Multimodality Imaging to Predict Response to Systemic Treatment in Patients with Advanced Colorectal Cancer

被引:30
作者
Heijmen, Linda [1 ,2 ]
ter Voert, Edwin E. G. W. [2 ]
Oyen, Wim J. G. [2 ]
Punt, Cornelis J. A. [3 ]
van Spronsen, Dick Johan [4 ]
Heerschap, Arend [2 ]
de Geus-Oei, Lioe-Fee [2 ,5 ]
van Laarhoven, Hanneke W. M. [1 ,3 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Med Oncol, NL-6525 ED Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Dept Radiol & Nucl Med, NL-6525 ED Nijmegen, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Dept Med Oncol, Nijmegen, Netherlands
[4] Canisius Wilhelmina Hosp, Dept Med Oncol, Nijmegen, Netherlands
[5] Univ Twente, MIRA Inst Biomed Technol & Tech Med, NL-7500 AE Enschede, Netherlands
关键词
DIFFUSION-WEIGHTED MRI; LIVER METASTASES; TUMOR RESPONSE; F-18-FDG PET; FDG-PET/CT; CHEMOTHERAPY; BEVACIZUMAB; GRADE;
D O I
10.1371/journal.pone.0120823
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Aim Aim of this study was to investigate the potential of F-18-FDG PET, diffusion weighted imaging (DWI) and susceptibility-weighted (T2*) MRI to predict response to systemic treatment in patients with colorectal liver metastases. The predictive values of pretreatment measurements and of early changes one week after start of therapy, were evaluated. Methods Imaging was performed prior to and one week after start of first line chemotherapy in 39 patients with colorectal liver metastases. F-18-FDG PET scans were performed on a PET/CT scanner and DWI and T2* were performed on a 1.5T MR scanner. The maximum standardized uptake values (SUV), total lesion glycolysis (TLG), apparent diffusion coefficient (ADC) and T2* value were assessed in the same lesions. Up to 5 liver metastases per patient were analyzed. Outcome measures were progression free survival (PFS), overall survival (OS) and size response. Results Pretreatment, high SUVmax, high TLG, low ADC and high T2* were associated with a shorter OS. Low pretreatment ADC value was associated with shorter PFS. After 1 week a significant drop in SUVmax and rise in ADC were observed. The drop in SUV was correlated with the rise in ADC (r=-0.58, p=0.002). Neither change in ADC nor in SUV was predictive of PFS or OS. T2* did not significantly change after start of treatment. Conclusion Pretreatment SUVmax, TLG, ADC, and T2* values in colorectal liver metastases are predictive of patient outcome. Despite sensitivity of DWI and F-18-FDG PET for early treatment effects, change in these parameters was not predictive of long term outcome.
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