Objectives: Recently, in adult ALL patients, to improve prognosis, pediatric ALL protocols have been used in adolescent and young adults and positive results have been reported.
Methods: In this study, we aimed to evaluate retrospectively the demographic features, treatment responses, cytogenetic data and survival analyses of adult T-All cases followed up by the Department of Adult Hematology at Dokuz Eylul University Hospital.
Results: The mean survival time for patients receiving H-CVAD was 46.9 months (±12.9), and median survival time of patients receiving BFM treatment was 71.5 months (±11.4).The median OS of patients receiving BFM was statistically significantly longer than that of Hyper-CVAD (p=0.044).
Conclusion: The use of pediatric intensive chemotherapy regimens in adolescent and young adult (AYA) patients with low incidence and poor prognosis of ALL-type T-ALL, the inclusion of nelarabine in the first line treatment and the selection of new targeted therapies based on new genomic discoveries can increase effectiveness. The use of pediatric intensive chemotherapy regimens is promising for increased survival in adults.