Main info

Identificatie:

ALL Target ATTRACT

Sponsor:

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Included patients:

0

(of 17)

Active sites:

0

(of 1)

2 sites are pending

Title:

A PRECISION MEDICINE RANDOMIZED TRIAL FOR PATIENTS WITH RELAPSED OR REFRACTORY T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA BASED ON A FUNCTIONAL APPROACH.

Timeline

News

Details

Phase:

Select:

Monitoring Type:

Objectives:

het nut beoordelen van een op precisiegeneeskunde gebaseerde strategie (gerichte therapeutische opties (TTO’s)) op het percentage hematologische remissie bij patiënten met recidiverende/refractaire T-cel-acute lymfatische leukemie (T-ALL)
Het beoordelen van het voordeel en de tolerantie van de TTO's, zowel in het algemeen als voor elke TTO afzonderlijk
Het evalueren van de totale overleving, de recidiefvrije overleving en de gebeurtenisvrije overleving.
Het vergelijken van de kwaliteit van leven en patiëntgerelateerde uitkomsten (QOL, PROM) tussen de verschillende strategieën en tussen de specifieke TTO's.
Het onderzoeken van de mechanismen van een recidief.
Het analyseren van de toewijzing van TTO's.

Eligibility

Inclusion Criteria:

1. Patients aged 15y or more (under 18y only for France)
2. Signed informed consent for patients aged ≥ 18 years and signed informed consent from both parents for patients aged between ≥ 15 years and < 18 years (only for France).
3. Patients with T-cell acute lymphoblastic leukemia in first or second relapse or in the refractory phase.
a) Patients with first relapses are eligible if relapse occurred within 24 months post complete remission achievement and if nelarabine is not considered as appropriate salvage therapy.
b) Patients with second and all subsequent relapses are eligible.
c) Refractory patients are defined as patients not responding after at least 2 lines of chemotherapy (induction + salvage).
d) Patients with relapses post-transplant and post CART-cells treatments are eligible.
4. Blast cells in blood and/or bone marrow to allow the shipment to one of the 3 reference laboratories in France, Spain and The Netherlands or An informative biological assessment already performed within 10 days prior to inclusion in one of the three reference laboratories in France, Spain or The Netherlands with at least one targeted therapeutic option validated (TTO1, venetoclax + tofacitinib; TTO2, venetoclax+ everolimus + enrylaze; TTO3, venetoclax + 5azacytidine) by one of the three National Validation Committees.
5. Adequate ECOG score (0-3).
6. Patients must be affiliated to a National Health systems (see countrybased specificity).
7. Patients must not have a contra-indication for venetoclax, tofacitinib, everolimus, glutaminolytic agents (enrylaze) or 5-azacytidine.
8. Willingness of women of child-bearing potential (WOCBP) or of male patients whose sexual partners are WOCBP to use an effective form of contraception during the study and at least 3 thereafter (see Annex 13.9).

Exclusion Criteria:

1. Patients in palliative care.
2. Patients with late relapses after the first complete remission (> 24 months post complete remission).
3. Patients with extramedullary only relapses or with clinically symptomatic central nervous system (CNS) involvement.
4. Pregnant or lactating women.
5. Participation in another clinical trial with an investigative drug at the time of study enrolment.
6. Individuals with another active uncontrolled malignancy.
7. Known active HBV-, HCV and HIV related diseases.
8. Patient under curatorship or deprived of liberty (except for minors). 9. Patients with contra-indication to chemotherapy except if considered related to the ALL:  ASAT (SGOT) and/or ALAT (SGPT) > 5 x ULN Total bilirubin ≥ 2.5 x ULN  Estimated glomerular filtration rate (GFR) < 50 mL/mn using the MDRD equation
10. Administration of live or live-attenuated vaccines within 4 weeks prior to the first dose of study treatment (see Annex 13.10)
11. Subject presenting with psychiatric disorders or any other condition that impair their ability to cooperate with study procedures.

Participating Sites

= Active hospitals

= Inactive hospitals