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Dilemmas Over the Decision to Perform Repeat Prostate Biopsies

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Korean Journal of Urology

The Korean Urological Association, 2014 227 Korean J Urol 2014;55:227

http://crossmark.crossref.org/dialog/?doi=10.4111/kju.2014.55.4.227&domain=pdf&date_stamp=2014-04-17

www.kjurology.org

http://dx.doi.org/10.4111/kju.2014.55.4.227

Editorial

Dilemmas Over the Decision to Perform Repeat Prostate Biopsies

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Regardless of age, patients with persistently elevated pros- tate-specific antigen (PSA) levels and/or a suspicious result on a digital rectal exam but with a previous history of a neg- ative prostate biopsy result usually present a dilemma to urologists. Published reports have shown that the positive rate of repeat prostate biopsy in men suspected of having prostate cancer and at least 1 previous negative biopsy is around 10% to 35% [1,2]. Potential reasons for previous negative findings in men who have cancer detected in re- peat biopsies include inadequacy of the initial biopsies (fewer cores taken) or the presence of precancerous lesions, such as atypical small acinar proliferation. As a result of concerns over missed cancer, urologists frequently resort to repeat biopsy. However, in reality, the aforementioned positive rates in repeat biopsies demonstrate that the re- sults of most repeat biopsies will prove to be negative. In addition to causing significant anxiety, prostate biopsies can result in complications that can sometimes be severe.

Some investigators have even reported that the rate of hos- pitalization for infection following prostate biopsies is on the rise [3]. Furthermore, in a Western series, it was shown that about 1 in 10 men refuse a repeat biopsy or require an- algesia or sedation for the procedure [4]. Overall, it would be safe to say that the decision to recommend a repeat pros- tate biopsy is never an easy one for urologists to make.

So how can urologists overcome such a dilemma? It may just be that we are digging a hole for us to be buried in by recommending PSA testing to the wrong group of men, spe- cifically, younger men, in the first place. A recently pub- lished American Urological Association (AUA) guideline on prostate cancer detection recommends against PSA screen- ing in men aged <40 years [5]. Also, despite causing some controversy, the same AUA guideline states that routine screening is not recommended in men aged 40 to 54 years and at average risk. Such statements may well have been made for the following reasons: a low prevalence of prostate cancer in younger men, absence of evidence for PSA screen- ing in younger men, and risk of harm from biopsies and treatments. Accordingly, to avoid the dilemma of agonizing over the decision to perform repeat biopsy in younger men, we should be more judicious in recommending PSA testing

initially. Although we should not actively discourage PSA testing in younger men on the whole (especially among those with a family history or other risk factors), a more careful approach in PSA screening would eventually prove beneficial in lessening the dilemma over repeat biopsies.

Also, newly developed markers, such as PCA3, phi, and 4Kscore (although not yet available worldwide), will likely be helpful in decision-making for prostate biopsies. In addi- tion, multiparametric magnetic resonance imaging has been frequently mentioned to increase the probability of a positive repeat biopsy. Applications of these tools would cer- tainly be helpful in lessening urologists’ burden over repeat biopsy decisions in the future. However, unless a break- through occurs in the detection of prostate cancer, which al- lows us to do away with PSA testing completely, we will nev- er be 100% freed from the dilemma over repeat biopsies.

Despite the current overall sentiment towards PSA testing, the fear of missed tumors will always linger.

Sung Kyu Hong, MD, PhD Associate Editor Department of Urology, Seoul National University Bundang Hospital, 82 Gumi-ro 173beon-gil, Bundang-gu, Seongnam 463-707, Korea E-mail: [email protected]

REFERENCES

1. Chun FK, Epstein JI, Ficarra V, Freedland SJ, Montironi R, Montorsi F, et al. Optimizing performance and interpretation of prostate biopsy: a critical analysis of the literature. Eur Urol 2010;58:851-64.

2. Kirby R, Fitzpatrick JM. Optimising repeat prostate biopsy deci- sions and procedures. BJU Int 2012;109:1750-4.

3. Nam RK, Saskin R, Lee Y, Liu Y, Law C, Klotz LH, et al. Increasing hospital admission rates for urological complications after trans- rectal ultrasound guided prostate biopsy. J Urol 2010;183:963-8.

4. Seymour H, Perry MJ, Lee-Elliot C, Dundas D, Patel U. Pain after transrectal ultrasonography-guided prostate biopsy: the advan- tages of periprostatic local anaesthesia. BJU Int 2001;88: 540-4.

5. Carter HB, Albertsen PC, Barry MJ, Etzioni R, Freedland SJ, Greene KL, et al. Early detection of prostate cancer: AUA Guideline. J Urol 2013;190:419-26.

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