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Press release 127/24 - 21.11.2024

New insights into the risk assessment of rare, aggressive tumours in children

New insights into the risk assessment of rare, aggressive tumours in children

An international research team with the significant involvement of Augsburg 伟德国际_伟德国际1946$娱乐app游戏 伟德国际_伟德国际1946$娱乐app游戏icine has made significant progress in the risk assessment and treatment of extracranial malign rhabdoid tumours. Recently published in the renowned journal “Clinical Cancer Research,” the study, “Clinical and Molecular Risk Factors in Extracranial Malignant Rhabdoid Tumours: Toward an Integrated Model of High-Risk Tumours,” shows how clinical and molecular factors can influence disease progression and contribute to improvements in individual treatment.

Scientists from the Experimental Pediatric Oncology and Tumor Epigenetics research group. AG Experimentelle p?diatrische Onkologie und Tumorepigenetik

Malign rhabdoid tumours are rare and affect around 35 children a year in Germany, in particular infants and toddlers. Due to the aggressive nature of the disease and the high rate of recurrence in this type of cancer, treatment is often difficult. As there has been no established model of prognosis for these tumours up until now, there has often been a lack of targeted treatment options that consider individual disease progression. The new research results now enable a more precise assessment of the risk and of individually adapted therapies that increase the chances of recovery for young patients.

A thorough molecular analysis was conducted in the study in which the research team analysed the genetic and epigenetic composition of the tumours. Data from a total of 213 patients from the EU-RHAB register was used. Through the analysis of tumour DNA and a modern machine learning process, the team were able to identify three subgroups with different risk profiles: a subgroup with improved chances of survival (“eMRT standard risk”) and two subgroups with increased risk of recurrence. These subgroups should support clinical decision-making by the early identification of high-risk patients.?

Professor Dr med. Pascal Johann, one of the leaders of the study at the 伟德国际_伟德国际1946$娱乐app游戏 Hospital Augsburg, and professor for experimental paediatrics at the Faculty of 伟德国际_伟德国际1946$娱乐app游戏icine, explains: “Our research results show that clinical as well as genetic factors have a significant influence on disease progression.” Professor Dr Dr med. Michael C. Frühwald, director of the Swabian Children’s Cancer Centre and co-author of the study, adds: “This study represents an important step towards personalised medicine in the treatment of children with malign rhabdoid tumours. Through a better understanding of the risk factors, we want to increase the chances of therapeutic success and the chances of recovery for seriously ill children.”

On behalf of the study, the two first-authors, Victoria E. Finke and Mona Steinbügl, were recently awarded a prize for outstanding scientific publications by the Dr. Wolfbauer-Stiftung in the context of the 伟德国际_伟德国际1946$娱乐app游戏 Hospital Augsburg’s 2024 Science Day.

In addition to pure research, the 伟德国际_伟德国际1946$娱乐app游戏 Hospital Augsburg is also running the clinical study EURHAB, which is specifically concerned with the research and treatment of rhabdoid tumours. As a European Assistance Centre for all cases of rhabdoid tumours, the 伟德国际_伟德国际1946$娱乐app游戏 Hospital Augsburg plays a central role in the further development of individual treatment strategies for this serious disease and is actively committed to the further development of therapeutic options and improvement in the prognosis of affected children.

To the study:

Title: Clinical and Molecular Risk Factors in Extracranial Malignant Rhabdoid Tumors: Toward an Integrated Model of High-Risk Tumors.

Published in: Clinical Cancer Research – AACR Journals

Authors: Victoria E. Fincke1,2, Mona Steinbügl1,2, Hye-Jung E. Chun3, Karolina Nemes1,2, Marlena Mucha1,2, Maurice Lo?ner1,2, Felix Dorn1,2, Katharina Gastberger1,2, Sebastian Bühner1,2, Martin Sill5, Thomas Kr?ncke4,5, Reiner Siebert6, Patrick Melchior7, Rhoikos Furtw?ngler8, Matthias Schlesner9, Christian Vokuhl10, Christoph R?cken11, Pascal D. Johann1,2,5, and Michael C. Frühwald1,2

1 Pediatrics and Adolescent 伟德国际_伟德国际1946$娱乐app游戏icine, Swabian Children’s Cancer Center, 伟德国际_伟德国际1946$娱乐app游戏 Hospital Augsburg, Augsburg, Germany. 2 Bavarian Cancer Research Center (BZKF), Augsburg, Germany. 3 Department of Biomedical Informatics, Harvard 伟德国际_伟德国际1946$娱乐app游戏ical School, Boston, Massachusetts. 4 Department of Diagnostic and Interventional Radiology, 伟德国际_伟德国际1946$娱乐app游戏 伟德国际_伟德国际1946$娱乐app游戏ical Center Augsburg, Augsburg, Germany. 5 Division of Pediatric Neurooncology, Hopp Children’s Cancer Center (KiTZ) Heidelberg, German Cancer Consortium (DKTK), German Cancer Research Center (DKFZ), Heidelberg, Germany. 6 Institute of Human Genetics, Ulm 伟德国际_伟德国际1946$娱乐app游戏 and Ulm 伟德国际_伟德国际1946$娱乐app游戏 伟德国际_伟德国际1946$娱乐app游戏ical Center, Ulm, Germany. 7 Department of Radiation Oncology, Saarland 伟德国际_伟德国际1946$娱乐app游戏 Hospital, Homburg, Germany. 8 Division of Pediatric Hematology and Oncology, Children’s Hospital, Inselspital Bern 伟德国际_伟德国际1946$娱乐app游戏, Bern, Switzerland. 9 Faculty of Applied Computer Sciences, Biomedical Informatics, Data Mining and Data Analytics, 伟德国际_伟德国际1946$娱乐app游戏 of Augsburg, Augsburg, Germany. 10 Section of Pediatric Pathology, Department of Pathology, 伟德国际_伟德国际1946$娱乐app游戏 Hospital Bonn, Bonn, Germany. 11 Department of Pathology, Kiel 伟德国际_伟德国际1946$娱乐app游戏 and 伟德国际_伟德国际1946$娱乐app游戏 伟德国际_伟德国际1946$娱乐app游戏ical Center Schleswig-Holstein, Kiel, Germany.

Download: http://aacrjournals.org/clincancerres/article-pdf/30/20/4667/3504475/ccr-23-3489.pdf by 伟德国际_伟德国际1946$娱乐app游戏 of Augsburg user on 19 November 2024

Scientific contact

Prof. Dr. Pascal Johann
Professor für Experimentelle P?diatrie
Pediatrics and Adolescent 伟德国际_伟德国际1946$娱乐app游戏icine

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伟德国际_伟德国际1946$娱乐app游戏ia contact

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Communications and 伟德国际_伟德国际1946$娱乐app游戏ia Relations

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