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Abstract:

Introduction: the main indicator that determines the prognosis of cancer is the degree of prevalence of tumor process at the time of detection. In terms of the growth of primary morbidity among urological cancers, bladder cancer ranks third, and prostate cancer is second. Treatment of patients in advanced stages is palliative and aimed at improving the quality of life and increasing its duration.

Bleeding from the bladder or prostate in such cases is a life-threatening complication and one of the most common causes of death in advanced cancer.

Aim: was to evaluate the effectiveness of embolization of arteries of the bladder and prostate in cancer patients with bleeding from the lower urinary tract as a preparatory stage for the subsequent specialized therapy of the oncological process.

Materials and methods: from 2019 to August 2021, 38 embolizing interventions were performed in 36 patients with recurrent bleeding from the bladder with ineffective conservative hemostatic therapy. Of these, there were 30 men and 6 women. The average age was 63 ± 2,6 years. All patients at the prehospital stage were diagnosed with pelvic cancer with invasion of the bladder wall without the possibility of radical treatment. Particles with a size of 300-500 µm, embolization coils and fragmentated hemostatic sponge were used for embolization.

Results: immediate angiographic success in the form of stagnation of blood flow through the target arteries was achieved in 100% of operations. In most cases, the relief of macrohematuria was achieved at day 4 (average values of erythrocytes in urine are 3,66 in p/sp). 2 patients (5,6%) underwent a second endovascular intervention during hospitalization due to the many small afferents suppluying the bladder tumor from the a. pudenta interna. Bleeding stopped in these patients by the 8th day of hospital stay. The early postoperative period in 100% of patients was accompanied by mild postembolization syndrome, which was stopped by symptomatic therapy within 24 hours.

Conclusions: endovascular embolization in patients with oncopathology using the superselective technique has shown efficacy in stopping urological oncological bleeding, allows to achieve stable hemostasis in a short time and to continue specific treatment of cancer in patients of the 2nd clinical group.

  

References

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2.     Schuhrke TD, Barr JW. Intractable bladder hemorrhage: therapeutic angiographic embolization of the hypogastric arteries. J Urol. 1976; 116(4): 523-525.

https://doi.org/10.1016/s0022-5347(17)58892-8

3.     Granov AM, Karelin MI, Tarazov PG. X-ray endovascular surgery in oncourology. Bulletin of roentgenology and radiology. 1996; 1: 35-37 [In Russ].

4.     Taha DE, Shokeir AA, Aboumarzouk OA. Selective embolisation for intractable bladder haemorrhages: A systematic review of the literature. Arab J Urol. 2018; 16(2): 197-205.

https://doi.org/10.1016/j.aju.2018.01.004

5.     Mohan S, Kumar S, Dubey D, et al. Superselective vesical artery embolization in the management of intractable hematuria secondary to hemorrhagic cystitis. World J Urol. 2019; 37(10): 2175 - 2182.

https://doi.org/10.1007/s00345-018-2604-0

6.     Tibilov AM, Baymatov MS, Kulchiev AA, et al. Arterial embolization in the treatment of inoperable bladder tumors complicated by bleeding. Materials of the V Russian Congress of Interventional Cardioangiologists. 2013; 35: 79 [In Russ].

7.     Bilhim T, Pisco JM, Tinto HR, et al. Prostatic arterial supply: anatomic and imaging findings relevant for selective arterial embolization. J. Vasc. Interv. Radiol. 2012; 23 (11): 1403-1415.

https://doi.org/10.1016/j.jvir.2012.07.028

8.     Bilhim T, Pereira JA, Tinto HR, et al. Middle rectal artery: myth or reality? Retrospective study with CT angiography and digital subtraction angiography. Surg Radiol Anat. 2013; 35(6): 517-522.

https://doi.org/10.1007/s00276-012-1068-y

9.     Korkmaz M, Sanal B, Aras B, et al. The short- and long-term effectiveness of transcatheter arterial embolization in patients with intractable hematuria. Diagn Interv Imaging. 2016; 97: 197-201.

https://doi.org/10.1016/j.diii.2015.06.020

10.   Liguori G, Amodeo A, Mucelli FP, et al. Intractable haematuria: long-term results after selective embolization of the internal iliac arteries. BJU Int. 2010; 106: 500-503.

https://doi.org/10.1111/j.1464-410X.2009.09192.x

 

11.   Karpov VK, Kapranov SA, Shaparov BM, Kamalov AA. Superselective embolization of urinary bladder arteries in the treatment of recurrent gross hematuria in bladder tumors. Urology. 2020; 5: 133-138 [In Russ].

https://doi.org/10.18565/urology.2020.5.133-138

 

Abstract:

Background: the optimal method for radiological diagnosis of prostate cancer (PCa) in planning multifocal biopsy is multiparametric magnetic resonance imaging (mpMRI)

Aim: was to improve the diagnosis of clinically significant PCa (csPCa) in patients with a negative primary biopsy, proceeding from mpMRI findings analysis based on results of the repeated procedure (24 cores) with targeted sampling of suspicious lesions.

Materials and methods: 732 patients were examined, 714 of them had been included in data of analysis. Prostatic mpMRI found suspicious foci with PI-RADS 3-5 in 396/714 (55.5%) patients. Results: The detection of PCa with a Gleason score of >7, PI-RADS 4 and 5 accounted for 65.9% and 80.0%, respectively Diagnostic sensitivity of mpMRI with a PI-RADS >4 in the diagnosis of PCa in patients with suspicious foci (n=396) was 83.6%, specificity - 84.9%; in the whole of 714 patients it was 46.4% and 86.7%, with a Gleason score of >7 - 75.3% and 89.3%, respectively In 73/290 (25.2%) patients with PI-RADS 3-5, PCa was detected in a systematic rather than in targeted biopsy, 17/73 (23.3%) of them having Gleason score >7. In 70/318 (22.0%) patients with PI-RADS 1-2, PCa was detected in systematic biopsy, in 11/70 (15.7%) cases Gleason score being >7.

Conclusion: mpMRI diagnostic accuracy for csPCa in patients with negative primary biopsy making it possible to refrain from repeated biopsy in males with PI-RADS 1-3; if repeated biopsy is necessary, the systematic one may be recommended.

 

References

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3.      Mottet N, Bellmunt J, Bolla M. et al. EAU-ESTRO-SIOG Guidelines on prostate cancer. Part 1: Screening, diagnosis, and local treatment with curative intent. Eur. Urol. 2017; 71 (4): 618-629.

4.      Standardized indicators of oncoepidemiological situation 2016. Evraziyskiy onkologicheskiy zhurnal. 2018; 6(2). Avaiable at: http://cisoncology.org/files/stat_oncology_2016.pdf (accessed 31 July 2018) [In Russ].

5.      Parker C, Gillessen S, Heidenreich A, Horwich A. Cancer of the prostate: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. of Oncol. 2015; 26 (suppl. 5): v69-v77.

6.      NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) with NCCN Evidence Blocks™. Prostate Cancer. 2018; Ver. 3. Available at: https://www.nccn.org/evidenceblocks/ (accessed 31 July 2018).

7.      Karman AV, Leusik EA. Comprehensive diagnostics for prostate cancer patients with negative primary biopsy. Early findings of a prospective study. Onkologicheskiy zhurnal. 2013; 7 (4): 65-71 [In Russ].

8.      Karman AV, Leusik EA. Diagnostic potential of PI-RADS for patients with negative results of initial multifocal biopsy. Onkologicheskii zhurnal. 2014; 8 (2): 20-27 [In Russ].

9.      Futterer JJ, Briganti A, de Visschere P. et al. Can clinically significant prostate cancer be detected with multiparametric magnetic resonance imaging? A systematic review of the literature. Eur. Urol. 2015; 68 (6): 1045-1053.

10.    Karman AV, Krasny SA, Leusik EA. et al. Our experience in employing the second version of PI-RADS scale in prostate cancer diagnosis in patients with negative initial multifocal biopsy. Onkologicheskiy zhurnal. 2015; 9 (2): 63-69 [In Russ].

11.    Kasel-Seibert M, Lehmann T, Aschenbach R. et al. Assessment of PI-RADS v2 for the Detection of Prostate Cancer. Eur. J. Radiol. 2016; 85 (4): 726-731.

12.    Moldovan PC, van den Broeck T, Sylvester R. et al. What Is the Negative Predictive Value of Multiparametric Magnetic Resonance Imaging in Excluding Prostate Cancer at Biopsy? A Systematic Review and Meta-analysis from the European Association of Urology Prostate Cancer Guidelines Panel. Eur. Urol. 2017; 72 (2): 250-266.

13.    Karman AV, Krasnyy SA, Shimanets SV. Targeted histology sampling from atypical small acinar proliferation area detected by repeat transrectal prostate biopsy. Onkourologiya. 2017; 3 (1): 91-100 [In Russ].

14.    Boesen L, Noergaard N, Chabanova E. et al. Early experience with multiparametric magnetic resonance imaging-targeted biopsies under visual transrectal ultrasound guidance in patients suspicious for prostate cancer undergoing repeated biopsy. Scand. J. Urol. 2015; 49 (1): 25-34.

15.    Junker D, Schwfer G, HeideggerI. et al. Multiparametric magnetic resonance imaging/transrectal ultrasound fusion targeted biopsy of the prostate: preliminary results of a prospective single-centre study. Urol. Int. 2015; 94 (3): 313-318.

16.    Prostate Imaging Reporting and Data System (PI-RADS). Available at: http://www.acr.org/Quality- Safety/Resources/PIRADS/ (accessed 31 July 2018).

17.    Bjurlin MA, Meng X, Le Nobin J. et al. Optimization of prostate biopsy: the role of magnetic resonance imaging targeted biopsy in detection, localization and risk assessment. J. Urol. 2014; 192 (3): 648-658.

18.    Franiel T, Stephan C, Erbersdobler A. et al. Areas suspicious for prostate cancer: MR-guided biopsy in patients with at least one transrectal US-guided biopsy with a negative finding - multiparametric MR imaging for detection and biopsy planning. Radiology. 2011; 259 (1): 162-172.

19.    Karman AV, Leusik EA., Dudarev VS. Saturation transrectal biopsy in prostate cancer diagnosing in men with negative primary multifocal biopsy. Onkologicheskij zhurnal. 2014; 8 (31): 31-40 [In Russ].

20.    Simmons LAM., Kanthabalan A, Arya M. et al. The PICTURE study: diagnostic accuracy of multiparametric MRI in men requiring a repeat prostate biopsy. Br. J. Cancer. 2017; 116 (9): 1159-1165.

21.    Brown LC, Ahmed HU, Faria R. et al. Multiparametric MRI to improve detection of prostate cancer compared with transrectal ultrasound-guided prostate biopsy alone: the PROMIS study. Health Technol. Assess. 2018; 22 (39): 1-176.

 

Abstract:

The prostate cancer is one of the most widespread forms of malignant new growths at men. Brachytherapy I125 is a modern, hi-tech, effective, rather safe and easily reproduced method of prostate cancer treatment. In the Russian Scientific Center of Roentgenoradiology implantation of microsources I125 in patients with localized and widespread prostate cancer is carried out by since 2003. For the last period 689 implantations of sources I125 were spent. The tumor-specific survival rate after brachytherapy significantly didn't differ from a tumor-specific survival rate after radical prostatectomy. Thus, brachytherapy is a hi-tech, modern method of treatment in patients with prostate cancer and quantity of undesirable postbeam effects is less than after radical prostatectomy.

 

References

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2.     Сивков А.В., Ощепков В.Н., Патаки К.В. Интерстициальная лучевая терапия I125 локализованного рака предстательной железы. Урология. 2004; 1: 21–25.

3.     Чиссов В.И., Старинский В.В. Злокачественные новообразования в России в 2008 г. (заболеваемость и смертность). 2010; 256.

4.     Stone N.H. et al. Prospective assessment of patient-reported long-term urinary morbidity and associated quality of life changes after I125 rostate brahytherapy. Brachytherapy. 2003; 2 (1): 32–39.

5.     De Reijke T.M., Laguna M.P. Department of Urology, Academic Medical Centre, Amsterdam. The Netherlands. Long-term complications of brachy-therapy in local prostate cancer. BJU International. 2003; 92 (8): 869–873.

 


 

Abstract:

Purpose. Was to determine the possibilities of transrectal ultrasound research (TUR) in grayscale-mode with the use of ultrasound angiography in diagnostics of rectitis and in monitoring its treatment in patients with prostate cancet (PC) after radiation therapy.

Materials and methods. The research consists of 62 patients with verified localized prostatic cancer (T13N01M0), which have already obtained conformed radiation therapy (RT) as a radical strategy. To estimate expressive radiation reaction patients were underwent transrectal ultrasound research before, during and after (in 3, 6, 12 months) radiation therapy. During the experiment, using grayscale-mode, the thickness of rectum front wall, its structure and echogenicity, and prostata capsula propria (lat.) tracking were estimated in dynamics. Vascularization of rectum front wall and pararectal cellulose was also analyzed in dynamics. Results of transrectal ultrasound were compared with clinical symptoms during the whole period of supervision, and were registered on the basis of patient’s personal note during and after treatment.

Results. Based on patients complaints we have noticed development of radiation rectitis (radiation therapy after-effect) which can be registered as higher thickness of rectum front wall, changes in its structure, decreasement of echogenicity and increased vascularization. The major part of patients with these changes noticed that such symptoms were therapeutically eliminated during supervision. Such echo-graphic changes won’t appear in case of prostate cancer progression and it can be used as a differential diagnostics between radiation therapy after-effect and prostate cancer growth.

Conclusion. Transrectal ultrasound allows to visualize early radiation rectitis implications in patients with prostatic cancer during radiation theraphy, and can promote the necessary treatment correction and advanced symptomatic therapy. 

 

References

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2.    Гранов А.М., Матякин Г.Г., Зубарев А.В. и др. Возможности современных методов лучевой диагностики и лечения рака предстательной железы. Кремл. мед. клин. вест. 2004; 16: 9–12.

3.    Давыдов М.И., Аксель Е.М. Статистика злокачественных новообразований в России и в странах СНГ в 2007 г. Вестник РОНЦ им. Н.Н. Блохина РАМН. 2009; 20 (3 – прил. 1): 8–138.

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Abstract:

The aim of the study was to demonstrate possibilities of magnetic resonance imaging (MRI) with contrast enhancement and calculation of «index of contrast agent accumulation» in diagnostics of prostate cancer. Accumulation of contrast agent in malignant and benign tissues were analyzed in comparison and in details. Efficiency of provided method of diagnosis and definition of pathologic process localization is proved.

 

Reference

1.     Franiel Т., Stephan C., Erbersdobler A., Dietz E. Maxeiner A. et al. Areas suspicious for prostate cancer: MR-guided biopsy in patients with at least one transrectal US-guided biopsy with a negative finding-multiparametric MR imaging for detection and biopsy planning. Radiology. 2011; 259:162-172.

2.     Kitajima K., Kaji Y, Fukabori Y, Yoshida K., Suganuma N. et al. Prostate cancer detection with 3T MRI: comparison of diffusion-weighted imaging and dynamic contrast-enhanced MRI in combination with T2-weighted imaging. J. Magn. Reson. Imaging. 2010; 31: 625-631.

3.     Futterer J.J., Heijmink S.W., Scheenen T.W., Veltman J., Huisman H.J. et al. Prostate cancer localization with dynamic contrastenhanced MR imaging and proton MR spectroscopic imaging. Radiology. 2006; 241:449-458.

4.     Tanimoto A., Nakashima J., Kohno H., Shinmoto H., Kuribayashi S. Prostate cancer screening: the clinical value of diffusionweighted imaging and dynamic MR imaging in combination with T2-weighted imaging. J. Magn. Reson. Imaging. 2007; 25:146-152.

5.     EL-Gabry E.A., Halpern E.J., Strup S.E., et al. Imaging prostate cancer; current and future applications. Oncology Huntingt. 2001; 15: 325-336.

6.     Engelbrecht MR, Huisman HJ, Laheij R.J. MR imaging Radiology 2003; 229: 248-254.

7.     Hara N., Okuizumi M. Koike H., Kawaguchi M., Bilim V. Dynamic contrast-enhanced magnetic resonance imaging (DCEMRI) is a useful modality for the precise detection and staging of early prostate cancer. Eur. Radiol. 2012; 22: 746-757.

8.     Nicholson B., Schaefer G., Theodorescu D. Angiogenesis in prostate cancer: biology and therapeutic opportunities. Cancer Metastasis Rev. 2001; 20: 297-319.

9.     Beyersdorff D., Taupitz M., Winkelmann B. et al. Patients with a history of elevated prostate-specific antigen levels and negative transrectal US-guided quadrant or sextant biopsy results: value of MR imaging. Radiology. 2002; 224: 701-706.

10.   Pasquier D., Hugentobler A., Masson P Which imaging methods should be used before salvage radiotherapy after prostatectomy for prostate cancer? Eur. Radiol. 2012; 22: 746-757.

11.   Cirillo S., Petracchini M., Scotti L. et al. Endorectal magnetic resonance imaging at 1.5 Tesla to assess local recurrence following radical prostatectomy using T2-weighted and contrast-enhanced imaging. Eur. Radiol. 2009; 19: 761-769

12.     ESUR prostate MR guidelines 2012 Jelle O. Barentsz & Jonathan Richenberg & Richard Clements & Peter Choyke & Sadhna Verma & Geert Villeirs & Olivier Rouviere & Vibeke Logager & Jurgen J. F^tere^ Engelbrecht M.R., Huisman H.J., Laheij R.J., et al. Discrimination of prostate cancer from normal peripheral zone and central gland tissue by using dynamic contrast enhanced MR imaging. Radiology. 2003; 229: 248-254 

 

Abstract:

Literature review is dedicated to the diagnosis of prostate cancer (PCa), namely the use of Fusion-technology, a technique which allows you to combine real-time data of magnetic resonance imaging (MRI) and transrectal ultrasound (TRUS), as well as to perform biopsy of the prostate, taking into consideration previously detected changes.

Review includes russian-language and foreign articles that discuss not only benefits, but also limit of the use of methods of prostate biopsy in verification of malignant pathology Review is based on data of main online resources: PubMed, Scientific Electronic Library (elibrary), SciVerse (ScienceDirect), Scopus.

During analysis of available literature, authors discuss the problem of prostate cancer diagnostics, difficulties encountered when using of traditional biopsy methods.

Review pays special attention to MRI/TRUS Fusion-navigation in diagnosis of prostate cancer as an alternative to other, more widely used in practice methods as for initial biopsy and for repeated manipulations

Conclusions: A key aspect of the application of MRI/TRUS Fusion-navigation is the ability to perform precisely targeted biopsy of suspicious sites by the presence of malignant changes ir prostate tissue, which increases the accuracy of diagnosis of tumors. Above described method of biopsy is extremely promising as part of specifying diagnostics of localized forms of prostate cancer. Methodics appeared informative in identifying clinically significant prostate cancer and accurate for localization of process, especially in front parts of the prostate, compared with 12 traditional points of biopsy At the same time, this manipulation, compared with traditional biopsy technique, requires advanced equipment and highly skilled personnel. 

 

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8.      Taira A.V., Merrick G.S., Galbreath R.W., et al. Performance of transperineal template-guided mapping biopsy in detecting prostate cancer in the initial and repeat biopsy setting. Prostate Cancer Prostatic Dis. 2010; 13:71-77.

9.      Javed S.I., Chadwick E., Edwards A.A., et al. Does prostate HistoScanning™ play a role in detecting prostate cancer in routine clinical practice? Results from three independent studies. BJU Int. 2013 Nov 13. doi: 10.1111/bju.12568.

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12.    Hambrock Т., Somford D.M., Hoeks C., Bouwense S.A.W., et al. Magnetic resonance imaging guided prostate biopsy in men with repeat negative biopsies and increased prostate specific antigen. Journal of Urology. 2010 Feb; 183(2):520-7.

13.    Hambrock T., Hoeks C., Hulsbergen-Van de Kaa et al.; Prospective Assessment of Prostate Cancer Aggressiveness Using 3-T Diffusion-Weighted Magnetic Resonance Imaging-Guided Biopsies Versus a Systematic 10-Core Transrectal Ultrasound Prostate Biopsy Cohort. Eur. Urol. 2012 Jan; 61(1):177-84.

14.    Kaplan I., Oldenburg N.E., Meskell P., et al. Real time MRI-ultrasound image guided stereotactic prostate biopsy. Magn. Reson. Imaging. 2002;20:295-299.

15.    Singh A.K., Kruecker J., Xu S., et al. Initial clinical experience with real-time transrectal ultrasonography-magnetic resonance imaging fusion-guided prostate biopsy. BJUInt. 2007;101:841-845.

16.    Pinto P.A., Chung PH., Rastinehad A.R., et al. Magnetic resonance imaging/ultrasound fusion guided prostate biopsy improves cancer detection following transrectal ultrasound biopsy and correlates with multiparametric magnetic resonance imaging. J.Urol. 2011; 186:1281-1285.

17.    Miyagawa T., Ishikawa S., Kimura T., et al. Real-time virtual sonography for navigation during targeted prostate biopsy using magnetic resonance imaging data. Int.J. Urol. 2010; 17: P855-860.

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19.    Bax J., Cool D., Gardi L., et al. Mechanically assisted 3D ultrasound guided prostate biopsy system. Med. Phys. 2008; 35: 5397-5410.

20.    Mozer P, Rouprrt M., Le Cossec C., et al. First round of targeted biopsies with magnetic resonance imaging/ultrasound-fusion images compared to conventional ultrasound-guided transrectal biopsies for the diagnosis of localised prostate cancer. J Urol. 2014 Jul;192(1): 127-8.

21.    Sonn G.A., Margolis D.J., Marks L.S. Target detection: Magnetic resonance imaging-ultrasound fusion-guided prostate biopsy. Urol Oncol. 2014 Aug;32(6):903-11

22.    Schoots I.G., Bangma C.H. MRI/US-fusion for targeted prostate biopsy. Ned. Tijdschr Geneeskd. 2014; 158.

23.    Rastinehad A.R., Turkbey B., Salami S.S., et al. Improving Detection of Clinically Significant Prostate Cancer: Magnetic Resonance Imaging/Transrectal Ultrasound Fusion Guided Prostate Biopsy. J Urol. 2014 Jun;191(6): 1749-54.

24.    Volkin D., Turkbey B., Hoang A.N., et al. Multiparametric MRI and Subsequent MR/Ultrasound Fusion-Guided Biopsy Increase the Detection of Anteriorly Located Prostate Cancers. BJU Int. 2014 Dec;114(6b):E43-9.

25.    Siddiqui M.M., Rais-Bahrami S., Truong H., et al. Magnetic resonance imaging/ultrasound-fusion biopsy significantly upgrades prostate cancer versus systematic 12-core transrectal ultrasound biopsy. Eur Urol. 2013 Nov;64(5):713-9.

26.    Walton Diaz A., Hoang A.N., Turkbey B., et al. Can magnetic resonance-ultrasound fusion biopsy improve cancer detection in enlarged prostates? J Urol. 2013 Dec;190(6):2020-5.

27.    Sonn G.A., Chang E., Natarajan S., et al. Value of targeted prostate biopsy using magnetic resonance-ultrasound fusion in men with prior negative biopsy and elevated prostate-specific antigen. Eur Urol. 2014 Apr;65(4): 809-15.

28.    Lawrence EM1, Tang SY Barrett T et al. Prostate cancer: performance characteristics of combined T2W and DW-MRI scoring in the setting of template transperineal re-biopsy using MR-TRUS fusion. Eur Radiol. 2014 Jul;24(7): 1497-505.

29.    Durmus T., Stephan C., Grigoryev M., et al. Detection of prostate cancer by real-time MR/ultrasound fusion-guided biopsy: 3T MRI and state of the art sonography. Rofo. 2013 May;185(5):428-33.

30.    Hu J.C., Chang E., Natarajan S., et al. Targeted Prostate Biopsy to Select Men for Active Surveillance: Do the Epstein Criteria Still Apply? J Urol. 2014 Aug;192(2): 385-90

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