Fritz Sörgel

Fritz Sörgel


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2019 in Journal of Pharmaceutical and Biomedical Analysis
Verified
Journal Article
Closed access
FSFritz Sörgel
Fritz Sörgel
MKMartina Kinzig
Martina Kinzig
MAMona Abdel-Tawab
Mona Abdel-Tawab
CBClemens Bidmon
Clemens Bidmon
ASAndré Schreiber
André Schreiber
UHUlrike Holzgrabe
Ulrike Holzgrabe

1 December 2010 in BioDrugs
Verified
Journal Article
Closed access
PDF file
FSFritz Sörgel
Fritz Sörgel
HLHelmut Lerch
Helmut Lerch
TLThomas Lauber
Thomas Lauber

1 August 2019 in Journal of Pharmaceutical and Biomedical Analysis
Verified
Journal Article
Closed access
OSOliver ScherfClavel
Oliver ScherfClavel
MKMartina Kinzig
Martina Kinzig
ABAxel Besa
Axel Besa
ASAndré Schreiber
André Schreiber
CBClemens Bidmon
Clemens Bidmon
UHUlrike Holzgrabe
Ulrike Holzgrabe

3 April 2015 in BioDrugs
Verified
Journal Article
Open access
PDF file
FSFritz Sörgel
Fritz Sörgel
ASArnd Schwebig
Arnd Schwebig
JHJohann Holzmann
Johann Holzmann
SPStefan Prasch
Stefan Prasch
PSPritibha Singh
Pritibha Singh
MKMartina Kinzig
Martina Kinzig
Biosimilars provide safety, purity, and potency similar to those of a reference biologic product.

21 November 2019 in Journal of Clinical Medicine
Verified
Journal Article
Open access
PDF file
PZPia S. Zeiner
Pia S. Zeiner
MKMartina Kinzig
Martina Kinzig
IDIris Divé
Iris Divé
GMGabriele Maurer
Gabriele Maurer
KFKatharina Filipski
Katharina Filipski
MRMichael W. Ronellenfitsch
Michael W. Ronellenfitsch
(1) Background: The phase 2 Regorafenib in Relapsed Glioblastoma (REGOMA) trial indicated a survival benefit for patients with first recurrence of a glioblastoma when treated with the multikinase inhibitor regorafenib (REG) instead of lomustine. The aim of this retrospective study was to investigate REG penetration to cerebrospinal fluid (CSF), treatment efficacy, and effects on magnetic resonance imaging (MRI) in patients with recurrent high-grade gliomas. (2) Methods: Patients were characterized by histology, adverse events, steroid treatment, overall survival (OS), and MRI growth pattern. REG and its two active metabolites were quantified by liquid chromatography/tandem mass spectrometry in patients’ serum and CSF. (3) Results: 21 patients mainly with IDH-wildtype glioblastomas who had been treated with REG were retrospectively identified. Thirteen CFS samples collected from 3 patients of the cohort were available for pharmacokinetic testing. CSF levels of REG and its metabolites were significantly lower than in serum. Follow-up MRI was available in 19 patients and showed progressive disease (PD) in all but 2 patients. Two distinct MRI patterns were identified: 7 patients showed classic PD with progression of contrast enhancing lesions, whereas 11 patients showed a T2-dominant MRI pattern characterized by a marked reduction of contrast enhancement. Median OS was significantly better in patients with a T2-dominant growth pattern (10 vs. 27 weeks respectively, p = 0.003). Diffusion restrictions were observed in 13 patients. (4) Conclusion: REG and its metabolites were detectable in CSF. A distinct MRI pattern that might be associated with an improved OS was observed in half of the patient cohort. Treatment response in the total cohort was poor.

24 May 2020 in ACS Pharmacology & Translational Science
Verified
Journal Article
Closed access
Cornelia B. LandersdorferCornelia B. Landersdorfer
Cornelia B. Landersdorfer
MKMartina Kinzig
Martina Kinzig
RHRainer Höhl
Rainer Höhl
PKPeter Kempf
Peter Kempf
RNRoger L. Nation
Roger L. Nation
FSFritz Sörgel
Fritz Sörgel