Recommendations for the Treatment of Children With Acute Lymphoblastic Leukemia in the GFAOP

ConditionChildhood ALL
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 18
SponsorFrench Africa Pediatric Oncology Group

About this trial

The LALGFA2019 Recommendations redefine the standard risk criteria and propose to introduce anthracycline induction in so-called high-risk forms (LAL line T and LAL line B with leukocytosis greater than or equal to 50 G/L or in children less than 1 year of age or more than 10 years of age) as well as Endoxan and Methotrexate in high dose consolidation.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

0 to 18 years of age presenting for treatment in any of the unit selected to carry out the recommandations

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Feasibility of these recommendations

Availability of drugs. This is part of the project as we are working with Low or low to Middle Income countries.

Time frame
This can be initially reviewed after the first 2 years and will be evaluated at the end for the community.
2

Correct application of therapeutic recommendations

Availability of drugs and adherence to protocol: Some centers may at times have to find locally the chemiotherapy for application of the protocol. The capacity of the units to do this is alos being studied. By looking at why treatment was not given. Was it because of lack of discipline regarding the attendance at the units for treatment, transport, accommodation, or medication not available ?

Time frame
5 weeks
3

Complete Remission Rate (CR) close to 85% after induction

Evaluation of the CR j34 or J42 depending on the risk level High or standard.

Time frame
J 34 or j42 post start of induction treatment for all children studied.
4

Ability to follow treatment:

The number of children who stop treatment without the consent of the doctor.

Time frame
5 weeks

Secondary outcomes

1

Survival without relapse of patients

the number of children in complete remission without relapse at the end of treatment .

Time frame
first evaluation starts in 2026 so that enough time has elapsed to evaluate.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

French Africa Pediatric Oncology Group

Lead sponsor

Gustave Roussy, Cancer Campus, Grand Paris

Collaborator