|Year : 2009 | Volume
| Issue : 2 | Page : 177-184
The routine use of prostate-specific antigen for early detection of cancer prostate in India: Is it justified?
Department of Urology, SGPGIMS, Rae Bareli Road, Lucknow-226 014, India
|Date of Web Publication||24-Jun-2009|
Department of Urology, SGPGIMS, Rae Bareli Road, Lucknow-226 014
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background: The use of prostate-specific antigen (PSA) for early detection of prostate cancer is a widely debated issue. The average Indian urologist is faced with the dilemma of whether PSA testing should be routinely offered to men over 50 years of age. The Urological Society of India is yet to issue any guidelines on PSA testing. This article attempts to explore scientific evidence dealing with this controversial subject.
Materials and Methods: A MEDLINE search was performed using the words 'PSA screening', 'prostate cancer statistics', and 'PSA screening guidelines'. The relevant articles were then analysed for evidence regarding the utility of PSA screening.
Results: Prostate cancer does not qualify to be categorized as a major health problem in India. The natural history of screen-detected cancer is not known. Prostate-specific antigen testing for early detection of prostate cancer has questionable benefits and has a potential to cause harm to asymptomatic individuals. There is no consensus amongst learned medical societies as to what should be the best approach for PSA testing. Most organizations caution against widespread PSA screening and emphasize on informed consent and patient counseling with regard to PSA testing. Randomized prospective trials are ongoing to assess to the true impact of screening on prostate cancer mortality.
Conclusions: There is no scientific rationale to advocate routine use of PSA for early detection of prostate cancer in Indian males. Results of randomized screening trials are awaited to clarify on this issue.
Keywords: Prostate cancer, prostate-specific antigen, screening
|How to cite this article:|
Dubey D. The routine use of prostate-specific antigen for early detection of cancer prostate in India: Is it justified?. Indian J Urol 2009;25:177-84
|How to cite this URL:|
Dubey D. The routine use of prostate-specific antigen for early detection of cancer prostate in India: Is it justified?. Indian J Urol [serial online] 2009 [cited 2019 Jun 17];25:177-84. Available from: http://www.indianjurol.com/text.asp?2009/25/2/177/52908
| Introduction|| |
The last couple of decades have been witness to a revolution in the methods used for the diagnosis and management of prostate cancer. One of the most hotly debated issues has been the use of prostate-specific antigen (PSA) for early detection of prostate cancer. Literature regarding early detection of prostate cancer emanates predominantly from American and Western European centers, regions where the incidence of prostatic carcinoma is amongst the highest in the World. Use of PSA for screening of prostate cancer has largely been a North American endeavor. , However, even in the USA, which has the highest incidence of prostate cancer, there is no consensus regarding PSA screening. The American Cancer Society  and the American Urological Association  recommend an annual PSA test for asymptomatic men above the age of 50 years. The American College of Preventive Medicine  and the US Preventive services task force  conclude that there is an insufficient evidence to recommend routine population screening with DRE or PSA. The National Health Service of the United Kingdom does not recommend screening,  even though the burden of prostate cancer is significant in that country. It is therefore evident that the medical community is deeply split on the benefits of PSA screening even in countries where prostate cancer is a major health problem.
Given this background, most Indian urologists are unsure about the real implications of ordering a PSA test to an asymptomatic Indian male aged above 50 years. This article attempts to explore the issue of use of PSA for early detection of prostate cancer, which should hopefully provide the Indian urologist with a correct perspective on this highly controversial topic.
| Principles of Screening|| |
Early detection attempts to identify preclinical and asymptomatic cases of a disease in a population at risk using a suitable test, rather than making a diagnosis based on a patient's presentation at a later stage with symptoms and signs. This objective can be achieved by employing screening methods, which can be broadly categorized into two types: 
- Organized screening: A large number of populations at risk are invited for screening and the process is monitored by an independent authority.
- Opportunistic screening: Patient asks doctor or doctor orders a test on the patient. This process is unmonitored.
In India and other parts of the world, most urologists and general physicians resort to 'Opportunistic screening' whilst ordering for a PSA test. This article debates the use of both organized and opportunistic screening for prostate cancer in India. The question to be answered is: Does routine testing for PSA in asymptomatic men make any sense from a public health perspective?
To answer this question there are seven key questions that need to be addressed:
Is the disease a substantial health problem in Indian males?
Prostate cancer is the most commonly diagnosed male malignancy and the second leading cause of male cancer death in the USA.  However, the incidence of prostate cancer varies from country to country, with the highest incidence being found in the Western world and the lowest in the Asian countries. Data obtained from the International Agency for Cancer Research (IARC) suggests very low incidence of prostate cancer in East Asian countries  [Figure 1]. In India, prostate cancer is also identified as only the 10th common malignancy affecting men.  Numerous factors like contrasting genetic, environmental, and dietary influences may be responsible for the low incidence of prostate cancer amongst Asian populations. Recent studies have demonstrated a significant impact of diet on prostate cancer. , East Asian diets have been traditionally vegetarian and low in fat content. A diet rich in phytoestrogens, which is found in vegetarian diets, and soy products has been associated with a protective mechanism against prostate cancer.  There is a growing evidence that curcumin (turmeric) and a diet rich in vegetables has a significant protective effect on prostate cancer growth. ,, These dietary factors could be responsible for the low incidence of prostate cancer in India.
The indian cancer registry
There is no comprehensive information available on the actual incidence of prostate cancer in India. Efforts have been made by the Indian Council of Medical Research (ICMR) to collect data through the National Cancer Registry. The boost for cancer registration in India began in 1982, through initiation of the National Cancer Registry Program (NCRP) by the Indian Council of Medical Research. The NCRP began with three population-based registries (existing Bombay registry and new registries at Bangalore and Madras) and three hospital-based registries (at Chandigarh, Dibrugarh, and Trivandrum). The data from cancer registries helped in highlighting the magnitude and common sites of cancer in India, and was useful in planning the National Cancer Control Program. The network of population-based cancer registries under NCRP is proposed to be expanded.
There are limited data on cancer incidence available from population-based cancer registries in India which have been published by the ICMR. The most established cancer registry for rural areas in India is at the Nargis Dutt Memorial Hospital at Barshi, Sholapur, Maharashtra. The 'Population-Based Rural Cancer Registry' was commenced under the auspices of ICMR under the NCRP in 1987. At this hospital, the top five male cancers that were identified were hypopharynx, oesophagus, rectum, lung and liver.  Similarly, a population-based cancer registry in rural Tamil Nadu showed extremely low incidence of prostate cancer with more than 50% cancers in males involving the head and neck region.  The Kolkata population-based cancer registry recorded prostate cancer as the sixth most common cause of cancer in males with the highest incidence of lung cancer followed by cancers of the oral cavity.  In cancer registries of Mumbai, Ahmedabad, Chennai, and Bangalore, prostate cancer was the fourth, ninth, ninth, and fifth most common cancer, respectively, amongst males, clearly highlighting the fact that prostate cancer is not a major health problem in India.  This data, though skewed, provides some insight into the burden of prostate cancer in India. It is therefore reasonable to conclude that there is no evidence to suggest that prostate cancer is public health problem in India which is in stark contrast to the situation in Western countries.
Is the natural history of the disease well understood?
Many men have a greater chance of dying with, rather than because of, prostate cancer. Whilst the lifetime risk of having a microscopic focus of prostate cancer at the age of 50 years is 42%, the risk of dying from prostate cancer is 3%.  Thus, a large number of prostate cancers follow an indolent course, without presenting clinically. Two longitudinal studies with more than 15-year follow-up have demonstrated that, in the large majority of cases detected (by palpation) in the pre-PSA era, prostate cancer progressed very slowly, with death due to other causes most commonly intervening before the cancer becomes life-threatening. , Short-term monitoring studies of highly selected older men with PSA-detected, nonpalpable, localized prostate cancer do not suggest that delayed or no treatment leads to poor health outcomes. , Prostate-specific antigen screening results in over-detection (of cases which would otherwise not have been detected) and introduces a lead-time (the time difference between screen detection and clinical detection) in the absence of screening, which may be of the order of 10 years or more. It is therefore logical to assume that the natural history of screen-detected cancer would follow a more prolonged course than that of clinically detected cancer from the pre-PSA era. This is important for men faced with the choice between conservative and curative treatment. In comparison with clinically detected disease, men with screen-detected cancers will have longer to endure any adverse effects of curative treatment and longer to wait for any beneficial effect on survival to emerge.
Whilst there is currently no standard definition for 'clinically significant' prostate cancer, this term may include prostate cancers at risk of progression and which, without screening, would be lethal.  Cancers are considered insignificant if their volume is <0.5 cc and there is absence of Gleason 4 or 5. It is likely that a large proportion of screen-detected prostate cancers may never become clinically significant, as shown in a recent analysis from the European Randomized Study of Screening for Prostate Cancer (ERSPC).  Prostate cancer screening programs should ideally detect a low proportion of 'insignificant' cancers;  however, it is estimated that between 18 and 85% of screen-detected prostate cancers may never become clinically significant, , representing a considerable burden of 'overdiagnosis' and potential overtreatment. Not more than approximately 1 in 8 screen-detected prostate cancers is likely to cause mortality if left untreated. 
The knowledge of the natural history of prostate cancer is, however, currently limited to clinically diagnosed cases, whilst little is known of the natural history of screen-detected prostate cancer. It is hoped that greater insight regarding the natural history of screen-detected cancer will soon be obtained from analysis of ongoing randomized trials in Europe and the United States. ,
Does performing the test improve patient outcomes?
Once prostate cancer is detected on biopsy, it remains unclear as to what is the best treatment option. The traditional approach includes radical prostatectomy, radical radiotherapy, brachytherapy or watchful waiting. Bill-Axelson et al.,  conducted a randomized prospective trial comparing watchful waiting with radical prostatectomy (RP) for the management of localized prostate cancer. This trial demonstrated that prostate cancer mortality was significantly lower in the RP group (30 of 347, 8.6%) vs watchful waiting (50 of 358, 14.4%). The absolute risk in reduction of death from prostate cancer was small (approx. 5%); however, reductions in risk of progression and metastasis was substantial. In a recent update of the trial, there was no extended benefit in survival and metastasis, even after a 10-year follow-up.  The 5% absolute improvement in 10-year survival was achieved at the expense of a 35% absolute increase in the risk of erectile dysfunction and a 28% absolute increase in the risk of urinary leakage.  Only 12% of patients in the Scandinavian trial had stage T1c disease, and as many as 19% of patients had a PSA level of >20 ng/mL. How can the outcome data, based largely on clinically detected prostate cancer, be applied to men with screen-detected disease? At present, insufficient time has elapsed to observe the natural history of screen-detected prostate cancer; however, it is interesting to compare the 10-year prostate cancer-specific mortality rate of 14.9% for watchful waiting reported by Bill-Axelson et al., , with the 15-year rate of 7.4-11.6% for screen-detected disease predicted by Nicholson and Harland. 
Given the more favorable natural history of screen-detected disease, it seems likely that the absolute survival benefit of treatment will be less compared to treatment of clinically detected prostate cancer. There are two ongoing randomized trials that will address this issue. , The results of these trials will be important in helping to define the magnitude of the survival benefit for the radical treatment of screen-detected, rather than clinically detected, prostate cancer.
In terms of 10-year freedom from distant metastasis, the absolute benefit of surgery vs watchful waiting was 10% (84.8 vs 74.6%, P = 0.004).  Hence it could be argued that 90% of patients did not benefit significantly from RP. Is it possible to identify these patients before surgery? One approach to this problem is active surveillance, in which radical treatment is targeted to those patients with biochemical or histological progression during a close-observation period.  This is by contrast to traditional watchful waiting, as specified in the Scandinavian trial, according to which palliative treatment is given to those with symptomatic progression.
Is the test accurate (high sensitivity and specificity)?
Although PSA is the most commonly performed screening test for the early detection of prostate cancer, its performance is very poor. There is no specific cut-off level for PSA to reliably detect prostate cancer. The normal accepted cut-off of 4.0 ng/ml is being seriously challenged because at this level PSA has a sensitivity of only 67.5-80%.  In other words, approximately 20-30% of tumors will be missed if PSA alone is used. Also the specificity of PSA testing is 60-70%  when the PSA level is 4.0 ng/ml. Prostate cancer may be present in significant proportion of men with a serum PSA <4.0 ng/ml. In a recent prostate biopsy series, positive biopsy rates for prostate cancer in men with serum PSA 2-4 ng/ml are nearly the same as a serum PSA of 2-20 ng/ml.  In fact, positive prostate biopsy rates consistently increase with age at PSA levels between 4 and 10 ng/ml with normal digital rectal examinations.  Stamey et al. (2004) concluded that PSA in the range of 4-10 ng/ml correlates more strongly with benign prostatic hyperplasia (BPH) than with prostate cancer.
Between 1995 and 2001, a large American study screened 6691 men for prostate cancer using PSA. The study showed that the diagnostic performance of total PSA using a threshold of 4 ng/ml was poor. The results indicated that if biopsies were performed only when the PSA was higher than 4 ng/ml, then 82 and 65% of cancers in men below 60 years of age and over 60 years of age, respectively, would be missed.  It was demonstrated that as PSA threshold is lowered, there is an improvement in sensitivity with a trade-off in specificity.
An analysis of the prostate cancer prevention (PCP) trial  also demonstrated low sensitivity with a PSA cut-off of 4.0 ng/ml: with this cut-off only 20.5% of the prostate cancer cases tested positive and nearly 80% cancers would have been missed. Lowering the PSA threshold for screening increases detection of aggressive cancer at an earlier stage; however, it has the unavoidable trade-off of increased detection of biologically irrelevant cancers.  Therefore, a positive screening test does not necessarily mean that an individual is certain to have a cancer, nor does a negative screening test result always confirm the absence of a cancer. Hence PSA, when used alone as a screening test has a poor specificity and sensitivity. Given the above limitations, serum PSA alone does not fulfil the criteria to be labeled as a valid screening test for prostate cancer.
There is evidence that prostate cancer screening decreases mortality
If it were to be convincingly demonstrated that screening reduces prostate cancer mortality then, the case could be made to implement screening and early detection protocols. However, this has not been forthcoming as yet. Widespread PSA screening in the USA began in the early1990s and toward the end of the decade, prostate cancer mortality has shown a declining trend. , Many authors advocate this decline in mortality due to aggressive PSA screening. Such a sudden decline so soon after the introduction of a screening test for a cancer known for its long latency is unexpected, and is unusual when one considers that the test was in use in the context of controlled clinical trials rather than among the general public until the late 1980s. One cannot exclude the potential contribution of the lead-time and length biases, increased awareness of prostate cancer, increased awareness of screening for prostate cancer, and improved surgical, radiation, and hormonal treatment for early and advanced prostate cancer, to the observed decline in mortality.
Other factors like the increased use of cholesterol-lowering agents (statins), which have an inhibitory effect on prostate cancer and dietary and lifestyle changes may partly account for this decline in mortality. 
There has been a paucity of properly conducted prospective clinical trials to observe the impact of screening on prostate cancer mortality.
Prostate cancer mortality in the Tyrol region of Austria, where PSA testing was widely available and encouraged, was compared with mortality in the rest of Austria where the test was not introduced.  A reduction in prostate cancer mortality was observed in the Tyrol region compared with the rest of Austria, but the reduction occurred far sooner than may be expected from the application of screening alone.  Recently, a study of two cohorts of men from regions with different practice patterns in the United States was reported.  Men in Seattle-Puget Sound received a higher exposure to screening and aggressive treatment for prostate cancer than men in Connecticut, with a five-fold difference in PSA testing and RP; however, no significant reduction in the adjusted rate ratio of prostate cancer mortality was observed.
Two randomized controlled trials for prostate cancer screening have been performed. The Quebec trial  commenced in 1988 and recruited men aged 45-80 years registered on the 1985 electoral rolls of Metropolitan Quebec City, Canada, and traceable on the health registries. A total of 46 193 men were randomized; 2 : 1 in favor of being invited to screening. Prostate cancer mortality was the primary outcome measured at 11-years follow-up. Eleven years after the commencement of the study, the authors of the Quebec study reported the relative risk of death from prostate cancer to be 0.39 (95% CI: 0.19-0.65) in men who are screened.
The Quebec study was limited by the lack of adherence to screening from participants randomized to the screening group. Although 31 133 men were randomized to receive screening for prostate cancer, only 23% of participants in this group actually complied with the randomization and were screened. Similarly, approximately 7% of men randomized to the control group were screened for prostate cancer. Therefore, crossover between groups was a significant problem in this trial. Data analysis was also compromised; mortality data was not analysed according to the intention-to-screen principle. The authors of the trial reported a reduction in prostate cancer-specific mortality by comparing mortality in men who were screened to that of men who were not screened, regardless of their initial randomization. Conversely, when this data was analysed, according to the intention-to-screen principle, no significant difference in mortality between the two groups was demonstrated. , Due to these methodological issues, results from this trial do not give a clear indication of any true benefits or harms associated with screening for prostate cancer.
The Norrkoping trial  commenced in 1987 and recruited men from Norrkoping, Sweden, aged 50-69 years registered on the 1987 national population register. A total of 9026 men were identified, with every sixth man 'randomized' to screening. This study was also criticized due to its methodological flaws. Furthermore, the quasi-random method of allocation, lack of allocation concealment, and potentially unblinded outcome assessment compromise the quality of the trial. Both the Quebec and Norrkoping studies have on critical appraisal  been found to be biased in terms of methodology. There are two ongoing randomized clinical trials to assess the impact of screening on prostate cancer mortality (the ERSPC, Rotterdam and PLCO, USA). Results from these studies would throw some light on this controversial aspect.
Adequate facilities exist to cope with abnormalities detected
Prostate-specific antigen is obtained from different laboratories in India and there is no standardization. Once PSA is abnormal, there is a need to perform ultrasound-guided transrectal prostatic biopsy. However, this facility is limited to very few centers in India. Also, further treatment in the form of radical prostectomy/radical radiotherapy is not standardized in various centers across India. Given this scenario, it is evident that facilities are inadequate to cope with abnormalities detected in PSA screening program. Therefore mass screening and especially the trend amongst general physicians to order for a PSA test should be discouraged.
Will performing the test likely to cause harm to individuals?
A large number of patients with an elevated PSA are unlikely to have prostate cancer. However, once they know that PSA elevation can be associated with prostate cancer, they resort to regular and frequent PSA checks and this becomes a source of anxiety. Moreover, prostate biopsy is also associated with complications. Radical treatment for prostate cancer may also be associated with harmful side-effects. A randomized control trial demonstrated that RP for palpable disease offers a 5% absolute benefit in terms of 10-year survival; but a 35 and 28% absolute increase in the risk of erectile dysfunction and urinary incontinence, respectively. Studies investigating the impact of screening on healthy individuals , have demonstrated that PSA screening can cause significant psychological harm to individuals who have false-positive PSA tests. A recent review has concluded that PSA screening is associated with psychological harms and its potential benefits remain uncertain. 
Given these arguments, it is evident that prostate cancer is not a major health problem in India, the natural history of screen-detected prostate cancer remains unknown, the PSA test is not reliable for the diagnosis of prostate cancer, and there is no convincing evidence that screening for prostate cancer decreases mortality. Also PSA screening has been found to be associated with significant psychological harm amongst those without prostate cancer. There appears to be no justification for mass or opportunistic screening for prostate cancer in India.
| The Position Adopted by Various Learned Societies Worldwide on the Issue of PSA Screening|| |
In spite of the high incidence of prostate cancer in North America and Europe, there is a significant difference of opinion amongst learned medical societies and government organizations regarding the use of PSA screening [Table 1].
What does this mean for urologists in India, should they order a PSA test for men older than 50 years?
With so much hype regarding PSA screening, many elderly patients are concerned whether they should undergo a routine PSA test. The American Urological Association  and the American Cancer Society  recommend PSA testing as a part of 'shared decision-making' between the patient and the urologist. This means that the urologist should explain both the advantages and disadvantages of undergoing a PSA test and offer it only as a part of informed consent. However, there seems to be no consensus regarding what should be conveyed to the patient as a part of the informed consent. , Moreover, the opinion regarding informed consent for PSA testing is divided among urologists with there being no widely accepted guideline. , The British Association of Urologists  suggests the following points to be incorporated while counseling a patient for the PSA test.
The recommendations of the Department of Health, Govt of UK , are indicated in [Table 2].
- The test may detect a cancer and a stage where curative treatment can be offered
- That the test may detect early prostate cancer in around 5% of men aged 50-65 years
- That the test will fail to detect some early tumors
- Prostate-specific antigen testing and subsequent treatment of early prostate cancer may incur risk and may not improve life expectancy in all men
Studies indicate that very few patients are actually informed about the PSA test. In a survey published in 2001, hardly 17% of physicians reported that they would decide whether to order a PSA test based on patient preferences.  Another study reported that only two-thirds of men who are screened even know that they have been tested.  These data suggest that minimal shared decision-making is occurring. Whether informed consent should be used for the average Indian patient is debatable as people in this country are less aware about prostate cancer as compared to their Western counterparts.
This issue is especially pertinent when applied to the majority of Indian patients, especially those with lower level of education and those belonging to the lower socioeconomic class. Interestingly, when informed consent was used for PSA testing in members of the lower socioeconomic class, they were found to be significantly less interested in undergoing the PSA test as compared to those who were not offered informed consent. 
Dr Steven Wolf, in an editorial in the American Journal of Family Medicine  makes a succinct comment regarding this dilemma: 'Just as the patient must decide, based on personal values, whether the benefits outweigh the risks, the physician must decide whether what is gained by circumventing the challenges of shared decision making is offset by its harms to the patient and physician. It is a personal choice that only conscience, not guidelines, can dictate.'
Given this scenario, it behooves upon tertiary medical institutions which have an interest in prostate cancer, to conduct epidemiological studies on prostate cancer in India, to document the true burden of disease rather than pursue a policy which is increasingly being questioned in the West. In the authors institution, well over 2000 patients have had their PSA done for 'opportunistic screening' and the pick-up rate of prostate cancer is merely approximately 12% (unpublished data), which could be attributed to a chance alone. In spite of using opportunistic screening for the vast majority of elderly males visiting the urology department, there have been not more than 25 radical prostatectomies performed in the author's institution in the last 5 years and the majority have been for clinically detected and locally advanced disease (unpublished data). In spite of routine use of PSA for early detection, no center in India has published results of RP series for screen-detected cancer prostate, indicating the relatively low incidence of disease which corroborates with data from the Indian Cancer Registry, as cited in the article.
| Conclusions|| |
Given the low incidence of cancer prostate in India and the doubtful utility of screening in populations with a high incidence of prostate cancer, it is not appropriate to advocate routine use of PSA for early detection of prostate cancer in the majority of Indian males. In case a patient requests for a PSA test, or the physician initiates the testing, the patient should be counseled about its benefits and limitations. However, before counseling the patients, it is important that urologists in India are themselves well informed about the benefits and limitations of PSA testing so that they can make individual decisions in the best interests of a particular patient.
| References|| |
|1.||Prostate-specific antigen (PSA) best practice policy. American Urological Association. Oncology 2000;14:267-72. Available from: http://auanet.org. [last accessed on 2008 Aug 8]. |
|2.||Smith RA, Cokkinides V, Eyre HJ. Cancer screening in the United States, 2007: A review of current guidelines, practices and prospects.CA Cancer J Clin 2007;57:90-104. [PUBMED] [FULLTEXT]|
|3.||Harris R and Lohr KN. US Preventive services task force: Screening for prostate cancer: Recommendation and rationale. Ann Intern Med 2002;137:917-29. |
|4.||Ferrini R, Woolf SH. Screening for prostate cancer in American men. American College of Preventive Medicine Practice policy statement. Available from: http://www.acpm.org/prostate.htm [last accessed on 2008 Aug 9]. |
|5.||Weston R, Parr N. New NHS guidelines for PSA testing in primary care. Lancet 2003;361:89-90. [PUBMED] [FULLTEXT]|
|6.||Nielsen C, Lang RS. Principles of screening. Med Clin N Am 1999;83:1323-38. [PUBMED] |
|7.||Landis SH, Murray T, Boldon S, Wingo PA. Cancer Statistics, 1999. CA Cancer J Clin 1999;49:8-31. |
|8.||Parkin DM, Whelan SL, Ferlay J, Raymond L, Teppo L, Thomas DB, editors. Cancer Incidence in Five Continents. Vol 8. Lyon: International Agency for Research on Cancer; International Association of Cancer Registries; 2002. |
|9.||Chan JM, Gann PH, Giovannucci EL. Role of diet in prostate cancer development and progression. J Clin Oncol 2005;23:8152-60. [PUBMED] [FULLTEXT]|
|10.||Sinha R, Andersen DE, McDonald SS, Greenwald P. Cancer Risk and Diet in India. J Postgrad Med 2003;49:222-8. [PUBMED] |
|11.||Rajaram S, Sabate J. Health benefits of a vegetarian diet. Nutrition 2000;16:531-3. |
|12.||Srivastava RK, Chen O, Siddiqui I, Sarva K, Shankar S. Linkage of curcumin induced cell cycle arrest and apoptosis by cyclin dependent kinase inhibitor p21(WAF1/CIP1). Cell Cycle 2007;6:2953-61. |
|13.||Khan N, Afaq F, Mukhtar H. Cancer prevention through dietary antioxidants: Progress and promise. Antioxid Redox Signal 2008;10:475-510. [PUBMED] [FULLTEXT]|
|14.||Agarwal BB, Kumar A, Bharti AC. Anticancer potential of curcumin: Preclinical and clinical studies. Anticancer Res 2003;23:363-98. |
|15.||Nandakumar A, Gupta PC, Gangadharan P, Visweswara RN. Development of an Atlas of Cancer in India, First ALL India Report: 2001-2002. Bangalore, India: National Cancer Registry; 2004. |
|16.||Rajkumar R, Sankaranarayanan R, Esmi A, Jayaraman R, Cherian J, Parkin DM. Leads to cancer control based on cancer patterns in a rural population in South India. Cancer Causes Control 2000;11:433-9. [PUBMED] [FULLTEXT]|
|17.||Sen U, Sankaranarayanan R, Mandal S, Ramanakumar AV, Parkin DM, Siddiqui M. Cancer patterns in eastern India: The first report of the Kolkata cancer registry. Int J Cancer 2002;100:86-91. |
|18.||Whitmore WF. Localised prostatic cancer: Management and detection issues. Lancet 1994;343:1263-7. |
|19.||Albertsen PC, Hanley JA, Gleason DF, Barry MJ. Competing risk analysis of men aged 55 to 74 years at diagnosis managed conservatively for clinically localized prostate cancer. JAMA 1998;280:975-80. [PUBMED] [FULLTEXT]|
|20.||Johansson JE, Andren O, Andersson SO, Dickman PW, Holmberg L, Magnuson A, et al . 20-year outcomes following conservative management of clinically localised prostate cancer. JAMA 2005;293:2095-101. |
|21.||Roemeling S, Roobol MJ, Postma R, Gosselar C, van der Kwast TH, Bangma CH, et al . Management and survival of screen detected prostate cancer patients who might have been suitable for active surveillance. Eur Urol 2006;50:475-82. |
|22.||Hardie C, Parker C, Norman A, Eeles R, Horwich A, Huddart R, et al . Early outcomes of active surveillance for localised prostate cancer. BJU Int 2005;95:956-60. |
|23.||Draisma G, Boer R, Otto SJ, van der Cruijsen IW, Damhuis RA, Schrφder FH, et al . Lead times and over detection due to prostate specific antigen screening: Estimates from the European Randomized Study of Screening for Prostate Cancer. J Natl Cancer Inst 2003;95:868-78. |
|24.||de Koning HJ, Essink-Bot ML, Schroder FH. Screening for prostate cancer. In: Abel E-NLPD, editor. Prostate cancer. Clinical and scientific aspects-bridging the gap. London, United Kingdom: Imperial College Press; 2003. p. 683-708. |
|25.||Steyerberg EW, Roobol MJ, Kattan MW, van der Kwast TH, de Koning HJ, Schroder FH. Prediction of indolent prostate cancer: Validation and updating of a prognostic nomogram. J Urol 2007;177:107-12. |
|26.||Stamey TA, Caldwell M, McNeal JE, Rosalie N, Hemenez M, Downs J. The Prostate specific Antigen era in the United States is over for prostate cancer: What happened in the last 20 years? J Urol 2004;172:1297-301. |
|27.||Etzioni R, Penson DF, Legler JM, di Tommaso D, Boer R, Gann PH, et al . Overdiagnosis due to prostate-specific antigen screening: Lessons from US prostate cancer incidence trends. J Natl Cancer Inst 2002;94:981-90. [PUBMED] [FULLTEXT]|
|28.||McGregor M, Hanley JA, Boivin JF, McLean RG. Screening for prostate cancer: Estimating the magnitude of overdetection. CMAJ 1998;159:1368-72. [PUBMED] [FULLTEXT]|
|29.||Wilt TJ, Brawer MK. The Prostate Cancer Intervention Versus Observation Trial (PIVOT): A randomized trial comparing radical prostatectomy versus expectant management for the treatment of clinically localised prostate cancer. Cancer 1995;75:1963-8. |
|30.||Donovan J, Hamdy F, Neal D, Peters T, Oliver S, Brindle L, et al . Prostate Testing for Cancer and Treatment (ProtecT) feasibility study. Health Technol Assess 2003;7:1-88. |
|31.||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;352:19-24. |
|32.||Bill-Axelson A, Holmberg L, Filιn F, Ruutu M, Garmo H, Busch C, et al . Radical prostatectomy versus watchful waiting in localized prostate cancer: The Scandinavian prostate cancer group-4 randomized trial. J Natl Cancer Inst 2008;100:1144-54. |
|33.||Steineck G, Helgesen F, Adolfsson J, Dickman PW, Johansson JE, Norlιn BJ, et al . Quality of life after radical prostatectomy or watchful waiting. N Engl J Med 2002;347:790-6. |
|34.||Nicholson PW, Harland SJ. Survival prospects after screen-detection of prostate cancer. BJU Int 2002;90:686-93. [PUBMED] [FULLTEXT]|
|35.||Parker C. Active surveillance: Towards a new paradigm in the management of early prostate cancer. Lancet Oncol 2004;5:101-6. [PUBMED] [FULLTEXT]|
|36.||Catalona WJ, Smith DS, Ornstein DK. Prostate cancer detection in men with serum PSA concentrations of 2.6 to 4.0 ng/ml and benign prostate examination; Enhancement of specificity with free PSA measurement. JAMA 1977;277:1452-5. |
|37.||Brawer MK. Prostate specific antigen: Current status. CA Cancer J Clin 1999;49:264-81. [PUBMED] [FULLTEXT]|
|38.||Veltri RW, Miller MC, O′Dowd GJ, Partin AW. Impact of age on total and complexed prostate-specific antigen cut-offs in a constemporary referral series of men with prostate cancer. Urology 2002;60;47-9. |
|39.||Orozco R, Kummel B, O′Dowd GJ, Stamey TA. Positive biopsy rate consistently increases with age at the same prostate-specific antigen level in patients with normal digital rectal examination. Urology 1998;51:531-4. |
|40.||Punglia RS, D′Amico AV, Catalona WJ, Roehl KA and Kuntz KM. Effect of verification bias on screening prostate cancer by measurement of postate-specific antigen. N Engl J Med 2003;349:335-42. |
|41.||Thompson IM, Pauler DK, Goodman PJ, Tangen CM, Lucia MS, Parnes HL, et al . Prevalence of prostate cancer among men with a prostate-specific antigen level < or = 4.0 ng per millilitre. N Engl J Med 2004;350: 2239-46. |
|42.||Ankerst DP, Thompson IM. Sensitivity and Specificity of prostate-specific antigen for prostate cancer detection with high rates of biopsy verification. Arch Ital Urol Androl 2006;78:125-9. |
|43.||McDavid K, Lee J, Fulton JP, Tonita J, Thompson TD. Prostate cancer incidence and mortality rates and trends in the United States and Canada. Public Health Rep 2004;119:174-86 [PUBMED] [FULLTEXT]|
|44.||Hankey BF, Feuer EJ, Clegg LX, Hayes RB, Legler JM, Prorok PP, et al . Cancer surveillance rates: i0 nterpreting trends in prostate cancer-part 1: Evidence of effects of screening in recent prostate cancer inceidence and mortality and survival rates. J Natl Cancer Inst 1999;91:1017-24. |
|45.||Colli JL, Amling CL. Exploring causes for declining prostate cancer mortality in the United States. Urol Oncol 2008;26:627-33. [PUBMED] [FULLTEXT]|
|46.||Bartsch G, Horninger W, Klocker H, Reissigl A, Oberaigner W, Schφnitzer D, et al . Prostate cancer mortality after introduction of prostate-specific antigen mass screening in the Federal State of Tyrol, Austria. Urology 2001;58:417-24. |
|47.||Carter HB. Rationale for earlier and less frequent prostate cancer screening. Urology 2001;58:639-41. [PUBMED] [FULLTEXT]|
|48.||Lu-Yao G, Albertsen PC, Stanford JL, Stukel TA, Walker-Corkery ES, Barry MJ. Natural experiment examining impact of aggressive screening and treatment on prostate cancer mortality in two fixed cohorts from Seattle area and Connecticut. BMJ 2002;325:740-3. [PUBMED] [FULLTEXT]|
|49.||Labrie F, Candas B, Dupont A, Cusan L, Gomez JL, Suburu RE, et al . Screening decreases prostate cancer death: First analysis of the 1988 Quebec prospective randomized controlled trial. Prostate 1999; 38:83-91. [PUBMED] [FULLTEXT]|
|50.||Boer R, Schroder FH. Quebec randomized controlled trial on prostate cancer screening shows no evidence for mortality reduction. Prostate 1999;40:130-4. |
|51.||Ilic D, O′Connor D, Green S, Wilt T. Screening for prostate cancer: A Cochrane systematic review. Cancer Causes Control 2007;18:279-85. [PUBMED] [FULLTEXT]|
|52.||Sandblom G, Varenhorst E, Lofman O, Rosell J, Carlsson P. Clinical consequences of screening for prostate cancer: 15 years follow-up of a randomised controlled trial in Sweden. Eur Urol 2004;46:717-23. |
|53.||McNaughton-Collins M, Fowler FJ Jr, Caubet JF, Bates DW, Lee JM, Hauser A, et al . Psychological effects of a suspicious prostate cancer screening test followed by a benign biopsy result. Am J Med 2004;117:719-25. [PUBMED] [FULLTEXT]|
|54.||Fowler FJ Jr, Barry MJ, Walker-Corkery B, Caubet JF, Bates DW, Lee JM, et al . The impact of a suspicious prostate biopsy on patients psychological, socio-behavioral and medical care outcomes. J Gen Intern Med 2006;21:715-21. [PUBMED] [FULLTEXT]|
|55.||Lin K, Lipsitz R, Miller T, Janakiraman S; US preventive services task force. Benefits and harms of prostate-specific antigen screening for for prostate cancer: a0 n evidence update for the US preventive services task force. Ann Intern Med 2008;149:192-9. |
|56.||Canadian Task Force on the Periodic Health Examination. Available from: http://www.ctfphc.org/index.html) [last accessed on 2008 Aug 19]. |
|57.||National Cancer Institute. Available from: http://www.cancer.gov/cancertopics/pdq/screening/prostate/HealthProfessional /page2. |
|58.||American academy of family physicians. Available from: http://www.aafp.org/afp/20000815/practice.html. [last accessed on 2008 Aug 19]. |
|59.||American College of Physicians. Clinical guideline part III: Screening for prostate cancer. Ann Intern Med 1997;126:480-4. [PUBMED] [FULLTEXT]|
|60.||American Medical Association Available from: http://www.ama-assn.org/ama/pub/category/13604.html. [last accessed on 2008 Aug 15]. |
|61.||The Royal College of Radiologists′, Clinical Oncology Information Network. British Association of Urological Surgeons: Guidelines on the management of prostate cancer. A document for local expert groups in the United Kingdom preparing prostate management policy documents . BJU Int 1999;84:987-1014. |
|62.||Heidenreich A, Aus G, Bolla M, Joniau S, Matveev VB, Scmid HP. EAU Guidelines on Prostate Cancer. Eur Urol 2008;53:68-80. |
|63.||Advisory committee on Cancer prevention. Recommendations on cancer screening in the European Union. Eur J Cancer 2000;36:1473-8. [PUBMED] [FULLTEXT]|
|64.||Canadian Urological Association. Early detection of prostate cancer. Canadian Urological Association-position statement. Winnipeg: 1994. |
|65.||Gann PH. Informed consent for prostate-specific antigen testing. Urology 2003;61:5-6. [PUBMED] [FULLTEXT]|
|66.||Talcott JA. What patients should be told before agreeing to a blood test that could change their lives. Urology 2003;61:7-9. [PUBMED] [FULLTEXT]|
|67.||Catalona WJ. Informed consent for prostate-specific antigen screening. Urology 2003;61:17-19. [PUBMED] [FULLTEXT]|
|68.||Ito K, Schrder FH. Informed consent for prostate-specific antigen-based screening-European view. Urology 2003;61:20-22. [PUBMED] [FULLTEXT]|
|69.||DH(2002a) Prostate cancer risk management programme: r0 eference booklet. Department of health. Available from: http://www.cancerscreening.nhs.uk [last accessed on 2008 Aug 13]. |
|70.||DH (2002b) Prostate cancer risk management programme: p0 atient information sheet. Department of health. Available from: http://www.cancerscreening.nhs.uk [last accessed on 2008 Aug 13]. |
|71.||Dunn AS, Shridharani KV, Lou W, Bernstein J, Horowitz CR. Physician-patient discussions of controversial cancer screening tests. Am J Prev Med 2001;20:130-4. [PUBMED] [FULLTEXT]|
|72.|| Lamplugh M, Gilmore P, Quinlan T, Cornford P. PSA testing: a0 re patients aware of what lies ahead? Ann R Coll Surg Engl 2006;8:284-8. |
|73.||Wolf AM, Naser JF, Wolf AM, Schorling JB. The impact of informed consent on patient interest in prostate-specific antigen screening. Arch Intern Med 1996;156:1333-6. |
|74.||Woolf SH, Krist A. The liability of giving patients a choice: Shared decision making and prostate cancer. Am Fam Physician 2005;71:1871-2. [PUBMED] [FULLTEXT]|
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