Childhood Cancer Survivor Study
Launched by ST. JUDE CHILDREN'S RESEARCH HOSPITAL · May 7, 2010
Trial Information
Current as of August 22, 2025
Recruiting
Keywords
ClinConnect Summary
The Childhood Cancer Survivor Study (CCSS) is a research project that aims to understand the long-term effects of cancer and its treatments on young people who survived cancer. This study will look at about 50,000 survivors who were diagnosed with cancer before they turned 21, between 1970 and 1999, and it will also include 10,000 of their siblings as a comparison group. The researchers want to learn more about how treatments like chemotherapy, radiation, and surgery might lead to health problems later in life for these survivors.
To be eligible, participants need to have survived specific types of cancer, such as leukemia or lymphoma, for at least five years after their diagnosis. They should have been diagnosed before turning 21 years old and should speak either English or Spanish while living in the U.S. or Canada at the time of their diagnosis. Participants will be asked about their health and experiences after treatment, which will help researchers identify any late health issues that may arise. This study is important because it can provide insights that help improve the care and support for childhood cancer survivors in the future.
Gender
ALL
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 St. Jude Children's Research Hospital
St. Jude Children's Research Hospital is a premier pediatric research institution dedicated to advancing the treatment and understanding of catastrophic diseases in children, particularly cancer and other life-threatening conditions. Renowned for its innovative clinical trials and cutting-edge research, St. Jude integrates patient care with scientific discovery to develop new therapies and improve outcomes for young patients. The hospital is committed to ensuring that no family receives a bill for treatment, travel, housing, or food, fostering a holistic approach to pediatric care. Through collaboration with global research networks, St. Jude aims to share its findings and expertise to enhance treatment options worldwide, making significant strides in pediatric medicine.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Rochester, Minnesota, United States
Minneapolis, Minnesota, United States
Chicago, Illinois, United States
Philadelphia, Pennsylvania, United States
Buffalo, New York, United States
Boston, Massachusetts, United States
Pittsburgh, Pennsylvania, United States
Orange, California, United States
Memphis, Tennessee, United States
Duarte, California, United States
Stanford, California, United States
Boston, Massachusetts, United States
Los Angeles, California, United States
Houston, Texas, United States
San Francisco, California, United States
Washington, District Of Columbia, United States
Dallas, Texas, United States
Aurora, Colorado, United States
Columbus, Ohio, United States
Fort Worth, Texas, United States
Seattle, Washington, United States
Houston, Texas, United States
Pittsburgh, Pennsylvania, United States
Minneapolis, Minnesota, United States
Los Angeles, California, United States
Toronto, Ontario, Canada
Birmingham, Alabama, United States
Atlanta, Georgia, United States
Chicago, Illinois, United States
Indianapolis, Indiana, United States
Ann Arbor, Michigan, United States
Minneapolis, Minnesota, United States
Saint Louis, Missouri, United States
New York, New York, United States
Toronto, Ontario, Canada
Patients applied
Trial Officials
Gregory T. Armstrong, MD, MSCE
Principal Investigator
St. Jude Children's Research Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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