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  • Pietsch, Torsten (7)
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IMMU-28. Deciphering the AT/RT ligandome (2018)
Marcu, Ana ; Trautwein, Nico ; Stevanovic, Stefan ; Johann, Pascal-David ; Technau, Antje ; Lager, Johanna ; Monoranu, Camelia-Maria ; Henkel, Lisa ; Krauß, Jürgen ; Ebinger, Martin ; Schuhmann, Martin ; Thomale, Ulrich ; Pietsch, Torsten ; Wölfl, Matthias ; Schlegel, Paul Gerhardt ; Frühwald, Michael C. ; Oyen, Florian ; Reisner, Yair ; Rammensee, Hans-Georg ; Eyrich, Matthias
Strategies to improve the quality of survival for childhood brain tumour survivors (2015)
Tallen, Gesche ; Resch, Anika ; Calaminus, Gabriele ; Wiener, Andreas ; Leiss, Ulrike ; Pletschko, Thomas ; Friedrich, Carsten ; Langer, Thorsten ; Grabow, Desiree ; Driever, Pablo Hernáiz ; Kortmann, Rolf-Dieter ; Timmermann, Beate ; Pietsch, Torsten ; Warmuth-Metz, Monika ; Bison, Brigitte ; Thomale, Ulrich-Wilhelm ; Krauss, Jürgen ; Mynarek, Martin ; Hoff, Katja von ; Ottensmeier, Holger ; Frühwald, Michael C. ; Kramm, Christof M. ; Temming, Petra ; Müller, Hermann L. ; Witt, Olaf ; Kordes, Uwe ; Fleischhack, Gudrun ; Gnekow, Astrid K. ; Rutkowski, Stefan
Local and systemic therapy of recurrent ependymoma in children and adolescents: short- and long-term result of the E-HIT-REZ 2005 study (2021)
Adolph, Jonas E. ; Fleischhack, Gudrun ; Mikasch, Ruth ; Zeller, Julia ; Warmuth-Metz, Monika ; Bison, Brigitte ; Mynarek, Martin ; Rutkowski, Stefan ; Schüller, Ulrich ; von Hoff, Katja ; Obrecht, Denise ; Pietsch, Torsten ; Pfister, Stefan M. ; Pajtler, Kristian W. ; Witt, Olaf ; Witt, Hendrik ; Kortmann, Rolf-Dieter ; Timmermann, Beate ; Krauß, Jürgen ; Frühwald, Michael C. ; Faldum, Andreas ; Kwiecien, Robert ; Bode, Udo ; Tippelt, Stephan
High frequency of disease progression in pediatric spinal cord low-grade glioma (LGG): management strategies and results from the German LGG study group (2020)
Perwein, Thomas ; Benesch, Martin ; Kandels, Daniela ; Pietsch, Torsten ; Schmidt, René ; Quehenberger, Franz ; Bison, Brigitte ; Warmuth-Metz, Monika ; Timmermann, Beate ; Krauss, Jürgen ; Thomale, Ulrich-Wilhelm ; Kortmann, Rolf-Dieter ; Driever, Pablo Hernáiz ; Gnekow, Astrid Katharina
Natural and cryptic peptides dominate the immunopeptidome of atypical teratoid rhabdoid tumors (2021)
Marcu, Ana ; Schlosser, Andreas ; Keupp, Anne ; Trautwein, Nico ; Johann, Pascal-David ; Wölfl, Matthias ; Lager, Johanna ; Monoranu, Camelia Maria ; Walz, Juliane S ; Henkel, Lisa M ; Krauß, Jürgen ; Ebinger, Martin ; Schuhmann, Martin ; Thomale, Ulrich Wilhelm ; Pietsch, Torsten ; Klinker, Erdwine ; Schlegel, Paul G ; Oyen, Florian ; Reisner, Yair ; Rammensee, Hans-Georg ; Eyrich, Matthias
[18F]FET-PET in children and adolescents with central nervous system tumors: does it support difficult clinical decision-making? (2023)
Kertels, Olivia ; Krauß, Jürgen ; Monoranu, Camelia Maria ; Samnick, Samuel ; Dierks, Alexander ; Kircher, Malte ; Mihovilovic, Milena I. ; Pham, Mirko ; Buck, Andreas K. ; Eyrich, Matthias ; Schlegel, Paul-Gerhardt ; Frühwald, Michael C. ; Bison, Brigitte ; Lapa, Constantin
Purpose Positron emission tomography (PET) with O-(2-[18F]fluoroethyl)-L-tyrosine ([18F]FET) is a well-established tool for non-invasive assessment of adult central nervous system (CNS) tumors. However, data on its diagnostic utility and impact on clinical management in children and adolescents are limited. Methods Twenty-one children and young adults (13 males; mean age, 8.6 ± 5.2 years; range, 1–19 at initial diagnosis) with either newly diagnosed (n = 5) or pretreated (n = 16) CNS tumors were retrospectively analyzed. All patients had previously undergone neuro-oncological work-up including cranial magnetic resonance imaging. In all cases, [18F]FET-PET was indicated in a multidisciplinary team conference. The impact of PET imaging on clinical decision-making was assessed. Histopathology (n = 12) and/or clinical and imaging follow-up (n = 9) served as the standard of reference. Results The addition of [18F]FET-PET to the available information had an impact on further patient management in 14 out of 21 subjects, with avoidance of invasive surgery or biopsy in four patients, biopsy guidance in four patients, change of further treatment in another five patients, and confirmation of diagnosis in one patient. Conclusion [18F]FET-PET may provide important additional information for treatment guidance in pediatric and adolescent patients with CNS tumors.
Adaption of neurosurgical resection patterns for pediatriclow-grade glioma spanning two decades: report from the German LGG-studies 1996–2018 (2024)
Kelety, Tibor ; Thomale, Ulrich‐Wilhelm ; Kandels, Daniela ; Schuhmann, Martin U. ; El Damaty, Ahmed ; Krauss, Jürgen ; Frühwald, Michael C. ; Hernáiz Driever, Pablo ; Witt, Olaf ; Bison, Brigitte ; Warmuth‐Metz, Monika ; Pietsch, Torsten ; Schmidt, René ; Gnekow, Astrid K.
Introduction Neurosurgery is considered the mainstay of treatment for pediatric low-grade glioma (LGG); the extent of resection determines subsequent stratification in current treatment protocols. Yet, surgical radicality must be balanced against the risks of complications that may affect long-term quality of life. We investigated whether this consideration impacted surgical resection patterns over time for patients of the German LGG studies. Patients and Methods Four thousand two hundred and seventy pediatric patients from three successive LGG studies (median age at diagnosis 7.6 years, neurofibromatosis (NF1) 14.7%) were grouped into 5 consecutive time intervals (TI1-5) for date of diagnosis and analyzed for timing and extent of first surgery with respect to tumor site, histology, NF1-status, sex, and age. Results The fraction of radiological LGG diagnoses increased over time (TI1 12.6%; TI5 21.7%), while the extent of the first neurosurgical intervention (3440/4270) showed a reduced fraction of complete/subtotal and an increase of partial resections from TI1 to TI5. Binary logistic regression analysis for the first intervention within the first year following diagnosis confirmed the temporal trends (p < 0.001) and the link with tumor site for each extent of resection (p < 0.001). Higher age is related to more complete resections in the cerebellum and cerebral hemispheres. Conclusions The declining extent of surgical resections over time was unrelated to patient characteristics. It paralleled the evolution of comprehensive treatment algorithms; thus, it may reflect alignment of surgical practice to recommendations in respect to age, tumor site, and NF1-status integrated as such into current treatment guidelines. Further investigations are needed to understand how planning, performance, or tumor characteristics impact achieving surgical goals.
Leptomeningeal dissemination in choroid plexus tumors: magnetic resonance imaging appearance and risk factors (2025)
Nunes do Espirito Santo, Daniel ; Warmuth-Metz, Monika ; Monoranu, Camelia-Maria ; Hasselblatt, Martin ; Thomas, Christian ; Pietsch, Torsten ; Krauß, Jürgen ; Schweitzer, Tilmann ; Bison, Brigitte ; Eyrich, Matthias ; Kordes, Uwe ; Obrecht-Sturm, Denise ; Pham, Mirko ; Quenzer, Annika
Background: Intracranial choroid plexus tumors (CPT) are rare and primarily affect young children. Leptomeningeal dissemination (LMD) has been reported not only in high-grade choroid plexus carcinoma (CPC) but also in lower histological grades; however, a systematic evaluation of CPT-specific imaging characteristics remains lacking. Methods: We analyzed the imaging characteristics of LMD in a single-center pediatric cohort of 22 CPT patients (thirteen choroid plexus papilloma (CPP), six atypical choroid plexus papilloma (aCPP), three CPC), comparing LMD features with those of the primary tumor. Additionally, we examined the correlation between resection status and LMD development during follow-up. Results: At diagnosis, we observed true LMD in three (two CPCs, one CPP) and pseudo-LMD in one case (CPP). During follow-up, two CPP patients developed cystic LMD, and one aCPP patient developed a solid metastasis. LMD had characteristics of the primary tumor in 3/4 cases. Incomplete resection was associated with a higher risk of LMD ( p = 0.025). Conclusions: LMD can occur in both high- and lower-grade CPT, presenting at diagnosis as well as in relapsed lower-grade cases. Notable MR-imaging features include pseudo-LMD at diagnosis and cystic LMD in relapsed CPP cases. Incomplete tumor resection may increase the risk of LMD, although further validation is needed.
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