Prostate biopsy explained

Prostate biopsy
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Prostate biopsy is a procedure in which small hollow needle-core samples are removed from a man's prostate gland to be examined for the presence of prostate cancer. It is typically performed when the result from a PSA blood test is high.[1] It may also be considered advisable after a digital rectal exam (DRE) finds possible abnormality. PSA screening is controversial as PSA may become elevated due to non-cancerous conditions such as benign prostatic hyperplasia (BPH), by infection, or by manipulation of the prostate during surgery or catheterization. Additionally many prostate cancers detected by screening develop so slowly that they would not cause problems during a man's lifetime, making the complications due to treatment unnecessary.

The most frequent side effect of the procedure is blood in the urine (31%). Other side effects may include infection (0.9%) and death (0.2%).[2]

Ultrasound-guided prostate biopsy

The procedure may be performed transrectally, through the urethra or through the perineum. The most common approach is transrectally, and historically this was done with tactile finger guidance.[3] The most common method of prostate biopsy was transrectal ultrasound-guided prostate (TRUS) biopsy.[4]

Extended biopsy schemes take 12 to 14 cores from the prostate gland through a thin needle in a systematic fashion from different regions of the prostate.[5]

A biopsy procedure with a higher rate of cancer detection is template prostate mapping (TPM) or transperineal template-guided mapping biopsy (TTMB), whereby typically 50 to 60 samples are taken of the prostate through the outer skin between the rectum and scrotum, to thoroughly sample and map the entire prostate, through a template with holes every 5 mm, usually under a general or spinal anaesthetic.[6] [7]

Antibiotics are usually prescribed to minimize the risk of infection.[4] [8] A healthcare provider may also prescribe an enema to be taken in the morning of the procedure. During the transrectal procedure, an ultrasound probe is inserted into the rectum to assist in guiding the biopsy needles. Following this, a local anesthetic, such as lidocaine, is administered into the tissue surrounding the prostate. Subsequently, a spring-loaded biopsy needle is inserted into the prostate, resulting in a clicking sound. When the local anesthetic is effective, any discomfort experienced is minimal.

MRI-guided targeted biopsy

MRI-US fusion biopsy

Since the mid-1980s, TRUS biopsy has been used to diagnose prostate cancer in essentially a blind fashion because prostate cancer cannot be seen on ultrasound due to poor soft tissue resolution. However, multi-parametric magnetic resonance imaging (mpMRI) has since about 2005 been used to better identify and characterize prostate cancer.[9] A study correlating MRI and surgical pathology specimens demonstrated a sensitivity of 59% and specificity of 84% in identifying cancer when T2-weighted, dynamic contrast enhanced, and diffusion-weighted imaging were used together.[10] Many prostate cancers missed by conventional biopsy are detectable by MRI-guided targeted biopsy.[11] In fact, a side-by-side comparison of TRUS versus MRI-guided targeted biopsy that was conducted as a prospective, investigator-blinded study demonstrated that MRI-guided biopsy improved detection of significant prostate cancer by 17.7%, and decreased the diagnosis of insignificant or low-risk disease by 89.4%.[12]

Two methods of MRI-guided, or "targeted" prostate biopsy, are available: (1) direct "in-bore" biopsy within the MRI tube, and (2) fusion biopsy using a device that fuses stored MRI with real-time ultrasound (MRI-US). Visual or cognitive MRI-US fusion have been described.[13]

When MRI is used alone to guide prostate biopsy, it is done by an interventional radiologist. Correlation between biopsy and final pathology is improved between MRI-guided biopsy as compared to TRUS.[14]

In the fusion MRI-US prostate biopsy, a prostate MRI is performed before biopsy and then, at the time of biopsy, the MRI images are fused to the ultrasound images to guide the urologist to the suspicious targets. Fusion MRI-US biopsies can be achieved in an office setting with a variety of devices.

MRI-guided prostate biopsy appears to be superior to standard TRUS-biopsy in prostate cancer detection. Several groups in the U.S.,[15] and Europe,[16] [17] have demonstrated that targeted biopsies obtained with fusion imaging are more likely to reveal cancer than blind systematic biopsies. In 2015, AdMeTech Foundation, American College of Radiology and European Society of Eurogenital Radiology developed Prostate Imaging Reporting and Data System (PI-RADS v2) for global standardization of image acquisition and interpretation, which similarly to BI-RADS standardization of breast imaging, is expected to improve patient selection for biopsies and precisely-targeted tissue sampling.[18] [19] PI-RADS v2 created standards for optimal mpMRI image reporting and graded the level of suspicion based on the score of one to five, with the goal to improve early detection (and exclusion) of clinically significant (or aggressive) prostate cancer.[20] The higher suspicion on mpMRI and the higher PI-RADS v2 score, the greater the likelihood of aggressive prostate cancer on targeted biopsy. Considerable experience and training is required by the reader of prostate mpMRI studies.

Up to 2013, indications for targeted biopsy have included mainly patients for whom traditional TRUS biopsies have been negative despite concern for rising PSA, as well as for patients enrolling in a program of active surveillance who may benefit from a confirmatory biopsy and/or the added confidence of more accurate non-invasive monitoring.[21] Increasingly, men undergoing initial biopsy are requesting targeted biopsy, and thus, the use of pre-biopsy MRI is growing rapidly.

Clinical trials of mpMRI and PI-RADS v2, including NIH-funded studies are underway to further clarify the benefits of targeted prostate biopsy.[22]

Side effects

Side effects of a TRUS or TPM biopsy include:[23] [6] [24]

Gleason score

See main article: Gleason score. The tissue samples are examined under a microscope to determine whether cancer cells are present, and to evaluate the microscopic features (or Gleason score) of any cancer found. Gleason score, PSA, and digital rectal examination together determine clinical risk, which then dictates treatment options.

Tumor markers

See main article: Tumor markers. Tissue samples can be stained for the presence of PSA and other tumor markers in order to determine the origin of malignant cells that have metastasized.[25]

Notes and References

  1. Ilic D, Djulbegovic M, Jung JH, Hwang EC, Zhou Q, Cleves A, Agoritsas T, Dahm P . 6 . Prostate cancer screening with prostate-specific antigen (PSA) test: a systematic review and meta-analysis . BMJ . 362 . k3519 . September 2018 . 30185521 . 6283370 . 10.1136/bmj.k3519 .
  2. Bell N, Connor Gorber S, Shane A, Joffres M, Singh H, Dickinson J, Shaw E, Dunfield L, Tonelli M . 6 . Recommendations on screening for prostate cancer with the prostate-specific antigen test . CMAJ . 186 . 16 . 1225–34 . November 2014 . 25349003 . 4216256 . 10.1503/cmaj.140703 .
  3. Ghei M, Pericleous S, Kumar A, Miller R, Nathan S, Maraj BH . Finger-guided transrectal biopsy of the prostate: a modified, safer technique . Annals of the Royal College of Surgeons of England . 87 . 5 . 386–7 . September 2005 . 16402467 . 1963966 .
  4. Roberts MJ, Bennett HY, Harris PN, Holmes M, Grummet J, Naber K, Wagenlehner FM . Prostate Biopsy-related Infection: A Systematic Review of Risk Factors, Prevention Strategies, and Management Approaches . Urology . 104 . 11–21 . June 2017 . 28007492 . 10.1016/j.urology.2016.12.011 .
  5. Patel AR, Jones JS . Optimal biopsy strategies for the diagnosis and staging of prostate cancer . Current Opinion in Urology . 19 . 3 . 232–7 . May 2009 . 19365892 . 10.1097/MOU.0b013e328329a33e .
  6. PROMIS - Prostate MRI Imaging Study. An evaluation of multi-parametric magnetic resonance imaging in the diagnosis and characterisation of prostate cancer. (UK) Medical Research Council - Clinical Trials Unit - PROMIS Trials Office. MRC: PR11, 2 February 2012
  7. Taira AV, Merrick GS, Galbreath RW, Andreini H, Taubenslag W, Curtis R, Butler WM, Adamovich E, Wallner KE . 6 . Performance of transperineal template-guided mapping biopsy in detecting prostate cancer in the initial and repeat biopsy setting . Prostate Cancer and Prostatic Diseases . 13 . 1 . 71–7 . March 2010 . 19786982 . 2834351 . 10.1038/pcan.2009.42 .
  8. Yaghi MD, Kehinde EO . Oral antibiotics in trans-rectal prostate biopsy and its efficacy to reduce infectious complications: Systematic review . Urology Annals . 7 . 4 . 417–27 . 2015 . 26538868 . 4660689 . 10.4103/0974-7796.164860 . free .
  9. Bonekamp D, Jacobs MA, El-Khouli R, Stoianovici D, Macura KJ . Advancements in MR imaging of the prostate: from diagnosis to interventions . Radiographics . 31 . 3 . 677–703 . May–June 2011 . 21571651 . 3093638 . 10.1148/rg.313105139 .
  10. Isebaert S, Van den Bergh L, Haustermans K, Joniau S, Lerut E, De Wever L, De Keyzer F, Budiharto T, Slagmolen P, Van Poppel H, Oyen R . 6 . Multiparametric MRI for prostate cancer localization in correlation to whole-mount histopathology . Journal of Magnetic Resonance Imaging . 37 . 6 . 1392–401 . June 2013 . 23172614 . 10.1002/jmri.23938 . free .
  11. Marks L, Young S, Natarajan S . MRI-ultrasound fusion for guidance of targeted prostate biopsy . Current Opinion in Urology . 23 . 1 . 43–50 . January 2013 . 23138468 . 3581822 . 10.1097/MOU.0b013e32835ad3ee .
  12. Pokorny MR, de Rooij M, Duncan E, Schröder FH, Parkinson R, Barentsz JO, Thompson LC . Prospective study of diagnostic accuracy comparing prostate cancer detection by transrectal ultrasound-guided biopsy versus magnetic resonance (MR) imaging with subsequent MR-guided biopsy in men without previous prostate biopsies . European Urology . 66 . 1 . 22–9 . July 2014 . 24666839 . 10.1016/j.eururo.2014.03.002 .
  13. Moore CM, Kasivisvanathan V, Eggener S, Emberton M, Fütterer JJ, Gill IS, Grubb Iii RL, Hadaschik B, Klotz L, Margolis DJ, Marks LS, Melamed J, Oto A, Palmer SL, Pinto P, Puech P, Punwani S, Rosenkrantz AB, Schoots IG, Simon R, Taneja SS, Turkbey B, Ukimura O, van der Meulen J, Villers A, Watanabe Y . 6 . Standards of reporting for MRI-targeted biopsy studies (START) of the prostate: recommendations from an International Working Group . European Urology . 64 . 4 . 544–52 . October 2013 . 23537686 . 10.1016/j.eururo.2013.03.030 .
  14. Hambrock T, Hoeks C, Hulsbergen-van de Kaa C, Scheenen T, Fütterer J, Bouwense S, van Oort I, Schröder F, Huisman H, Barentsz J . 6 . 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 . European Urology . 61 . 1 . 177–84 . January 2012 . 21924545 . 10.1016/j.eururo.2011.08.042 . 2066/109206 . 7076555 . free .
  15. Vourganti S, Rastinehad A, Yerram N, Nix J, Volkin D, Hoang A, Turkbey B, Gupta GN, Kruecker J, Linehan WM, Choyke PL, Wood BJ, Pinto PA . 6 . Multiparametric magnetic resonance imaging and ultrasound fusion biopsy detect prostate cancer in patients with prior negative transrectal ultrasound biopsies . The Journal of Urology . 188 . 6 . 2152–2157 . December 2012 . 23083875 . 3895467 . 10.1016/j.juro.2012.08.025 .
  16. Kuru TH, Roethke MC, Seidenader J, Simpfendörfer T, Boxler S, Alammar K, Rieker P, Popeneciu VI, Roth W, Pahernik S, Schlemmer HP, Hohenfellner M, Hadaschik BA . 6 . Critical evaluation of magnetic resonance imaging targeted, transrectal ultrasound guided transperineal fusion biopsy for detection of prostate cancer . The Journal of Urology . 190 . 4 . 1380–6 . October 2013 . 23608676 . 10.1016/j.juro.2013.04.043 .
  17. Fiard G, Hohn N, Descotes JL, Rambeaud JJ, Troccaz J, Long JA . Targeted MRI-guided prostate biopsies for the detection of prostate cancer: initial clinical experience with real-time 3-dimensional transrectal ultrasound guidance and magnetic resonance/transrectal ultrasound image fusion . Urology . 81 . 6 . 1372–8 . June 2013 . 23540865 . 10.1016/j.urology.2013.02.022 .
  18. Web site: AdMeTech. www.admetech.org. 2015-09-28.
  19. Web site: Prostate Imaging Reporting and Data System (PI-RADS) - American College of Radiology. www.acr.org. 2015-09-28.
  20. Weinreb JC, Barentsz JO, Choyke PL, Cornud F, Haider MA, Macura KJ, Margolis D, Schnall MD, Shtern F, Tempany CM, Thoeny HC, Verma S . 6 . PI-RADS Prostate Imaging - Reporting and Data System: 2015, Version 2 . European Urology . 69 . 1 . 16–40 . January 2016 . 26427566 . 6467207 . 10.1016/j.eururo.2015.08.052 .
  21. Sonn GA, Natarajan S, Margolis DJ, MacAiran M, Lieu P, Huang J, Dorey FJ, Marks LS . 6 . Targeted biopsy in the detection of prostate cancer using an office based magnetic resonance ultrasound fusion device . The Journal of Urology . 189 . 1 . 86–91 . January 2013 . 23158413 . 3561472 . 10.1016/j.juro.2012.08.095 .
  22. Web site: Search of: prostate mri biopsy - List Results - ClinicalTrials.gov. www.clinicaltrials.gov.
  23. Roberts MJ, Bennett HY, Harris PN, Holmes M, Grummet J, Naber K, Wagenlehner FM . Prostate Biopsy-related Infection: A Systematic Review of Risk Factors, Prevention Strategies, and Management Approaches . Urology . 104 . 11–21 . June 2017 . 28007492 . 10.1016/j.urology.2016.12.011 .
  24. Web site: Five Tips for a Safe Endocavity Biopsy . EDM Medical Solutions. 21 September 2018 .
  25. Chuang AY, DeMarzo AM, Veltri RW, Sharma RB, Bieberich CJ, Epstein JI . 11535862 . Immunohistochemical differentiation of high-grade prostate carcinoma from urothelial carcinoma . The American Journal of Surgical Pathology . 31 . 8 . 1246–55 . August 2007 . 17667550 . 10.1097/PAS.0b013e31802f5d33 .