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The Swedish childhood tumor biobank: systematic collection and molecular characterization of all pediatric CNS and other solid tumors in Sweden
The Swedish Childhood Tumor Biobank (BTB) is a nonprofit national infrastructure for collecting tissue samples and genomic data from pediatric patients diagnosed with central nervous system (CNS) and other solid tumors. The BTB is built on a multidisciplinary network established to provide the scien...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10204274/ https://www.ncbi.nlm.nih.gov/pubmed/37221626 http://dx.doi.org/10.1186/s12967-023-04178-4 |
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author | Díaz de Ståhl, Teresita Shamikh, Alia Mayrhofer, Markus Juhos, Szilvester Basmaci, Elisa Prochazka, Gabriela Garcia, Maxime Somarajan, Praveen Raj Zielinska-Chomej, Katarzyna Illies, Christopher Øra, Ingrid Siesjö, Peter Sandström, Per-Erik Stenman, Jakob Sabel, Magnus Gustavsson, Bengt Kogner, Per Pfeifer, Susan Ljungman, Gustaf Sandgren, Johanna Nistér, Monica |
author_facet | Díaz de Ståhl, Teresita Shamikh, Alia Mayrhofer, Markus Juhos, Szilvester Basmaci, Elisa Prochazka, Gabriela Garcia, Maxime Somarajan, Praveen Raj Zielinska-Chomej, Katarzyna Illies, Christopher Øra, Ingrid Siesjö, Peter Sandström, Per-Erik Stenman, Jakob Sabel, Magnus Gustavsson, Bengt Kogner, Per Pfeifer, Susan Ljungman, Gustaf Sandgren, Johanna Nistér, Monica |
author_sort | Díaz de Ståhl, Teresita |
collection | PubMed |
description | The Swedish Childhood Tumor Biobank (BTB) is a nonprofit national infrastructure for collecting tissue samples and genomic data from pediatric patients diagnosed with central nervous system (CNS) and other solid tumors. The BTB is built on a multidisciplinary network established to provide the scientific community with standardized biospecimens and genomic data, thereby improving knowledge of the biology, treatment and outcome of childhood tumors. As of 2022, over 1100 fresh-frozen tumor samples are available for researchers. We present the workflow of the BTB from sample collection and processing to the generation of genomic data and services offered. To determine the research and clinical utility of the data, we performed bioinformatics analyses on next-generation sequencing (NGS) data obtained from a subset of 82 brain tumors and patient blood-derived DNA combined with methylation profiling to enhance the diagnostic accuracy and identified germline and somatic alterations with potential biological or clinical significance. The BTB procedures for collection, processing, sequencing, and bioinformatics deliver high-quality data. We observed that the findings could impact patient management by confirming or clarifying the diagnosis in 79 of the 82 tumors and detecting known or likely driver mutations in 68 of 79 patients. In addition to revealing known mutations in a broad spectrum of genes implicated in pediatric cancer, we discovered numerous alterations that may represent novel driver events and specific tumor entities. In summary, these examples reveal the power of NGS to identify a wide number of actionable gene alterations. Making the power of NGS available in healthcare is a challenging task requiring the integration of the work of clinical specialists and cancer biologists; this approach requires a dedicated infrastructure, as exemplified here by the BTB. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-023-04178-4. |
format | Online Article Text |
id | pubmed-10204274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102042742023-05-24 The Swedish childhood tumor biobank: systematic collection and molecular characterization of all pediatric CNS and other solid tumors in Sweden Díaz de Ståhl, Teresita Shamikh, Alia Mayrhofer, Markus Juhos, Szilvester Basmaci, Elisa Prochazka, Gabriela Garcia, Maxime Somarajan, Praveen Raj Zielinska-Chomej, Katarzyna Illies, Christopher Øra, Ingrid Siesjö, Peter Sandström, Per-Erik Stenman, Jakob Sabel, Magnus Gustavsson, Bengt Kogner, Per Pfeifer, Susan Ljungman, Gustaf Sandgren, Johanna Nistér, Monica J Transl Med Research The Swedish Childhood Tumor Biobank (BTB) is a nonprofit national infrastructure for collecting tissue samples and genomic data from pediatric patients diagnosed with central nervous system (CNS) and other solid tumors. The BTB is built on a multidisciplinary network established to provide the scientific community with standardized biospecimens and genomic data, thereby improving knowledge of the biology, treatment and outcome of childhood tumors. As of 2022, over 1100 fresh-frozen tumor samples are available for researchers. We present the workflow of the BTB from sample collection and processing to the generation of genomic data and services offered. To determine the research and clinical utility of the data, we performed bioinformatics analyses on next-generation sequencing (NGS) data obtained from a subset of 82 brain tumors and patient blood-derived DNA combined with methylation profiling to enhance the diagnostic accuracy and identified germline and somatic alterations with potential biological or clinical significance. The BTB procedures for collection, processing, sequencing, and bioinformatics deliver high-quality data. We observed that the findings could impact patient management by confirming or clarifying the diagnosis in 79 of the 82 tumors and detecting known or likely driver mutations in 68 of 79 patients. In addition to revealing known mutations in a broad spectrum of genes implicated in pediatric cancer, we discovered numerous alterations that may represent novel driver events and specific tumor entities. In summary, these examples reveal the power of NGS to identify a wide number of actionable gene alterations. Making the power of NGS available in healthcare is a challenging task requiring the integration of the work of clinical specialists and cancer biologists; this approach requires a dedicated infrastructure, as exemplified here by the BTB. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-023-04178-4. BioMed Central 2023-05-23 /pmc/articles/PMC10204274/ /pubmed/37221626 http://dx.doi.org/10.1186/s12967-023-04178-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Díaz de Ståhl, Teresita Shamikh, Alia Mayrhofer, Markus Juhos, Szilvester Basmaci, Elisa Prochazka, Gabriela Garcia, Maxime Somarajan, Praveen Raj Zielinska-Chomej, Katarzyna Illies, Christopher Øra, Ingrid Siesjö, Peter Sandström, Per-Erik Stenman, Jakob Sabel, Magnus Gustavsson, Bengt Kogner, Per Pfeifer, Susan Ljungman, Gustaf Sandgren, Johanna Nistér, Monica The Swedish childhood tumor biobank: systematic collection and molecular characterization of all pediatric CNS and other solid tumors in Sweden |
title | The Swedish childhood tumor biobank: systematic collection and molecular characterization of all pediatric CNS and other solid tumors in Sweden |
title_full | The Swedish childhood tumor biobank: systematic collection and molecular characterization of all pediatric CNS and other solid tumors in Sweden |
title_fullStr | The Swedish childhood tumor biobank: systematic collection and molecular characterization of all pediatric CNS and other solid tumors in Sweden |
title_full_unstemmed | The Swedish childhood tumor biobank: systematic collection and molecular characterization of all pediatric CNS and other solid tumors in Sweden |
title_short | The Swedish childhood tumor biobank: systematic collection and molecular characterization of all pediatric CNS and other solid tumors in Sweden |
title_sort | swedish childhood tumor biobank: systematic collection and molecular characterization of all pediatric cns and other solid tumors in sweden |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10204274/ https://www.ncbi.nlm.nih.gov/pubmed/37221626 http://dx.doi.org/10.1186/s12967-023-04178-4 |
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