ClinicalTrials.gg
RecruitingNCT05407480GFAOPLH2019Updated Mar 2, 2026

Thereapeutic Recommendantion for Children With a Hodgkin Lymphoma

An observational study in Staging and Therapeutic Recommendations, sponsored by French Africa Pediatric Oncology Group. Recruiting at 1 site in France. Open to participants aged 0 Months to 18 Years. Per ClinicalTrials.gov, last updated 2026-03-02.

Sponsored by French Africa Pediatric Oncology Group · Observational

From the registry’s dates

  • Started Nov 2022; still recruiting 3 years 11 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
250
Ages
0 Months to 18 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Staging
  • Therapeutic Recommendations
03

In context

Lead sponsor

French Africa Pediatric Oncology Group is the lead sponsor of 6 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
0 Months to 18 Years
Sexes eligible
All
Sampling method
Non-probability sample

Study population

All children arriving in one of the participating units :

under 18 years of age at diagnosis and suffering from "classical" Hodgkin's disease according to the WHO classification.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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 or constitutional or acquired immune deficiencies

Exclusion criteria

Exclusion Criteria:

  • Over 18 years of age at diagnosis
  • A history of hematological or a history of constitutional or a history of acquired immune deficiencies
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
250 participants (estimated)
Patient registry
No

Interventions

  • OtherObservational

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

06

What researchers measure

Primary outcomes

  1. Patient status

    Dead or Alive

    Time frame: 24 months

  2. Drugs

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

    Time frame: 24 months

07

Study locations

1 of 1 sites recruiting
  • Brenda Mallon
    Paris, France 94805, France
    Recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Nov 2022 (actual). Primary completion is estimated for Dec 2028, 73 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 2, 2022
First posted
Jun 7, 2022
StartActual
Nov 15, 2022
Primary completionEst.
Dec 31, 2028
CompletionEst.
Dec 31, 2030
Last update
Mar 2, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05407480
Lead sponsor
French Africa Pediatric Oncology Group
Responsible party
Sponsor
First posted
Jun 7, 2022
Start date
Nov 15, 2022
Primary completion
Dec 31, 2028 (estimated)
Completion
Dec 31, 2030 (estimated)
Last update
Mar 2, 2026

Study contacts

Brenda MS MALLON
Contact
brenda.mallon@gustaveroussy.fr
0033 142115411
FATEN Ben Ayed, Professeur
Contact
faten.fedhila@yahoo.fr
FATEN Ben Ayed, Professeur
principal investigator · French Africa Pediatric Oncology Group

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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