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 inJournal of magnetic resonance imaging Vol. 28; no. 3; pp. 720 - 726
Main Authors Tamada, Tsutomu, Sone, Teruki, Jo, Yoshimasa, Toshimitsu, Shinya, Yamashita, Takenori, Yamamoto, Akira, Tanimoto, Daigo, Ito, Katsuyoshi
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.09.2008
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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.
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.
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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.
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  article-title: Correlation between metabolite ratios and ADC values of prostate in men with increased PSA level
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  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
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  start-page: 654
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  article-title: Endorectal diffusion‐weighted imaging in prostate cancer to differentiate malignant and benign peripheral zone tissue
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  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
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  year: 2008
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  article-title: T2‐weighted MR imaging of prostate cancer: multishot echo‐planar imaging vs fast spin‐echo imaging
  publication-title: Eur Radiol
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  year: 2000
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  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
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  article-title: Combined diffusion‐weighted and dynamic contrast‐enhanced MRI for prostate cancer diagnosis—correlation with biopsy and histopathology
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  article-title: Measurement of cell density and necrotic fraction in human melanoma xenografts by diffusion weighted magnetic resonance imaging
  publication-title: Magn Reson Med
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  year: 2001
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  article-title: Prostate cancer: what is the future role for imaging?
  publication-title: AJR Am J Roentgenol
– volume: 42
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Snippet Purpose 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
URI https://api.istex.fr/ark:/67375/WNG-9P1MPPQV-Z/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjmri.21503
https://www.ncbi.nlm.nih.gov/pubmed/18777532
https://www.proquest.com/docview/69553387
Volume 28
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