Martin T. Freitag

Martin T. Freitag

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Martin T. Freitag

Department of Nuclear Medicine, Medical Center—University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

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28 October 2015 in European Journal of Nuclear Medicine and Molecular Imaging
Verified
Journal Article
Closed access
PDF file
MFMartin T. Freitag
Martin T. Freitag
JRJan P. Radtke
Jan P. Radtke
BHBoris A. Hadaschik
Boris A. Hadaschik
AKA. Kopp-Schneider
A. Kopp-Schneider
MEMatthias Eder
Matthias Eder
AAAli Afshar-Oromieh
Ali Afshar-Oromieh

17 December 2016 in European Journal of Nuclear Medicine and Molecular Imaging
Verified
Journal Article
Closed access
PDF file
MFMartin T. Freitag
Martin T. Freitag
JRJan P. Radtke
Jan P. Radtke
AAAli Afshar-Oromieh
Ali Afshar-Oromieh
MRMatthias C. Roethke
Matthias C. Roethke
BHBoris A. Hadaschik
Boris A. Hadaschik
Antonia Dimitrakopoulou-StraussAntonia Dimitrakopoulou-Strauss
Antonia Dimitrakopoulou-Strauss

17 August 2017 in PLOS ONE
Verified
Journal Article
Open access
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THThorsten Heußer
Thorsten Heußer
PMPhilipp Mann
Philipp Mann
CRChristopher M. Rank
Christopher M. Rank
MSMartin Schäfer
Martin Schäfer
Antonia Dimitrakopoulou-StraussAntonia Dimitrakopoulou-Strauss
Antonia Dimitrakopoulou-Strauss
MFMartin T. Freitag
Martin T. Freitag
Combined positron emission tomography (PET) and magnetic resonance imaging (MRI) targeting the prostate-specific membrane antigen (PSMA) with a 68Ga-labelled PSMA-analog (68Ga-PSMA-11) is discussed as a promising diagnostic method for patients with suspicion or history of prostate cancer. One potential drawback of this method are severe photopenic (halo-) artifacts surrounding the bladder and the kidneys in the scatter-corrected PET images, which have been reported to occur frequently in clinical practice. The goal of this work was to investigate the occurrence and impact of these artifacts and, secondly, to evaluate variants of the standard scatter correction method with regard to halo-artifact suppression. Experiments using a dedicated pelvis phantom were conducted to investigate whether the halo-artifact is modality-, tracer-, and/or concentration-dependent. Furthermore, 31 patients with history of prostate cancer were selected from an ongoing 68Ga-PSMA-11-PET/MRI study. For each patient, PET raw data were reconstructed employing six different variants of PET scatter correction: absolute scatter scaling, relative scatter scaling, and relative scatter scaling combined with prompt gamma correction, each of which was combined with a maximum scatter fraction (MaxSF) of MaxSF = 75% or MaxSF = 40%. Evaluation of the reconstructed images with regard to halo-artifact suppression was performed both quantitatively using statistical analysis and qualitatively by two independent readers. The phantom experiments did not reveal any modality-dependency (PET/MRI vs. PET/CT) or tracer-dependency (68Ga vs. 18F-FDG). Patient- and phantom-based data indicated that halo-artifacts derive from high organ-to-background activity ratios (OBR) between bladder/kidneys and surrounding soft tissue, with a positive correlation between OBR and halo size. Comparing different variants of scatter correction, reducing the maximum scatter fraction from the default value MaxSF = 75% to MaxSF = 40% was found to efficiently suppress halo-artifacts in both phantom and patient data. In 1 of 31 patients, reducing the maximum scatter fraction provided new PET-based information changing the patient’s diagnosis. Halo-artifacts are particularly observed for 68Ga-PSMA-11-PET/MRI due to 1) the biodistribution of the PSMA-11-tracer resulting in large OBRs for bladder and kidneys and 2) inaccurate scatter correction methods currently used in clinical routine, which tend to overestimate the scatter contribution. If not compensated for, 68Ga-PSMA-11 uptake pathologies may be masked by halo-artifacts leading to false-negative diagnoses. Reducing the maximum scatter fraction was found to efficiently suppress halo-artifacts.

16 October 2017 in European Journal of Nuclear Medicine and Molecular Imaging
Verified
Journal Article
Closed access
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MFMartin T. Freitag
Martin T. Freitag
CKClaudia Kesch
Claudia Kesch
JCJens Cardinale
Jens Cardinale
PFPaul Flechsig
Paul Flechsig
RFRalf Floca
Ralf Floca
FGFrederik Giesel
Frederik Giesel

1 March 2017 in EJNMMI Physics
Verified
Journal Article
Open access
PDF file
THThorsten Heußer
Thorsten Heußer
CRChristopher M. Rank
Christopher M. Rank
Yannick BerkerYannick Berker
Yannick Berker
MFMartin T. Freitag
Martin T. Freitag
MKMarc Kachelrieß
Marc Kachelrieß
Accurate PET quantification demands attenuation correction (AC) for both patient and hardware attenuation of the 511 keV annihilation photons. In hybrid PET/MR imaging, AC for stationary hardware components such as patient table and MR head coil is straightforward, employing CT-derived attenuation templates. AC for flexible hardware components such as MR-safe headphones and MR radiofrequency (RF) surface coils is more challenging. Registration-based approaches, aligning CT-based attenuation templates with the current patient position, have been proposed but are not used in clinical routine. Ignoring headphone or RF coil attenuation has been shown to result in regional activity underestimation values of up to 18%. We propose to employ the maximum-likelihood reconstruction of attenuation and activity (MLAA) algorithm to estimate the attenuation of flexible hardware components. Starting with an initial attenuation map not including flexible hardware components, the attenuation update of MLAA is applied outside the body outline only, allowing to estimate hardware attenuation without modifying the patient attenuation map. Appropriate prior expectations on the attenuation coefficients are incorporated into MLAA. The proposed method is investigated for non-TOF PET phantom and 18F-FDG patient data acquired with a clinical PET/MR device, using headphones or RF surface coils as flexible hardware components. Although MLAA cannot recover the exact physical shape of the hardware attenuation maps, the overall attenuation of the hardware components is accurately estimated. Therefore, the proposed algorithm significantly improves PET quantification. Using the phantom data, local activity underestimation when neglecting hardware attenuation was reduced from up to 25% to less than 3% under- or overestimation as compared to reference scans without hardware present or to CT-derived AC. For the patient data, we found an average activity underestimation of 7.9% evaluated in the full brain and of 6.1% for the abdominal region comparing the uncorrected case with MLAA. MLAA is able to provide accurate estimations of the attenuation of flexible hardware components and can therefore be used to significantly improve PET quantification. The proposed approach can be readily incorporated into clinical workflow.

1 November 2017 in European Journal of Radiology
Verified
Journal Article
Closed access
MFMartin T. Freitag
Martin T. Freitag
MFMatthias Fenchel
Matthias Fenchel
PBPhilipp Bäumer
Philipp Bäumer
THThorsten Heußer
Thorsten Heußer
CRChristopher M. Rank
Christopher M. Rank
FMFlorian Maier
Florian Maier