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Clinico-biological features of 5202 patients with acute lymphoblastic leukemia enrolled in the Italian AIEOP and GIMEMA protocols and stratified in age cohorts
Authors:Sabina Chiaretti  Antonella Vitale  Gianni Cazzaniga  Sonia Maria Orlando  Daniela Silvestri  Paola Fazi  Maria Grazia Valsecchi  Loredana Elia  Anna Maria Testi  Francesca Mancini  Valentino Conter  Geertruy te Kronnie  Felicetto Ferrara  Francesco Di Raimondo  Alessandra Tedeschi  Giuseppe Fioritoni  Francesco Fabbiano  Giovanna Meloni  Giorgina Specchia  Giovanni Pizzolo  Franco Mandelli  Anna Guarini  Giuseppe Basso  Andrea Biondi  Robin Foà
Abstract:The outcome of children and adults with acute lymphoblastic leukemia is markedly different. Since there is limited information on the distribution of clinico-biological variables in different age cohorts, we analyzed 5202 patients with acute lymphoblastic leukemia enrolled in the Italian multicenter AIEOP and GIMEMA protocols and stratified them in nine age cohorts. The highest prevalence of acute lymphoblastic leukemia was observed in children, although a second peak was recorded from the 4th decade onwards. Interestingly, the lowest incidence was found in females between 14–40 years. Immunophenotypic characterization showed a B-lineage in 85.8% of patients: a pro-B stage, associated with MLL/AF4 positivity, was more frequent in patients between 10–50 years. T-lineage leukemia (14.2%) was rare among small children and increased in patients aged 10–40 years. The prevalence of the BCR/ABL1 rearrangement increased progressively with age starting from the cohort of patients 10–14 years old and was present in 52.7% of cases in the 6th decade. Similarly, the MLL/AF4 rearrangement constantly increased up to the 5th decade, while the ETV6/RUNX1 rearrangement disappeared from the age of 30 onwards. This study shows that acute lymphoblastic leukemia in adolescents and young adults is characterized by a male prevalence, higher percentage of T-lineage cases, an increase of poor prognostic molecular markers with aging compared to cases in children, and conclusively quantified the progressive increase of BCR/ABL+ cases with age, which are potentially manageable by targeted therapies.
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