ORIGINAL RESEARCH article
Front. Oncol.
Sec. Pediatric Oncology
Volume 15 - 2025 | doi: 10.3389/fonc.2025.1614445
This article is part of the Research TopicDiagnosis and Therapy Pediatric Hematological Malignancies - Recent Progress - Volume IIView all 6 articles
Impact of Standardized Immunophenotyping and MRD Monitoring on Early Mortality Reduction in Childhood Leukemia: A Step Towards Addressing Healthcare Disparities in Vulnerable Populations from Southern Mexico
Provisionally accepted- 1Laboratorio de Citómica del Cáncer Infantil, Centro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social, Puebla, Puebla, Mexico
- 2Facultad de Ciencias Químicas. Benemérita Universidad Autónoma de Puebla, Puebla, Puebla, Mexico
- 3Coordinación de Atención Oncológica, Instituto Mexicano del Seguro Social, Mexico City, México, Mexico
- 4Unidad de Investigación Médica en Epidemiología Clínica, UMAE, Hospital de Pediatría 'Dr. Silvestre Frenk Freund', CMN Siglo XXI, Instituto Mexicano del Seguro Social (IMSS), Mexico City, Mexico., Mexico City, México, Mexico
- 5Tecnológico Nacional de México, Instituto Tecnológico de Ciudad de Madero, División de Estudios de Posgrado e Investigación, Ciudad Madero, Tamaulipas, Mexico
- 6Facultad de Medicina, Universidad Popular Autónoma del Estado de Puebla, Puebla, Mexico., Puebla, Puebla, Mexico
- 7Centro de Investigación Oncológica Una Nueva Esperanza, Universidad Popular Autónoma del Estado de Puebla, Puebla, Mexico., Puebla, Puebla, Mexico
- 8Secretaría de Ciencia, Humanidades, Tecnología e Innovación (SECIHTI), Mexico City, Mexico
- 9Coordinación de Investigación en Salud, Instituto Mexicano del Seguro Social, Oaxaca, Oaxaca, Mexico
- 10Coordinación Clínica de Educación e Investigación en Salud de la UMF No. 1, Instituto Mexicano del Seguro Social, Oaxaca, Oaxaca, Mexico
- 11Servicio de Oncohematología Pediátrica, Hospital para el Niño Poblano, Secretaria de Salud (SS), Puebla, Puebla, Mexico
- 12Servicio de Oncohematología Pediátrica, IMSS UMAE CMN Hospital de Especialidades Dr. Manuel Ávila Camacho, Puebla, Puebla, Mexico
- 13Servicio de Hematología, Instituto Mexicano del Seguro (IMSS) Unidad Médica de Alta Especialidad (UMAE) Centro Médico Nacional (CMN) Hospital de Especialidades Dr. Manuel Ávila Camacho, Puebla, Mexico
- 14Departamento de Enseñanza e Investigación, Instituto de Seguridad y Servicios Sociales de los Trabajadores al Servicio de los Poderes del Estado de Puebla (ISSSTEP), Puebla, Mexico
- 15Servicio de Oncohematología Pediátrica, Instituto de Seguridad y Servicios Sociales de los Trabajadores al Servicio de los Poderes del Estado de Puebla (ISSSTEP), Puebla, Mexico, Puebla, Puebla, Mexico
- 16Servicio de Hematología Pediátrica, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado (ISSSTE), Puebla, Puebla, Mexico
- 17Servicio de Oncohematología, Hospital General del Sur Dr. Eduardo Vázquez Navarro, Secretaria de Salud (SS), Puebla, Puebla, Mexico
- 18Departamento de Pediatría, Hospital Universitario de Puebla (BUAP), Puebla, Mexico
- 19Servicio de Oncología Pediátrica, Hospital Infantil de Tlaxcala, Secretaria de Salud (SS), Tlaxcala, Tlaxcala, Mexico
- 20Servicio de Hemato-Oncología Pediátrica, Hospital de la Niñez Oaxaqueña 'Dr. Guillermo Zárate Mijangos', Secretaria de Salud y Servicios de Salud Oaxaca (SSO), Oaxaca, Oaxaca, Mexico
- 21Servicio de Oncocrean, Hospital General de Zona 01 'Dr. Demetrio Mayoral Pardo' Instituto Mexicano del Seguro Social (IMSS), Oaxaca, Oaxaca, Mexico
- 22Facultad Mexicana de Medicina, Universidad La Salle, Mexico City, México, Mexico
- 23Facultad de Medicina, Universidad Nacional Autónoma de México, UNAM, Mexico City, México, Mexico
- 24Unidad de Investigación Médica en Genética Humana, UMAE Hospital de Pediatría 'Dr. Silvestre Frenk Freund', Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social (IMSS), Mexico City, México, Mexico
- 25Dirección de Educación e Investigación, UMAE Hospital de Pediatría 'Dr. Silvestre Frenk Freund', Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social (IMSS), Mexico City, México, Mexico
- 26Laboratorio de Genómica Funcional del Cáncer, Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City, Mexico
- 27Laboratorio de Bioquímica y Biología Molecular. Centro de Química. Instituto de Ciencias. Benemérita Universidad Autónoma de Puebla, Puebla, Mexico
- 28Unidad de Educación e Investigación, Instituto Mexicano del Seguro Social, Mexico City, Mexico
- 29División de Investigación en Salud, UMAE Hospital de Pediatría “Dr. Silvestre Frenk Freund”, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, México, Mexico
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Despite high cure rates for pediatric B-cell acute lymphoblastic leukemia (B-ALL) in high-income countries, early mortality remains unacceptably high in low-and middle-income countries (LMICs), due to limited access to risk-adapted therapy and response monitoring. Southern Mexico, a region marked by socioeconomic vulnerability, is emblematic of this disparity. In 2022 the Childhood Cancer Cytomics Laboratory (CCCL) started the implementation of standardized protocols for immunophenotyping and measurable residual disease (MRD) monitoring of B-ALL patients from this region. Objective: To evaluate the impact of implementing standardized immunophenotyping and MRD monitoring on early mortality in children with B-ALL treated in public hospitals in southern Mexico. Methods: Public hospitals were invited to participate (between 2022 and 2024), and standardized protocols for sample collection, handling, and transportation were implemented. 298 newly diagnosed children with B-ALL were enrolled and followed throughout treatment. Patients were stratified based on whether immunophenotyping and MRD were performed at the CCCL. MRD was assessed at the end of induction therapy using standardized EuroFlow-based protocols. Early mortality-defined as death occurring within the first year after diagnosis-was evaluated. Adjusted hazard ratios (aHR) and 95% confidence intervals (CI) were estimated using multivariable Cox regression. Results: Early mortality was significantly lower among patients who underwent MRD at the CCCL (10.8%) compared to those who did not (24.8%, p<0.01). One-year overall survival was also higher in patients evaluated at the CCCL (89.6% vs. 75.2%, p<0.001). In the regression analysis, patients who underwent MRD monitoring at the CCCL showed a significantly lower risk of early mortality during the first year of treatment (aHR) 0.41; 95% CI: 0.22-0.77; p < 0.01), after adjusting for sex, NCI risk classification, treatment abandonment, and early relapse. MRD positivity was associated with a CD34⁺ ProB immunophenotype, suggesting a more treatment-resistant leukemic profile. Conclusion: Centralized, standardized MRD at the CCCL was associated with a reduction in early mortality and improved one-year survival in children with B-ALL from a socioeconomically vulnerable population. These findings demonstrate the clinical value and feasibility of implementing MRD-informed response assessment in LMICs and highlight the potential of centralized diagnostic platforms to reduce survival disparities in childhood leukemia.
Keywords: pediatric B-cell acute lymphoblastic leukemia, Immunophenotyping, measurable residual disease (MRD), early-mortality, low-and middle -income countries
Received: 18 Apr 2025; Accepted: 25 Jun 2025.
Copyright: © 2025 Alfaro-Hernández, Ramírez-Ramírez, Romo-Rodríguez, Ayala, Del Campo-Martínez, López-Aguilar, Flores Lujano, Allende-López, Alarcón-Ruiz, Banos-Lara, Casique-Aguirre, Elizarrarás-Rivas, López-Aquino, GARRIDO, Olvera-Caraza, Terán-Cerqueda, Solís-Poblano, Aristil-Chery, Alvarez-Rodríguez, Herrera-Olivares, Chávez Aguilar, Márquez-Toledo, Cano-Cuapio, Luna-Silva, Martínez-Martell, Ramírez-Ramírez, Rodríguez-Espinosa, Medina-León, Rodríguez-Díaz, Mata-Rocha, Olivares-Sosa, Rosas-Vargas, Mejia-Arangure, Millán-Pérez-Peña, Pelayo and Núñez-Enríquez. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Rosana Pelayo, Unidad de Educación e Investigación, Instituto Mexicano del Seguro Social, Mexico City, Mexico
Juan Carlos Núñez-Enríquez, División de Investigación en Salud, UMAE Hospital de Pediatría “Dr. Silvestre Frenk Freund”, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, México, Mexico
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