Sebastian Bauer

ORCID: 0000-0001-5949-8120
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About
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Research Areas
  • Gastrointestinal Tumor Research and Treatment
  • Sarcoma Diagnosis and Treatment
  • Gastric Cancer Management and Outcomes
  • Gastrointestinal disorders and treatments
  • Peptidase Inhibition and Analysis
  • Vascular Tumors and Angiosarcomas
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Chronic Myeloid Leukemia Treatments
  • Cardiac tumors and thrombi
  • Cancer Genomics and Diagnostics
  • Neurofibromatosis and Schwannoma Cases
  • Platelet Disorders and Treatments
  • Metastasis and carcinoma case studies
  • Cancer, Hypoxia, and Metabolism
  • Cancer, Lipids, and Metabolism
  • Lymphoma Diagnosis and Treatment
  • Lung Cancer Treatments and Mutations
  • Bone Tumor Diagnosis and Treatments
  • Musculoskeletal synovial abnormalities and treatments
  • Histone Deacetylase Inhibitors Research
  • Extracellular vesicles in disease
  • Advanced Breast Cancer Therapies
  • Multiple Myeloma Research and Treatments
  • Radiopharmaceutical Chemistry and Applications

Essen University Hospital
2016-2025

Deutschen Konsortium für Translationale Krebsforschung
2016-2025

University of Duisburg-Essen
2016-2025

German Cancer Research Center
2016-2025

West Cancer Center
2016-2025

Brigham and Women's Hospital
2005-2024

Heidelberg University
1990-2024

West German Heart and Vascular Center Essen
2015-2024

TU Dortmund University
2013-2024

Science for Life Laboratory
2023-2024

Soft tissue sarcomas (STSs) gather over 80 histological entities, with even more molecular subsets, characterised by a low to very incidence in all populations. The majority of arise from the soft (close 75%), ∼15% gastrointestinal stromal tumours (GISTs) and 10% bone sarcomas. These ESMO–EURACAN (European Society for Medical Oncology–European Reference Network rare adult solid cancers) Clinical Practice Guidelines cover STSs, while GISTs are covered dedicated [1.Casali P.G. Abecassis N....

10.1093/annonc/mdy096 article EN publisher-specific-oa Annals of Oncology 2018-03-28

<h3>Context</h3>Adjuvant imatinib administered for 12 months after surgery has improved recurrence-free survival (RFS) of patients with operable gastrointestinal stromal tumor (GIST) compared placebo.<h3>Objective</h3>To investigate the role administration duration as adjuvant treatment who have a high estimated risk GIST recurrence surgery.<h3>Design, Setting, and Patients</h3>Patients KIT-positive removed at were entered between February 2004 September 2008 to this randomized, open-label...

10.1001/jama.2012.347 article EN JAMA 2012-03-27

Gastrointestinal stromal tumours (GISTs) are rare tumours, with an estimated unadjusted incidence of around 1/100 000/year [1.Nilsson B. Bümming P. Meis-Kindblom J.M. et al.Gastrointestinal tumors: the incidence, prevalence, clinical course, and prognostication in preimatinib mesylate era–a population-based study western Sweden.Cancer. 2005; 103: 821-829Crossref PubMed Scopus (1027) Google Scholar]. This only covers clinically relevant GISTs, since, if investigated, a much higher number...

10.1093/annonc/mdy095 article EN publisher-specific-oa Annals of Oncology 2018-03-28

10.1016/j.annonc.2021.07.006 article EN publisher-specific-oa Annals of Oncology 2021-07-22

Primary bone tumours are rare, accounting for < 0.2% of malignant neoplasms registered in the EUROCARE (European Cancer Registry based study on survival and care cancer patients) database [1.Stiller C.A. Trama A. Serraino D. Descriptive epidemiology sarcomas Europe: report from RARECARE project.Eur J Cancer. 2013; 49: 684-695Abstract Full Text PDF PubMed Scopus (265) Google Scholar]. Different tumour subtypes have distinct patterns incidence, each has no more than 0.3 incident cases per 100...

10.1093/annonc/mdy310 article EN publisher-specific-oa Annals of Oncology 2018-08-02

10.1016/j.annonc.2021.08.1995 article EN publisher-specific-oa Annals of Oncology 2021-09-06

Leiomyosarcoma (LMS) is an aggressive mesenchymal malignancy with few therapeutic options. The mechanisms underlying LMS development, including clinically actionable genetic vulnerabilities, are largely unknown. Here we show, using whole-exome and transcriptome sequencing, that tumors characterized by substantial mutational heterogeneity, near-universal inactivation of TP53 RB1, widespread DNA copy number alterations chromothripsis, frequent whole-genome duplication. Furthermore, detect...

10.1038/s41467-017-02602-0 article EN cc-by Nature Communications 2018-01-04

Three years of adjuvant imatinib therapy are recommended for patients with GI stromal tumor (GIST) high-risk features, according to survival findings in the Scandinavian Sarcoma Group XVIII/AIO (Arbeitsgemeinschaft Internistische Onkologie) trial. To investigate whether benefits have persisted, we performed second planned analysis trial.Eligible had macroscopically completely excised, KIT-positive GIST a high risk recurrence, as determined by using modified National Institutes Health...

10.1200/jco.2015.62.9170 article EN Journal of Clinical Oncology 2015-11-03

Abstract The clinical relevance of comprehensive molecular analysis in rare cancers is not established. We analyzed the profiles and outcomes 1,310 patients (rare cancers, 75.5%) enrolled a prospective observational study by German Cancer Consortium that applies whole-genome/exome RNA sequencing to inform care adults with incurable cancers. On basis 472 single six composite biomarkers, cross-institutional tumor board provided evidence-based management recommendations, including diagnostic...

10.1158/2159-8290.cd-21-0126 article EN Cancer Discovery 2021-06-10

Little is known about whether the duration of adjuvant imatinib influences prognostic significance KIT proto-oncogene receptor tyrosine kinase (KIT) and platelet-derived growth factor α (PDGFRA) mutations.To investigate effect PDGFRA mutations on recurrence-free survival (RFS) in patients with gastrointestinal stromal tumors (GISTs) treated surgery imatinib.This exploratory study based Scandinavian Sarcoma Group VIII/Arbeitsgemeinschaft Internistische Onkologie (SSGXVIII/AIO) multicenter...

10.1001/jamaoncol.2016.5751 article EN JAMA Oncology 2017-03-24
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