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Clinical Efficacy of Ovarian Cancer Screening

Various trials of ovarian cancer screening programs have been reported worldwide. In 2011, one of the most famous papers indicated that annual screening using CA125/transvaginal sonography (TVS) did not reduce ovarian cancer mortality in the United States of America (USA). To investigate the validit...

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Autores principales: Koshiyama, Masafumi, Matsumura, Noriomi, Konishi, Ikuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4934039/
https://www.ncbi.nlm.nih.gov/pubmed/27390606
http://dx.doi.org/10.7150/jca.14615
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author Koshiyama, Masafumi
Matsumura, Noriomi
Konishi, Ikuo
author_facet Koshiyama, Masafumi
Matsumura, Noriomi
Konishi, Ikuo
author_sort Koshiyama, Masafumi
collection PubMed
description Various trials of ovarian cancer screening programs have been reported worldwide. In 2011, one of the most famous papers indicated that annual screening using CA125/transvaginal sonography (TVS) did not reduce ovarian cancer mortality in the United States of America (USA). To investigate the validity of ovarian cancer screening, we verified the analyses of previous reports. At first, we obtained the USA datasets that were used for the analyses and identified many patients in whom cancers were accidentally detected several years after the screening period. We thus performed a new prognostic comparison between the screening group (cancers that were detected through screening or within one year after screening) and the control group (cancers that were found more than one year after screening, without screening, or in the original control group). The results showed that the prognoses of the screening group were significantly better than those of the control group (p=0.0017). In addition, the screening group contained significantly fewer stage IV cases than the control group (p=0.005). In another screening in the United Kingdom, ovarian cancer was detected at a relatively earlier stage (stage I/II: 44%), while the rate of stage IV detection was low (4%). Very recently, this team showed significant difference in the rates with and without screening (p=0.021) when prevalent cases were excluded and indicated the delayed effect of screening. These results contrasted with the USA data. In other studies in the USA and Japan, annual screening was also associated with a decreased stage at detection. New histopathological, molecular and genetic studies have recently provided two categories of ovarian carcinogenesis. Type I carcinomas are slow-growing neoplasms that often develop from benign ovarian cysts. Type II carcinomas are high-grade clinically aggressive neoplasms. The rate of type II carcinomas is significantly higher in Europe and the USA than in Asia (p<0.001). Conversely, type I carcinomas are relatively common in Asia. These data theoretically imply that annual screening would be more effective in Asia.
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spelling pubmed-49340392016-07-07 Clinical Efficacy of Ovarian Cancer Screening Koshiyama, Masafumi Matsumura, Noriomi Konishi, Ikuo J Cancer Perspective Various trials of ovarian cancer screening programs have been reported worldwide. In 2011, one of the most famous papers indicated that annual screening using CA125/transvaginal sonography (TVS) did not reduce ovarian cancer mortality in the United States of America (USA). To investigate the validity of ovarian cancer screening, we verified the analyses of previous reports. At first, we obtained the USA datasets that were used for the analyses and identified many patients in whom cancers were accidentally detected several years after the screening period. We thus performed a new prognostic comparison between the screening group (cancers that were detected through screening or within one year after screening) and the control group (cancers that were found more than one year after screening, without screening, or in the original control group). The results showed that the prognoses of the screening group were significantly better than those of the control group (p=0.0017). In addition, the screening group contained significantly fewer stage IV cases than the control group (p=0.005). In another screening in the United Kingdom, ovarian cancer was detected at a relatively earlier stage (stage I/II: 44%), while the rate of stage IV detection was low (4%). Very recently, this team showed significant difference in the rates with and without screening (p=0.021) when prevalent cases were excluded and indicated the delayed effect of screening. These results contrasted with the USA data. In other studies in the USA and Japan, annual screening was also associated with a decreased stage at detection. New histopathological, molecular and genetic studies have recently provided two categories of ovarian carcinogenesis. Type I carcinomas are slow-growing neoplasms that often develop from benign ovarian cysts. Type II carcinomas are high-grade clinically aggressive neoplasms. The rate of type II carcinomas is significantly higher in Europe and the USA than in Asia (p<0.001). Conversely, type I carcinomas are relatively common in Asia. These data theoretically imply that annual screening would be more effective in Asia. Ivyspring International Publisher 2016-06-25 /pmc/articles/PMC4934039/ /pubmed/27390606 http://dx.doi.org/10.7150/jca.14615 Text en © Ivyspring International Publisher. Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. See http://ivyspring.com/terms for terms and conditions.
spellingShingle Perspective
Koshiyama, Masafumi
Matsumura, Noriomi
Konishi, Ikuo
Clinical Efficacy of Ovarian Cancer Screening
title Clinical Efficacy of Ovarian Cancer Screening
title_full Clinical Efficacy of Ovarian Cancer Screening
title_fullStr Clinical Efficacy of Ovarian Cancer Screening
title_full_unstemmed Clinical Efficacy of Ovarian Cancer Screening
title_short Clinical Efficacy of Ovarian Cancer Screening
title_sort clinical efficacy of ovarian cancer screening
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4934039/
https://www.ncbi.nlm.nih.gov/pubmed/27390606
http://dx.doi.org/10.7150/jca.14615
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