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The Pediatric Acute Leukemia (PedAL) Screening Trial - A Study to Test Bone Marrow and Blood in Children With Leukemia That Has Come Back After Treatment or Is Difficult to Treat - A Leukemia & Lymphoma Society and Children's Oncology Group Study

Mixed Phenotype Acute Leukemia | Myelodysplastic Syndrome | Acute Myeloid Leukemia | Acute Lymphoblastic...

This study aims to use clinical and biological characteristics of acute leukemias to screen for patient eligibility for available pediatric leukemia sub-trials. Testing bone marrow and blood from patients with leukemia that has come back after treatment or is difficult to treat may provide information about the patient's leukemia that is important when deciding how to best treat it, and may help doctors find better ways to diagnose and treat leukemia in children, adolescents, and young adults.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    0 to 22

Participation Criteria

Inclusion Criteria:

* Patients must be less than 22 years of age at the time of study enrollment
* Patient must have one of the following at the time of study enrollment:

* Patient has known or suspected relapsed/refractory (including primary refractory) AML as defined in protocol

* This includes isolated myeloid sarcoma
* Patient has known or suspected relapsed/refractory (including primary refractory) myeloid leukemia of Down syndrome (ML-DS)
* Patient has known or suspected relapsed ALL as defined in protocol that meets one of the following criteria:

* Second or greater B-ALL medullary relapse, excluding KMT2Ar
* Any first or greater B-ALL medullary relapse involving KMT2Ar
* Any first or greater T-ALL medullary relapse with or without KMT2Ar
* Patient has known or suspected relapsed/refractory (including primary refractory) mixed phenotype acute leukemia (MPAL) as defined in protocol
* Patient has known or suspected de novo or relapsed/refractory (including primary refractory) treatment-related AML (t-AML)
* Patient has known or suspected de novo or relapsed/refractory (including primary refractory) myelodysplastic syndrome (MDS) or treatment-related myelodysplastic syndrome (t-MDS)

* Note: Relapsed/refractory disease includes stable disease, progressive disease, and disease relapse.
* Patient has known or suspected de novo or relapsed/refractory (including primary refractory) juvenile myelomonocytic leukemia (JMML)

* Note: Relapsed/refractory disease includes stable disease, progressive disease, and disease relapse.
* All patients and/or their parents or legal guardians must sign a written informed consent
* All institutional, Food and Drug Administration (FDA), and National Cancer Institute (NCI) requirements for human studies must be met

Study Location

CancerCare Manitoba
CancerCare Manitoba
Winnipeg, Manitoba
Canada

Contact Study Team

Primary Contact

Site Public Contact

[email protected]
866-561-1026
Hospital for Sick Children
Hospital for Sick Children
Toronto, Ontario
Canada

Contact Study Team

Primary Contact

Site Public Contact

[email protected]
416-813-7654
British Columbia Children's Hospital
British Columbia Children's Hospital
Vancouver, British Columbia
Canada

Contact Study Team

Primary Contact

Site Public Contact

604-875-2345
Children's Hospital of Eastern Ontario
Children's Hospital of Eastern Ontario
Ottawa, Ontario
Canada

Contact Study Team

Primary Contact

Site Public Contact

613-737-7600
Centre Hospitalier Universitaire de Sherbrooke-Fleurimont
Centre Hospitalier Universitaire de Sherbrooke-Fleurimont
Sherbrooke, Quebec
Canada

Contact Study Team

Primary Contact

Site Public Contact

[email protected]
819-820-6480
Alberta Children's Hospital
Alberta Children's Hospital
Calgary, Alberta
Canada

Contact Study Team

Primary Contact

Site Public Contact

[email protected]
403-220-6898
IWK Health Centre
IWK Health Centre
Halifax, Nova Scotia
Canada

Contact Study Team

Primary Contact

Site Public Contact

[email protected]
902-470-8520
The Montreal Children's Hospital of the MUHC
The Montreal Children's Hospital of the MUHC
Montreal, Quebec
Canada

Contact Study Team

Primary Contact

Site Public Contact

[email protected]
514-412-4445
Centre Hospitalier Universitaire Sainte-Justine
Centre Hospitalier Universitaire Sainte-Justine
Montreal, Quebec
Canada

Contact Study Team

Primary Contact

Site Public Contact

[email protected]
514-345-4931
University of Alberta Hospital
University of Alberta Hospital
Edmonton, Alberta
Canada

Contact Study Team

Primary Contact

Site Public Contact

[email protected]
780-407-8798
Children's Hospital
Children's Hospital
London, Ontario
Canada

Contact Study Team

Primary Contact

Site Public Contact

519-685-8306
Study Sponsored By
LLS PedAL Initiative, LLC
Participants Required
More Information
Study ID: NCT04726241