%0 Journal Article %A Ribera, Josep-Maria %A Morgades, Mireia %A Montesinos, Pau %A Tormo, Mar %A Martínez-Carballeira, Daniel %A González-Campos, José %A Gil, Cristina %A Barba, Pere %A García-Boyero, Raimundo %A Coll, Rosa %A Pedreño, María %A Ribera, Jordi %A Mercadal, Santiago %A Vives, Susana %A Novo, Andrés %A Genescà, Eulàlia %A Hernández-Rivas, Jesús-María %A Bergua, Juan %A Amigo, María-Luz %A Vall-Llovera, Ferran %A Martínez-Sánchez, Pilar %A Calbacho, María %A García-Cadenas, Irene %A Garcia-Guiñon, Antoni %A Sánchez-Sánchez, María-José %A Cervera, Marta %A Feliu, Evarist %A Orfao, Alberto %A PETHEMA Group, Spanish Society of Hematology %T A pediatric regimen for adolescents and young adults with Philadelphia chromosome-negative acute lymphoblastic leukemia: Results of the ALLRE08 PETHEMA trial. %D 2020 %U http://hdl.handle.net/10668/15048 %X Pediatric-based or -inspired trials have improved the prognosis of adolescents and young adults (AYA) with Philadelphia chromosome-negative (Ph-neg) acute lymphoblastic leukemia (ALL). This study reports the results of treatment of the ALLRE08 trial, a full pediatric trial for AYA aged 15-30 years with standard-risk (SR) ALL. From 2008 to 2018, 89 patients (38 adolescents [15-18 years] and 51 young adults [YA, 19-30 years], median age: 20 [15-29] years) were enrolled in the ALLRE08 trial. The complete response (CR) was 95%. Twenty-two patients were transferred to a high-risk (HR) protocol because of poor marrow response on day 14 (n = 20) or high-level of end-induction minimal residual response (MRD ≥ 0.25%, n = 2). Cumulative incidence of relapse (CIR) at 5 years was 35% (95%CI: 23%-47%), with significant differences between adolescents and YA: 13% (4%-28%) vs 52% (34%-67%), P = .012. No treatment-related mortality was observed in 66/66 patients following the ALLRE08 trial vs 3/23 patients moved to a HR trial. The estimated 5-year overall survival (OS) was 74% (95%CI: 63%-85%), with significantly higher rates for adolescents vs YA: 87% (95%CI: 74%-100%) vs 63% (46%-80%), P = .021. Although CIR or OS were lower in patients who were transferred to a HR trial, the differences were not statistically significant (CIR: 34% [21%-47%] vs 37% [14%-61%]; OS: 78% [66%-90%] vs 61% [31%;91%]). A full pediatric trial is feasible and effective for AYA with Ph-neg, SR-ALL, with better results for adolescents than for YA. Outcome of patients with poor early response rescued with a HR trial was not significantly inferior. %K acute lymphoblastic leukemia %K adolescents and young adults %K pediatric treatment %~