FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W1880596512> ?p ?o ?g. }

• W1880596512 endingPage "1480" @default.
• W1880596512 startingPage "1479" @default.
• W1880596512 abstract "Dear Editor, Recently, Tabuchi et al. (Cancer Sci 2015; 106: 108–14)1 investigated “determinants of prostate-specific antigen (PSA)-based screening participation while simultaneously taking into account factors associated with fecal occult blood test (FOBT).” They found “three factors related to healthy-user bias: i.e., older age, a technical or junior college education, and adherence to doctors' suggestions,” and concluded that “it may be necessary to increase participation in the former (FOBT) and decrease it in the latter (PSA testing).” However, their observations appeared to be associated with the characteristics of screenees, but do not seem to be a solid reason for reducing participation in PSA-based screening. It appears that no problem exists in the statement for FOBT, but seems at least premature for PSA testing. Prostate cancer (PCa) was very rare 30–40 years ago in Japan. The incidence has been rapidly growing,2 and PCa is now one of the major cancers. It is predicted to become the second most common cancer by 2020, following lung cancer, according to Globocan 2012.3 Not only primary prevention but also secondary prevention is crucial. However, because no definite preventive or risk factors for PCa are known,4 convincing primary prevention is unavailable at present. Thus, there is nothing else to adopt for early detection and treatments, including digital rectal examination, transrectal ultrasound examination, and PSA testing. Of these, PSA-based screening seems the most useful. Randomized controlled trials (RCTs) were conducted to evaluate a PCa mortality-lowering effect of PSA testing; the findings were controversial in two major RCTs carried out in European countries (European Randomized Study of Screening for Prostate Cancer [ERSPC]),5 and the USA (US Prostate, Lung, Colorectal, and Ovarian [PLCO] Cancer Screening Trial).6 Both RCTs should be criticized in view of their limitations, statistical power, observation period, or biases. The higher contamination (or self-selection) of participation in PSA testing in the control arm in the US PLCO Cancer Screening Trial, in particular, poses a serious problem.7 Formerly, the Japanese Urological Association recommended PSA testing8 in line with the results of the ERSPC study, which were confirmed by the inclusion of follow-up data up to 13 years.9 On the other hand, as also discussed by the authors, the US Preventive Services Task Force (USPSTF) declared an opposite statement,10 mostly based on the findings of the US PLCO Cancer Screening Trial. According to the guideline, which depended on a systematic literature review by a research group11 under the auspices of the Ministry of Health, Labour and Welfare, Japan, the Ministry decided not to include PSA testing as a population-based screening program for PCa.12 For the PSA test performance with a cut-off figure of 4.0 ng/mL, the sensitivity was reported to be approximately 20%, specificity ~90%, and a positive predictive value of ~30%.13 The values appear rather low, but are acceptably robust. Problems include the fact that it detects certain latent/low-risk PCa along with prostate hypertrophy and inflammation as well as PCa to be treated; that is, there are some over-diagnoses and over-treatments. However, the USPSTF acknowledged: “This recommendation does not include the use of the PSA test for surveillance after diagnosis or treatment of PCa,”10 suggesting that the test is useful. Accordingly, PSA testing appears to be a double-edged sword, so we must handle it properly. At least two proposals could be made regarding PSA-based screening. Provided that RCT is actually impractical, a case–control study should be conducted to assess the effectiveness of PSA screening in Japanese men having specific genetic backgrounds and lifestyle factors, while the prevalence of PCa and PSA testing remain low/lower. In order to reduce PCa mortality, prolong patients' healthy life, and improve quality of life, while lessening undue medical expenditure, risk communication (informed decision-making) on the screening should be undertaken among physicians, patients, and responsible parties, including work-site, municipal, and governmental health sectors. The author has no conflict of interest." @default.
• W1880596512 created "2016-06-24" @default.
• W1880596512 creator A5020187477 @default.
• W1880596512 date "2015-10-01" @default.
• W1880596512 modified "2023-09-26" @default.
• W1880596512 title "Re: Determinants of participation in prostate cancer screening: A simple analytical framework to account for healthy‐user bias" @default.
• W1880596512 cites W2007824082 @default.
• W1880596512 cites W2011382825 @default.
• W1880596512 cites W2077506728 @default.
• W1880596512 cites W2095761465 @default.
• W1880596512 cites W2110873856 @default.
• W1880596512 cites W2120357482 @default.
• W1880596512 cites W2132528779 @default.
• W1880596512 cites W2134793522 @default.
• W1880596512 cites W586565687 @default.
• W1880596512 doi "https://doi.org/10.1111/cas.12753" @default.
• W1880596512 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4638014" @default.
• W1880596512 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26498113" @default.
• W1880596512 hasPublicationYear "2015" @default.
• W1880596512 type Work @default.
• W1880596512 sameAs 1880596512 @default.
• W1880596512 citedByCount "0" @default.
• W1880596512 crossrefType "journal-article" @default.
• W1880596512 hasAuthorship W1880596512A5020187477 @default.
• W1880596512 hasBestOaLocation W18805965121 @default.
• W1880596512 hasConcept C121608353 @default.
• W1880596512 hasConcept C126322002 @default.
• W1880596512 hasConcept C143998085 @default.
• W1880596512 hasConcept C151730666 @default.
• W1880596512 hasConcept C168563851 @default.
• W1880596512 hasConcept C2775941076 @default.
• W1880596512 hasConcept C2776463041 @default.
• W1880596512 hasConcept C2777267654 @default.
• W1880596512 hasConcept C2778435480 @default.
• W1880596512 hasConcept C2779158730 @default.
• W1880596512 hasConcept C2780101318 @default.
• W1880596512 hasConcept C2780192828 @default.
• W1880596512 hasConcept C2781406297 @default.
• W1880596512 hasConcept C29456083 @default.
• W1880596512 hasConcept C512399662 @default.
• W1880596512 hasConcept C526805850 @default.
• W1880596512 hasConcept C71924100 @default.
• W1880596512 hasConcept C86803240 @default.
• W1880596512 hasConceptScore W1880596512C121608353 @default.
• W1880596512 hasConceptScore W1880596512C126322002 @default.
• W1880596512 hasConceptScore W1880596512C143998085 @default.
• W1880596512 hasConceptScore W1880596512C151730666 @default.
• W1880596512 hasConceptScore W1880596512C168563851 @default.
• W1880596512 hasConceptScore W1880596512C2775941076 @default.
• W1880596512 hasConceptScore W1880596512C2776463041 @default.
• W1880596512 hasConceptScore W1880596512C2777267654 @default.
• W1880596512 hasConceptScore W1880596512C2778435480 @default.
• W1880596512 hasConceptScore W1880596512C2779158730 @default.
• W1880596512 hasConceptScore W1880596512C2780101318 @default.
• W1880596512 hasConceptScore W1880596512C2780192828 @default.
• W1880596512 hasConceptScore W1880596512C2781406297 @default.
• W1880596512 hasConceptScore W1880596512C29456083 @default.
• W1880596512 hasConceptScore W1880596512C512399662 @default.
• W1880596512 hasConceptScore W1880596512C526805850 @default.
• W1880596512 hasConceptScore W1880596512C71924100 @default.
• W1880596512 hasConceptScore W1880596512C86803240 @default.
• W1880596512 hasIssue "10" @default.
• W1880596512 hasLocation W18805965121 @default.
• W1880596512 hasLocation W18805965122 @default.
• W1880596512 hasLocation W18805965123 @default.
• W1880596512 hasLocation W18805965124 @default.
• W1880596512 hasOpenAccess W1880596512 @default.
• W1880596512 hasPrimaryLocation W18805965121 @default.
• W1880596512 hasRelatedWork W1600028657 @default.
• W1880596512 hasRelatedWork W1824199679 @default.
• W1880596512 hasRelatedWork W1893851373 @default.
• W1880596512 hasRelatedWork W1992694633 @default.
• W1880596512 hasRelatedWork W2036403910 @default.
• W1880596512 hasRelatedWork W2071638686 @default.
• W1880596512 hasRelatedWork W2125413300 @default.
• W1880596512 hasRelatedWork W2402308151 @default.
• W1880596512 hasRelatedWork W2432937838 @default.
• W1880596512 hasRelatedWork W2461736489 @default.
• W1880596512 hasVolume "106" @default.
• W1880596512 isParatext "false" @default.
• W1880596512 isRetracted "false" @default.
• W1880596512 magId "1880596512" @default.
• W1880596512 workType "article" @default.