1996
DOI: 10.1159/000473833
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Screening and Early Detection of Prostate Cancer Will Decrease Morbidity and Mortality from Prostate Cancer: The Argument Against

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Cited by 20 publications
(8 citation statements)
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“…HPC1 (1q24-q25), PCaP (1q42-q43), HPCX (Xq27-q28), CAPB (1p36), HPC20 (20q13), HPC2/ECAC2 (17p11) and 10q25 [32][33][34][35][36][37][38][39][40], but confirmatory studies at these loci have produced discordant results. Although an autosomal dominant model has been shown to provide the best model of the familial aggregation of prostate cancer in many studies [41][42][43][44][45][46], some analyses suggest that multiple alleles, each conferring modest risks such as RNASEL variants [47], may be responsible for most inherited disease [48]. The involvement of low-penetrance alleles whose effect may be modified by environmental effects, together with locus heterogeneity, provides an explanation for the difficulties with identifying a gene through linkage.…”
Section: Discussionmentioning
confidence: 99%
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“…HPC1 (1q24-q25), PCaP (1q42-q43), HPCX (Xq27-q28), CAPB (1p36), HPC20 (20q13), HPC2/ECAC2 (17p11) and 10q25 [32][33][34][35][36][37][38][39][40], but confirmatory studies at these loci have produced discordant results. Although an autosomal dominant model has been shown to provide the best model of the familial aggregation of prostate cancer in many studies [41][42][43][44][45][46], some analyses suggest that multiple alleles, each conferring modest risks such as RNASEL variants [47], may be responsible for most inherited disease [48]. The involvement of low-penetrance alleles whose effect may be modified by environmental effects, together with locus heterogeneity, provides an explanation for the difficulties with identifying a gene through linkage.…”
Section: Discussionmentioning
confidence: 99%
“…There is now increased concern about the early detection of prostate cancer, heightened by the ageing population. However, the conclusion that prostate-cancer screening applied to the general population is costeffective is contentious [46,47]. Most studies have found no evidence for a significant difference between familial and sporadic forms of prostate cancer in terms of either clinicopathological features, response to treatment, or outcome [48][49][50][51].…”
Section: Discussionmentioning
confidence: 99%
“…There remain many uncertainties surrounding the early detection of prostate cancer. From some perspectives, the lack of randomized controlled trial data is sufficient reason to limit introduction of PSA testing, but for most, the key issue relates to problems of potential overdiagnosis 43–45 …”
Section: Early Detection Of Prostate Cancermentioning
confidence: 99%
“…Although the efficacy of screening for PCa is under continuous debate [4,5], the advent of TRUS has improved visualization of prostate lesions. Hypoechoic lesions found during TRUS, as well as high levels of serum prostate-specific antigen (PSA) and abnormal digital rectal examination (DRE) findings, are the typical findings considered to be suspicious for PCa, and TRUS-guided prostate biopsy is generally recommended.…”
Section: Introductionmentioning
confidence: 99%