EDITORIAL article
Front. Oncol.
Sec. Pediatric Oncology
This article is part of the Research TopicImmunological Therapies in Pediatric Cancers: A Latin American PerspectiveView all 6 articles
The Rise of Immunotherapy for Childhood Cancer in Latin America
Provisionally accepted- National Institute of Pediatrics (Mexico), Mexico City, Mexico
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Immunotherapy has reshaped the global landscape of pediatric oncology, emerging as one of the most transformative therapeutic domains for children with relapsed, refractory, or high-risk malignancies. From bispecific antibodies to cell-based therapies and immunemodulating agents, these strategies-once confined to highly specialized centers in highincome countries-are now expanding into low-and middle-income regions. Latin America, a region marked by scientific talent but persistent structural inequalities, has entered a crucial phase in the adoption, evaluation, and local development of immunological therapies for childhood cancers.Despite economic, logistical, and regulatory challenges, a growing network of pediatric oncology centers across Mexico, Brazil, Argentina, Chile, and Colombia is advancing innovative models for implementing antibody-based therapies, post-transplant immune modulation, and emerging cellular therapies. These pioneering efforts not only address the clinical needs of the region but also generate evidence that reflects unique epidemiologic patterns, resource constraints, and population-specific disease biology. This special issue, Immunological Therapies in Pediatric Cancers: A Latin American Perspective, brings together a series of original contributions that illuminate the opportunities, challenges, and breakthroughs shaping the regional immunotherapy landscape. Each article offers a window into how Latin American institutions are reimagining care pathways for children with cancer through immunologic innovation.Highlights of the Special Issue 1. Blinatumomab-induced remission followed by haploidentical transplantation in pediatric relapsed/refractory pre-B ALL: a multicenter study in Mexico This multicenter Mexican study demonstrates that the integration of blinatumomab as a bridge-to-transplant strategy can yield high remission rates and successful transition to haploidentical hematopoietic stem-cell transplantation (HSCT). The findings highlight both the feasibility and effectiveness of bispecific T-cell engager therapy in resource-limited settings while underscoring the growing regional expertise in haploidentical transplant platforms.2. High-risk neuroblastoma in Mexico: from multimodal therapy to immunotherapy-Experience with the first patient treated with naxitamabThe introduction of anti-GD2 immunotherapy in Mexico marks a milestone in the treatment of high-risk neuroblastoma. This case-based report contextualizes the first use of naxitamab in the country, illustrating how rigorous multimodal management combined with targeted immunotherapy can be successfully implemented in Latin American pediatric oncology units. It lays essential for broader national expansion of anti-GD2 treatment.3. Haploidentical, matched-related, and matched-unrelated donor HSCT for pediatric acute leukemias during the early years of haploidentical implementation in a developing country with a large donor registry This contribution provides a comparative experience across donor types during the initial phase of haploidentical transplant adoption. The study reveals encouraging outcomes for haploidentical HSCT, supported by the presence of a robust national unrelated donor registry. These observations reinforce the critical role of donor availability, local infrastructure, and early expertise in accelerating the growth of cellular therapy in middleincome countries. Post-transplant maintenance therapy is a rapidly evolving field, particularly in acute leukemias with high relapse risk. This Brazilian report provides real-world insight into maintenance strategies such as targeted agents, immune-modulating therapies, and precision-guided approaches tailored to relapse biology. The work reflects a growing Latin American commitment to extending curative potential beyond HSCT by adopting posttransplant immunologic interventions. This innovative investigation explores the anti-inflammatory and pro-apoptotic properties of pentoxifylline as an adjunctive immunomodulatory agent in ALL. The demonstration of early remission and enhanced leukemic apoptosis invites further exploration of costeffective, accessible immunologic strategies that may complement standard therapy in lowresource environments. Taken together, the contributions in this issue underscore a dynamic era for pediatric immuno-oncology in Latin America. Across diverse institutions, immunotherapy is increasingly viewed not as imported technology but as a domain ripe for regional innovation, clinical leadership, and context-specific solutions.However, significant challenges remain:-Equitable access to high-cost immunotherapies -Regulatory adaptability for advanced biologics and cell-based products -Sustainable financing models compatible with public health systems -Manufacturing capacity for CAR-T and other cell therapies -Specialized training to support rapidly evolving clinical technologies A Vision for the Future The rise of immunotherapy in Latin America is more than a scientific advancement-it is a movement toward health equity and therapeutic justice. As local experts implement and generate evidence for cutting-edge therapies, they redefine the global narrative of what is possible in pediatric oncology outside high-income settings. This special issue stands as a testament to the resilience, creativity, and scientific commitment that characterize pediatric oncology across the region. It invites researchers, clinicians, policymakers, and advocates to work collectively toward a future in which every child with cancer-regardless of geography-has access to life-saving immunological therapies.
Keywords: pediatric cancer, Latin America, pediatric Immunotherapy, anti-GD2 antibodies, haploidenitcal stem cell transplantation
Received: 11 Nov 2025; Accepted: 26 Nov 2025.
Copyright: © 2025 Olaya Vargas. 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: Alberto Olaya Vargas
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