8 results match your criteria: "German Cancer Institute[Affiliation]"
Intensive Care Med
August 2024
Laboratory for Computational Physiology, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Neuro Oncol
December 2023
Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany.
Background: The prognosis for Li-Fraumeni syndrome (LFS) patients with medulloblastoma (MB) is poor. Comprehensive clinical data for this patient group is lacking, challenging the development of novel therapeutic strategies. Here, we present clinical and molecular data on a retrospective cohort of pediatric LFS MB patients.
View Article and Find Full Text PDFEur J Cancer
June 2022
Research Department of Pathology, University College London, London, UK; Department of Histopathology, Royal National Orthopaedic Hospital, Stanmore, HA7 4LP, UK. Electronic address:
Aim: Osteosarcoma (OS) is the most common primary bone tumour in children and adolescents. Circulating free (cfDNA) and circulating tumour DNA (ctDNA) are promising biomarkers for disease surveillance and prognostication in several cancer types; however, few such studies are reported for OS. The purpose of this study was to discover and validate methylation-based biomarkers to detect plasma ctDNA in patients with OS and explore their utility as prognostic markers.
View Article and Find Full Text PDFClin Cancer Res
June 2022
Neurology Department, Brain Tumor Center, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
Purpose: In a post hoc analysis of the CATNON trial (NCT00626990), we explored whether adding temozolomide to radiotherapy improves outcome in patients with IDH1/2 wildtype (wt) anaplastic astrocytomas with molecular features of glioblastoma [redesignated as glioblastoma, isocitrate dehydrogenase-wildtype (IDH-wt) in the 2021 World Health Organization (WHO) classification of central nervous system tumors].
Patients And Methods: From the randomized phase III CATNON study examining the addition of adjuvant and concurrent temozolomide to radiotherapy in anaplastic astrocytomas, we selected a subgroup of IDH1/2wt and H3F3Awt tumors with presence of TERT promoter mutations and/or EGFR amplifications and/or combined gain of chromosome 7 and loss of chromosome 10. Molecular abnormalities including MGMT promoter methylation status were determined by next-generation sequencing, DNA methylation profiling, and SNaPshot analysis.
Neuropathol Appl Neurobiol
October 2021
Department of Neuropathology, Institute of Pathology, Hannover Medical School, Hannover, Germany.
Aims: Brain invasion (BI) was firstly defined as a single criterion of atypia in otherwise benign meningiomas in the revised fourth edition of 2016 WHO classification of brain tumours after being previously inconsistently addressed. However, recent studies have raised doubts about the prognostic significance of BI in otherwise benign meningiomas. In our study, we investigate the reproducibility of such a prognostic effect.
View Article and Find Full Text PDFActa Neuropathol
March 2020
Department of Neurology, University Hospital and University of Zurich, Zurich, Switzerland.
Acta Neuropathol
November 2018
Department of Neurology, University Hospital and University of Zurich, Zurich, Switzerland.
J Am Soc Nephrol
December 2001
Departments of *Nephrology and Hypertension and Vascular Medicine, University Medical Center, Utrecht, The Netherlands; Department of Cellular and Molecular Pathology, German Cancer Institute, Heidelberg, Germany; and Department of Pharmacology, Pharmacy Faculty, Utrecht, The Netherlands.
Chronic nitric oxide (NO) synthase inhibition in rats causes hypertension, renal vascular injury, and proteinuria. NO deficiency increases superoxide (O(2)(-)) activity, but the effects of antioxidant treatment on renal injury have not been studied in this model. Exposure of rats to N omega-nitro-L-arginine (L-NNA) for 4 d markedly decreased NO-dependent relaxation in aortic rings and increased glomerular and renal interstitial monocyte influx, but renal O(2)(-) activity was not increased.
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