Author/Authors :
Weikert, Thomas Department of Radiology - University Hospital Basel - University of Basel - Petersgraben - Basel, Switzerland , Christopher Maas, Ole Cantonal Hospital St. Gallen - Clinic of Radiology and Nuclear Medicine - Rorschacher - Gallen, Switzerland , Haas, Tanja Department of Radiology - University Hospital Basel - University of Basel - Petersgraben - Basel, Switzerland , Klarhofer, Markus Siemens Healthcare AG - Freilagerstrasse - Zurich, Switzerland , Bremerich, Jens Department of Radiology - University Hospital Basel - University of Basel - Petersgraben - Basel, Switzerland , Forrer, Flavio Cantonal Hospital St. Gallen - Clinic of Radiology and Nuclear Medicine - Rorschacher - Gallen, Switzerland , Walter Sauter, Alexander Department of Radiology - University Hospital Basel - University of Basel - Petersgraben - Basel, Switzerland , Sommer, Gregor Department of Radiology - University Hospital Basel - University of Basel - Petersgraben - Basel, Switzerland
Abstract :
The purpose of this study was to determine if parameters derived from diffusion-weighted (DW-) and dynamic contrast-enhanced
(DCE-) magnetic resonance imaging (MRI) can help to assess early response to peptide receptor radionuclide therapy (PRRT)
with 90Y-DOTATOC in neuroendocrine hepatic metastases (NET-HM). Twenty patients (10 male; 10 female; mean age: 59.2
years) with NET-HM were prospectively enrolled in this single-center imaging study. DW-MRI and DCE-MRI studies were
performed just before and 48 hours after therapy with 90Y-DOTATOC. Abdominal SPECT/CT was performed 24 hours after
therapy. This MRI imaging and therapy session was repeated after a mean interval of 10 weeks. Up to four lesions per patient were
evaluated. Response to therapy was evaluated using metastasis sizes at the first and second therapy session as standard for
comparison (regressive, stable, and progressive). DW-MRI analysis included the apparent diffusion coefficient (ADC) and
parameters related to intravoxel incoherent motion (IVIM), namely, diffusion (D), perfusion fraction (f) and pseudo-diffusion
(D∗). DCE-MRI analysis comprised Ktrans, ve and kep. For statistical analysis of group differences, one-way analysis of variance
(ANOVA) and appropriate post hoc testing was performed. A total of 51 lesions were evaluated. Seven of 51 lesions (14%) showed
size progression, 18/51 (35%) regression, and 26/51 (51%) remained stable. The lesion-to-spleen uptake ratio in SPECT showed a
decrease between the two treatment sessions that was significantly stronger in regressive lesions compared with stable (p = 0.013)
and progressive lesions (p = 0.021). ANOVA showed significant differences in mean ADC after 48 h (p = 0.026), with higher
ADC values for regressive lesions. Regarding IVIM, highest values for D at baseline were seen in regressive lesions (p = 0.023). In
DCE-MRI, a statistically significant increase in ve after 10 weeks (p = 0.046) was found in regressive lesions. No differences were
observed for the transfer constants Ktrans and kep. Diffusion restriction quantified as ADC was able to differentiate regressive from
progressive NET-HMs as early as 48 hours after PRRT. DW-MRI therefore may complement scintigraphy/SPECT for early
assessment of response to PRRT. Assessment of perfusion parameters using IVIM and DCE-MRI did not show an
additional benefit.