Quantitative Assessment of Bone Metastasis in Prostate Cancer Using Synthetic Magnetic Resonance Imaging

被引:52
作者
Arita, Yuki [1 ,2 ]
Takahara, Taro [3 ]
Yoshida, Soichiro [4 ]
Kwee, Thomas C. [5 ]
Yajima, Shugo [4 ]
Ishii, Chikako [2 ]
Ishii, Ryota [6 ]
Okuda, Shigeo [1 ]
Jinzaki, Masahiro [1 ]
Fujii, Yasuhisa [4 ]
机构
[1] Keio Univ, Sch Med, Dept Diagnost Radiol, Tokyo, Japan
[2] Yaesu Clin, Adv Imaging Ctr, Dept Radiol, Tokyo, Japan
[3] Tokai Univ, Sch Engn, Dept Biomed Engn, Hiratsuka, Kanagawa, Japan
[4] Tokyo Med & Dent Univ, Grad Sch, Dept Urol, Tokyo, Japan
[5] Univ Med Ctr Groningen, Dept Radiol Nucl Med & Mol Imaging, Groningen, Netherlands
[6] Keio Univ Hosp, Clin & Translat Res Ctr, Biostat Unit, Tokyo, Japan
基金
日本学术振兴会;
关键词
magnetic resonance imaging; bone marrow; sclerosis; protons; biomarkers; RELAXATION-TIMES; PROTON-DENSITY; QUANTIFICATION; BRAIN; SURVIVAL; MRI;
D O I
10.1097/RLI.0000000000000579
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Objectives The aims of this study were to evaluate the feasibility of quantitative synthetic magnetic resonance imaging (SyMRI) for characterizing bone lesions in prostate cancer and to discriminate viable progressive osteoblastic bone metastasis from nonviable bone metastases with treatment-induced sclerosis during the treatment course. Materials and Methods This institutional review board-approved prospective study included 96 consecutive prostate cancer patients who underwent whole-body MRI including diffusion-weighted imaging at the time of staging at diagnosis or starting a new line of anticancer treatment. Additional synthetic MRI of the lumbosacral spine, pelvis, and proximal femurs was performed. A region of interest of 1.0 cm in diameter was set in each bone lesion by 2 independent readers who were blinded to bone lesions' diagnosis. Differences in SyMRI variables between the different bone lesions were compared with the Wilcoxon rank sum test, and associations of SyMRI variables with active disease were analyzed with logistic regression analysis. Performance of T1, T2, and proton density (PD) for diagnosing active disease was assessed using the area under the receiver operating characteristic curve. Results Ninety-three bone lesions were eligible for analysis. The PD values of active (viable) bone metastatic lesions were significantly higher than those of inactive (nonviable) bone metastatic lesions without sclerosis and those of red bone marrow (P < 0.001 for both readers). The PD values of inactive bone metastatic lesions with sclerosis were significantly lower than those of inactive bone metastatic lesions without sclerosis and red bone marrow (P < 0.001 for both readers). The PD value proved to be an independent significant indicator (P < 0.001) for differentiating bone lesions. The areas under the curve of T1/T2/PD for identifying active disease were 0.81/0.69/0.93 for reader 1 and 0.78/0.70/0.92 for reader 2, respectively. Conclusions Signal quantification on SyMRI provides objective assessment of bone lesions in the lower trunk. The PD value can be useful to determine the viability of bone metastases in prostate cancer.
引用
收藏
页码:638 / 644
页数:7
相关论文
共 21 条
[1]   Synthetic MRI of the brain in a clinical setting [J].
Blystad, I. ;
Warntjes, J. B. M. ;
Smedby, O. ;
Landtblom, A-M ;
Lundberg, P. ;
Larsson, E-M .
ACTA RADIOLOGICA, 2012, 53 (10) :1158-1163
[2]   Feasibility of synthetic MRI in knee imaging in routine practice [J].
Boudabbous, Sana ;
Neroladaki, Angeliki ;
Bagetakos, Ilias ;
Hamard, Marion ;
Delattre, Benedicte M. A. ;
Vargas, Maria Isabel .
ACTA RADIOLOGICA OPEN, 2018, 7 (05)
[3]   Prostate-specific antigen (PSA) as a surrogate end point for survival in prostate cancer clinical trials [J].
Collette, Laurence .
EUROPEAN UROLOGY, 2008, 53 (01) :6-9
[4]   MR imaging relaxation times of abdominal and pelvic tissues measured in vivo at 3.0 T: Preliminary results [J].
de Bazelaire, CMJ ;
Duhamel, GD ;
Rofsky, NM ;
Alsop, DC .
RADIOLOGY, 2004, 230 (03) :652-659
[5]   Chemical shift imaging: preliminary experience as an alternative sequence for defining the extent of a bone tumor [J].
Del Grande, Filippo ;
Tatizawa-Shiga, Ney ;
Farahani, Sahar Jalali ;
Chalian, Majid ;
Fayad, Laura Marie .
QUANTITATIVE IMAGING IN MEDICINE AND SURGERY, 2014, 4 (03) :173-180
[6]   Bone Scan Index: A Quantitative Treatment Response Biomarker for Castration-Resistant Metastatic Prostate Cancer [J].
Dennis, Elizabeth R. ;
Jia, Xiaoyu ;
Mezheritskiy, Irina S. ;
Stephenson, Ryan D. ;
Schoder, Heiko ;
Fox, Josef J. ;
Heller, Glenn ;
Scher, Howard I. ;
Larson, Steven M. ;
Morris, Michael J. .
JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (05) :519-524
[7]   New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1) [J].
Eisenhauer, E. A. ;
Therasse, P. ;
Bogaerts, J. ;
Schwartz, L. H. ;
Sargent, D. ;
Ford, R. ;
Dancey, J. ;
Arbuck, S. ;
Gwyther, S. ;
Mooney, M. ;
Rubinstein, L. ;
Shankar, L. ;
Dodd, L. ;
Kaplan, R. ;
Lacombe, D. ;
Verweij, J. .
EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) :228-247
[8]   Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012 [J].
Ferlay, Jacques ;
Soerjomataram, Isabelle ;
Dikshit, Rajesh ;
Eser, Sultan ;
Mathers, Colin ;
Rebelo, Marise ;
Parkin, Donald Maxwell ;
Forman, David ;
Bray, Freddie .
INTERNATIONAL JOURNAL OF CANCER, 2015, 136 (05) :E359-E386
[9]   Impact of the Site of Metastases on Survival in Patients with Metastatic Prostate Cancer [J].
Gandaglia, Giorgio ;
Karakiewicz, Pierre I. ;
Briganti, Alberto ;
Passoni, Niccolo Maria ;
Schiffmann, Jonas ;
Trudeau, Vincent ;
Graefen, Markus ;
Montorsi, Francesco ;
Sun, Maxine .
EUROPEAN UROLOGY, 2015, 68 (02) :325-334
[10]   The evolutionary history of lethal metastatic prostate cancer [J].
Gundem, Gunes ;
Van Loo, Peter ;
Kremeyer, Barbara ;
Alexandrov, Ludmil B. ;
Tubio, Jose M. C. ;
Papaemmanuil, Elli ;
Brewer, Daniel S. ;
Kallio, Heini M. L. ;
Hoegnas, Gunilla ;
Annala, Matti ;
Kivinummi, Kati ;
Goody, Victoria ;
Latimer, Calli ;
O'Meara, Sarah ;
Dawson, Kevin J. ;
Isaacs, William ;
Emmert-Buck, Michael R. ;
Nykter, Matti ;
Foster, Christopher ;
Kote-Jarai, Zsofia ;
Easton, Douglas ;
Whitaker, Hayley C. ;
Neal, David E. ;
Cooper, Colin S. ;
Eeles, Rosalind A. ;
Visakorpi, Tapio ;
Campbell, Peter J. ;
McDermott, Ultan ;
Wedge, David C. ;
Bova, G. Steven .
NATURE, 2015, 520 (7547) :353-+