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Genetic Analysis in Identifying Late-Occurring Complications in Childhood Cancer Survivors

Childhood Malignant Neoplasm

This 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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Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    0 and up

Critères de participation

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

Lieu de l'étude

CancerCare Manitoba
CancerCare Manitoba
Winnipeg, Manitoba
Canada

Contactez l'équipe d'étude

Primary Contact

Site Public Contact

[email protected]
866-561-1026
Children's Hospital
Children's Hospital
London, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Site Public Contact

519-685-8306
Centre Hospitalier Universitaire Sainte-Justine
Centre Hospitalier Universitaire Sainte-Justine
Montreal, Quebec
Canada

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Primary Contact

Site Public Contact

514-345-4931
British Columbia Children's Hospital
British Columbia Children's Hospital
Vancouver, British Columbia
Canada

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The Montreal Children's Hospital of the MUHC
The Montreal Children's Hospital of the MUHC
Montreal, Quebec
Canada

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Kingston Health Sciences Centre
Kingston Health Sciences Centre
Kingston, Ontario
Canada

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Primary Contact

Site Public Contact

[email protected]
613-549-6666
IWK Health Centre
IWK Health Centre
Halifax, Nova Scotia
Canada

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Primary Contact

Site Public Contact

902-470-6767
Children's Hospital of Eastern Ontario
Children's Hospital of Eastern Ontario
Ottawa, Ontario
Canada

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Primary Contact

Site Public Contact

613-738-3931
Allan Blair Cancer Centre
Allan Blair Cancer Centre
Regina, Saskatchewan
Canada

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University of Alberta Hospital
University of Alberta Hospital
Edmonton, Alberta
Canada

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Primary Contact

Site Public Contact

[email protected]
780-407-6615
McMaster Children's Hospital at Hamilton Health Sciences
McMaster Children's Hospital at Hamilton Health Sciences
Hamilton, Ontario
Canada

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Primary Contact

Site Public Contact

905-521-2100
Hospital for Sick Children
Hospital for Sick Children
Toronto, Ontario
Canada

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Primary Contact

Site Public Contact

[email protected]
416-813-7654
Saskatoon Cancer Centre
Saskatoon Cancer Centre
Saskatoon, Saskatchewan
Canada

Contactez l'équipe d'étude

Primary Contact

Site Public Contact

306-655-2914
Étude parrainée par
Children's Oncology Group
Participants recherchés
Plus d'informations
ID de l'étude: NCT00082745