Academic Journal

The relapsed acute lymphoblastic leukemia network (ReALLNet) : a multidisciplinary project from the spanish society of pediatric hematology and oncology (SEHOP)

التفاصيل البيبلوغرافية
العنوان: The relapsed acute lymphoblastic leukemia network (ReALLNet) : a multidisciplinary project from the spanish society of pediatric hematology and oncology (SEHOP)
المؤلفون: Velasco, Pablo, Bautista, Francisco Jose, Rubio, Alba, Aguilar, Yurena, Rives, Susana, Dapena, Jose L, Pérez, Antonio, Ramirez, Manuel, Saiz-Ladera, Cristina, Izquierdo, Elisa, Escudero, Adela, Camós, Mireia, Vega-García, Nerea, Ortega, Margarita, Hidalgo-Gómez, Gloria, Palacio, Carlos, Menéndez, Pablo, Bueno, Clara, Montero, Joan, Romecín, Paola A., Zazo, Santiago, Alvarez, Federico, Parras, Juan, Ortega-Sabater, Carmen, Chulián, Salvador, Rosa, María, Cirillo, Davide, García, Elena, García, Jorge, Manzano-Muñoz, Albert, Minguela, Alfredo, Fuster, José Luis
سنة النشر: 2023
المجموعة: Universitat Autònoma de Barcelona: Dipòsit Digital de Documents de la UAB
مصطلحات موضوعية: Relapsed acute lymphoblastic leukemia, Precision medicine, Cancer registry, Artificial intelligence, Functional assay
الوصف: Acute lymphoblastic leukemia (ALL) is the most common pediatric cancer, with survival rates exceeding 85%. However, 15% of patients will relapse; consequently, their survival rates decrease to below 50%. Therefore, several research and innovation studies are focusing on pediatric relapsed or refractory ALL (R/R ALL). Driven by this context and following the European strategic plan to implement precision medicine equitably, the Relapsed ALL Network (ReALLNet) was launched under the umbrella of SEHOP in 2021, aiming to connect bedside patient care with expert groups in R/R ALL in an interdisciplinary and multicentric network. To achieve this objective, a board consisting of experts in diagnosis, management, preclinical research, and clinical trials has been established. The requirements of treatment centers have been evaluated, and the available oncogenomic and functional study resources have been assessed and organized. A shipping platform has been developed to process samples requiring study derivation, and an integrated diagnostic committee has been established to report results. These biological data, as well as patient outcomes, are collected in a national registry. Additionally, samples from all patients are stored in a biobank. This comprehensive repository of data and samples is expected to foster an environment where preclinical researchers and data scientists can seek to meet the complex needs of this challenging population. This proof of concept aims to demonstrate that a network-based organization, such as that embodied by ReALLNet, provides the ideal niche for the equitable and efficient implementation of "what's next" in the management of children with R/R ALL.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
تدمد: 85173436
Relation: Frontiers in Pediatrics; Vol. 11 (september 2023); https://ddd.uab.cat/record/289764; urn:10.3389/fped.2023.1269560; urn:oai:ddd.uab.cat:289764; urn:scopus_id:85173436838; urn:oai:pubmedcentral.nih.gov:10547895; urn:pmid:37800011; urn:pmc-uid:10547895; urn:pmcid:PMC10547895
الاتاحة: https://ddd.uab.cat/record/289764
Rights: open access ; Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. ; https://creativecommons.org/licenses/by/4.0/
رقم الانضمام: edsbas.D9B4A8A8
قاعدة البيانات: BASE