Management and outcome of children with high-risk neuroblastoma: insights from the Spanish Society of Pediatric Hematology and Oncology (SEHOP) neuroblastoma group on refractory and relapse/progressive disease
Immunotherapy; Neuroblastoma; Relapse
| Autores: | , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2025 |
| País: | España |
| Institución: | Departament de Salut de la Generalitat de Catalunya (DS) |
| Repositorio: | Scientia. Dipòsit d'Informació Digital del Departament de Salut |
| OAI Identifier: | oai:scientiasalut.gencat.cat:11351/13792 |
| Acceso en línea: | http://hdl.handle.net/11351/13792 |
| Access Level: | acceso abierto |
| Palabra clave: | Infants Neuroblastoma - Tractament Neuroblastoma - Recaiguda NAMED GROUPS::Persons::Age Groups::Child DISEASES::Neoplasms::Neoplasms by Histologic Type::Neoplasms, Germ Cell and Embryonal::Neuroectodermal Tumors::Neoplasms, Neuroepithelial::Neuroectodermal Tumors, Primitive::Neuroectodermal Tumors, Primitive, Peripheral::Neuroblastoma Other subheadings::Other subheadings::/therapy DISEASES::Neoplasms::Neoplastic Processes::Neoplasm Recurrence, Local DENOMINACIONES DE GRUPOS::personas::Grupos de Edad::niño ENFERMEDADES::neoplasias::neoplasias por tipo histológico::neoplasias de células germinales y embrionarias::tumores neuroectodérmicos::neoplasias neuroepiteliales::tumores neuroectodérmicos primitivos::tumores neuroectodérmicos primitivos periféricos::neuroblastoma Otros calificadores::Otros calificadores::/terapia ENFERMEDADES::neoplasias::procesos neoplásicos::recurrencia neoplásica local |
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| dc.title.none.fl_str_mv |
Management and outcome of children with high-risk neuroblastoma: insights from the Spanish Society of Pediatric Hematology and Oncology (SEHOP) neuroblastoma group on refractory and relapse/progressive disease |
| title |
Management and outcome of children with high-risk neuroblastoma: insights from the Spanish Society of Pediatric Hematology and Oncology (SEHOP) neuroblastoma group on refractory and relapse/progressive disease |
| spellingShingle |
Management and outcome of children with high-risk neuroblastoma: insights from the Spanish Society of Pediatric Hematology and Oncology (SEHOP) neuroblastoma group on refractory and relapse/progressive disease Martinez de las Heras, Blanca Infants Neuroblastoma - Tractament Neuroblastoma - Recaiguda NAMED GROUPS::Persons::Age Groups::Child DISEASES::Neoplasms::Neoplasms by Histologic Type::Neoplasms, Germ Cell and Embryonal::Neuroectodermal Tumors::Neoplasms, Neuroepithelial::Neuroectodermal Tumors, Primitive::Neuroectodermal Tumors, Primitive, Peripheral::Neuroblastoma Other subheadings::Other subheadings::/therapy DISEASES::Neoplasms::Neoplastic Processes::Neoplasm Recurrence, Local DENOMINACIONES DE GRUPOS::personas::Grupos de Edad::niño ENFERMEDADES::neoplasias::neoplasias por tipo histológico::neoplasias de células germinales y embrionarias::tumores neuroectodérmicos::neoplasias neuroepiteliales::tumores neuroectodérmicos primitivos::tumores neuroectodérmicos primitivos periféricos::neuroblastoma Otros calificadores::Otros calificadores::/terapia ENFERMEDADES::neoplasias::procesos neoplásicos::recurrencia neoplásica local |
| title_short |
Management and outcome of children with high-risk neuroblastoma: insights from the Spanish Society of Pediatric Hematology and Oncology (SEHOP) neuroblastoma group on refractory and relapse/progressive disease |
| title_full |
Management and outcome of children with high-risk neuroblastoma: insights from the Spanish Society of Pediatric Hematology and Oncology (SEHOP) neuroblastoma group on refractory and relapse/progressive disease |
| title_fullStr |
Management and outcome of children with high-risk neuroblastoma: insights from the Spanish Society of Pediatric Hematology and Oncology (SEHOP) neuroblastoma group on refractory and relapse/progressive disease |
| title_full_unstemmed |
Management and outcome of children with high-risk neuroblastoma: insights from the Spanish Society of Pediatric Hematology and Oncology (SEHOP) neuroblastoma group on refractory and relapse/progressive disease |
| title_sort |
Management and outcome of children with high-risk neuroblastoma: insights from the Spanish Society of Pediatric Hematology and Oncology (SEHOP) neuroblastoma group on refractory and relapse/progressive disease |
| dc.creator.none.fl_str_mv |
Martinez de las Heras, Blanca Rubio-Aparicio, Pedro M Mazorra Roig, Paula López Almaraz, Ricardo RUBIO-SAN-SIMON, Alba Moreno, Lucas |
| author |
Martinez de las Heras, Blanca |
| author_facet |
Martinez de las Heras, Blanca Rubio-Aparicio, Pedro M Mazorra Roig, Paula López Almaraz, Ricardo RUBIO-SAN-SIMON, Alba Moreno, Lucas |
| author_role |
author |
| author2 |
Rubio-Aparicio, Pedro M Mazorra Roig, Paula López Almaraz, Ricardo RUBIO-SAN-SIMON, Alba Moreno, Lucas |
| author2_role |
author author author author author |
| dc.contributor.none.fl_str_mv |
Institut Català de la Salut [Martínez de las Heras B] Pediatric Hemato-Oncology Department, Hospital Universitario y Politécnico La Fe, European Reference Network PAEDCAN member, Valencia, Spain. Clinical and Translational Oncology Research Group, Investigation Institute La Fe, Valencia, Spain. [Rubio Aparicio PM] Pediatric Hemato-Oncology Department, Hospital Universitario La Paz, European Reference Network PAEDCAN member, Madrid, Spain. [Rubio San Simón A] Pediatric Hemato-Oncology Department, Hospital Infantil Universitario Niño Jesús, Madrid, Spain. [Moreno L, Mazorra P] Servei de Pediatria, Vall d’Hebron Hospital Universitari, Barcelona, Spain. European Reference Network PAEDCAN member, Barcelona, Spain. [López Almaraz R] Pediatric Onco-Hematology Unit, Hospital Cruces, and Pediatric Oncology Group Vall d'Hebron Barcelona Hospital Campus |
| dc.subject.none.fl_str_mv |
Infants Neuroblastoma - Tractament Neuroblastoma - Recaiguda NAMED GROUPS::Persons::Age Groups::Child DISEASES::Neoplasms::Neoplasms by Histologic Type::Neoplasms, Germ Cell and Embryonal::Neuroectodermal Tumors::Neoplasms, Neuroepithelial::Neuroectodermal Tumors, Primitive::Neuroectodermal Tumors, Primitive, Peripheral::Neuroblastoma Other subheadings::Other subheadings::/therapy DISEASES::Neoplasms::Neoplastic Processes::Neoplasm Recurrence, Local DENOMINACIONES DE GRUPOS::personas::Grupos de Edad::niño ENFERMEDADES::neoplasias::neoplasias por tipo histológico::neoplasias de células germinales y embrionarias::tumores neuroectodérmicos::neoplasias neuroepiteliales::tumores neuroectodérmicos primitivos::tumores neuroectodérmicos primitivos periféricos::neuroblastoma Otros calificadores::Otros calificadores::/terapia ENFERMEDADES::neoplasias::procesos neoplásicos::recurrencia neoplásica local |
| topic |
Infants Neuroblastoma - Tractament Neuroblastoma - Recaiguda NAMED GROUPS::Persons::Age Groups::Child DISEASES::Neoplasms::Neoplasms by Histologic Type::Neoplasms, Germ Cell and Embryonal::Neuroectodermal Tumors::Neoplasms, Neuroepithelial::Neuroectodermal Tumors, Primitive::Neuroectodermal Tumors, Primitive, Peripheral::Neuroblastoma Other subheadings::Other subheadings::/therapy DISEASES::Neoplasms::Neoplastic Processes::Neoplasm Recurrence, Local DENOMINACIONES DE GRUPOS::personas::Grupos de Edad::niño ENFERMEDADES::neoplasias::neoplasias por tipo histológico::neoplasias de células germinales y embrionarias::tumores neuroectodérmicos::neoplasias neuroepiteliales::tumores neuroectodérmicos primitivos::tumores neuroectodérmicos primitivos periféricos::neuroblastoma Otros calificadores::Otros calificadores::/terapia ENFERMEDADES::neoplasias::procesos neoplásicos::recurrencia neoplásica local |
| description |
Immunotherapy; Neuroblastoma; Relapse |
| publishDate |
2025 |
| dc.date.none.fl_str_mv |
2025 2025 2025 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11351/13792 |
| url |
http://hdl.handle.net/11351/13792 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Clinical and Translational Oncology;27 https://doi.org/10.1007/s12094-025-03853-w |
| dc.rights.none.fl_str_mv |
Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ info:eu-repo/semantics/openAccess |
| rights_invalid_str_mv |
Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
application/pdf |
| dc.publisher.none.fl_str_mv |
Springer |
| publisher.none.fl_str_mv |
Springer |
| dc.source.none.fl_str_mv |
Scientia reponame:Scientia. Dipòsit d'Informació Digital del Departament de Salut instname:Departament de Salut de la Generalitat de Catalunya (DS) |
| instname_str |
Departament de Salut de la Generalitat de Catalunya (DS) |
| reponame_str |
Scientia. Dipòsit d'Informació Digital del Departament de Salut |
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Scientia. Dipòsit d'Informació Digital del Departament de Salut |
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| _version_ |
1869404015877423104 |
| spelling |
Management and outcome of children with high-risk neuroblastoma: insights from the Spanish Society of Pediatric Hematology and Oncology (SEHOP) neuroblastoma group on refractory and relapse/progressive diseaseMartinez de las Heras, BlancaRubio-Aparicio, Pedro MMazorra Roig, PaulaLópez Almaraz, RicardoRUBIO-SAN-SIMON, AlbaMoreno, LucasInfantsNeuroblastoma - TractamentNeuroblastoma - RecaigudaNAMED GROUPS::Persons::Age Groups::ChildDISEASES::Neoplasms::Neoplasms by Histologic Type::Neoplasms, Germ Cell and Embryonal::Neuroectodermal Tumors::Neoplasms, Neuroepithelial::Neuroectodermal Tumors, Primitive::Neuroectodermal Tumors, Primitive, Peripheral::NeuroblastomaOther subheadings::Other subheadings::/therapyDISEASES::Neoplasms::Neoplastic Processes::Neoplasm Recurrence, LocalDENOMINACIONES DE GRUPOS::personas::Grupos de Edad::niñoENFERMEDADES::neoplasias::neoplasias por tipo histológico::neoplasias de células germinales y embrionarias::tumores neuroectodérmicos::neoplasias neuroepiteliales::tumores neuroectodérmicos primitivos::tumores neuroectodérmicos primitivos periféricos::neuroblastomaOtros calificadores::Otros calificadores::/terapiaENFERMEDADES::neoplasias::procesos neoplásicos::recurrencia neoplásica localImmunotherapy; Neuroblastoma; RelapseImmunoteràpia; Neuroblastoma; RecaigudaInmunoterapia; Neuroblastoma; RecaídaPurpose Outcome for children with refractory and relapse/progressive high-risk neuroblastoma (HR-NB) remains poor, without an internationally agreed standard second-line approach. Heterogeneity in patients’ disease and treatment strategies challenges clinical management. The survival rate for patients with resistant disease does not exceed 20% at 5 years. The study’s aim was to analyze refractory and progressive HR-NB patients in a real-world setting to evaluate current clinical practices and optimize future approaches. Methods Data from patients diagnosed with refractory and relapse/progressive (R/R-P) HR-NB between January 2019 and December 2021 at six of the major Spanish neuroblastoma treating hospitals were collected and analyzed. Results A total of 67 episodes of R/R-P HR-NB were included. Treatments applied included chemotherapy (97%), immunotherapy (48%), consolidation (21%), local treatment (surgery and/or radiotherapy) (45%) and maintenance (16%), and were administered within a clinical trial (CT) in 34% of the episodes. Biopsy was performed in 37% of the tumors and 30% were profiled. Event-free survival (EFS) in our cohort was 20.9% and overall survival (OS) 32%. Significant survival advantage (in both OS and EFS) was observed in refractory episodes compared to relapse/progressive, in first events compared to successive, and when response or disease stabilization was achieved. MYCN status, presence of lymph node metastases, use of irinotecan or topotecan, and radiotherapy were also univariate predictors of OS. Conclusions Treatment of refractory and relapse/progressive HR-NB is highly heterogeneous. We confirm a poor outcome, although certain epidemiological and treatment-related factors have prognostic value. Molecular profiling and inclusion in CTs should be improved.This study has been co-funded by Instituto de Salud Carlos III (ISCIII) through the project ‘ICI21/00098’ with funds from Plan de Recuperación, Transformación y Resiliencia and ‘Funded by the European Union - NextGenerationEU’.SpringerInstitut Català de la Salut[Martínez de las Heras B] Pediatric Hemato-Oncology Department, Hospital Universitario y Politécnico La Fe, European Reference Network PAEDCAN member, Valencia, Spain. Clinical and Translational Oncology Research Group, Investigation Institute La Fe, Valencia, Spain. [Rubio Aparicio PM] Pediatric Hemato-Oncology Department, Hospital Universitario La Paz, European Reference Network PAEDCAN member, Madrid, Spain. [Rubio San Simón A] Pediatric Hemato-Oncology Department, Hospital Infantil Universitario Niño Jesús, Madrid, Spain. [Moreno L, Mazorra P] Servei de Pediatria, Vall d’Hebron Hospital Universitari, Barcelona, Spain. European Reference Network PAEDCAN member, Barcelona, Spain. [López Almaraz R] Pediatric Onco-Hematology Unit, Hospital Cruces, and Pediatric Oncology GroupVall d'Hebron Barcelona Hospital Campus202520252025info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/11351/13792Scientiareponame:Scientia. Dipòsit d'Informació Digital del Departament de Salutinstname:Departament de Salut de la Generalitat de Catalunya (DS)InglésClinical and Translational Oncology;27https://doi.org/10.1007/s12094-025-03853-wAttribution 4.0 Internationalhttp://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessoai:scientiasalut.gencat.cat:11351/137922026-06-12T09:38:37Z |
| score |
15.812429 |