Cargando…
Retrospective analysis of outcomes for pediatric acute lymphoblastic leukemia in South American centers
INTRODUCTION: Acute lymphoblastic Leukemia (ALL) is the most common pediatric malignancy. While the survival rate for childhood ALL exceeds 90% in high-income countries, the estimated survival in low-and middle-income countries ranges from 22-79%, depending on the region and local resources. METHODS...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10643117/ https://www.ncbi.nlm.nih.gov/pubmed/38023200 http://dx.doi.org/10.3389/fonc.2023.1254233 |
_version_ | 1785134284211748864 |
---|---|
author | Duffy, Caitlyn Graetz, Dylan E. Lopez, Arturo M. Zapata Carrillo, Angela K. Job, Godwin Chen, Yichen Devidas, Meenakshi Leon, Sandra Alarcón Bonzi, Sol Aponte Flores, Pedro Cardona Torres, Lizeth Escobar Broncano, Eddy Hernández Jaramillo, Soledad Jiménez Zelada, Ma Ofelia Novoa, Romulo Reaño Samudio, Angelica Sánchez-Fernandez, Gissela Villanueva, Erika Metzger, Monika L. Friedrich, Paola Jeha, Sima |
author_facet | Duffy, Caitlyn Graetz, Dylan E. Lopez, Arturo M. Zapata Carrillo, Angela K. Job, Godwin Chen, Yichen Devidas, Meenakshi Leon, Sandra Alarcón Bonzi, Sol Aponte Flores, Pedro Cardona Torres, Lizeth Escobar Broncano, Eddy Hernández Jaramillo, Soledad Jiménez Zelada, Ma Ofelia Novoa, Romulo Reaño Samudio, Angelica Sánchez-Fernandez, Gissela Villanueva, Erika Metzger, Monika L. Friedrich, Paola Jeha, Sima |
author_sort | Duffy, Caitlyn |
collection | PubMed |
description | INTRODUCTION: Acute lymphoblastic Leukemia (ALL) is the most common pediatric malignancy. While the survival rate for childhood ALL exceeds 90% in high-income countries, the estimated survival in low-and middle-income countries ranges from 22-79%, depending on the region and local resources. METHODS: This study retrospectively reviewed demographic, biological, and clinical parameters of children under 18 years of age with newly diagnosed ALL presenting between 2013-2017 across five pediatric centers in 4 countries in South America. Survival analyses were estimated using the Kaplan-Meier method. RESULTS: Across the five centers, 752 patients were analyzed (Bolivia [N=9], Ecuador [N=221], Paraguay [N=197], Peru [N=325]) and 92.1% (n=690) patients were diagnosed with B-cell and 7.5% (n= 56) with T-cell ALL. The median age was 5.5 years old (IQR 7.29). At diagnosis, 47.8% of patients were categorized as standard and 51.9% as high risk per their institutional regimen. Advanced diagnostics availability varied between modalities. MRD was evaluated in 69.1% of patients; molecular testing was available for ETV6-RUNX, BCR-ABL1, TCF3-PBX1, and KMT2A-rearranged ALL in 75-81% of patients; however, karyotyping and evaluation for iAMP21 were only performed in 42-61% of patients. Central nervous system (CNS) involvement was evaluated at diagnosis in 57.3% (n=429) patients; of these, 93.7% (n=402) were CNS 1, 1.6% (n=7) were CNS 2, 0.7% (n=11) were CNS3, 1.9% (n=8) had cranial nerve palsy, and 2.1% (n=9) results unavailable. Chemotherapy delays >2 weeks were reported in 56.0% (n=421) patients during treatment. Delays were attributed to infection in 63.2% (n=265), drug-related toxicities in 47.3% (n=198), and resource constraints, including lack of bed availability in 23.2% (n=97) of patients. The 3-year Abandonment-sensitive EFS and OS were 61.0±1.9% and 67.2±1.8%, respectively. The 3-year EFS and OS were 71.0±1.8% and 79.6±1.7%, respectively. DISCUSSION: This work reveals opportunities to improve survival, including addressing severe infections, treatment interruptions, and modifications due to drug shortages. In 2018, healthcare professionals across South America established the Pediatric Oncology Latin America (POLA) group in collaboration with St. Jude Children’s Research Hospital. POLA collaborators developed an evidence-based, consensus-derived, adapted treatment guideline, informed by preliminary results of this evaluation, to serve as the new standard of care for pediatric ALL in participating institutions. |
format | Online Article Text |
id | pubmed-10643117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106431172023-01-01 Retrospective analysis of outcomes for pediatric acute lymphoblastic leukemia in South American centers Duffy, Caitlyn Graetz, Dylan E. Lopez, Arturo M. Zapata Carrillo, Angela K. Job, Godwin Chen, Yichen Devidas, Meenakshi Leon, Sandra Alarcón Bonzi, Sol Aponte Flores, Pedro Cardona Torres, Lizeth Escobar Broncano, Eddy Hernández Jaramillo, Soledad Jiménez Zelada, Ma Ofelia Novoa, Romulo Reaño Samudio, Angelica Sánchez-Fernandez, Gissela Villanueva, Erika Metzger, Monika L. Friedrich, Paola Jeha, Sima Front Oncol Oncology INTRODUCTION: Acute lymphoblastic Leukemia (ALL) is the most common pediatric malignancy. While the survival rate for childhood ALL exceeds 90% in high-income countries, the estimated survival in low-and middle-income countries ranges from 22-79%, depending on the region and local resources. METHODS: This study retrospectively reviewed demographic, biological, and clinical parameters of children under 18 years of age with newly diagnosed ALL presenting between 2013-2017 across five pediatric centers in 4 countries in South America. Survival analyses were estimated using the Kaplan-Meier method. RESULTS: Across the five centers, 752 patients were analyzed (Bolivia [N=9], Ecuador [N=221], Paraguay [N=197], Peru [N=325]) and 92.1% (n=690) patients were diagnosed with B-cell and 7.5% (n= 56) with T-cell ALL. The median age was 5.5 years old (IQR 7.29). At diagnosis, 47.8% of patients were categorized as standard and 51.9% as high risk per their institutional regimen. Advanced diagnostics availability varied between modalities. MRD was evaluated in 69.1% of patients; molecular testing was available for ETV6-RUNX, BCR-ABL1, TCF3-PBX1, and KMT2A-rearranged ALL in 75-81% of patients; however, karyotyping and evaluation for iAMP21 were only performed in 42-61% of patients. Central nervous system (CNS) involvement was evaluated at diagnosis in 57.3% (n=429) patients; of these, 93.7% (n=402) were CNS 1, 1.6% (n=7) were CNS 2, 0.7% (n=11) were CNS3, 1.9% (n=8) had cranial nerve palsy, and 2.1% (n=9) results unavailable. Chemotherapy delays >2 weeks were reported in 56.0% (n=421) patients during treatment. Delays were attributed to infection in 63.2% (n=265), drug-related toxicities in 47.3% (n=198), and resource constraints, including lack of bed availability in 23.2% (n=97) of patients. The 3-year Abandonment-sensitive EFS and OS were 61.0±1.9% and 67.2±1.8%, respectively. The 3-year EFS and OS were 71.0±1.8% and 79.6±1.7%, respectively. DISCUSSION: This work reveals opportunities to improve survival, including addressing severe infections, treatment interruptions, and modifications due to drug shortages. In 2018, healthcare professionals across South America established the Pediatric Oncology Latin America (POLA) group in collaboration with St. Jude Children’s Research Hospital. POLA collaborators developed an evidence-based, consensus-derived, adapted treatment guideline, informed by preliminary results of this evaluation, to serve as the new standard of care for pediatric ALL in participating institutions. Frontiers Media S.A. 2023-10-30 /pmc/articles/PMC10643117/ /pubmed/38023200 http://dx.doi.org/10.3389/fonc.2023.1254233 Text en Copyright © 2023 Duffy, Graetz, Lopez, Carrillo, Job, Chen, Devidas, Leon, Bonzi, Flores, Torres, Broncano, Jaramillo, Zelada, Novoa, Samudio, Sánchez-Fernandez, Villanueva, Metzger, Friedrich and Jeha https://creativecommons.org/licenses/by/4.0/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) and the copyright owner(s) 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. |
spellingShingle | Oncology Duffy, Caitlyn Graetz, Dylan E. Lopez, Arturo M. Zapata Carrillo, Angela K. Job, Godwin Chen, Yichen Devidas, Meenakshi Leon, Sandra Alarcón Bonzi, Sol Aponte Flores, Pedro Cardona Torres, Lizeth Escobar Broncano, Eddy Hernández Jaramillo, Soledad Jiménez Zelada, Ma Ofelia Novoa, Romulo Reaño Samudio, Angelica Sánchez-Fernandez, Gissela Villanueva, Erika Metzger, Monika L. Friedrich, Paola Jeha, Sima Retrospective analysis of outcomes for pediatric acute lymphoblastic leukemia in South American centers |
title | Retrospective analysis of outcomes for pediatric acute lymphoblastic leukemia in South American centers |
title_full | Retrospective analysis of outcomes for pediatric acute lymphoblastic leukemia in South American centers |
title_fullStr | Retrospective analysis of outcomes for pediatric acute lymphoblastic leukemia in South American centers |
title_full_unstemmed | Retrospective analysis of outcomes for pediatric acute lymphoblastic leukemia in South American centers |
title_short | Retrospective analysis of outcomes for pediatric acute lymphoblastic leukemia in South American centers |
title_sort | retrospective analysis of outcomes for pediatric acute lymphoblastic leukemia in south american centers |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10643117/ https://www.ncbi.nlm.nih.gov/pubmed/38023200 http://dx.doi.org/10.3389/fonc.2023.1254233 |
work_keys_str_mv | AT duffycaitlyn retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT graetzdylane retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT lopezarturomzapata retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT carrilloangelak retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT jobgodwin retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT chenyichen retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT devidasmeenakshi retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT leonsandraalarcon retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT bonzisolaponte retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT florespedrocardona retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT torreslizethescobar retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT broncanoeddyhernandez retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT jaramillosoledadjimenez retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT zeladamaofelia retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT novoaromuloreano retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT samudioangelica retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT sanchezfernandezgissela retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT villanuevaerika retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT metzgermonikal retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT friedrichpaola retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters AT jehasima retrospectiveanalysisofoutcomesforpediatricacutelymphoblasticleukemiainsouthamericancenters |