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Taking people in SwedenNo phase

Expert panel advises treatment choices for young people with returning blood cancers

Experts advise treatment choices for children and young adults with returning blood cancers.

Plain-language title generated from the registry record
Registry title: International Leukemia Target Board

Key facts

Where
Gothenburg, SwedenSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 0 and 25 years old?
  • What type of cancer has the patient been diagnosed with?
  • Is this cancer newly diagnosed, or has it come back or not responded to treatment?

Source: NCT05270096, who can take part

Where in Sweden

  • Queen SilviaGothenburg, SwedenTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Princess Maxima Center for Pediatric Oncology
Trial code
NCT05270096
Record updated
9 January 2026
Original description
The iLTB is a proof-of-concept initiative for children with r/r hematological malignancies, in which available treatment options will be prioritized by actionable events in a harmonized and uniform setting across Europe by a team of biologists, bio-statisticians, bio-informaticians, disease experts, geneticists, flow-experts, clinical trial physicians and also the treating physician.Read full original descriptionShow less

International Concerted Action to Allocate Children, Adolescents and Young Adults With Relapsed and Refractory Leukemia/Lymphoma to the Right Therapy.

The iLTB is a proof-of-concept initiative for children with r/r hematological malignancies, in which available treatment options will be prioritized by actionable events in a harmonized and uniform setting across Europe by a team of biologists, bio-statisticians, bio-informaticians, disease experts, geneticists, flow-experts, clinical trial physicians and also the treating physician.

The iLTB will discuss molecular (genetic lesions), immunophenotypic/surface antigen markers information and, if available, drug response profiles to prioritize these events taking into account the treatment history and treatment intention (bridging to hematopoietic stem cell transplanation/CAR-T or palliative) of each patient followed by a registry to monitor how often iLTB advice has been followed, which other therapy was chosen (off-label, compassionate use) and what the patient outcome is at an aggregated level.

As such the iLTB is non-interventional as it mainly provides advice and registers data on patients discussed in the iLTB.

Inclusion: The patient has been diagnosed with a R/R hematological malignancy; The patient is less than 18 years of age at the time of first diagnosis and less than 25 years at the time of inclusion with relapse/refractory hematological malignancy; The patient is treated in a pediatric/AYA setting or study protocol, with no current standard of care treatment; The patients' life expectancy is at least 6 weeks; The patient has undergone any sort of molecular profiling of his/her tumor and the re-sults of this analysis are available; The patient has undergone flow cytometry in a certified lab and results are available; Written informed consent of patient and/or parent(s)/guardian(s) to discuss the patient in the iLTB according to local law and legislation has been obtained.

ClinicalTrials.gov NCT05270096