Observational
OtherOBSERVAITON OF THE CAPACITY OF THE GROUP TO TREAT ACCORDING TO THE PROTOCOLE AND LOOK AT OUTCOME FOR STAGE I AND II DISEASE
NCT Number: NCT04425421
This is the 4th LMB study by the French African Pediatric Oncology Group (GFAOP). The study hopes to be able to evaluate children earlier with stage I and II disease and to evaluate treatment response earlier so that the units can decide if a change in treatment is necessary, it is also hoped to provide an intensification of treatment for the stage IV disease.
Interested in participating?
Request InfoUp to 18 year
All sexes
Observational
Hopital Yalgado Ouedraogo, Ouagadougou, Burkina Faso
This is the 4th Burkitt's Lymphoma (LMB) study by the GFAOP group. This study hopes to include at least 14 Sub Saharian countries some of whom have never participated in a LMB study. The evaluation of improvement in early diagnosis should be possible in this study. The study hopes to be able to evaluate children earlier, with stage I and II disease and to evaluate treatment response earlier so that the units can decide if a change in treatment is necessary, it is also hoped to provide an intensification of treatment for children with a stage IV disease. Starting from 2026 we now have the possibility of introducing rituximab into the treatment of African children with Burkitt lymphoma, starting from 15/03/2026. This amendment will prospectively evaluate the toxicity and effectiveness of adding rituximab to the current therapeutic recommendations. These results will be compared with those observed during the first years of implementation in two GFAOP units: specifically, the unit at CHU Yalgado Ouagadougou in Burkina Faso and CHU Treichville in Abidjan, Ivory Coast.
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Clinical diagnosis of Burkitt's Lymphoma: all location. Diagnosis by cytology or histology. Not possible to follow all the treatment.
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Exclusion criteria
Not a B Cell tumor. Child has been previously treated. Child has also another illness which would render the treatment incompatible. Parents refusal.
OBSERVAITON OF THE CAPACITY OF THE GROUP TO TREAT ACCORDING TO THE PROTOCOLE AND LOOK AT OUTCOME FOR STAGE I AND II DISEASE
Time frame: 5 years
evaluating the initial clinical reports and later histological reports to confirm the diagnosis and the stage.
Time frame: 5 Years
evaluating the initial clinical reports and later histological reports to confirm the stage and the diagnosis.
Time frame: 5 Years
Comparison of treatment given and recommended treatment.
Time frame: 5 Years
How many children alive or dead after treatment
Time frame: 5 years
The evaluation and the treatment of relapse and outcome
Time frame: 5 years
Evaluations of the correct application of recommendations
Contact information is provided by the study sponsor or research team.
BRENDA MALLON, MSc PhD
CONTACT
Chantal Ms BOUDA, Dr.
CONTACT
French Africa Pediatric Oncology Group
Other
Acronym: GFALMB2019
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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