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A modified CALGB 10403 in adolescents and young adults with acute lymphoblastic leukemia in Central America

Mexico and Central America have a high incidence of acute lymphoblastic leukemia (ALL) in adolescents and young adults. Historically, this patient group has been treated using adult-based regimens, which entails a high rate of treatment-related mortality and a poor overall survival (OS). The use of...

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Detalles Bibliográficos
Autores principales: Rangel-Patiño, Juan, Lee-Tsai, Yu Ling, Urbalejo-Ceniceros, Victor Itaí, Luna-Perez, Maria Elena Monserrat, Espinosa-Bautista, Karla Adriana, Amador, Lauro Fabian, Cabrera-García, Álvaro, Balderas-Delgado, Carolina, Inclan-Alarcon, Sergio I, Neme-Yunes, Yvette, Sanchez-Albarrán, Jose Manuel, Apodaca, Elia Ixel, Meillon-García, Luis, Stock, Wendy, Demichelis-Gómez, Roberta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society of Hematology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10500455/
https://www.ncbi.nlm.nih.gov/pubmed/37307212
http://dx.doi.org/10.1182/bloodadvances.2023009754
Descripción
Sumario:Mexico and Central America have a high incidence of acute lymphoblastic leukemia (ALL) in adolescents and young adults. Historically, this patient group has been treated using adult-based regimens, which entails a high rate of treatment-related mortality and a poor overall survival (OS). The use of the CALGB 10403, a pediatric-inspired regimen, has been proven effective in this patient subgroup. Nonetheless, low- and middle-income countries (LMICs) may present limited access to standard care treatments implemented elsewhere, warranting the need for further research to improve outcomes among vulnerable populations. In this study, we present the outcomes in terms of safety and effectiveness of using a modified CALGB 10403 regimen to reflect drug and resource availability in LMICs. Modifications included the use of Escherichia coli asparaginase,6-mercaptopurine instead of thioguanine and the use of rituximab among patients with CD20(+). A total of 95 patients with a median age of 23 (range, 14-49) years treated with this modified scheme were prospectively assessed at 5 centers in Mexico and 1 in Guatemala. Among these, 87.8% achieved a complete response after induction. During follow-up, 28.3% of patients relapsed. Two-year OS rate was 72.1%. Factors associated with worse OS included hyperleukocytosis (hazard ratio [HR], 4.28; 95% confidence interval [CI], 1.81-10.10) and postinduction minimal residual disease (HR, 4.67; 95% CI, 1.75-12.44). Most patients presented hepatotoxicity (51.6% and 53.7% during induction and consolidation, respectively), and the treatment-related mortality was 9.5%. Overall, results highlight that implementing a modified CALGB 10403 regimen in Central America is feasible, and it is associated with improvements in clinical outcomes and a manageable safety profile.