Oncology: State-of-the-Art Research in Austria

A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Cancer Therapy".

Deadline for manuscript submissions: 31 May 2025 | Viewed by 2576

Special Issue Editors


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Guest Editor
1. Karl Landsteiner University of Health Sciences, Dr. Karl-Dorrek-Straße 30, 3500 Krems, Austria
2. Department of General and Thoracic Surgery, University Hospital Krems, Mitterweg 10, 3500 Krems, Austria
Interests: thoracic surgery; solitary fibrous tumor; mesothelioma; lung cancer; orphan disease biomarker
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Guest Editor
Division of Thoracic Surgery, Department of Surgery, Comprehensive Cancer Centre Vienna, Medical University Vienna, 1090 Vienna, Austria
Interests: thoracic oncology; minimal invasive and robotic oncologic surgery interventional bronchoscopy; lung cancer ; pleural mesothelioma; lung metastasis; cancer staging; cancer biology
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Special Issue Information

Dear Colleagues,

Cancer remains one of the leading causes of death worldwide. Austrian scientists were among the pioneers in cancer research, and today, the scientific output of our small country is internationally acknowledged. Furthermore, the clinical outcome of cancer patients in our country is among the best worldwide, and thus Austrian clinicians and scientists can look back on a great history and forward to a promising future. In the present Special Issue, we want to focus on modern Austrian cancer research in times of personalized and multimodal medicine. Nationwide and international collaborations will be our focus. All types of research, from basic to translational to clinical, as well as relevant review articles summarizing state-of-the-art knowledge, are welcome for submission. The full spectrum of cancer research and malignant diseases will be considered for publication. Also, historic articles looking back to the past of Austrian cancer research are welcome for submission. This Special Issue provides a platform to present the high quality of research and standard of care for the Austrian cancer research community.

Dr. Bahil Ghanim
Dr. Mir Alireza Hoda
Guest Editors

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Keywords

  • oncology
  • cancer
  • research
  • tumor
  • Austria

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Published Papers (2 papers)

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Research

11 pages, 1096 KiB  
Article
Overexpression of Fibroblast Growth Factor 8 Is a Predictor of Impaired Survival in Esophageal Squamous Cell Carcinoma and Correlates with ALK/EML4 Alteration
by Gerd Jomrich, Dagmar Kollmann, Winny Yan, Daniel Winkler, Matthias Paireder, Lisa Gensthaler, Hannah Christina Puhr, Aysegül Ilhan-Mutlu, Reza Asari and Sebastian F. Schoppmann
Cancers 2024, 16(21), 3624; https://doi.org/10.3390/cancers16213624 - 27 Oct 2024
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Abstract
FGF8, ALK, and EML4 have been identified as promising biomarkers in a number of malignancies. The aim of this study was to examine the prognostic role of FGF8, ALK, and EML4 in esophageal squamous cell carcinoma (ESCC). Methods: Consecutive patients with ESCC who [...] Read more.
FGF8, ALK, and EML4 have been identified as promising biomarkers in a number of malignancies. The aim of this study was to examine the prognostic role of FGF8, ALK, and EML4 in esophageal squamous cell carcinoma (ESCC). Methods: Consecutive patients with ESCC who underwent upfront resection were included in this study. ALK and EML4 gene status was evaluated by fluorescence in situ hybridization (FISH) using a triple-color break-apart single-fusion probe and a probe against 2p11. FGF8, ALK, and EML4 protein expression was determined by immunohistochemistry. Results: A total of 122 patients were included in this study. Multivariate analysis revealed that FGF8 overexpression is an independent negative prognostic factor for patients’ overall survival (OS) (p = 0.04). Furthermore, a significant correlation between the expression of FGF8, and ALK (p = 0.04) and EML4 (p = 0.01) alteration was found. Conclusions: FGF8 overexpression is an adverse independent prognostic factor in patients with upfront resected ESCC. Furthermore, FGF8 expression significantly correlates with ALK and EML4 amplification and may therefore qualify as a future therapeutic target. Full article
(This article belongs to the Special Issue Oncology: State-of-the-Art Research in Austria)
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20 pages, 2539 KiB  
Article
Real-World Treatment Patterns and Timeliness of Clinical Care Pathway for Non-Small Cell Lung Cancer Patients in Austria: The PRATER Retrospective Study
by Maximilian Hochmair, Angelika Terbuch, David Lang, Christian Trockenbacher, Florian Augustin, Bahil Ghanim, Dominik Maurer, Hossein Taghizadeh, Christoph Kamhuber, Robert Wurm, Jörg Lindenmann, Petra Braz, Tatjana Bundalo, Merjem Begic, Johanna Bauer, Patrick Reimann, Nino Müser, Florian Huemer, Verena Schlintl, Daniela Bianconi, Bernhard Baumgartner, Peter Schenk, Markus Rauter and Konrad Hötzeneckeradd Show full author list remove Hide full author list
Cancers 2024, 16(14), 2586; https://doi.org/10.3390/cancers16142586 - 19 Jul 2024
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Abstract
This was a retrospective study of the profile and initial treatments of adults diagnosed with early-stage (ES) non-small cell lung cancer (NSCLC) during January 2018–December 2021 at 16 leading hospital institutions in Austria, excluding patients enrolled in clinical trials. In total, 319 patients [...] Read more.
This was a retrospective study of the profile and initial treatments of adults diagnosed with early-stage (ES) non-small cell lung cancer (NSCLC) during January 2018–December 2021 at 16 leading hospital institutions in Austria, excluding patients enrolled in clinical trials. In total, 319 patients were enrolled at a planned ~1:1:1 ratio across StI:II:III. Most tested biomarkers were programmed death ligand 1 (PD-L1; 58% expressing), Kirsten rat sarcoma virus (KRAS; 22% positive), and epidermal growth factor receptor (EGFR; 18% positive). Of 115/98/106 StI/II/III patients, 82%/85%/36% underwent surgery, followed by systemic therapy in 9%/45%/47% of those [mostly chemotherapy (ChT)]. Unresected treated StIII patients received ChT + radiotherapy [43%; followed by immune checkpoint inhibitors (ICIs) in 39% of those], ICI ± ChT (35%), and ChT-alone/radiotherapy-alone (22%). Treatment was initiated a median (interquartile range) of 24 (7–39) days after histological confirmation, and 55 (38–81) days after first medical visit. Based on exploratory analyses of all patients newly diagnosed with any stage NSCLC during 2018–2021 at 14 of the sites (N = 7846), 22%/10%/25%/43% had StI/II/III/IV. The total number was not significantly different between pre-COVID-19 (2018–2019) and study-specific COVID-19 (2020–2021) periods, while StI proportion increased (21% vs. 23%; p = 0.012). Small differences were noted in treatments. In conclusion, treatments were aligned with guideline recommendations at a time which preceded the era of ICIs and targeted therapies in the (neo)adjuvant setting. Full article
(This article belongs to the Special Issue Oncology: State-of-the-Art Research in Austria)
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