo
Memorial-Sloan Kettering Cancer Center, New York
OhioNationwide Children's Hospital, Columbus
PennsylvaniaChildren's Hospital of Philadelphia, Philadelphia
Children's Hospital of Pittsburgh, Pittsburgh
TennesseeSt. Jude Children's Research Hospital, Memphis
TexasCook Children's Medical Center, Fort Worth
M.D. Anderson Cancer Center, Houston
Texas Children's Hospital, Houston
WashingtonSeattle Children's Hospital, Seattle

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.