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Can Fam Physician
Vol. 53, No. 6, June 2007, pp.989 - 992
Copyright © 2007 by The College of Family Physicians of Canada
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Debates

Should Canadians be offered systematic prostate cancer screening?

YES

Yves Fradet, MD FRCSC
Professor and Head of Surgery and Urology at Laval University in Quebec

Correspondence to: Dr Yves Fradet, Centre de recherche, L’Hôtel-Dieu-de-Québec, 11 côte du Palais, Québec, QC G1R 2J6; telephone 418 525-4444, extension 15561; fax 418 691-5562; e-mail yves.fradet{at}crhdq.ulaval.ca

The justification for systematically screening asymptomatic patients for a condition is based on the severity of the disease, the existence of an effective method of detection, the efficacy of treatment, and a demonstrated substantial effect on mortality.1 In my view, all of these conditions are met with prostate cancer screening, and men have the right to be informed of the potential benefit to their health.

Severity of disease

The severity of prostate cancer is undeniable. Every year in Canada, some 20 000 new cases are diagnosed, and 20% of these men die from prostate cancer. These numbers are comparable to the numbers for breast cancer, and mortality and health care costs will increase proportionally with the rapid increase in life expectancy.

Effective method of detection

Prostate cancer screening is now possible thanks to a combination of the prostate specific antigen (PSA) test, which helps to identify those at greater risk of cancer, and development of a biopsy procedure guided by trans-rectal ultrasound. Approximately 6% of men aged 50 and older will have PSA levels higher than 4 µg/mL, and 16% will have levels between 2.5 and 4 µg/mL. Ultrasound-guided biopsies are well tolerated under local anesthetic and have a specificity of nearly 100% and a sensitivity of about 85%. About 15% of cancers are detected during a second biopsy.2

Efficacy of treatment

The efficacy of treatment for prostate cancer is well documented. A Swedish study3 demonstrated that surgical treatment of localized prostate cancer had reduced cancer mortality by more than 50% at 10 years and had had no negative effects on quality of life. No other cancer treatment can claim these results. Several other studies and observations show that screening significantly reduces mortality from prostate cancer. A study conducted in the Tyrol4 reported a statistically significant decrease in mortality among men who agreed to at least one systematic screening compared with men in other parts of Austria who were not screened. In Quebec city, a 67% decrease in mortality was observed among 7155 men (23% of 30 958 who were offered screening) who were systematically screened compared with those who turned down screening.5 Another European randomized pilot study of 2367 men showed a 75% decrease in cancer mortality at 10 years.6 We have also seen close to a 25% decrease in prostate cancer mortality in both Canada and the United States as well as in England, Austria, and several European countries since the PSA test was introduced, despite an increase in longevity.7 Regions in which the PSA test is used less extensively, such as Scandinavia and Australia, continue to experience an increase in prostate cancer mortality.

Comparison with screening for other diseases

While prostate cancer screening was being made available, screening for several other cancers was introduced on the basis of similar, even inferior data. For example, systematic screening for cervical cancer was implemented on the basis of similar observations and was never subjected to controlled studies.1 Among the many studies that have evaluated the efficacy of breast cancer screening, only 1 Swedish study was able to demonstrate a significant reduction in mortality and only in women older than 50. Breast cancer screening, however, is widely practised. The same is true for colon cancer; only 1 American study has demonstrated the efficacy of fecal occult blood screening. Even though studies are still trying to evaluate the efficacy of colonoscopy at the present time, it is widely used for screening purposes.

So, why isn’t screening for prostate cancer being promoted by family physicians as strongly as screening for these other cancers?

Clearly, advocacy for cancers specific to men has been much less effective than advocacy for cancers specific to women or cancers that affect both men and women. The biggest objection to prostate cancer screening is the potential detection of cancers that are not clinically significant and that will not result in death. It is becoming increasingly evident that low-grade cancers (Gleason =6) with a PSA of <10 carry a low risk of death, even without treatment.8 In Canada, close monitoring is increasingly recommended for this type of low-risk cancer.9 Moreover, this type of cancer seems to respond to hormone therapy and changes in diet and lifestyle, areas in which family physicians should play a predominant role. It would make sense to try to minimize the psychological and medical effects of a diagnosis of low-risk prostate cancer rather than to deprive some men of an effective means of detecting and treating a high-risk cancer just because we are afraid of adversely affecting a whole lot of other men.


KEY POINTS

  • Prostate cancer is common (the most common cancer in men) and serious (third cause of death due to cancer).
  • Effective treatment exists.
  • Screening reduces mortality due to prostate cancer.
  • Morbidity rates related to the detection of low-risk cancer can be decreased through close surveillance.

 

References

  1. Rimer BK, Schildkrait JM, Hiatt RA. Cancer screening. In: DeVita VT, Hellman S, Rosenberg SA, editors. Cancer: principles and practice of oncology. 7 ed. Philadelphia, Pa: Lippincott, Williams and Wilkins; 2004.
  2. Thompson IM, Ankerst DP, Chi C, Goodman PJ, Tangen CM, Lucia MS, et al. Assessing prostate cancer risk: results from the Prostate Cancer Prevention Trial. J Natl Cancer Inst 2006;98:506-7.[Free Full Text]
  3. Bill-Axelson A, Holmberg L, Ruutu M, Haggman M, Andersson SO, Bratell S, et al. Radical prostatectomy versus watchful waiting in early prostate cancer. N Engl J Med 2005;353:1298-300.[Free Full Text]
  4. Horninger W, Berger A, Pelzer A, Klocker H, Oberaigner W, Schönitzer D, et al. Screening for prostate cancer: updated experience from the Tyrol study. Can J Urol 2005;12(Suppl_1):7-13.[Medline]
  5. Candas B, Cusan L, Gomez JL, Diamond P, Suburu RE, Levesque J, et al. Evaluation of prostatic specific antigen and digital rectal examination as screening tests for prostate cancer. Prostate 2004;45:19-35.
  6. Schröder FH, Roobol MJ, Damhuis RAM, de Koning HJ, Blijenberg BG, Van der Kwast, et al. Rotterdam randomized pilot studies of screening for prostate cancer—an overview after 10 years. J Natl Cancer Inst 2005;97:696.[Free Full Text]
  7. Oliver SE, May MT, Gunnell D. International trends in prostate-cancer mortality in the "PSA ERA. Int J Cancer 2001;92:893-8.[Medline]
  8. Albertsen PC, Hanley JA, Fine J. 20-year outcomes following conservative management of clinically localized prostate cancer. JAMA 2005;293:2095-101.[Abstract/Free Full Text]
  9. Klotz L. Active surveillance with selective delayed intervention: using natural history to guide treatment in good risk prostate cancer. J Urol 2004;172(5 Pt 2):S48-50. discussion S50–1.[Medline]

Related articles in CFP:

Devrait-on offrir aux Canadiens le dépistage systématique du cancer de la prostate?: OUI
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CFP 2007 53: 994-997. [Full Text]  

Devrait-on offrir aux Canadiens le dépistage systématique du cancer de la prostate?: NON
Michel Labrecque, France Légaré, and Michel Cauchon
CFP 2007 53: 994-997. [Full Text]  



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