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Prostate tumor volume measurement with combined T2-weighted imaging and diffusion-weighted MR: correlation with pathologic tumor volume

UROLOGICAL SURVEY

Imaging

Prostate tumor volume measurement with combined T2-weighted imaging and diffusion-weighted MR: correlation with pathologic tumor volume

Mazaheri Y, Hricak H, Fine SW, Akin O, Shukla-Dave A, Ishill NM, Moskowitz CS, Grater JE, Reuter VE, Zakian KL, Touijer KA, Koutcher JA

Department of Medical Physics, Memorial Sloan-Kettering Cancer Center, New York, NY, USA

Radiology. 2009; 252: 449-57

PURPOSE: To retrospectively determine the accuracy of diffusion-weighted (DW) magnetic resonance (MR) imaging for identifying cancer in the prostate peripheral zone (PZ) and to assess the accuracy of tumor volume measurements made with T2-weighted imaging and combined T2-weighted and DW MR imaging by using surgical pathologic examination as the reference standard.

MATERIALS AND METHODS: The institutional review board issued a waiver of informed consent for this HIPAA-compliant study. Forty-two patients underwent endorectal MR at 1.5 T before undergoing radical prostatectomy for prostate cancer and had at least one PZ tumor larger than 0.1 cm(3) at surgical pathologic examination. On T2-weighted images, an experienced radiologist outlined suspected PZ tumors. Two apparent diffusion coefficient (ADC) cutoff values were identified by using the Youden index and published literature. Image cluster analysis was performed on voxels within the suspected tumor regions. Associations between volume measurements from imaging and from pathologic examination were assessed by using concordance correlation coefficients (CCCs). The sensitivity and specificity of ADCs for identifying malignant PZ voxels were calculated.

RESULTS: In identifying malignant voxels, respective ADC cutoff values of 0.0014 and 0.0016 mm(2)/sec yielded sensitivity of 82% and 95% and specificity of 85% and 65%, respectively. Sixty PZ cancer lesions larger than 0.1 cm(3) were found at pathologic examination; 43 were detected by the radiologist. CCCs between imaging and pathologic tumor volume measurements were 0.36 for T2-weighted imaging, and 0.46 and 0.60 for combined T2-weighted and DW MR imaging with ADC cutoffs of 0.0014 and 0.0016 mm(2)/sec, respectively; the CCC of combined T2-weighted and DW MR imaging (ADC cutoff, 0.0016 mm(2)/sec) was significantly higher (P = .006) than that of T2-weighted imaging alone.

CONCLUSION: Adding DW MR to T2-weighted imaging can significantly improve the accuracy of prostate PZ tumor volume measurement. Supplemental MATERIAL: http://radiology.rsnajnls.org/cgi/content/full/252/2/449/DC1.

Editorial Comment

The authors showed that the combination of anatomic information obtained with conventional T2-weighted image and functional study technique, obtained with diffusion-weighted image, significantly improves the accuracy of prostate peripheral zone tumor volume measurement. This information is interesting since multivariate analysis performed in other study showed that tumor volume, but not pathologic stage or baseline PSA level, was independently predictive of post-prostatectomy disease recurrence (1). In other words, measurement of prostate cancer tumor volume may provide information on prognosis that is independent of direct morphologic assessment of extraprostatic extension. Other studies have shown that pathologic tumor volume correlates also with pathologic stage, Gleason score, margin status, vascular invasion and metastases (2). So far, imaging estimation of prostate cancer tumor volume has been obtained with the combination of conventional MRI and spectroscopic imaging (3). This combined technique however is more effective in tumors larger than 0.5 cm3. Although the results of this study might be useful in daily clinical practice, we agree with the authors that determination of tumor volume should be better accomplished by using of multiparametric MRI prostate evaluation (combination of conventional T2-weighted image, diffusion-weighted image and dynamic contrast-enhanced studies).

References

1. Stamey TA, McNeal JE, Yemoto CM, Sigal BM, Johnstone IM: Biological determinants of cancer progression in men with prostate cancer. JAMA 1999: 281; 1395-400.

2. Bostwick DG, Graham SD Jr, Napalkov P, Abrahamsson PA, di Sant'agnese PA, et al.: Staging of early prostate cancer: a proposed tumor volume-based prognostic index. Urology 1993:41; 403-11.

3. Coakley FV, Kurhanewicz J, Lu Y, Jones KD, Swanson MG, Chang SD, et al.: Prostate cancer tumor volume measurement with e-MRI and MRSI. Radiology 2002; 223: 91-97.

Dr. Adilson Prando

Chief, Department of Radiology and

Diagnostic Imaging, Vera Cruz Hospital

Campinas, São Paulo, Brazil

E-mail: adilson.prando@gmail.com

  • 1. Stamey TA, McNeal JE, Yemoto CM, Sigal BM, Johnstone IM: Biological determinants of cancer progression in men with prostate cancer. JAMA 1999: 281; 1395-400.
  • 2. Bostwick DG, Graham SD Jr, Napalkov P, Abrahamsson PA, di Sant'agnese PA, et al.: Staging of early prostate cancer: a proposed tumor volume-based prognostic index. Urology 1993:41; 403-11.
  • 3. Coakley FV, Kurhanewicz J, Lu Y, Jones KD, Swanson MG, Chang SD, et al.: Prostate cancer tumor volume measurement with e-MRI and MRSI. Radiology 2002; 223: 91-97.

Publication Dates

  • Publication in this collection
    15 Jan 2010
  • Date of issue
    Dec 2009
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