Jürgen Frank Schäfer

Prof. Dr. Jürgen Frank Schäfer

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Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

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

Representative Publications

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1 August 2004 in Radiology
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Journal Article
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JSJürgen Frank Schäfer
Jürgen Frank Schäfer
JVJoachim Vollmar
Joachim Vollmar
FSFritz Schick
Fritz Schick
RVReinhard Vonthein
Reinhard Vonthein
MSMarcus D. Seemann
Marcus D. Seemann
CCClaus D. Claussen
Claus D. Claussen
PURPOSE: To determine whether dynamic contrast material–enhanced magnetic resonance (MR) imaging with use of kinetic and morphologic parameters reveals statistically significant differences between malignant and benign solitary pulmonary nodules. MATERIALS AND METHODS: Fifty-eight patients met the inclusion criteria of a solitary 5–40-mm pulmonary nodule without calcification or fat at computed tomography. Fifty-one patients were examined successfully; 46 received a histologic diagnosis, and five received a diagnosis by means of observation over 2 years. Dynamic MR images were acquired every 10 seconds for a total of 4 minutes. Diagnostic characteristics for differentiation were examined by using threshold values for maximum peak enhancement, slope of enhancement, and washout. Receiver operating characteristic curves were calculated to test the usefulness of these parameters. The diagnostic performance of a combination of curve profiles and morphologic contrast material distribution were tested by using a...

10 June 2023 in Journal of Clinical Oncology
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Journal Article
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TFTim Flaadt
Tim Flaadt
RLRuth Ladenstein
Ruth Ladenstein
MEMartin Ebinger
Martin Ebinger
Holger N. LodeHolger N. Lode
Holger N. Lode
HAHelga Björk Arnardóttir
Helga Björk Arnardóttir
Peter LangPeter Lang
Peter Lang
PURPOSE: Patients with relapsed high-risk neuroblastoma (rHR-NB) have a poor prognosis. We hypothesized that graft-versus-neuroblastoma effects could be elicited by transplantation of haploidentical stem cells (haplo-SCT) exploiting cytotoxic functions of natural killer cells and their activation by the anti-GD2 antibody dinutuximab beta (DB). This phase I/II trial assessed safety, feasibility, and outcomes of immunotherapy with DB plus subcutaneous interleukin-2 (scIL2) after haplo-SCT in patients with rHR-NB.METHODS: Patients age 1-21 years underwent T-/B-cell–depleted haplo-SCT followed by DB and scIL2. The primary end point ‘success of treatment’ encompassed patients receiving six cycles, being alive 180 days after end of trial treatment without progressive disease, unacceptable toxicity, acute graft-versus-host-disease (GvHD) ≥grade 3, or extensive chronic GvHD.RESULTS: Seventy patients were screened, and 68 were eligible for immunotherapy. Median number of DB cycles was 6 (range, 1-9). Median number of scIL2 cycles was 3 (1−6). The primary end point was met by 37 patients (54.4%). Median observation time was 7.8 years. Five-year event-free survival (EFS) and overall survival from start of trial treatment were 43% (95% CI, 31 to 55) and 53% (95% CI, 41 to 65), respectively. Five-year EFS among patients in complete remission (CR; 52%; 95% CI, 31 to 69) or partial remission (44%; 95% CI, 27 to 60) before immunotherapy were significantly better compared with patients with nonresponse/mixed response/progressive disease (13%; 95% CI, 1 to 42; P = .026). Overall response rate in 43 patients with evidence of disease after haplo-SCT was 51% (22 patients), with 15 achieving CR (35%). Two patients developed GvHD grade 2 and 3 each. No unexpected adverse events occurred.CONCLUSION: DB therapy after haplo-SCT in patients with rHR-NB is feasible, with low risk of inducing GvHD, and results in long-term remissions likely attributable to increased antineuroblastoma activity by donor-derived effector cells.

19 April 2006 in European Radiology
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JSJürgen Frank Schäfer
Jürgen Frank Schäfer
HSHeinz-Peter W. Schlemmer
Heinz-Peter W. Schlemmer

28 May 2020 in Pediatric Radiology
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Journal Article
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JSJürgen Frank Schäfer
Jürgen Frank Schäfer
CGClaudio Granata
Claudio Granata
TKThekla von Kalle
Thekla von Kalle
MKMartin Kyncl
Martin Kyncl
ALAnnemieke S. Littooij
Annemieke S. Littooij
OEOn Behalf Of The Oncology Task Force Of The Espr
On Behalf Of The Oncology Task Force Of The Espr
The purpose of this recommendation of the Oncology Task Force of the European Society of Paediatric Radiology (ESPR) is to indicate reasonable applications of whole-body MRI in children with cancer and to address useful protocols to optimize workflow and diagnostic performance. Whole-body MRI as a radiation-free modality has been increasingly performed over the last two decades, and newer applications, as in screening of children with germ-line mutation cancer-related gene defects, are now widely accepted. We aim to provide a comprehensive outline of the diagnostic value for use in daily practice. Based on the results of our task force session in 2018 and the revision in 2019 during the ESPR meeting, we summarized our group’s experiences in whole-body MRI. The lack of large evidence by clinical studies is challenging when focusing on a balanced view regarding the impact of whole-body MRI in pediatric oncology. Therefore, the final version of this recommendation was supported by the members of Oncology Task Force.

31 July 2006 in Lung Cancer
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JSJürgen Frank Schäfer
Jürgen Frank Schäfer
VSVincent Schneider
Vincent Schneider
JVJoachim Vollmar
Joachim Vollmar
MWManfred Wehrmann
Manfred Wehrmann
HAHermann Aebert
Hermann Aebert
CCClaus D. Claussen
Claus D. Claussen

5 May 2020 in Radiology
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Journal Article
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ATAshok J. Theruvath
Ashok J. Theruvath
FSFlorian Siedek
Florian Siedek
AMAnne M. Muehe
Anne M. Muehe
JGJordi Garcia-Diaz
Jordi Garcia-Diaz
JKJulian Kirchner
Julian Kirchner
HDHeike E Daldrup-Link
Heike E Daldrup-Link
Our data showed significant agreement between response assessments at whole-body diffusion-weighted MRI and fluorine 18 fluorodeoxyglucose PET/MRI after induction chemotherapy; the agreement after ... Background Whole-body diffusion-weighted (DW) MRI can help detect cancer with high sensitivity. However, the assessment of therapy response often requires information about tumor metabolism, which ...