Use of PERCIST for prediction of progression-free and overall survival after radioembolization for liver metastases from pancreatic cancer

Marlies Michl, Sebastian Lehner, Philipp M. Paprottka, Harun Ilhan, Peter Bartenstein, Volker Heinemann, Stefan Boeck, Nathalie L. Albert, Wolfgang P. Fendler

Publikation: Beitrag in FachzeitschriftArtikelBegutachtung

22 Zitate (Scopus)

Abstract

We evaluated the prognostic accuracy of established PET response criteria in patients with liver metastases from pancreatic cancer after treatment with 90Y microspheres. Methods: Seventeen patients underwent 18F-FDG PET/CT before and 3 mo after radioembolization for liver metastases from pancreatic cancer. Overall survival, progression-free survival, and time to intrahepatic progression were among other factors correlated with metabolic response as revealed by PERCIST 1.0-defined declining SUVpeak and total-lesion glycolysis. Results: Metabolic response by change in SUVpeak (7/17) and change in total-lesion glycolysis (7/17) was a predictor for overall survival (P = 0.039; hazard ratio [HR], 0.24; 95% confidence interval [CI], 0.06-0.93), progression-free survival (P = 0.016; HR, 0.15; 95% CI, 0.03-0.69), and time to intrahepatic progression (P = 0.010; HR, 0.16; 95% CI, 0.04-0.65). A summed baseline CT diameter of less than 8 cm for the 2 largest liver metastases predicted time to intrahepatic progression (P = 0.013; HR, 0.21; 95% CI, 0.06-0.72) but did not predict overall or progression-free survival. Patient outcome was not predicted by other parameters, including baseline SUVpeak, baseline total-lesion glycolysis, or change in serum level of carcinoembryonic antigen or carbohydrate antigen 19-9 from baseline to followup (each, P > 0.05). Conclusion: Metabolic response by 18F-FDG PET/CT predicts overall survival, progression-free survival, and time to intrahepatic progression after radioembolization for liver metastases from pancreatic cancer.

OriginalspracheEnglisch
Seiten (von - bis)355-360
Seitenumfang6
FachzeitschriftJournal of Nuclear Medicine
Jahrgang57
Ausgabenummer3
DOIs
PublikationsstatusVeröffentlicht - 1 März 2016
Extern publiziertJa

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