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NCT Number: NCT05407480

Thereapeutic Recommendantion for Children With a Hodgkin Lymphoma

The GFAOP propose a simple and reproducible staging according to clinical, biological and radiological data.

Develop standardized but different therapeutic recommendations based on the availability or lack of radiation therapy in the pilot unites who will adapt these recommendations.

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Key information

Age range

0 month–18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Brenda Mallon

Paris, France, 94805

Location status: Recruiting

Location contact

Aléine BUDIONGO, DR

SUB_INVESTIGATOR

Aïssata BARRY, DR

CONTACT

[email protected]

0033 6 61 51 94 74

Chantal BOUDA, DR

SUB_INVESTIGATOR

FATEN FEDHILA DR BEN AYED, PROF

CONTACT

Dr. FEDHILA BEN AYED Faten Tunis <[email protected]>

Fatou-Binetou DIAGNE AKONDE, DR

SUB_INVESTIGATOR

Mbola RAKOTOMAHEFA, PROF

SUB_INVESTIGATOR

About this study

In high-income countries, therapeutic outcomes exceed 90% and therapeutic de-escalation is necessary to reduce mainly the effects of long-term radiotherapy. Within the same country, there are also differences between the therapeutic protocols used in the different centres.

The Experience of Sub-Saharan African Units of the Franco-African Paediatric Oncology Group (GFAOP) in the treatment of pediatric Hodgkin lymphoma in 104 patients was based on chemotherapy alone. The latter was based on COPP/ABV cures without complementary irradiation adapted to the initial stratification and modulated according to the morphological response. Overall survival at 5 years was 82% at 30 months after a median decrease of 17 months.

It seemed appropriate to bring together in a single committee the representatives of the various pilot units in order to standardize the therapeutic protocols in the African countries.

So with this recommendation the GFAOP propose a simple and reproducible staging according to clinical, biological and radiological data.

  • Develop standardized but different therapeutic recommendations based on the availability or lack of radiation therapy in the pilot unit.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

under 18 years of age at diagnosis

  • suffering from "classical" Hodgkin's disease according to the WHO classification.
  • with no history of hematological malignancies or constitutional or acquired immune deficiencies

Exclusion criteria

  • Over 18 years of age at diagnosis
  • A history of hematological malignancies or a history of constitutional or a history of acquired immune deficiencies

Treatment and study plan

Observational

Other

Descriptive data will be collected to evaluation compliance with the protocol and to evaluate outcome

Primary outcomes

  1. Patient status

    Time frame: 24 months

    Dead or Alive

  2. Drugs

    Time frame: 24 months

    The evaluation of the number of children who remain untreated because of lack of acess to chemotherapy

Study contacts

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

Brenda MS MALLON

CONTACT

[email protected]

0033 142115411

FATEN Ben Ayed, Professeur

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

French Africa Pediatric Oncology Group

Other

Collaborators

  • Gustave Roussy, Cancer Campus, Grand Paris

Registry information

Official study title

Therapeutic Recommendations for Children Registered in the RFAOP Register and With a Hodgkin Lymphoma

Acronym: GFAOPLH2019

Important dates

Study start
2022
Primary completion
2028
Study completion
2030
First posted
Jun 7, 2022
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.

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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