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

Author:

Rangel-Patiño Juan1,Lee-Tsai Yu Ling2,Urbalejo-Ceniceros Victor Itaí3ORCID,Luna-Perez Maria Elena Monserrat3,Espinosa-Bautista Karla Adriana4,Amador Lauro Fabian5,Cabrera-García Álvaro6ORCID,Balderas-Delgado Carolina6,Inclan-Alarcon Sergio I7,Neme-Yunes Yvette7,Sanchez-Albarrán Jose Manuel1,Apodaca Elia Ixel1ORCID,Meillon-García Luis7,Stock Wendy8,Demichelis-Gómez Roberta1

Affiliation:

1. 1Hematology and Oncology Department, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico

2. 2Hospital General San Juan de Dios, Guatemala, Guatemala

3. 3Hematology Department, Instituto Nacional de Cancerología, Mexico City, Mexico

4. 4Hematology Department, Comisión Coordinadora de Institutos Nacionales de Salud y Hospitales de Alta Especialidad, Mexico City, Mexico

5. 5Hematology Department, Hospital Regional de Alta Especialidad del Bajío, León, Mexico

6. 6Hematology Department, Hospital Regional de Alta Especialidad de Ixtapaluca, Estado de Mexico, Mexico

7. 7Centro Médico ABC, Mexico City, Mexico

8. 8Department of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL

Abstract

Abstract 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.

Publisher

American Society of Hematology

Subject

Hematology

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