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NCT Number: NCT04425421

Recommendations for the Treatment of Children With Burkitt's Lymphoma

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.

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Key information

Age range

Up to 18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Hopital Yalgado Ouedraogo, Ouagadougou, Burkina Faso

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About this study

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.

Who can participate

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.

Treatment and study plan

Observational

Other

OBSERVAITON OF THE CAPACITY OF THE GROUP TO TREAT ACCORDING TO THE PROTOCOLE AND LOOK AT OUTCOME FOR STAGE I AND II DISEASE

Primary outcomes

  1. Evaluation of the number of cases with local disease.

    Time frame: 5 years

    evaluating the initial clinical reports and later histological reports to confirm the diagnosis and the stage.

  2. Evaluation of the number of cases by stage at the time of diagnosis.

    Time frame: 5 Years

    evaluating the initial clinical reports and later histological reports to confirm the stage and the diagnosis.

  3. Evaluating the treatment given.

    Time frame: 5 Years

    Comparison of treatment given and recommended treatment.

  4. Evaluating the follow up after treatment.

    Time frame: 5 Years

    How many children alive or dead after treatment

  5. Number of relapse cases

    Time frame: 5 years

    The evaluation and the treatment of relapse and outcome

Secondary outcomes

  1. Application of therapeutic recommendations

    Time frame: 5 years

    Evaluations of the correct application of recommendations

Study contacts

Contact information is provided by the study sponsor or research team.

BRENDA MALLON, MSc PhD

CONTACT

[email protected]

0033142115411

Chantal Ms BOUDA, Dr.

CONTACT

[email protected]

00(226)70 10 01 30

Sponsors and collaborators

Lead sponsor

French Africa Pediatric Oncology Group

Other

Registry information

Acronym: GFALMB2019

Important dates

Study start
2020
Primary completion
2028
Study completion
2030
First posted
Jun 11, 2020
Registry last updated
Mar 2, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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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