Hanbali Amr, Saad Ayman, Ahmed Syed Osman, Alfayez Mansour, Madien Heba, Alfaqawi Samar, Aleid Manar, Hamad Alaa, Desai Sameer, Alsarami Leena, Alahmari Ali, Alotaibi Ahmad, Alkhaldi Hanan, Alfraih Feras, Alhayli Saud, Alshaibani Alfadel, Albabtain Abdulwahab, Alamer Abdullah, Alotaibi Shaykhah, Shaheen Marwan, Albanyan Omar, Rasheed Walid, Alsharif Fahad, Chaudhri Naeem, Almohareb Fahad, Alzahrani Hazzaa, Fakih Riad El, Aljurf Mahmoud, Kotb Ahmed
Department of hematology and cellular therapy, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
Department of hematology and cellular therapy, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
Clin Lymphoma Myeloma Leuk. 2025 Jul 17. doi: 10.1016/j.clml.2025.07.006.
Adolescents and young adults (AYA) with Philadelphia-negative acute lymphoblastic leukemia (ALL) represent a distinct population with variable outcomes. This study assessed the real-world efficacy and safety of the AYA-15 protocol in this group.
A retrospective cohort of 149 AYA patients (median age: 18 years) treated with the AYA-15 protocol at a tertiary care center in the middle east was analyzed. Baseline characteristics, measurable residual disease (MRD) kinetics, toxicity profiles, and survival outcomes were examined. Multivariate Cox regression was performed to identify adverse prognostic factors.
Among the 149 patients, 74% had B-cell ALL and 10% had central nervous system (CNS) involvement. Day 28 MRD negativity was achieved in 76% of patients, increasing to 88% post-consolidation. The 5-year overall survival (OS), disease-free survival (DFS), and event-free survival (EFS) rates were 79%, 68%, and 59%, respectively. The most common grade ≥3 toxicities included febrile neutropenia, infections, hepatotoxicity, and hypersensitivity reactions to PEG-asparaginase. Multivariable analysis identified CNS involvement, post-consolidation MRD positivity, and elevated BMI as independent predictors of inferior outcomes.
The AYA-15 protocol demonstrated favorable survival and MRD response rates in a real-world cohort of Philadelphia-negative AYA ALL patients. Certain baseline and treatment-related factors were associated with poorer outcomes, highlighting the importance of individualized risk stratification.