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B1+ field correction of T1 estimation is necessary for quantitative breast DCE MRI even at 1.5T Poster No.: B-0424 Congress: ECR 2016 Type: Scientific Paper Authors: W. Tsai, K. Kao, K. Chang, C. E. Lin; Taipei/TW Keywords: Breast, Molecular imaging, MR, Ultrasound, Technical aspects, Cancer Any information contained in this pdf file is automatically generated from digital material submitted to EPOS by third parties in the form of scientific presentations. References to any names, marks, products, or services of third parties or hypertext links to thirdparty sites or information are provided solely as a convenience to you and do not in any way constitute or imply ECR's endorsement, sponsorship or recommendation of the third party, information, product or service. ECR is not responsible for the content of these pages and does not make any representations regarding the content or accuracy of material in this file. As per copyright regulations, any unauthorised use of the material or parts thereof as well as commercial reproduction or multiple distribution by any traditional or electronically based reproduction/publication method ist strictly prohibited. You agree to defend, indemnify, and hold ECR harmless from and against any and all claims, damages, costs, and expenses, including attorneys' fees, arising from or related to your use of these pages. Please note: Links to movies, ppt slideshows and any other multimedia files are not available in the pdf version of presentations. www.myESR.org Page 1 of 8 Purpose To quantify the effect of T1 estimation in fat by B1 correction in breast MRI at 1.5T, and to examine the subsequent quantitative dynamic contrast enhanced (DCE) parameters in breast cancer with and without B1 correction. Methods and materials + B1 field and variable flip angle (VFA) mapping were included in our DCE breast MRI protocol for a total of 72 breast cancer patients on a GE 450W MR system. We computed pre-contrast T1 relaxation in fat and breast tumors with and without B1 correction. The pharmacokinetic parameters of breast cancer were calculated using Tofts model with T1 value before and after B1 correction. The mean and median of B1, T1 values and DCE parameters were used for statistical analysis. Results The flip angle (FA) in the left breast is 18.99% higher and 2.97% lower, in the right, than the prescribed value. This 21.96% average FA difference created a 43.05% T1 estimation bias in fat between the breasts. The T1 variation in fat was reduced to 0.96% after B1 correction. There is 50% overestimate and 7% underestimate of tumor T1 at the left breast and the right, respectively, associated with B1 error. Assuming T1 after B1 correction represent the true tumor T1, 41% underestimation in the left breast and 10% trans overestimation in the right without B1 correction were seen in the DCE parameters(K ve, IAUGCBN90). Images for this section: Page 2 of 8 , Fig. 1: Figure 1. a. The relative flip angle variation in percentage in the left and right breasts in 72 breast MRI patients . The dotted line is the group median value. b. Comparison of flip angle variation in left and right breast in all 72 patients using a box plot. The central mark on each box is the median, the edges of the box are the 25th (Q1) and 75th (Q3) percentiles, the upper 'whisker' is the smaller of the maximum value and Q3+1.5xIQR, and the lower whisker is the larger of the minimum value and Q1-1.5xIQR, where IQR represents the interquartile range, i.e. Q3-Q1. © Radiology, Koo Foundation Sun Yat-Sen Cancer Center - Taipei/TW Fig. 2: Figure 2. Comparison of T1 estimation in fat without (a)and with (b) correction of B1 inhomogeneity in 72 breast MRI patients. Page 3 of 8 © Radiology, Koo Foundation Sun Yat-Sen Cancer Center - Taipei/TW Fig. 3: Figure 3. Comparison of T10 estimation in breast cancer without (a)and with (b) correction of B1 inhomogeneity in 72 breast MRI patients. © Radiology, Koo Foundation Sun Yat-Sen Cancer Center - Taipei/TW Page 4 of 8 Fig. 4: Figure 4. Comparison of percentage of T1 estimation error induced percentage of estimation error in the pharmacokinetic parameters (a) Ktrans, (b) kep, (c) ve, (d) vp, (e) IAUGCBN90 in 72 patients. The red curves are equivalent to the model P(TT)/P(TB)=(TT/ TB)-1.3(p-value <2e-16). © Radiology, Koo Foundation Sun Yat-Sen Cancer Center - Taipei/TW Table 1: Table1.Patients and tumor characteristics (n=72) © Radiology, Koo Foundation Sun Yat-Sen Cancer Center - Taipei/TW Page 5 of 8 Conclusion The B1 inhomogeneity induced T1 estimation error can cause significant pharmacokinetic parameter bias in breast cancer at 1.5T DCE MRI. B1 correction for more accurate T1 value should be considered for quantitative DCE breast MRI even at 1.5 Tesla to correct the significant systemic error unless the B1 homogeneity is verified to be accurate beforehand. Personal information 1,2 WanChen Tsai MD 4 3 3 , Kuo-Jang Kao MD PhD , Kai-Ming Chang PhD , Chen-Fang Hung 5 6 7 MS , Qing Yang PhD , Chien-Yuan E Lin PhD , Chii-Ming Chen MD 1 2 Department of Radiology, Koo Foundation Sun Yat-Sen Cancer Center; School of 3 4 Medicine, National Yang-Ming University; Department of Research, Department of 5 Clinical Research, Koo Foundation Sun Yat-Sen Cancer Center; Apollo Medical Imaging 6 Technology Pty Ltd, Melbourne, Australia Department of Research, GE Healthcare, 7 Taiwan; Department of Surgery, Koo Foundation Sun Yat-Sen Cancer Center Corresponding author: Wan-Chen Tsai, MD 125 Lider Rd, Pei-Tou district, Taipei 112 Taiwan Department of Radiology, Koo Foundation Sun Yat-Sen Cancer Center Phone: +886-2-28970011 ext. 1117 Fax: +886-2-28971100 Page 6 of 8 E-mail: [email protected] References 1. Padhani AR: Dynamic contrast-enhanced MRI in clinical oncology: current status and future directions. 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Liang J, Sammet S, Yang X, Jia G, Takayama Y, Knopp MV: Intraindividual in vivo comparison of gadolinium contrast agents for pharmacokinetic analysis using dynamic contrast enhanced magnetic resonance imaging. Invest Radiol 2010, 45(5):233-244. Page 8 of 8