Heribert Schmitt-Willich
Bayer HealthCare Pharmaceuticals
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Heribert Schmitt-Willich.
PLOS ONE | 2016
Erik Mittra; Norman Koglin; Camila Mosci; Meena Kumar; Aileen Hoehne; Khun Visith Keu; Andrei Iagaru; Andre Mueller; Mathias Berndt; Santiago Bullich; Matthias Friebe; Heribert Schmitt-Willich; Volker Gekeler; Luder Fels; Claudia Bacher-Stier; Dae Hyuk Moon; Frederick T. Chin; Andrew Stephens; Ludger Dinkelborg; Sanjiv S. Gambhir
Purpose (S)-4-(3-[18F]Fluoropropyl)-L-glutamic acid (18F-FSPG) is a novel radiopharmaceutical for Positron Emission Tomography (PET) imaging. It is a glutamate analogue that can be used to measure xC- transporter activity. This study was performed to assess the feasibility of 18F-FSPG for imaging orthotopic brain tumors in small animals and the translation of this approach in human subjects with intracranial malignancies. Experimental Design For the small animal study, GS9L glioblastoma cells were implanted into brains of Fischer rats and studied with 18F-FSPG, the 18F-labeled glucose derivative 18F-FDG and with the 18F-labeled amino acid derivative 18F-FET. For the human study, five subjects with either primary or metastatic brain cancer were recruited (mean age 50.4 years). After injection of 300 MBq of 18F-FSPG, 3 whole-body PET/Computed Tomography (CT) scans were obtained and safety parameters were measured. The three subjects with brain metastases also had an 18F-FDG PET/CT scan. Quantitative and qualitative comparison of the scans was performed to assess kinetics, biodistribution, and relative efficacy of the tracers. Results In the small animals, the orthotopic brain tumors were visualized well with 18F-FSPG. The high tumor uptake of 18F-FSPG in the GS9L model and the absence of background signal led to good tumor visualization with high contrast (tumor/brain ratio: 32.7). 18F-FDG and 18F-FET showed T/B ratios of 1.7 and 2.8, respectively. In the human pilot study, 18F-FSPG was well tolerated and there was similar distribution in all patients. All malignant lesions were positive with 18F-FSPG except for one low-grade primary brain tumor. In the 18F-FSPG-PET-positive tumors a similar T/B ratio was observed as in the animal model. Conclusions 18F-FSPG is a novel PET radiopharmaceutical that demonstrates good uptake in both small animal and human studies of intracranial malignancies. Future studies on larger numbers of subjects and a wider array of brain tumors are planned. Trial Registration ClinicalTrials.gov NCT01186601
Archive | 2009
Ananth Srinivasan; Mathias Berndt; Keith Graham; Matthias Friebe; Heribert Schmitt-Willich
Archive | 2009
Ludger Dinkelborg; Heribert Schmitt-Willich; Keith Graham; Norman Koglin; Mathias Berndt; Matthias Friebe; Andre Müller
Archive | 2006
Heiko Schirmer; Hanns-Joachim Weinmann; Johannes Platzek; Ludwig Zorn; Bernd Misselwitz; Joerg Meding; Heribert Schmitt-Willich; Thomas Brumby
Archive | 2002
Johannes Platzek; Heribert Schmitt-Willich; Günther Michl; Thomas Frenzel; Detlev Sülzle; Hans Bauer; Bernd Radüchel; Hanns-Joachim Weinmann; Heiko Schirmer
Archive | 1996
Thomas Frenzel; Andreas Mühler; Johannes Platzek; Bernd Radüchel; Heribert Schmitt-Willich
Archive | 2014
Ludger Dinkelborg; Heribert Schmitt-Willich; Keith Graham; Norman Koglin; Mathias Berndt; Matthias Friebe; Andre Müller
Archive | 2011
Heribert Schmitt-Willich; Ulrike Röhn; Matthias Friebe; Lutz Lehmann; Ansgar Dr. Fitzner; Sabine Krause; Damian Brockschnieder; Thomas Dyrks; Andrea Thiele; Ulf Bömer; Ursula Mönning; Tobias Heinrich
Archive | 2008
Heiko Schirmer; Hanns-Joachim Weinmann; Johannes Platzek; Ludwig Zorn; Bernd Misselwitz; Jörg Meding; Heribert Schmitt-Willich; Thomas Brumby
Archive | 2011
Heribert Schmitt-Willich; Niels Böhnke; Norman Koglin; Mathias Berndt; Matthias Friebe; Andre Müller