Apparent Diffusion Coefficient (ADC) predicts therapy response in pancreatic ductal adenocarcinoma

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作者
M. Trajkovic-Arsic
I. Heid
K. Steiger
A. Gupta
A. Fingerle
C. Wörner
N. Teichmann
S. Sengkwawoh-Lueong
P. Wenzel
A. J. Beer
I. Esposito
R. Braren
J. T. Siveke
机构
[1] Division of Solid Tumor Translational Oncology,
[2] West German Cancer Center,undefined
[3] University Hospital Essen,undefined
[4] German Cancer Consortium (DKTK,undefined
[5] partner site Essen) and German Cancer Research Center (DKFZ),undefined
[6] Institute of Radiology,undefined
[7] Klinikum Rechts der Isar,undefined
[8] Technical University of Munich,undefined
[9] Institute of Pathology,undefined
[10] TUM School of Medicine,undefined
[11] Technical University of Munich,undefined
[12] 2. Medizinische Klinik,undefined
[13] Klinikum Rechts der Isar,undefined
[14] Technical University of Munich,undefined
[15] Department of Nuclear Medicine,undefined
[16] Klinikum Rechts der Isar,undefined
[17] Technical University of Munich,undefined
[18] Department of Nuclear Medicine,undefined
[19] University Hospital of Ulm,undefined
[20] Institute of Pathology,undefined
[21] University Clinic Duesseldorf,undefined
[22] Heinrich-Heine University,undefined
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摘要
Recent advances in molecular subtyping of Pancreatic Ductal Adenocarcinoma (PDAC) support individualization of therapeutic strategies in this most aggressive disease. With the emergence of various novel therapeutic strategies and neoadjuvant approaches in this quickly deteriorating disease, robust approaches for fast evaluation of therapy response are urgently needed. To this aim, we designed a preclinical imaging-guided therapy trial where genetically engineered mice harboring endogenous aggressive PDAC were treated with the MEK targeting drug refametinib, which induces rapid and profound tumor regression in this model system. Multi-parametric non-invasive imaging was used for therapy response monitoring. A significant increase in the Diffusion-Weighted Magnetic Resonance Imaging derived Apparent Diffusion Coefficient (ADC) was noted already 24 hours after treatment onset. Histopathological analyses showed increased apoptosis and matrix remodeling at this time point. Our findings suggest the ADC parameter as an early predictor of therapy response in PDAC.
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