Apparent diffusion coefficient values in peripheral and transition zones of the prostate: Comparison between normal and malignant prostatic tissues and correlation with histologic grade
Purpose To investigate the utility of apparent diffusion coefficient (ADC) values for discriminating tumor in patients with prostate cancer from normal prostatic tissues in healthy adult men, and to identify correlations between ADC and histologic grade of prostate cancer. Materials and Methods A to...
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Published in | Journal of magnetic resonance imaging Vol. 28; no. 3; pp. 720 - 726 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.09.2008
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Subjects | |
Online Access | Get full text |
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Abstract | Purpose
To investigate the utility of apparent diffusion coefficient (ADC) values for discriminating tumor in patients with prostate cancer from normal prostatic tissues in healthy adult men, and to identify correlations between ADC and histologic grade of prostate cancer.
Materials and Methods
A total of 125 healthy male volunteers (mean age, 60 years; range, 50–86 years) and 90 prostate cancer patients (mean age, 71 years; range, 51–88 years) underwent diffusion‐weighted imaging (DWI) of the prostate with a single‐shot echo‐planar imaging sequence using b‐factors of 0 and 800 sec/mm2. ADC was measured from two locations in the peripheral zone (PZ) and two locations in the central gland (CG) in normal subjects, and tumor locations of PZ or transition zone (TZ) in patients with prostate cancer.
Results
Mean ADC values of tumor regions in both PZ (1.02 ± 0.25 × 10−3 mm2/sec) and TZ (0.94 ± 0.21 × 10−3 mm2/sec) were significantly lower than those in the corresponding normal regions (1.80 ± 0.27 × 10−3 mm2/sec and 1.34 ± 0.14 × 10−3 mm2/sec, respectively) (P < 0.0001 each). Furthermore, a significant negative correlation was identified between ADC in PZ cancer and tumor Gleason score (ρ = −0.497, P < 0.0001).
Conclusion
ADC values appear to provide acceptable diagnostic accuracy in both PZ and TZ. J. Magn. Reson. Imaging 2008;28:720–726. © 2008 Wiley‐Liss, Inc. |
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AbstractList | Purpose
To investigate the utility of apparent diffusion coefficient (ADC) values for discriminating tumor in patients with prostate cancer from normal prostatic tissues in healthy adult men, and to identify correlations between ADC and histologic grade of prostate cancer.
Materials and Methods
A total of 125 healthy male volunteers (mean age, 60 years; range, 50–86 years) and 90 prostate cancer patients (mean age, 71 years; range, 51–88 years) underwent diffusion‐weighted imaging (DWI) of the prostate with a single‐shot echo‐planar imaging sequence using b‐factors of 0 and 800 sec/mm2. ADC was measured from two locations in the peripheral zone (PZ) and two locations in the central gland (CG) in normal subjects, and tumor locations of PZ or transition zone (TZ) in patients with prostate cancer.
Results
Mean ADC values of tumor regions in both PZ (1.02 ± 0.25 × 10−3 mm2/sec) and TZ (0.94 ± 0.21 × 10−3 mm2/sec) were significantly lower than those in the corresponding normal regions (1.80 ± 0.27 × 10−3 mm2/sec and 1.34 ± 0.14 × 10−3 mm2/sec, respectively) (P < 0.0001 each). Furthermore, a significant negative correlation was identified between ADC in PZ cancer and tumor Gleason score (ρ = −0.497, P < 0.0001).
Conclusion
ADC values appear to provide acceptable diagnostic accuracy in both PZ and TZ. J. Magn. Reson. Imaging 2008;28:720–726. © 2008 Wiley‐Liss, Inc. To investigate the utility of apparent diffusion coefficient (ADC) values for discriminating tumor in patients with prostate cancer from normal prostatic tissues in healthy adult men, and to identify correlations between ADC and histologic grade of prostate cancer.PURPOSETo investigate the utility of apparent diffusion coefficient (ADC) values for discriminating tumor in patients with prostate cancer from normal prostatic tissues in healthy adult men, and to identify correlations between ADC and histologic grade of prostate cancer.A total of 125 healthy male volunteers (mean age, 60 years; range, 50-86 years) and 90 prostate cancer patients (mean age, 71 years; range, 51-88 years) underwent diffusion-weighted imaging (DWI) of the prostate with a single-shot echo-planar imaging sequence using b-factors of 0 and 800 sec/mm2. ADC was measured from two locations in the peripheral zone (PZ) and two locations in the central gland (CG) in normal subjects, and tumor locations of PZ or transition zone (TZ) in patients with prostate cancer.MATERIALS AND METHODSA total of 125 healthy male volunteers (mean age, 60 years; range, 50-86 years) and 90 prostate cancer patients (mean age, 71 years; range, 51-88 years) underwent diffusion-weighted imaging (DWI) of the prostate with a single-shot echo-planar imaging sequence using b-factors of 0 and 800 sec/mm2. ADC was measured from two locations in the peripheral zone (PZ) and two locations in the central gland (CG) in normal subjects, and tumor locations of PZ or transition zone (TZ) in patients with prostate cancer.Mean ADC values of tumor regions in both PZ (1.02+/-0.25x10(-3) mm2/sec) and TZ (0.94+/-0.21x10(-3) mm2/sec) were significantly lower than those in the corresponding normal regions (1.80+/-0.27x10(-3) mm2/sec and 1.34+/-0.14x10(-3) mm2/sec, respectively) (P<0.0001 each). Furthermore, a significant negative correlation was identified between ADC in PZ cancer and tumor Gleason score (rho=-0.497, P<0.0001).RESULTSMean ADC values of tumor regions in both PZ (1.02+/-0.25x10(-3) mm2/sec) and TZ (0.94+/-0.21x10(-3) mm2/sec) were significantly lower than those in the corresponding normal regions (1.80+/-0.27x10(-3) mm2/sec and 1.34+/-0.14x10(-3) mm2/sec, respectively) (P<0.0001 each). Furthermore, a significant negative correlation was identified between ADC in PZ cancer and tumor Gleason score (rho=-0.497, P<0.0001).ADC values appear to provide acceptable diagnostic accuracy in both PZ and TZ.CONCLUSIONADC values appear to provide acceptable diagnostic accuracy in both PZ and TZ. To investigate the utility of apparent diffusion coefficient (ADC) values for discriminating tumor in patients with prostate cancer from normal prostatic tissues in healthy adult men, and to identify correlations between ADC and histologic grade of prostate cancer. A total of 125 healthy male volunteers (mean age, 60 years; range, 50-86 years) and 90 prostate cancer patients (mean age, 71 years; range, 51-88 years) underwent diffusion-weighted imaging (DWI) of the prostate with a single-shot echo-planar imaging sequence using b-factors of 0 and 800 sec/mm2. ADC was measured from two locations in the peripheral zone (PZ) and two locations in the central gland (CG) in normal subjects, and tumor locations of PZ or transition zone (TZ) in patients with prostate cancer. Mean ADC values of tumor regions in both PZ (1.02+/-0.25x10(-3) mm2/sec) and TZ (0.94+/-0.21x10(-3) mm2/sec) were significantly lower than those in the corresponding normal regions (1.80+/-0.27x10(-3) mm2/sec and 1.34+/-0.14x10(-3) mm2/sec, respectively) (P<0.0001 each). Furthermore, a significant negative correlation was identified between ADC in PZ cancer and tumor Gleason score (rho=-0.497, P<0.0001). ADC values appear to provide acceptable diagnostic accuracy in both PZ and TZ. |
Author | Tamada, Tsutomu Jo, Yoshimasa Yamashita, Takenori Yamamoto, Akira Toshimitsu, Shinya Tanimoto, Daigo Ito, Katsuyoshi Sone, Teruki |
Author_xml | – sequence: 1 givenname: Tsutomu surname: Tamada fullname: Tamada, Tsutomu email: ttamada@med.kawasaki-m.ac.jp organization: Department of Radiology, Kawasaki Medical School, Okayama, Japan – sequence: 2 givenname: Teruki surname: Sone fullname: Sone, Teruki organization: Department of Radiology, Kawasaki Medical School, Okayama, Japan – sequence: 3 givenname: Yoshimasa surname: Jo fullname: Jo, Yoshimasa organization: Department of Urology, Kawasaki Medical School, Okayama, Japan – sequence: 4 givenname: Shinya surname: Toshimitsu fullname: Toshimitsu, Shinya organization: Department of Radiology, Hiroshima Heiwa Clinic, Hiroshima, Japan – sequence: 5 givenname: Takenori surname: Yamashita fullname: Yamashita, Takenori organization: Department of Radiology, Kawasaki Medical School, Okayama, Japan – sequence: 6 givenname: Akira surname: Yamamoto fullname: Yamamoto, Akira organization: Department of Radiology, Kawasaki Medical School, Okayama, Japan – sequence: 7 givenname: Daigo surname: Tanimoto fullname: Tanimoto, Daigo organization: Department of Radiology, Kawasaki Medical School, Okayama, Japan – sequence: 8 givenname: Katsuyoshi surname: Ito fullname: Ito, Katsuyoshi organization: Department of Radiology, Kawasaki Medical School, Okayama, Japan |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18777532$$D View this record in MEDLINE/PubMed |
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References | Thornbury JR, Ornstein DK, Choyke PL, Langlotz CP, Weinreb JC. Prostate cancer: what is the future role for imaging? AJR Am J Roentgenol 2001; 176: 17-22. Gibbs P, Tozer DJ, Liney GP, Turnbull LW. Comparison of quantitative T2 mapping and diffusion-weighted imaging in the normal and pathologic prostate. Magn Reson Med 2001; 46: 1054-1058. Sodickson DK, McKenzie CA. A generalized approach to parallel magnetic resonance imaging. Med Phys 2001; 28: 1629-1643. Yu KK, Hricak H. Imaging prostate cancer. Radiol Clin N Am 2000; 38: 59-85. Castillo M, Smith JK, Kwock L, Wilber K. Apparent diffusion coefficients in the evaluation of high-grade cerebral gliomas. AJNR Am J Neuroradiol 2001; 22: 60-64. Lyng H, Haraldseth O, Rofstad EK. Measurement of cell density and necrotic fraction in human melanoma xenografts by diffusion weighted magnetic resonance imaging. Magn Reson Med 2000; 43: 828-836. Wefer AE, Hricak H, Vigneron DB, et al. Sextant localization of prostate cancer: comparison of sextant biopsy, magnetic resonance imaging and magnetic resonance spectroscopic imaging with step section histology. J Urol 2000; 164: 400-404. Parivar F, Rajanayagam V, Waluch V, Eto RT, Jones LW, Ross BD. Endorectal surface coil MR imaging of prostatic carcinoma with the inversion-recovery sequence. J Magn Reson Imaging 1991; 1: 657-664. de Souza NM, Reinsberg SA, Scurr ED, Brewster JM, Payne GS. Magnetic resonance imaging in prostate cancer: the value of apparent diffusion coefficients for identifying malignant nodules. Br J Radiol 2007; 80: 90-95. Schiebler ML, Tomaszewski JE, Bezzi M, et al. Prostatic carcinoma and benign prostatic hyperplasia: correlation of high-resolution MR and histopathologic findings. Radiology 1989; 172: 131-137. Akin O, Sala E, Moskowitz CS, et al. Transition zone prostate cancers: features, detection, localization, and staging at endorectal MR imaging. Radiology 2006; 239: 784-792. McNeal JE, Redwine EA, Freiha FS, Stamey TA. Zonal distribution of prostatic adenocarcinoma. Correlation with histologic pattern and direction of spread. Am J Surg Pathol 1988; 12: 897-906. Gibbs P, Pickles MD, Turnbull LW. Diffusion imaging of the prostate at 3.0 Tesla. Invest Radiol 2006; 41: 185-188. Ikonen S, Kivisaari L, Tervahartiala P, Vehmas T, Taari K, Rannikko S. Prostatic MR imaging. Accuracy in differentiating cancer from other prostatic disorders. Acta Radiol 2001; 42: 348-354. Le Bihan D, Breton E, Lallemand D, et al. MR imaging of intravoxel incoherent motions: application to diffusion and perfusion in neurologic disorders. Radiology 1986; 161: 401-407. Tanimoto A, Nakashima J, Kohno H, Shinmoto H, Kuribayashi S. Prostate cancer screening: the clinical value of diffusion-weighted imaging and dynamic MR imaging in combination with T2-weighted imaging. J Magn Reson Imaging 2007; 25: 146-152. Turnbull LW, Buckley DL, Turnbull LS, Liney GP, Knowles AJ. Differentiation of prostatic carcinoma and benign prostatic hyperplasia: correlation between dynamic Gd-DTPA-enhanced MR imaging and histopathology. J Magn Reson Imaging 1999; 9: 311-316. Anderson AW, Xie J, Pizzonia J, Bronen RA, Spencer DD, Gore JC. Effects of cell volume fraction changes on apparent diffusion in human cells. Magn Reson Imaging 2000; 18: 689-695. Tamada T, Sone T, Nagai K, et al. T2-weighted MR imaging of prostate cancer: multishot echo-planar imaging vs fast spin-echo imaging. Eur Radiol 2004; 14: 318-325. Hosseinzadeh K, Schwarz SD. Endorectal diffusion-weighted imaging in prostate cancer to differentiate malignant and benign peripheral zone tissue. J Magn Reson Imaging 2004; 20: 654-661. Kim CK, Park BK, Han JJ, Kang TW, Lee HM. Diffusion-weighted imaging of the prostate at 3 T for differentiation of malignant and benign tissue in transition and peripheral zones: preliminary results. J Comput Assist Tomogr 2007; 31: 449-454. Pickles MD, Gibbs P, Sreenivas M, Turnbull LW. Diffusion-weighted imaging of normal and malignant prostate tissue at 3.0 T. J Magn Reson Imaging 2006; 23: 130-134. Stamey TA, McNeal JE, Yemoto CM, Sigal BM, Johnstone IM. Biological determinants of cancer progression in men with prostate cancer. JAMA 1999; 281: 1395-1400. Chan I, Wells W III, Mulkern RV, et al. Detection of prostate cancer by integration of line-scan diffusion, T2-mapping and T2-weighted magnetic resonance imaging; a multichannel statistical classifier. Med Phys 2003; 30: 2390-2398. Kumar V, Jagannathan NR, Kumar R, et al. Correlation between metabolite ratios and ADC values of prostate in men with increased PSA level. Magn Reson Imaging 2006; 24: 541-548. Zackrisson B, Aus G, Bergdahl S, et al. The risk of finding focal cancer (less than 3 mm) remains high on re-biopsy of patients with persistently increased prostate specific antigen but the clinical significance is questionable. J Urol 2004; 171: 1500-1503. Sato C, Naganawa S, Nakamura T, et al. Differentiation of noncancerous tissue and cancer lesions by apparent diffusion coefficient values in transition and peripheral zones of the prostate. J Magn Reson Imaging 2005; 21: 258-262. Catalona WJ, Richie JP, Ahmann FR, et al. Comparison of digital rectal examination and serum prostate specific antigen in the early detection of prostate cancer: results of a multicenter clinical trial of 6,630 men. J Urol 1994; 151: 1283-1290. Perrotti M, Han KR, Epstein RE, et al. Prospective evaluation of endorectal magnetic resonance imaging to detect tumor foci in men with prior negative prostastic biopsy: a pilot study. J Urol 1999; 162: 1314-1317. Bangma CH, Kranse R, Blijenberg BG, Schroder FH. The value of screening tests in the detection of prostate cancer. Part I: Results of a retrospective evaluation of 1726 men. Urology 1995; 46: 773-778. Grossfeld GD, Coakley FV. Benign prostatic hyperplasia: clinical overview and value of diagnostic imaging. Radiol Clin N Am 2000; 38: 31-47. Coakley FV, Kurhanewicz J, Lu Y, et al. Prostate cancer tumor volume: measurement with endorectal MR and MR spectroscopic imaging. Radiology 2002; 223: 91-97. Issa B. In vivo measurement of the apparent diffusion coefficient in normal and malignant prostatic tissues using echo-planar imaging. J Magn Reson Imaging 2002; 16: 196-200. Kozlowski P, Chang SD, Jones EC, Berean KW, Chen H, Goldenberg SL. Combined diffusion-weighted and dynamic contrast-enhanced MRI for prostate cancer diagnosis-correlation with biopsy and histopathology. J Magn Reson Imaging 2006; 24: 108-113. Reinsberg SA, Payne GS, Riches SF, et al. Combined use of diffusion-weighted MRI and 1H MR spectroscopy to increase accuracy in prostate cancer detection. AJR Am J Roentgenol 2007; 188: 91-98. 2002; 16 2004; 20 1991; 1 2000; 43 2007; 188 1994; 151 1998 1999; 162 1988; 12 2005; 21 2001; 28 2007; 31 2001; 22 2006; 239 2001; 46 2003; 30 2001; 42 1999; 9 2001; 176 2006; 41 2000; 18 2000; 38 2006; 23 2006; 24 1995; 46 2004; 14 2002; 223 1986; 161 1999; 281 2008; 27 2004; 171 2007; 80 1989; 172 2000; 164 2007; 25 e_1_2_5_26_2 e_1_2_5_24_2 e_1_2_5_25_2 e_1_2_5_22_2 e_1_2_5_23_2 e_1_2_5_20_2 e_1_2_5_21_2 e_1_2_5_28_2 e_1_2_5_29_2 Ikonen S (e_1_2_5_33_2) 2001; 42 e_1_2_5_14_2 e_1_2_5_37_2 e_1_2_5_13_2 e_1_2_5_9_2 e_1_2_5_16_2 e_1_2_5_35_2 e_1_2_5_8_2 e_1_2_5_15_2 e_1_2_5_36_2 e_1_2_5_7_2 e_1_2_5_10_2 e_1_2_5_6_2 e_1_2_5_34_2 e_1_2_5_5_2 e_1_2_5_12_2 e_1_2_5_31_2 e_1_2_5_4_2 e_1_2_5_11_2 e_1_2_5_32_2 e_1_2_5_3_2 e_1_2_5_2_2 e_1_2_5_18_2 e_1_2_5_17_2 e_1_2_5_19_2 e_1_2_5_30_2 Castillo M (e_1_2_5_27_2) 2001; 22 Brooks JD (e_1_2_5_38_2) 1998 |
References_xml | – reference: Bangma CH, Kranse R, Blijenberg BG, Schroder FH. The value of screening tests in the detection of prostate cancer. Part I: Results of a retrospective evaluation of 1726 men. Urology 1995; 46: 773-778. – reference: Grossfeld GD, Coakley FV. Benign prostatic hyperplasia: clinical overview and value of diagnostic imaging. Radiol Clin N Am 2000; 38: 31-47. – reference: Anderson AW, Xie J, Pizzonia J, Bronen RA, Spencer DD, Gore JC. Effects of cell volume fraction changes on apparent diffusion in human cells. Magn Reson Imaging 2000; 18: 689-695. – reference: Kumar V, Jagannathan NR, Kumar R, et al. Correlation between metabolite ratios and ADC values of prostate in men with increased PSA level. Magn Reson Imaging 2006; 24: 541-548. – reference: Lyng H, Haraldseth O, Rofstad EK. Measurement of cell density and necrotic fraction in human melanoma xenografts by diffusion weighted magnetic resonance imaging. Magn Reson Med 2000; 43: 828-836. – reference: Coakley FV, Kurhanewicz J, Lu Y, et al. Prostate cancer tumor volume: measurement with endorectal MR and MR spectroscopic imaging. Radiology 2002; 223: 91-97. – reference: Sato C, Naganawa S, Nakamura T, et al. Differentiation of noncancerous tissue and cancer lesions by apparent diffusion coefficient values in transition and peripheral zones of the prostate. J Magn Reson Imaging 2005; 21: 258-262. – reference: Thornbury JR, Ornstein DK, Choyke PL, Langlotz CP, Weinreb JC. Prostate cancer: what is the future role for imaging? AJR Am J Roentgenol 2001; 176: 17-22. – reference: Tamada T, Sone T, Nagai K, et al. T2-weighted MR imaging of prostate cancer: multishot echo-planar imaging vs fast spin-echo imaging. Eur Radiol 2004; 14: 318-325. – reference: Ikonen S, Kivisaari L, Tervahartiala P, Vehmas T, Taari K, Rannikko S. Prostatic MR imaging. Accuracy in differentiating cancer from other prostatic disorders. Acta Radiol 2001; 42: 348-354. – reference: Schiebler ML, Tomaszewski JE, Bezzi M, et al. Prostatic carcinoma and benign prostatic hyperplasia: correlation of high-resolution MR and histopathologic findings. Radiology 1989; 172: 131-137. – reference: Reinsberg SA, Payne GS, Riches SF, et al. Combined use of diffusion-weighted MRI and 1H MR spectroscopy to increase accuracy in prostate cancer detection. AJR Am J Roentgenol 2007; 188: 91-98. – reference: Sodickson DK, McKenzie CA. A generalized approach to parallel magnetic resonance imaging. Med Phys 2001; 28: 1629-1643. – reference: McNeal JE, Redwine EA, Freiha FS, Stamey TA. Zonal distribution of prostatic adenocarcinoma. Correlation with histologic pattern and direction of spread. Am J Surg Pathol 1988; 12: 897-906. – reference: Parivar F, Rajanayagam V, Waluch V, Eto RT, Jones LW, Ross BD. Endorectal surface coil MR imaging of prostatic carcinoma with the inversion-recovery sequence. J Magn Reson Imaging 1991; 1: 657-664. – reference: Yu KK, Hricak H. Imaging prostate cancer. Radiol Clin N Am 2000; 38: 59-85. – reference: Pickles MD, Gibbs P, Sreenivas M, Turnbull LW. Diffusion-weighted imaging of normal and malignant prostate tissue at 3.0 T. J Magn Reson Imaging 2006; 23: 130-134. – reference: Tanimoto A, Nakashima J, Kohno H, Shinmoto H, Kuribayashi S. Prostate cancer screening: the clinical value of diffusion-weighted imaging and dynamic MR imaging in combination with T2-weighted imaging. J Magn Reson Imaging 2007; 25: 146-152. – reference: Akin O, Sala E, Moskowitz CS, et al. Transition zone prostate cancers: features, detection, localization, and staging at endorectal MR imaging. Radiology 2006; 239: 784-792. – reference: Gibbs P, Tozer DJ, Liney GP, Turnbull LW. Comparison of quantitative T2 mapping and diffusion-weighted imaging in the normal and pathologic prostate. Magn Reson Med 2001; 46: 1054-1058. – reference: Kozlowski P, Chang SD, Jones EC, Berean KW, Chen H, Goldenberg SL. Combined diffusion-weighted and dynamic contrast-enhanced MRI for prostate cancer diagnosis-correlation with biopsy and histopathology. J Magn Reson Imaging 2006; 24: 108-113. – reference: Perrotti M, Han KR, Epstein RE, et al. Prospective evaluation of endorectal magnetic resonance imaging to detect tumor foci in men with prior negative prostastic biopsy: a pilot study. J Urol 1999; 162: 1314-1317. – reference: Chan I, Wells W III, Mulkern RV, et al. Detection of prostate cancer by integration of line-scan diffusion, T2-mapping and T2-weighted magnetic resonance imaging; a multichannel statistical classifier. Med Phys 2003; 30: 2390-2398. – reference: Castillo M, Smith JK, Kwock L, Wilber K. Apparent diffusion coefficients in the evaluation of high-grade cerebral gliomas. AJNR Am J Neuroradiol 2001; 22: 60-64. – reference: Zackrisson B, Aus G, Bergdahl S, et al. The risk of finding focal cancer (less than 3 mm) remains high on re-biopsy of patients with persistently increased prostate specific antigen but the clinical significance is questionable. J Urol 2004; 171: 1500-1503. – reference: de Souza NM, Reinsberg SA, Scurr ED, Brewster JM, Payne GS. Magnetic resonance imaging in prostate cancer: the value of apparent diffusion coefficients for identifying malignant nodules. Br J Radiol 2007; 80: 90-95. – reference: Hosseinzadeh K, Schwarz SD. Endorectal diffusion-weighted imaging in prostate cancer to differentiate malignant and benign peripheral zone tissue. J Magn Reson Imaging 2004; 20: 654-661. – reference: Turnbull LW, Buckley DL, Turnbull LS, Liney GP, Knowles AJ. Differentiation of prostatic carcinoma and benign prostatic hyperplasia: correlation between dynamic Gd-DTPA-enhanced MR imaging and histopathology. J Magn Reson Imaging 1999; 9: 311-316. – reference: Stamey TA, McNeal JE, Yemoto CM, Sigal BM, Johnstone IM. Biological determinants of cancer progression in men with prostate cancer. JAMA 1999; 281: 1395-1400. – reference: Issa B. In vivo measurement of the apparent diffusion coefficient in normal and malignant prostatic tissues using echo-planar imaging. J Magn Reson Imaging 2002; 16: 196-200. – reference: Catalona WJ, Richie JP, Ahmann FR, et al. Comparison of digital rectal examination and serum prostate specific antigen in the early detection of prostate cancer: results of a multicenter clinical trial of 6,630 men. J Urol 1994; 151: 1283-1290. – reference: Wefer AE, Hricak H, Vigneron DB, et al. Sextant localization of prostate cancer: comparison of sextant biopsy, magnetic resonance imaging and magnetic resonance spectroscopic imaging with step section histology. J Urol 2000; 164: 400-404. – reference: Le Bihan D, Breton E, Lallemand D, et al. MR imaging of intravoxel incoherent motions: application to diffusion and perfusion in neurologic disorders. Radiology 1986; 161: 401-407. – reference: Gibbs P, Pickles MD, Turnbull LW. Diffusion imaging of the prostate at 3.0 Tesla. Invest Radiol 2006; 41: 185-188. – reference: Kim CK, Park BK, Han JJ, Kang TW, Lee HM. Diffusion-weighted imaging of the prostate at 3 T for differentiation of malignant and benign tissue in transition and peripheral zones: preliminary results. J Comput Assist Tomogr 2007; 31: 449-454. – volume: 80 start-page: 90 year: 2007 end-page: 95 article-title: Magnetic resonance imaging in prostate cancer: the value of apparent diffusion coefficients for identifying malignant nodules publication-title: Br J Radiol – volume: 24 start-page: 541 year: 2006 end-page: 548 article-title: Correlation between metabolite ratios and ADC values of prostate in men with increased PSA level publication-title: Magn Reson Imaging – volume: 30 start-page: 2390 year: 2003 end-page: 2398 article-title: Detection of prostate cancer by integration of line‐scan diffusion, T2‐mapping and T2‐weighted magnetic resonance imaging; a multichannel statistical classifier publication-title: Med Phys – volume: 20 start-page: 654 year: 2004 end-page: 661 article-title: Endorectal diffusion‐weighted imaging in prostate cancer to differentiate malignant and benign peripheral zone tissue publication-title: J Magn Reson Imaging – volume: 46 start-page: 773 year: 1995 end-page: 778 article-title: The value of screening tests in the detection of prostate cancer. Part I: Results of a retrospective evaluation of 1726 men publication-title: Urology – volume: 27 start-page: 552 year: 2008 end-page: 556 article-title: Age‐related and zonal anatomical changes of apparent diffusion coefficient values in normal human prostatic tissues – volume: 14 start-page: 318 year: 2004 end-page: 325 article-title: T2‐weighted MR imaging of prostate cancer: multishot echo‐planar imaging vs fast spin‐echo imaging publication-title: Eur Radiol – volume: 31 start-page: 449 year: 2007 end-page: 454 article-title: Diffusion‐weighted imaging of the prostate at 3 T for differentiation of malignant and benign tissue in transition and peripheral zones: preliminary results publication-title: J Comput Assist Tomogr – volume: 38 start-page: 31 year: 2000 end-page: 47 article-title: Benign prostatic hyperplasia: clinical overview and value of diagnostic imaging publication-title: Radiol Clin N Am – volume: 24 start-page: 108 year: 2006 end-page: 113 article-title: Combined diffusion‐weighted and dynamic contrast‐enhanced MRI for prostate cancer diagnosis—correlation with biopsy and histopathology publication-title: J Magn Reson Imaging – volume: 162 start-page: 1314 year: 1999 end-page: 1317 article-title: Prospective evaluation of endorectal magnetic resonance imaging to detect tumor foci in men with prior negative prostastic biopsy: a pilot study publication-title: J Urol – volume: 43 start-page: 828 year: 2000 end-page: 836 article-title: Measurement of cell density and necrotic fraction in human melanoma xenografts by diffusion weighted magnetic resonance imaging publication-title: Magn Reson Med – volume: 239 start-page: 784 year: 2006 end-page: 792 article-title: Transition zone prostate cancers: features, detection, localization, and staging at endorectal MR imaging publication-title: Radiology – volume: 23 start-page: 130 year: 2006 end-page: 134 article-title: Diffusion‐weighted imaging of normal and malignant prostate tissue at 3.0 T publication-title: J Magn Reson Imaging – volume: 223 start-page: 91 year: 2002 end-page: 97 article-title: Prostate cancer tumor volume: measurement with endorectal MR and MR spectroscopic imaging publication-title: Radiology – start-page: 89 year: 1998 end-page: 128 – volume: 151 start-page: 1283 year: 1994 end-page: 1290 article-title: Comparison of digital rectal examination and serum prostate specific antigen in the early detection of prostate cancer: results of a multicenter clinical trial of 6,630 men publication-title: J Urol – volume: 176 start-page: 17 year: 2001 end-page: 22 article-title: Prostate cancer: what is the future role for imaging? publication-title: AJR Am J Roentgenol – volume: 42 start-page: 348 year: 2001 end-page: 354 article-title: Prostatic MR imaging. Accuracy in differentiating cancer from other prostatic disorders publication-title: Acta Radiol – volume: 25 start-page: 146 year: 2007 end-page: 152 article-title: Prostate cancer screening: the clinical value of diffusion‐weighted imaging and dynamic MR imaging in combination with T2‐weighted imaging publication-title: J Magn Reson Imaging – volume: 18 start-page: 689 year: 2000 end-page: 695 article-title: Effects of cell volume fraction changes on apparent diffusion in human cells publication-title: Magn Reson Imaging – volume: 12 start-page: 897 year: 1988 end-page: 906 article-title: Zonal distribution of prostatic adenocarcinoma. Correlation with histologic pattern and direction of spread publication-title: Am J Surg Pathol – volume: 38 start-page: 59 year: 2000 end-page: 85 article-title: Imaging prostate cancer publication-title: Radiol Clin N Am – volume: 46 start-page: 1054 year: 2001 end-page: 1058 article-title: Comparison of quantitative T2 mapping and diffusion‐weighted imaging in the normal and pathologic prostate publication-title: Magn Reson Med – volume: 21 start-page: 258 year: 2005 end-page: 262 article-title: Differentiation of noncancerous tissue and cancer lesions by apparent diffusion coefficient values in transition and peripheral zones of the prostate publication-title: J Magn Reson Imaging – volume: 1 start-page: 657 year: 1991 end-page: 664 article-title: Endorectal surface coil MR imaging of prostatic carcinoma with the inversion–recovery sequence publication-title: J Magn Reson Imaging – volume: 41 start-page: 185 year: 2006 end-page: 188 article-title: Diffusion imaging of the prostate at 3.0 Tesla publication-title: Invest Radiol – volume: 9 start-page: 311 year: 1999 end-page: 316 article-title: Differentiation of prostatic carcinoma and benign prostatic hyperplasia: correlation between dynamic Gd‐DTPA‐enhanced MR imaging and histopathology publication-title: J Magn Reson Imaging – volume: 171 start-page: 1500 year: 2004 end-page: 1503 article-title: The risk of finding focal cancer (less than 3 mm) remains high on re‐biopsy of patients with persistently increased prostate specific antigen but the clinical significance is questionable publication-title: J Urol – volume: 16 start-page: 196 year: 2002 end-page: 200 article-title: In vivo measurement of the apparent diffusion coefficient in normal and malignant prostatic tissues using echo‐planar imaging publication-title: J Magn Reson Imaging – volume: 281 start-page: 1395 year: 1999 end-page: 1400 article-title: Biological determinants of cancer progression in men with prostate cancer publication-title: JAMA – volume: 161 start-page: 401 year: 1986 end-page: 407 article-title: MR imaging of intravoxel incoherent motions: application to diffusion and perfusion in neurologic disorders publication-title: Radiology – volume: 164 start-page: 400 year: 2000 end-page: 404 article-title: Sextant localization of prostate cancer: comparison of sextant biopsy, magnetic resonance imaging and magnetic resonance spectroscopic imaging with step section histology publication-title: J Urol – volume: 188 start-page: 91 year: 2007 end-page: 98 article-title: Combined use of diffusion‐weighted MRI and 1H MR spectroscopy to increase accuracy in prostate cancer detection publication-title: AJR Am J Roentgenol – volume: 172 start-page: 131 year: 1989 end-page: 137 article-title: Prostatic carcinoma and benign prostatic hyperplasia: correlation of high‐resolution MR and histopathologic findings publication-title: Radiology – volume: 28 start-page: 1629 year: 2001 end-page: 1643 article-title: A generalized approach to parallel magnetic resonance imaging publication-title: Med Phys – volume: 22 start-page: 60 year: 2001 end-page: 64 article-title: Apparent diffusion coefficients in the evaluation of high‐grade cerebral gliomas publication-title: AJNR Am J Neuroradiol – ident: e_1_2_5_17_2 doi: 10.1002/jmri.20251 – ident: e_1_2_5_34_2 doi: 10.1148/radiology.172.1.2472644 – ident: e_1_2_5_18_2 doi: 10.1002/jmri.20626 – ident: e_1_2_5_8_2 doi: 10.1007/s00330-003-2118-y – ident: e_1_2_5_37_2 doi: 10.1016/S0033-8389(05)70148-2 – ident: e_1_2_5_35_2 doi: 10.1002/jmri.1880010607 – ident: e_1_2_5_36_2 doi: 10.1001/jama.281.15.1395 – ident: e_1_2_5_12_2 doi: 10.1016/S0022-5347(05)67370-3 – ident: e_1_2_5_24_2 doi: 10.1259/bjr/24232319 – ident: e_1_2_5_3_2 doi: 10.1016/S0022-5347(17)35233-3 – start-page: 89 volume-title: Campbell's urology year: 1998 ident: e_1_2_5_38_2 – ident: e_1_2_5_16_2 doi: 10.1002/jmri.20159 – ident: e_1_2_5_25_2 doi: 10.1097/01.rct.0000243456.00437.59 – ident: e_1_2_5_2_2 doi: 10.1016/S0090-4295(99)80342-2 – ident: e_1_2_5_9_2 doi: 10.1002/(SICI)1522-2586(199902)9:2<311::AID-JMRI24>3.0.CO;2-W – ident: e_1_2_5_6_2 doi: 10.1016/S0033-8389(05)70150-0 – ident: e_1_2_5_4_2 doi: 10.1097/01.ju.0000118052.59597.83 – ident: e_1_2_5_14_2 doi: 10.1002/jmri.10139 – ident: e_1_2_5_20_2 doi: 10.1097/01.rli.0000192418.30684.14 – ident: e_1_2_5_11_2 doi: 10.1148/radiol.2231010575 – ident: e_1_2_5_31_2 doi: 10.1002/jmri.21117 – volume: 22 start-page: 60 year: 2001 ident: e_1_2_5_27_2 article-title: Apparent diffusion coefficients in the evaluation of high‐grade cerebral gliomas publication-title: AJNR Am J Neuroradiol – ident: e_1_2_5_10_2 doi: 10.1016/S0022-5347(05)68275-4 – volume: 42 start-page: 348 year: 2001 ident: e_1_2_5_33_2 article-title: Prostatic MR imaging. 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To investigate the utility of apparent diffusion coefficient (ADC) values for discriminating tumor in patients with prostate cancer from normal... To investigate the utility of apparent diffusion coefficient (ADC) values for discriminating tumor in patients with prostate cancer from normal prostatic... |
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SubjectTerms | Aged Aged, 80 and over Algorithms apparent diffusion coefficient diffusion magnetic resonance imaging histologic type of neoplasm Humans Image Enhancement - methods Image Interpretation, Computer-Assisted - methods Male Middle Aged peripheral zone prostate cancer Prostatic Neoplasms - pathology Reference Values Reproducibility of Results Sensitivity and Specificity Statistics as Topic transition zone |
Title | Apparent diffusion coefficient values in peripheral and transition zones of the prostate: Comparison between normal and malignant prostatic tissues and correlation with histologic grade |
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