Thereapeutic Recommendantion for Children With a Hodgkin Lymphoma

NCT ID: NCT05407480

Last Updated: 2025-10-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

250 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-11-15

Study Completion Date

2034-11-20

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Staging Therapeutic Recommendations

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Observational

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

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

0 Months

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Gustave Roussy, Cancer Campus, Grand Paris

OTHER

Sponsor Role collaborator

French Africa Pediatric Oncology Group

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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FATEN Ben Ayed, Professeur

Role: PRINCIPAL_INVESTIGATOR

French Africa Pediatric Oncology Group

Locations

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Brenda Mallon

Paris, France, France

Site Status RECRUITING

Countries

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France

Central Contacts

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Brenda MS MALLON

Role: CONTACT

0033 142115411

FATEN Ben Ayed, Professeur

Role: CONTACT

Facility Contacts

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FATEN FEDHILA DR BEN AYED, PROF

Role: primary

Aïssata BARRY, DR

Role: backup

0033 6 61 51 94 74

Other Identifiers

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GFAOP LH 2019

Identifier Type: -

Identifier Source: org_study_id

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