PB1677 SIXTEEN YEAR'S EXPERIENCE OF THE EORTC 58951 PROTOCOL FOR THE TREATMENT OF CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA IN THE SOUTH OF TUNISIA

Abstract

Background:Childhood acute lymphoblastic leukemia (ALL) is an hematologic malignancies with high rate of cure. We report the experience of the clinical hematology department of Sfax‐Tunisia for the treatment of childhood ALL with the EORTC 58951 protocol.Aims:We report in this study the experience of the clinical hematology department of Sfax‐Tunisia for the treatment of childhood ALL with the EORTC 58951 protocol.Methods:From January 2000 to December 2015, we retrospectively studied the outcome of all childhood ALL treated with the EORTC 58951 pediatric protocol. For those patients we studied the leukemia characteristics (sex ratio, white blood cell counts WBC, blast's phenotype, cytogenetic abnormalities) and response to treatment: response to prophase, remission rate, risk group stratification, treatment related mortality (TRM) (induction and post induction death) and survival (overall survival OS, event free survival EFS and disease free survival DFS).Results: From January 2000 to December 2015, 193 children were treated with the EORTC 58951 protocol. Median age was 6 years (range: 13 months to 15 years). Sex ratio M/F was 1.47. WBC counts less than 10 G/l, from 10 to 100 G/L and more than 100 G/L were observed respectively in 42, 42 and 16% of cases. The blast's phenotype was B in 71% and T in 29%. Cytogenetic abnormalities were noted in 38% of cases. A good response to prophase was noted in 83% and complete remission in 96% of cases. The EORTC risk group stratification was Low Risk (LR) in 6%, Average Risk1 (AR1) in 46%, Average Risk2 (AR2) in 23.5% and Very High Risk (VHR) in 24.5%. TRM was 10.5%: induction rate death was 6% and post‐induction rate death was 4.5%. Nine patients from VHR group with familial donor underwent allograft. The relapse rate was 28% of all patients in remission; 8% for LR group, 32% for AR1 group, 18% for AR2 group and 44% for VHR group. At 5 years of follow up, OS and EFS were 66 and 60 respectively and DFS was 70%.Summary/Conclusion:At diagnosis, childhood ALL in our study had poor characteristics particularly higher rate of T phenotype of blasts, higher rate of leukocytosis more than 100 G/L, higher rate of VHR therapeutic group and higher rate of cortico‐resistant regarding occidental series. Despite the acceptable results concerning remission rate but survival rates remain lower than those observed in the literature, this is explained mainly by the high rate of relapse (28% vs ∼15%). It can be improved our results by detecting high risk patient with MRD study especially for AR1 risk group and doing allograft for VHR patients.