Hans‐Ulrich Schildhaus

ORCID: 0000-0002-9856-7050
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About
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Research Areas
  • Lung Cancer Treatments and Mutations
  • Gastrointestinal Tumor Research and Treatment
  • Sarcoma Diagnosis and Treatment
  • Cancer Genomics and Diagnostics
  • Gastric Cancer Management and Outcomes
  • Gastrointestinal disorders and treatments
  • HER2/EGFR in Cancer Research
  • Colorectal Cancer Treatments and Studies
  • Lung Cancer Research Studies
  • Cancer Immunotherapy and Biomarkers
  • Peptidase Inhibition and Analysis
  • Cholangiocarcinoma and Gallbladder Cancer Studies
  • Vascular Tumors and Angiosarcomas
  • Genetic factors in colorectal cancer
  • Metastasis and carcinoma case studies
  • Cardiac tumors and thrombi
  • Neurofibromatosis and Schwannoma Cases
  • Fibroblast Growth Factor Research
  • PI3K/AKT/mTOR signaling in cancer
  • Medical Imaging and Pathology Studies
  • Monoclonal and Polyclonal Antibodies Research
  • Pancreatic and Hepatic Oncology Research
  • Cancer therapeutics and mechanisms
  • Lung Cancer Diagnosis and Treatment
  • Epigenetics and DNA Methylation

Universitätsmedizin Göttingen
2015-2025

Essen University Hospital
2019-2024

Deutschen Konsortium für Translationale Krebsforschung
2020-2024

Institut für Hämatopathologie Hamburg
2024

University of Duisburg-Essen
2019-2024

Hesse (Germany)
2023-2024

Biomarker Technologies (China)
2024

Sunny BioDiscovery (United States)
2023

Bayer (France)
2023

Endocyte (United States)
2023

Martin Peifer Lynnette Fernández-Cuesta Martin L. Sos Julie George Danila Seidel and 88 more Lawryn H. Kasper Dennis Plenker Frauke Leenders Ruping Sun Thomas Zander Roopika Menon Mirjam Koker Ilona Dahmen Christian Müller Vincenzo Di Cerbo Hans‐Ulrich Schildhaus Janine Altmüller Ingelore Baessmann Christian Becker Bram De Wilde Jo Vandesompele Diana Böhm Sascha Ansén Franziska Gabler Ines Wilkening Stefanie Heynck Johannes M. Heuckmann Xin Lü Scott L. Carter Kristian Cibulskis Shantanu Banerji Gad Getz Kwon-Sik Park Daniel Rauh Christian Grütter Matthias Fischer Laura Pasqualucci Gavin Wright Zoe Wainer Prudence A. Russell Iver Petersen Yuan Chen Erich Stoelben Corinna Ludwig Philipp A. Schnabel Hans Hoffmann Thomas Muley Michael Brockmann Walburga Engel-Riedel Lucia Anna Muscarella Vito Michele Fazio Harry J.M. Groen Wim Timens Hannie Sietsma Erik Thunnissen Egbert F. Smit Daniëlle A.M. Heideman Peter J.F. Snijders Federico Cappuzzo Claudia Ligorio Stefania Damiani John K. Field Steinar Solberg Odd Terje Brustugun Marius Lund‐Iversen Jörg Sänger Joachim H. Clement Alex Soltermann Holger Moch Walter Weder Benjamin Solomon Jean‐Charles Soria Pierre Validire Benjamin Besse Élisabeth Brambilla Christian Brambilla Sylvie Lantuéjoul Philippe Lorimier Peter M. Schneider Michael Hallek William Pao Matthew Meyerson Julien Sage Jay Shendure Robert C. Schneider Reinhard Büttner Jürgen Wolf Peter Nürnberg Sven Perner Lukas C. Heukamp Paul K. Brindle Stefan A. Haas Roman K. Thomas

10.1038/ng.2396 article EN Nature Genetics 2012-09-02
Danila Seidel Thomas Zander Lukas C. Heukamp Martin Peifer Marc Bos and 95 more Lynnette Fernández-Cuesta Frauke Leenders Xin Lü Sascha Ansén Masyar Gardizi Chau Nguyen Johannes Berg Prudence A. Russell Zoe Wainer Hans‐Ulrich Schildhaus Toni-Maree Rogers Benjamin Solomon William Pao Scott L. Carter Gad Getz D. Neil Hayes Matthew D. Wilkerson Erik Thunnissen William D. Travis Sven Perner Gavin Wright Élisabeth Brambilla Reinhard Buettner Juergen Wolf Roman K. Thomas Franziska Gabler Ines Wilkening Christian Mueller Ilona Dahmen Roopika Menon Katharina Koenig Kerstin Albus Sabine Merkelbach‐Bruse Jana Fassunke Katja Schmitz Helen Kuenstlinger Michaela Angelika Kleine Elke Binot Silvia Querings Janine Altmueller Ingelore Boessmann Peter Nuemberg Peter M. Schneider Magdalena Bogus Alex Soltermann Holger Moch Odd Terje Brustugun Steinar Solberg Marius Lund‐Iversen Åslaug Helland Thomas Muley Hans Hoffmann Philipp A. Schnabel Yuan Chen Harry J.M. Groen Wim Timens Hannie Sietsma Joachim H. Clement Walter Weder Joerg Saenger Erich Stoelben Corinna Ludwig Walburga Engel-Riedel Egbert F. Smit Danille A. M. Heideman Peter J.F. Snijders Lucia Nogová Martin L. Sos Christian Mattonet Karin Toepelt Matthias Scheffler Eray Goekkurt Rainer Kappes Stefan Krueger Kato Kambartel Dirk Behringer Wolfgang Schulte Wolfgang Galetke Winfried Randerath Matthias Heldwein Andreas Schlesinger Monika Serke Khosro Hekmat Konrad Frank Roland Schnell Marcel Reiser Ali-Nuri Huenerlituerkoglu Stephan Schmitz Lisa Meffert Yon‐Dschun Ko Markus Litt-Lampe Ulrich Gerigk Rainer Fricke Benjamin Besse Christian Brambilla

The pattern of mutations in human lung cancer differs by tumor subtype and is a useful addition to histology for selecting targeted therapy improving patient survival.

10.1126/scitranslmed.3006802 article EN Science Translational Medicine 2013-10-30

Abstract Gastrointestinal stromal tumors (GIST) are characterized by a strong KIT receptor activation most often resulting from mutations. In smaller subgroup of without mutations, analogous activating mutations found in the platelet-derived growth factor α (PDGFRα) gene. Both PDGFRα and receptors targets tyrosine kinase inhibitor imatinib (Glivec) which has improved treatment advanced GISTs significantly. However, show secondary progress under therapy with after initial response. One...

10.1158/1078-0432.ccr-05-1211 article EN Clinical Cancer Research 2006-03-15

The approval of vemurafenib in the US 2011 and Europe 2012 improved therapy not resectable or metastatic melanoma. Patients carrying a substitution valine to glutamic acid at codon 600 (p.V600E) leucine (p.V600K) BRAF show complete partial response. Therefore, precise identification underlying somatic mutations is essential. Herein, we evaluate sensitivity, specificity feasibility six different methods for detection mutations. Samples harboring p.V600E as well rare exon 15 were compared...

10.1186/1471-2407-14-13 article EN cc-by BMC Cancer 2014-01-10

Atypical EGFR mutations occur in 10%-30% of non-small-cell lung cancer (NSCLC) patients with and their sensitivity to classical epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKI) is highly heterogeneous. Patients harboring one group uncommon, recurrent (G719X, S768I, L861Q) respond EGFR-TKI. Exon 20 insertions are mostly insensitive EGFR-TKI but display exon inhibitors. Clinical outcome data very rare point compound upon systemic treatments still sparse date.In this...

10.1016/j.annonc.2022.02.225 article EN cc-by Annals of Oncology 2022-03-07

Patients affected by neurofibromatosis type 1 (NF-1) have an increased risk of developing gastrointestinal stromal tumors (GIST). NF-1-associated GISTs are usually wild for c-KIT and platelet-derived growth factor receptor-alpha (PDGFR-alpha) mutations harbor a different oncogenic molecular mechanism. The lack data on imatinib activity raises the question whether to enroll these patients in clinical trials. We analyzed large series NF-1 related discuss therapeutic implications.Clinical,...

10.1158/1078-0432.ccr-08-0086 article EN Clinical Cancer Research 2008-07-15

MET is a potential therapeutic target in lung cancer and both tyrosine kinase inhibitors monoclonal antibodies have entered clinical trials. signaling can be activated by various mechanisms, including gene amplification. In this study, we aimed to investigate amplification status adeno- squamous cell carcinomas of the lung. We propose clearly defined scores provide epidemiologic data on cancer.We evaluated prevalence increased copy numbers 693 treatment-naïve cancers FISH, clear cutoff...

10.1158/1078-0432.ccr-14-0450 article EN Clinical Cancer Research 2014-12-10

Inflammatory fibroid polyps (IFPs) are mesenchymal tumours which arise in the submucosa and mucosa of gastrointestinal tract. To date, pathogenesis is unknown IFPs considered reactive non-neoplastic lesions. Investigating a series 23 IFPs, we made observation that consistently express PDGFRA. further elucidate pathogenetic role PDGFRA, performed mutational analyses exons 10, 12, 14, 18. As characterized by an inflammatory infiltrate rich eosinophils, used fluorescence situ hybridization...

10.1002/path.2393 article EN The Journal of Pathology 2008-06-13

Abstract Purpose: Although the mutational status in gastrointestinal stromal tumors (GIST) can predict response to treatment with tyrosine kinase inhibitors, role of tumor genotype as a prognostic factor remains controversial. The ConticaGIST study sought determine pathologic and molecular factors associated disease-free survival (DFS) patients operable, imatinib-naive GIST. Experimental Design: Clinicopathologic data from 1,056 localized GIST who underwent surgery curative intention (R0/R1)...

10.1158/1078-0432.ccr-14-1677 article EN Clinical Cancer Research 2014-10-08

Residual tumor cells remain beyond the margins of every glioblastoma (GBM) resection. Their resistance to postsurgical therapy is considered a major driving force mortality, but their biology remains largely uncharacterized. In this study, residual were derived via experimental biopsy resection margin after standard neurosurgery for direct comparison with samples from routinely resected tissue. vitro analysis proliferation, invasion, stem cell qualities, GBM-typical antigens, genotypes, and...

10.1002/ana.22036 article EN Annals of Neurology 2010-04-07

The first evaluation of pelvic extended lymph node dissection (pLND) in oligometastatic prostate cancer (PCa) detected by (68)Ga-PSMA PET/CT.Retrospective analysis 35 PCa patients underwent PET/CT affected biochemical recurrence (BCR) after curative treatment (n = 23) or before primary therapy high-risk 12). We performed pLND associated with pathologic imaging 17 men nodal PCa.Indicative lesions for were 91.4% (32 35) patients. Nodal, bone, visceral (pulmonary), and within the suspected...

10.1002/pros.23091 article EN The Prostate 2015-09-10

We recently reported fibroblast growth factor receptor-type 1 (FGFR1) amplification to be associated with therapeutically tractable FGFR1 dependency in squamous cell lung cancer. This makes a novel target for directed therapy these tumors. To reproducibly identify patients clinical studies, we developed standardized reading and evaluation strategy fluorescence in-situ hybridization (FISH) propose criteria, describe different patterns of low- high-level amplifications report on the prevalence...

10.1038/modpathol.2012.102 article EN cc-by-nc-nd Modern Pathology 2012-06-08

Fibroblast activation protein (FAP) is overexpressed in several solid tumors and therefore represents an attractive target for radiotheranostic applications. Recent investigations demonstrated rapid high uptake of small-molecule inhibitors FAP (68Ga-FAPI-46) PET imaging. Here, we report our initial experience the feasibility safety 90Y-FAPI-46 radioligand therapy extensively pretreated patients with tumors. Methods: Patients were considered if they showed both exhaustion all approved...

10.2967/jnumed.121.262468 article EN Journal of Nuclear Medicine 2021-08-12

<b>Introduction:</b> Bone and soft tissue sarcomas express fibroblast activation protein (FAP) on tumor cells associated fibroblast. Therefore, FAP is a promising therapeutic diagnostic target. Novel radio-labelled FAP-Inhibitors (e.g. <sup>68</sup>Ga-FAPI46) have shown high uptake in positron emission tomography (PET) sarcoma patients. Here we report endpoints of the FAPI-PET prospective observational trial. <b>Methods:</b> Forty-seven patients with bone or undergoing clinical...

10.2967/jnumed.121.262096 article EN Journal of Nuclear Medicine 2021-04-30

Performance of the new CE-IVD-marked HercepTest™ mAb pharmDx (Dako Omnis) assay (HercepTest (mAb)) was compared against PATHWAY® anti-HER-2/neu (4B5) (PATHWAY 4B5) using 119 pre-selected breast cancer samples covering entire range HER2 immunohistochemistry (IHC) expression scores (0, 1 + , 2 3 +). The sensitivity and specificity both assays were assessed based on consensus IHC amplification status, as determined by fluorescence in situ hybridization (FISH) according to 2018 ASCO/CAP testing...

10.1007/s00428-022-03378-5 article EN cc-by Virchows Archiv 2022-08-16

(1) Colorectal cancer (CRC) is a leading cause of cancer-related deaths globally. Cancer-associated fibroblasts (CAFs) are major components CRC’s tumour microenvironment (TME), but their biological background and interplay with the TME remain poorly understood. This study investigates CAF biology its impact on CRC progression. (2) The cohort comprises 155 cases, including CRC, diverse localizations, adenomas, inflammations, controls. Digital gene expression analysis examines genes associated...

10.3390/genes15020209 article EN Genes 2024-02-06

Aims and methods: Desmoid‐type fibromatosis (desmoid) is a fibroblastic tumour that shows locally aggressive growth. Mesenteric desmoid rare lesion shares morphological biological features with fibromatoses occurring in the abdominal wall or extraabdominal sites, but differs terms of gross appearance clinical presentation. We report on series 56 cases mesenteric desmoids from our consultation files compare them non‐mesenteric retroperitoneal fibrosis. Results: Primary diagnosis desmoid‐type...

10.1111/j.1365-2559.2012.04355.x article EN Histopathology 2012-08-09
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