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
This study, called PedAL, is for children and young people up to 22 years old who have certain types of leukaemia that have either returned after treatment or have been difficult to treat. Doctors will collect samples of blood and bone marrow from these patients. By carefully looking at these samples, they hope to learn more about the leukaemia itself. This deeper understanding can help doctors decide on the best way to treat each patient and also contribute to finding new and better treatments for young people with leukaemia in the future. It's a way to screen patients for other specific leukaemia studies.
At a glance
What is this study about?
This study, called PedAL (which stands for Pediatric Acute Leukemia Screening Trial), is for children and young people up to 22 years old who are dealing with certain types of leukaemia. This includes leukaemia that has returned after treatment or has been challenging to treat for a while. The main idea behind this research is to learn as much as possible about how these types of leukaemia behave.
To do this, doctors will collect samples of blood and bone marrow from patients taking part. By closely examining these samples, they hope to find out specific details about each patient's leukaemia. This information is really important because it can help doctors choose the most suitable treatments and even find specific studies that might be a good fit for that patient. Over time, gathering all this information helps the medical community understand leukaemia in young people much better.
Ultimately, the goal of this study is to improve the way we diagnose and treat leukaemia in children, teenagers, and young adults. It helps doctors gain knowledge that could lead to new, more effective ways to fight the disease, giving young patients the best possible chance.
Key takeaways
- This study helps doctors learn more about leukaemia in young people.
- It focuses on leukaemia that has returned or is hard to treat.
- Only blood and bone marrow samples are collected, no new medicines are given.
- Information gained could improve future leukaemia treatments.
- Patients under 22 with specific leukaemia types may be eligible.
- Participation involves sample collection and long-term follow-up.
Who may be eligible?
This study is looking for children and young people who are under 22 years old at the time they join. They must have certain types of leukaemia that have either come back after treatment, or have been hard to treat.
Specifically, this includes various forms of acute leukaemia (like Acute Lymphoblastic Leukaemia or Acute Myeloid Leukaemia), as well as Myelodysplastic Syndrome or Juvenile Myelomonocytic Leukaemia, especially if these conditions have returned or are proving difficult to manage. If you're not sure if your child's specific condition fits, it's best to ask their doctor.
All families and patients (if they are old enough) will need to give their permission in writing to take part in the study. Your medical team will explain everything fully before you make any decisions.
Could this study suit you?
Answer these quick questions to see if you may be eligible. This is a guide only — the research team makes the final call.
- Is the patient under 22 years old?
- Does the patient have Acute Lymphoblastic Leukaemia, Acute Myeloid Leukaemia, or Mixed Phenotype Acute Leukaemia that has come back or is difficult to treat?
- Does the patient have Myelodysplastic Syndrome or Juvenile Myelomonocytic Leukaemia that is new, has come back, or is hard to treat?
- Has the patient (or their parent/guardian) signed a consent form?
- Is the patient dealing with Myeloid Leukemia related to Down Syndrome that has come back or is hard to treat?
What does participation involve?
If you decide to take part, your child will have samples of their blood and/or bone marrow collected at the start of the study. These collections might also happen again during their treatment, or if their leukaemia returns or isn't responding well to treatment.
The study itself involves just the collection of these samples and no new medications or treatments will be given as part of *this* particular study. After the study collections are completed, the research team will keep in touch. They will check in every three months for the first two years, then every six months for another three years. This is to gather long-term information about the leukaemia, but it mostly involves just keeping records.
Potential risks and benefits
Locations (183)
- Children's Hospital of AlabamaVerified postcodeBirmingham, United States· Recruiting
- USA Health Strada Patient Care CenterVerified postcodeMobile, United States· Recruiting
- Providence Alaska Medical CenterVerified postcodeAnchorage, United States· Recruiting
- Banner Children's at DesertVerified postcodeMesa, United States· Recruiting
- Phoenix Childrens HospitalVerified postcodePhoenix, United States· Recruiting
- Banner University Medical Center - TucsonVerified postcodeTucson, United States· Recruiting
- Arkansas Children's HospitalVerified postcodeLittle Rock, United States· Recruiting
- Kaiser Permanente Downey Medical CenterVerified postcodeDowney, United States· Recruiting
- Loma Linda University Medical CenterVerified postcodeLoma Linda, United States· Recruiting
- Miller Children's and Women's Hospital Long BeachVerified postcodeLong Beach, United States· Recruiting
- Children's Hospital Los AngelesVerified postcodeLos Angeles, United States· Recruiting
- Valley Children's HospitalVerified postcodeMadera, United States· Recruiting
Common questions
What is the main goal of this study?
To learn more about the leukaemia in children and young people, especially when it has come back or is hard to treat, to help find better ways to diagnose and treat it.
Will my child receive new medicine in this study?
No, this study focuses on collecting blood and bone marrow samples; it does not involve giving new medicines or treatments.
How old do you have to be to join?
Patients must be under 22 years old when they join the study.
What kind of samples are needed?
Blood and/or bone marrow samples will be collected.
How long will doctors keep track of patients?
After the main part of the study, patients will be followed up for up to 5 years through regular check-ins.
How to find out more
Always speak to your GP or specialist before deciding to take part in a study.
Interested in taking part?
Discussion
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