Pharmacokinetic analysis based on dynamic contrast-enhanced MRI for evaluating tumor response to preoperative therapy for oral cancer

被引:55
作者
Chikui, Toru [1 ]
Kitamoto, Erina [1 ]
Kawano, Shintaro [2 ]
Sugiura, Tsuyoshi [3 ]
Obara, Makoto [4 ]
Simonetti, Arjan W. [5 ]
Hatakenaka, Masamitsu [6 ]
Matsuo, Yoshio [6 ]
Koga, Shoichi [7 ]
Ohga, Masahiro [7 ]
Nakamura, Katsumasa [6 ]
Yoshiura, Kazunori [1 ]
机构
[1] Kyushu Univ, Dept Oral & Maxillofacial Radiol, Fac Dent Sci, Fukuoka 812, Japan
[2] Kyushu Univ, Sect Oral & Maxillofacial Oncol, Div Maxillofacial Diagnost & Surg Sci, Fac Dent Sci, Fukuoka 812, Japan
[3] Kyushu Univ, Dept Maxillofacial Surg, Kyushu Univ Hosp, Fukuoka 812, Japan
[4] Philips Elect Japan, Konan Minato Ku, Tokyo, Japan
[5] Philips Healthcare, Imaging Syst, Best, Netherlands
[6] Kyushu Univ, Dept Clin Radiol, Grad Sch Med Sci, Fukuoka 812, Japan
[7] Kyushu Univ, Radiol Ctr, Kyushu Univ Hosp, Fukuoka 812, Japan
关键词
neoadjuvant radiotherapy; oral cancer; TK model; SQUAMOUS-CELL CARCINOMA; ARTERIAL INPUT FUNCTION; NECK-CANCER; KINETIC-PARAMETERS; RADIATION-THERAPY; BLOOD CAPILLARIES; DUODENAL VILLI; DCE MRI; HEAD; CHEMOTHERAPY;
D O I
10.1002/jmri.23704
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
Purpose: To evaluate whether a pharmacokinetic analysis is useful for monitoring the response of oral cancer to chemoradiotherapy (CRT). Materials and Methods: Twenty-nine patients were included. They underwent dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) before and after CRT. The DCE-MRI data were analyzed using a Tofts and Kermode (TK) model. The histological evaluation of the effects of CRT was performed according to Ohboshi and Shimosato's classification. Results: None of the pre-CRT parameters were significantly different between the responders and nonresponders. The post-CRT volume of the extravascular extracellular space (EES) per unit volume of tissue (ve) of responders (0.397 +/- 0.080) was higher than that of nonresponders (0.281 +/- 0.076) (P = 0.01). The change of the ve between the pre- and post-CRT of the responders (0.154 +/- 0.093) was larger than that of the nonresponders (0.033 +/- 0.073) (P = 0.001). Therefore, the increase in the ve strongly suggested a good tumor response to CRT, which reflected an increase of the EES secondary to the destruction of the cancer nest. The changes in the volume transfer constant (Ktrans) were significantly different between the responders and nonresponders (P = 0.018). Conclusion: Both the increase of the ve and the elevation of permeability (Ktrans) were indicative of a good tumor response to CRT. The pharmacokinetic analysis had potential for monitoring the histopathological response to CRT. J. Magn. Reson. Imaging 2012;36:589597. (C) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:589 / 597
页数:9
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