Background: The numbers needed to treat (NNT) and the corresponding confidence intervals for patients with prostate cancer and defined annual PSA increases (PSA velocity, PSAV) have not been described previously. Aim: The objective of this study is to assess NNT, numbers needed to treat to harm and corresponding confidence intervals for radical prostatectomy (RP) in patients with prostate cancer defined as a PSAV ≤2 ng/ml/year. Methods: NNT following RP were estimated in risk groups defined by PSAV using mortality statistics and hazard ratios obtained in a noncontrolled trial. As no suited control group and no appropriate randomized trials were available for doing this calculation and as such trials are unlikely to become available in the near future we have calculated our NNTs as published previously by using relative risk reduction from an earlier randomized trial (RCT) comparing RP with watchful waiting (WW) [Can J Urol 2006;13(suppl 1):48–55]. Results: For preoperative PSAV >2 ng/ml/year, NNT for RP were estimated at 25, whereas for preoperative PSAV ≤2 ng/ml/year, the estimate was 618. The lower 95% confidence limits (NNTBl) were 9 and 126, respectively (treatment with benefit). The implications emerging from these findings are discussed by comparison with published NNT values from other RCTs. The lower 95% confidence limit for preoperative PSAV ≤2 ng/ml/year was found to be large in comparison. Conclusion: The NNT estimate obtained here for PSAV >2 ng/ml/year and its lower 95% confidence interval is comparable to values in other studies on prostate cancer for therapies considered to be effective, while the estimated NNT for patients with PSAV ≤2 ng/ml/year is large in comparison. We conclude that the benefits of RP for localized prostate cancer with preoperative PSAV ≤2 ng/ml/year may be considered small. There are several limitations to our findings, the most important of which lies in the fact that while PSAV remains significantly associated with outcomes, the predictive value of PSA measurements is low. While PSAV >2 ng/ml/year clearly indicates a need for surgery, a PSAV ≤2 ng/ml/year should imply further decision making.

1.
Jemal A, Siegel R, Ward E, et al: Cancer Statistics 2006. CA Cancer J Clin 2006;56:106–130.
2.
Klotz L: Active surveillance with selective delayed intervention using PSA doubling time for good risk prostate cancer. Eur Urol 2005;47:16–21.
3.
Thompson, IM, Pauler, DK, Goodman PJ, et al: Prevalence of prostate cancer among men with a prostate-specific antigen level of <4.0 ng per milliliter. N Engl J Med 2004;350:2239–2246.
4.
D’Amico AV, Chen MH, Roehl KA, et al: Preoperative PSA velocity and the risk of death from prostate cancer after radical prostatectomy. N Engl J Med 2004;351:125–135.
5.
Klotz LH, Nam RK: Active surveillance with severe delayed intervention for favorable risk prostate cancer: clinical experience and a ‘number needed to treat’ analysis. Can J Urol 2006;13(suppl 1):48–55.
6.
Whitson JM, Carroll, PR: Active surveillance for early-stage prostate cancer. J Clin Oncol 2010;28:2807–2809.
7.
Bill-Axelson A, Holmberg L, Ruutu M, et al: Radical prostatectomy versus watchful waiting in early prostate cancer. N Engl J Med 2005;352:1977–1984.
8.
Altman DG, Andersen PK: Calculating the number needed to treat for trials where the outcome is time to an event. BMJ 1999;319:1492–1495.
9.
Altman DG: Education and debate. Confidence intervals for the number needed to treat. BMJ 1998;317:1309–1312.
10.
Pilepich MV, Winter K, Lawton CA, et al: Androgen suppression adjuvant to definitive radiotherapy in carcinomas of the prostate – long term results of phase III RTOG 85-31. Int J Radiat Oncol Biol Phys 2005;61:1285–1290.
11.
Bolla M, Collette L, Blank L, et al: Long-term results with immediate androgen suppression and external irradiation in patients with locally advanced prostate cancer (an EORTC study): a phase III randomised trial. Lancet 2002;360:103–108.
12.
Center for evidence-Based-Medicine Toronto: http://ktclearinghouse.ca/cebm/glossary/nnt/oncology, last accessed 14 Feb. 2011.
13.
Horwitz EM, Bae K, Hanks GE, et al: Ten-years follow-up of Radiation Therapy Oncology Group Protocol 92-02: a phase III trial of the duration of elective androgen deprivation in locally advanced prostate cancer. J Clin Oncol 2008;26:2497–2504.
14.
Messing EM, Manola J, Sarosdy M, et al: Immediate hormonal therapy compared with observation after radical prostatectomy and pelvic lymphadectomy in men with node-positive prostate cancer. N Engl J Med 1999;341:1781–1788.
15.
Messing EM, Manola J, Yao J, et al: Immediate versus deferred androgen deprivation treatment in patients with node-positive prostate cancer after radical prostatectomy and pelvic lymphadenectomy. Lancet Oncol 2006;7:472–479.
16.
Tannock IF, de Wit R, Berry WR, et al: Docetaxel plus prednisone or mitoxantrone plus prednisone for advanced prostate cancer. N Engl J Med 2004;351:1502–1512.
17.
Overgaard M, Hansen PS, Overgaard J, et al: Postoperative radiotherapy in high-risk premenopausal women with breast cancer who receive adjuvant chemotherapy. N Engl J Med 1997;337:949–955.
18.
Overgaard M, Jensen MB, Overgaard J, et al: Postoperative radiotherapy in high-risk postmenopausal breast-cancer patients given adjuvant tamoxifen: Danish Breast Cancer Cooperative Group DBCG 82c randomised trial. Lancet 1999;353:1641–1648.
19.
Steineck G, Helgesen, F, Adolfsson J, et al: Quality of life after radical prostatectomy or watchful waiting. N Engl J Med 2002;347:790–796.
20.
Weißbach L, Altwein J: Aktive Überwachung oder aktive Therapie? Dtsch Arztebl Int 2009;106:371–376.
21.
Interdisziplinäre Leitlinie S3 der Deutschen Gesellschaft für Urologie: http://www.aezq.de/aezq/publikationen/kooperation, last accessed July 2010.
22.
Loeb S, Vonesh EF, Metter J, et al: What is the true number needed to screen and treat to save a life with prostate-specific antigen testing? J Clin Oncol 2010;29:464–467.
23.
Carter HB, Ferucci L, Kettermann A, et al: Detection of lilfe-threatening prostate cancer with prostate-specific antigen velocity during the window of curability. J Natl Cancer Inst 2006;98:1521–1527.
24.
Sölétormos G, Semjonow A, Sibley PEC, et al: Biological variation of total prostate-specific antigen: a survey of published estimates and consequences for clinical practice. Clin Chem 2005;51:1342–1351.
25.
Fall K, Garmo H, Andrén O, et al: Prostate-specific antigen levels as a predictor of lethal prostate cancer. J Natl Cancer Inst 2007;99:526–532.
26.
Kumar-Sinha C, Tomlins SA, Chinnaiyan AM: Recurrent gene fusions in prostate cancer. Nat Rev Cancer 2008;8:497–511.
27.
Johansson JE, Andrén O, Andersson SO, et al: Natural history of early, localized prostate cancer. JAMA 2004;291:2713–2719.
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