TREATMENT OF ACUTE PROMYELOCYTIC LEUKEMIA WITH AIDA BASED REGIMEN

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Ramzi Jeddi *
Hèla Ghédira
Ramzi Ben Amor
Yosr Ben Abdennebi
Kacem Karima
Zarrouk Mohamed
Hend Ben Neji
Lamia Aissaoui
Raihane Ben Lakhal
Naouel Ben Salah
Samia Menif
Zaher Belhadjali
Hela Ben Abid
Emna Gouider
Raouf Hafsia
Ali Saad
Pierre Fenaux
Balkis Meddeb
(*) Corresponding Author:
Ramzi Jeddi | ramzi.jed@voila.fr

Abstract

In Tunisia, the ATRA era began in 1998 with the use, consecutively, of two regimens combining ATRA and an anthracycline with cytarabine (APL93), and without cytarabine (LPA99). From 2004, 51 patients with confirmed APL either by t(15;17) or PML/RARA were treated according to the PETHEMA LPA 99 trial. Forty three patients achieved CR (86%). The remaining seven patients had early death (one died before treatment onset): four caused by differentiation syndrome (DS) and three died from central nervous system hemorrhage. Multivariate analysis revealed that female gender (P=0.045), baseline WBC> 10 G/L ( P=0.041) and serum creatinine > 1.4mg/dl ( P=0.021) were predictive of mortality during induction. DS was observed in 16 patients (32%) after a median onset time of 15 days from treatment onset (range, 2–29). Body mass index ≥ 30 (P=0.01) was the only independent predictor of DS. Occurrence of hypertensive peaks significantly predicted occurrence of DS (P=0.011) and was significantly associated with high BMI (p=0.003). With a median follow-up of 50 months, 5 year cumulative incidence of relapse, event free and overall survival were 4.7%, 74% and 78%, respectively.


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Author Biographies

Ramzi Jeddi, Aziza Othmana University Hospital

-Hematology Department, Aziza Othmana University Hospital, Tunis, Tunisia2-Department of molecular analysis, Pasteur Institute, Tunis, Tunisia3-Department of cytogenetic analysis, Farhat Hached Hospital, Sousse, Tunisia4-Hematology Department, Avicenne Hospital, Assistance Publique Hôpitaux de Paris, Paris 13 University, Paris, France

Lamia Aissaoui

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Emna Gouider

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