Background. The aim of this study was to determine concordance rates for prostatectomy specimens and transrectal needle biopsy samples in various areas of the prostate in order to assess diagnostic accuracy of the transrectal biopsy approach, especially for presurgical detection of cancer in the prostatic apex. Materials and Methods. From 2006 to 2011, 158 patients whose radical prostatectomy specimens had been evaluated were retrospectively enrolled in this study. Concordance rates for histopathology results of prostatectomy specimens and needle biopsy samples were evaluated in 8 prostatic sections (apex, middle, base, and transitional zones bilaterally) from 73 patients diagnosed at this institution, besides factors for detecting apex cancer in total 118 true positive and false negative apex cancers. Results. Prostate cancer was found most frequently (85%) in the apex of all patients. Of 584 histopathology sections, 153 (49%) from all areas were false negatives, as were 45% of apex biopsy samples. No readily available preoperative factors for detecting apex cancer were identified. Conclusions. In Japanese patients, the most frequent location of prostate cancer is in the apex. There is a high false negative rate for transrectal biopsy samples. To improve the detection rate, transperitoneal biopsy or more accurate imaging technology is needed. 1. Introduction One of the most frequent location of cancer in the prostate gland is in the apex. Iremashvili et al. showed the incidence of carcinoma in prostatectomy specimens; 65.4% of all patients had apex carcinoma, 56.6% had middle carcinoma, 47.3% had base carcinoma [1]. Apex core specimens obtained by needle biopsy have been associated with the highest cancer detection rates [2]. However, to the best of our knowledge, there have been no previous reports of assessments of the sensitivity and specificity of transrectal biopsy procedures for detection of apical prostate cancer through determining correlations between histopathologic diagnoses of preoperative transrectal biopsy and subsequently resected tissue specimens, especially with regard to presurgical detection of prostate cancer localized to the apex. Recently, in Japan, prostate cancer (PCA) screening has spread and diagnostic imaging technology has improved. Detection of early stage PCA has been increasing [3, 4]. Kikuchi et al. reported that, in the United States after 1995, many smaller PCAs detected were located in the apex of the prostate: the frequency of apical cancer detection after 1995 had risen to 46% from 26%, a significant increase [5,
References
[1]
V. Iremashvili, L. Pelaez, M. Jorda et al., “Prostate sampling by 12-core biopsy: comparison of the biopsy results with tumor location in prostatectomy specimens,” Urology, vol. 79, no. 1, pp. 37–42, 2012.
[2]
A. S. Moussa, A. Meshref, L. Schoenfield et al., “Importance of additional “extreme” anterior apical needle biopsies in the initial detection of prostate cancer,” Urology, vol. 75, no. 5, pp. 1034–1039, 2010.
[3]
G. S. Jack, M. S. Cookson, C. S. Coffey et al., “Pathological parameters of radical prostatectomy for clinical stages T1c versus T2 prostate adenocarcinoma: decreased pathological stage and increased detection of transition zone tumors,” Journal of Urology, vol. 168, no. 2, pp. 519–524, 2002.
[4]
H. Augustin, P. G. Hammerer, M. Graefen et al., “Insignificant prostate cancer in radical prostatectomy specimen: time trends and preoperative prediction,” European Urology, vol. 43, no. 5, pp. 455–460, 2003.
[5]
E. Kikuchi, P. T. Scardino, T. M. Wheeler, K. M. Slawin, and M. Ohori, “Is tumor volume an independent prognostic factor in clinically localized prostate cancer?” Journal of Urology, vol. 172, no. 2, pp. 508–511, 2004.
[6]
J. Ishii, M. Ohori, P. Scardino, T. Tsuboi, K. Slawin, and T. Wheeler, “Significance of the craniocaudal distribution of cancer in radical prostatectomy specimens,” International Journal of Urology, vol. 14, no. 9, pp. 817–821, 2007.
[7]
R. Takashima, S. Egawa, S. Kuwao, and S. Baba, “Anterior distribution of Stage T1c nonpalpable tumors in radical prostatectomy specimens,” Urology, vol. 59, no. 5, pp. 692–697, 2002.
[8]
K. K. Hodge, J. E. McNeal, M. K. Terris, and T. A. Stamey, “Random systematic versus directed ultrasound guided transrectal core biopsies of the prostate,” Journal of Urology, vol. 142, no. 1, pp. 71–75, 1989.
[9]
A. S. Huo, T. Hossack, J. L. Symons et al., “Accuracy of primary systematic template guided transperineal biopsy of the prostate for locating prostate cancer: a comparison with radical prostatectomy specimens,” Journal of Urology, vol. 187, no. 6, pp. 2044–2049, 2012.
[10]
H. Rogatsch, W. Horninger, H. Volgger, G. Bartsch, G. Mikuz, and T. Mairinger, “Radical prostatectomy: the value of preoperative, individually labeled apical biopsies,” Journal of Urology, vol. 164, no. 3 I, pp. 754–758, 2000.
[11]
J. N. Kabalin, J. E. McNeal, H. M. Price, F. S. Freiha, and T. A. Stamey, “Unsuspected adenocarcinoma of the prostate in patients undergoing cystoprostatectomy for other causes: incidence, histology and morphometric observations,” Journal of Urology, vol. 141, no. 5, pp. 1091–1094, 1989.
[12]
J. E. McNeal and O. Haillot, “Patterns of spread of adenocarcinoma in the prostate as related to cancer volume,” Prostate, vol. 49, no. 1, pp. 48–57, 2001.
[13]
A. R. Patel and J. S. Jones, “Optimal biopsy strategies for the diagnosis and staging of prostate cancer,” Current Opinion in Urology, vol. 19, no. 3, pp. 232–237, 2009.
[14]
J. C. Presti Jr., G. J. O'Dowd, M. C. Miller, R. Mattu, and R. W. Veltri, “Extended peripheral zone biopsy schemes increase cancer detection rates and minimize variance in prostate specific antigen and age related cancer rates: results of a community multi-practice study,” Journal of Urology, vol. 169, no. 1, pp. 125–129, 2003.
[15]
R. J. Babaian, A. Toi, K. Kamoi et al., “A comparative analysis of sextant and an extended 11-core multisite directed biopsy strategy,” Journal of Urology, vol. 163, no. 1, pp. 152–157, 2000.
[16]
L. A. Eskew, R. L. Bare, D. L. McCullough, and T. A. Stamey, “Systematic 5 region prostate biopsy is superior to sextant method for diagnosing carcinoma of the prostate,” Journal of Urology, vol. 157, no. 1, pp. 199–203, 1997.
[17]
C. K. Naughton, D. C. Miller, and Y. Yan, “Impact of transrectal ultrasound guided prostate biopsy on quality of life: a prospective randomized trial comparing 6 versus 12 cores,” Journal of Urology, vol. 165, no. 1, pp. 100–103, 2001.
[18]
M. Inahara, H. Suzuki, S. Kojima et al., “Improved prostate cancer detection using systematic 14-core biopsy for large prostate glands with normal digital rectal examination findings,” Urology, vol. 68, no. 4, pp. 815–819, 2006.
[19]
K. Orikasa, A. Ito, S. Ishidoya, S. Saito, M. Endo, and Y. Arai, “Anterior apical biopsy: is it useful for prostate cancer detection?” International Journal of Urology, vol. 15, no. 10, pp. 900–904, 2008.
[20]
J. L. Wright and W. J. Ellis, “Improved prostate cancer detection with anterior apical prostate biopsies,” Urologic Oncology, vol. 24, no. 6, pp. 492–495, 2006.
[21]
A. J. Stephenson, D. P. Wood, M. W. Kattan et al., “Location, extent and number of positive surgical margins do not improve accuracy of predicting prostate cancer recurrence after radical prostatectomy,” Journal of Urology, vol. 182, no. 4, pp. 1357–1363, 2009.
[22]
T. Terakawa, H. Miyake, K. Tanaka, A. Takenaka, T. A. Inoue, and M. Fujisawa, “Surgical margin status of open versus laparoscopic radical prostatectomy specimens,” International Journal of Urology, vol. 15, no. 8, pp. 704–708, 2008.
[23]
L. Salomon, A. G. Anastasiadis, O. Levrel et al., “Location of positive surgical margins after retropubic, perineal, and laparoscopic radical prostatectomy for organ-confined prostate cancer,” Urology, vol. 61, no. 2, pp. 386–390, 2003.
[24]
P. A. Humphrey, “Tumor amount in prostatic tissues in relation to patient outcome andmanagement,” American Journal of Clinical Pathology, vol. 131, no. 1, pp. 7–10, 2009.
[25]
J. I. Epstein, “Prognostic significance of tumor volume in radical prostatectomy and needle biopsy specimens,” Journal of Urology, vol. 186, no. 3, pp. 790–797, 2011.
[26]
K. Kawamura, H. Suzuki, N. Kamiya et al., “Development of a new nomogram for predicting the probability of a positive initial prostate biopsy in Japanese patients with serum PSA levels less than 10 ng/mL,” International Journal of Urology, vol. 15, no. 7, pp. 598–603, 2008.