Allogreffe decellules souches hématopoïétiques dans les leucémies aigues myéloblastiques de l’enfant: Survieet rechute
DOI :
https://doi.org/10.62438/tunismed.v103i11.5353Mots-clés :
Acute myeloblastic leukemia, children, allogeneic stem cell transplantation, survival, relapseRésumé
Introduction: L’allogreffe de cellules souches hématopoïétiques (allo-CSH) est indiquée dans Les leucémies aigues myéloblastiques (LAM) de l’enfant à haut risque (HR).
Objectif: Evaluer la survie globale(SG) , survie sans événement(SSE),la rechute et la mortalité non liée à la rechute (NRM).
Méthodes: Etude descriptive rétrospective, ayant inclus les enfants (˂18ans) atteints de LAM allogreffés à partir d’un donneur géno-identique entre1999 et2023. Le conditionnement pré-greffe était de type Busulfan-cyclophosphamide(BuCy)ou irradiation corporelle totale-Cy. Le greffon était de type moelle osseuse(MO)ou cellules souches périphériques.
Résultats: Cinquante-deux enfants ont été inclus avec un âge médian de 13ans (3-17ans).Les patients étaient Classés HR dans 60,3% des cas. Le délai médian diagnostic-greffe était de 5 mois (3-40mois). En pré-greffe,75% des patients étaient en RC1. Le greffon était de type MO dans 84,6% des cas. Le conditionnement était de type BuCy dans 90,4% des cas. Le taux de rejet était de 5,8%. Les incidences cumulées (IC) de la GVHD aigue et de la GVHD chronique étaient de 20% et de 23,4%, respectivement. L’IC de la NRM était de7,7% et de la rechute était de 44,7%. Après un suivi médian de 30mois (39j-18ans),l aSG et la SSE à 3 ans étaient de 51,6%et47,8%, respectivement.
Conclusion: La rechute postallo-CSH demeure un problème majeur.Le renforcement du Conditionnement pré-greffe, l’étude de la pharmacocinétique du Bu et le développement des
Thérapies ciblées pourraient réduirece risque
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