Genetic Analysis in Identifying Late-Occurring Complications in Childhood Cancer Survivors
Childhood Malignant NeoplasmThis clinical trial studies cancer survivors to identify those who are at increased risk of developing late-occurring complications after undergoing treatment for childhood cancer. A patient's genes may affect the risk of developing complications, such as congestive heart failure, avascular necrosis, stroke, and second cancer, years after undergoing cancer treatment. Genetic studies may help doctors identify survivors of childhood cancer who are more likely to develop late complications.
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Participation Requirements
-
Sex:
ALL -
Eligible Ages:
0 and up
Participation Criteria
Inclusion Criteria:
* ELIGIBILITY CRITERIA - CASES
* Diagnosis of primary cancer at age 21 or younger, irrespective of current age
* No prior history of allogeneic (non-autologous) hematopoietic cell transplant
* Development of one of the following key adverse events at any time following initiation of cancer therapy:
* Cardiac dysfunction; please note: case enrollment has been closed due to achievement of target accrual
* Ischemic stroke (IS)
* Subsequent malignant neoplasm (SMN)
* Avascular necrosis (AVN); please note: case enrollment has been closed due to achievement of target accrual
* Submission of a blood specimen (or in certain cases a saliva specimen) to the Coordinating Center at the University of Alabama at Birmingham as per the requirements; please note: if a patient is currently receiving active cancer treatment, it is preferable to obtain the blood sample at a time when the patient's white blood cell (WBC) is \> 2,000
* Written informed consent from the patient and/or the patient's legally authorized guardian
* In active follow up by a COG institution; active follow up will be defined as date of last visit or contact by a COG institution within the past 24 months; any type of contact, including contact specifically for participation in ALTE03N1, qualifies as active follow-up; please note: treatment on a COG (or legacy group) therapeutic protocol for the primary cancer is NOT required
* ELIGIBILITY CRITERIA - CONTROLS
* CONTROL: Diagnosis of primary cancer at age 21 or younger, irrespective of current age
* CONTROLS: No prior history of allogeneic (non-autologous) hematopoietic cell transplant
* CONTROLS: No clinical evidence of any of the following key adverse events:
* Cardiac dysfunction (CD); please note: if a patient is currently receiving active cancer treatment, it is preferable to obtain the blood sample at a time when the patient's WBC is \> 2,000
* Ischemic stroke (IS)
* Avascular necrosis (AVN)
* Subsequent malignant neoplasm (SMN)
* CONTROLS: Submission of a blood specimen (or in certain cases a saliva specimen) to the Coordinating Center Laboratory at the University of Alabama at Birmingham as per the requirements
* CONTROLS: Written informed consent from the patient and/or the patient's legally authorized guardian
* CONTROLS: In active follow up by a COG institution; active follow up will be defined as date of last visit or contact by a COG institution within the past 24 months; any type of contact, including contact specifically for participation in ALTE03N1, qualifies as active follow-up; please note: treatment on a COG (or legacy group) therapeutic protocol for the primary cancer is NOT required
Study Location
CancerCare Manitoba
CancerCare ManitobaWinnipeg, Manitoba
Canada
Contact Study Team
Children's Hospital
Children's HospitalLondon, Ontario
Canada
Contact Study Team
Site Public Contact
519-685-8306Centre Hospitalier Universitaire Sainte-Justine
Centre Hospitalier Universitaire Sainte-JustineMontreal, Quebec
Canada
Contact Study Team
Site Public Contact
514-345-4931British Columbia Children's Hospital
British Columbia Children's HospitalVancouver, British Columbia
Canada
Contact Study Team
The Montreal Children's Hospital of the MUHC
The Montreal Children's Hospital of the MUHCMontreal, Quebec
Canada
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Kingston Health Sciences Centre
Kingston Health Sciences CentreKingston, Ontario
Canada
Contact Study Team
IWK Health Centre
IWK Health CentreHalifax, Nova Scotia
Canada
Contact Study Team
Site Public Contact
902-470-6767Children's Hospital of Eastern Ontario
Children's Hospital of Eastern OntarioOttawa, Ontario
Canada
Contact Study Team
Site Public Contact
613-738-3931Allan Blair Cancer Centre
Allan Blair Cancer CentreRegina, Saskatchewan
Canada
Contact Study Team
University of Alberta Hospital
University of Alberta HospitalEdmonton, Alberta
Canada
Contact Study Team
McMaster Children's Hospital at Hamilton Health Sciences
McMaster Children's Hospital at Hamilton Health SciencesHamilton, Ontario
Canada
Contact Study Team
Site Public Contact
905-521-2100Hospital for Sick Children
Hospital for Sick ChildrenToronto, Ontario
Canada
Contact Study Team
Saskatoon Cancer Centre
Saskatoon Cancer CentreSaskatoon, Saskatchewan
Canada
Contact Study Team
Site Public Contact
306-655-2914- Study Sponsored By
- Children's Oncology Group
- Participants Required
- More Information
- Study ID:
NCT00082745