Actively Recruiting
International Concerted Action to Allocate Children, Adolescents and Young Adults With Relapsed and Refractory Leukemia/Lymphoma to the Right Therapy
Led by Princess Maxima Center for Pediatric Oncology · Updated on 2026-01-09
600
Participants Needed
7
Research Sites
100 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating a new approach called the international Leukemia Target Board (iLTB) for children, adolescents, and young adults with relapsed or refractory blood cancers. The iLTB aims to bring together experts across Europe to review molecular, immunophenotypic, and drug response data from each patient to prioritize potential treatment options. This non-interventional study seeks to provide uniform advice to treating physicians and facilitate access to early phase clinical trials or alternative treatments when standard options are limited. The iLTB does not provide treatments directly but serves as a platform where experts discuss patients' genetic lesions, surface antigen markers, and drug response profiles. Patients eligible for discussion have relapsed or refractory hematological malignancies and have undergone molecular profiling and flow cytometry. The expert panel uses a prioritization algorithm to recommend potential therapies or trial options, considering each patient's treatment history and goals. Patient data is shared following informed consent and feedback is given to the treating physician. Participants are involved through data sharing and expert review of their tumor profiles, but no treatment is administered by the study itself. The study tracks how often physicians follow the iLTB advice, what therapies are chosen, and patient outcomes over time. The main measure is the proportion of patients receiving therapy aligned with iLTB recommendations, monitored over about 8 years. This long-term registry helps assess the impact of expert advice on treatment decisions and outcomes for this challenging patient group.
CONDITIONS
Brief Title
International Leukemia Target Board
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient has been diagnosed with a relapsed or refractory hematological malignancy
- Patient is less than 18 years old at first diagnosis and less than 25 years old at time of inclusion
- Patient is treated in a pediatric or adolescent/young adult setting with no current standard of care treatment
- Patient's life expectancy is at least 6 weeks
- Patient has molecular profiling results of their tumor available
- Patient has flow cytometry results from a certified lab available
- Written informed consent to discuss the patient in the international Leukemia Target Board has been obtained according to local laws
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 8 years
Participants who undergo routine care are observed through an international platform where experts review molecular profiling and other diagnostic information to advise on the most appropriate treatment options.
Data sharing and discussion occur as needed; no additional study visits required
Trial Site Locations
Total: 7 locations
1
UH Gent
Ghent, Belgium
Actively Recruiting
2
Righospitalet
Copenhagen, Denmark
Actively Recruiting
3
Semmelweis
Budapest, Hungary
Actively Recruiting
4
Princess Máxima Center for Pediatric Oncology
Utrecht, Utrecht, Netherlands, 3584CS
Actively Recruiting
5
Vall d'Hebron
Barcelona, Spain
Actively Recruiting
6
Queen Silvia
Gothenburg, Sweden
Actively Recruiting
7
Newcastle Hospital
Newcastle, United Kingdom
Actively Recruiting
Research Team
U
Uri Ilan, MD
A
Anne Elsinghorst
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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