Prospective study of Outcomes in Sporadic versus Hereditary breast cancer (POSH): study protocol

<p>Abstract</p> <p>Background</p> <p>Young women presenting with breast cancer are more likely to have a genetic predisposition to the disease than breast cancer patients in general. A genetic predisposition is known to increase the risk of new primary breast (and other...

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Main Authors: Ennis Sarah, Hammond Victoria, Simmonds Peter, Gerty Sue, Eccles Diana, Altman Douglas G
Format: Article
Language:English
Published: BMC 2007-08-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/7/160
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spelling doaj-48a286af16674fbd9130d42c1bfd128d2020-11-24T21:30:05ZengBMCBMC Cancer1471-24072007-08-017116010.1186/1471-2407-7-160Prospective study of Outcomes in Sporadic versus Hereditary breast cancer (POSH): study protocolEnnis SarahHammond VictoriaSimmonds PeterGerty SueEccles DianaAltman Douglas G<p>Abstract</p> <p>Background</p> <p>Young women presenting with breast cancer are more likely to have a genetic predisposition to the disease than breast cancer patients in general. A genetic predisposition is known to increase the risk of new primary breast (and other) cancers. It is unclear from the literature whether genetic status should be taken into consideration when planning adjuvant treatment in a young woman presenting with a first primary breast cancer. The primary aim of the POSH study is to establish whether genetic status influences the prognosis of primary breast cancer independently of known prognostic factors.</p> <p>Methods/design</p> <p>The study is a prospective cohort study recruiting 3,000 women aged 40 years or younger at breast cancer diagnosis; the recruiting period covers 1<sup>st </sup>June 2001 to 31<sup>st </sup>December 2007. Written informed consent is obtained at study entry. Family history and known epidemiological risk data are collected by questionnaire. Clinical information about diagnosis, treatment and clinical course is collected and blood is stored. Follow up data are collected annually after the first year. An additional recruitment category includes women aged 41 to 50 years who are found to be BRCA1 or BRCA2 gene carriers and were diagnosed with their first breast cancer during the study recruiting period.</p> <p>Discussion</p> <p>Power estimates were based on 10% of the cohort carrying a BRCA1 gene mutation. Preliminary BRCA1 and BRCA2 mutation analysis in a pilot set of study participants confirms we should have 97% power to detect a difference of 10% in event rates between gene carriers and sporadic young onset cases. Most of the recruited patients (>80%) receive an anthracycline containing adjuvant chemotherapy regimen making planned analyses more straightforward.</p> http://www.biomedcentral.com/1471-2407/7/160
collection DOAJ
language English
format Article
sources DOAJ
author Ennis Sarah
Hammond Victoria
Simmonds Peter
Gerty Sue
Eccles Diana
Altman Douglas G
spellingShingle Ennis Sarah
Hammond Victoria
Simmonds Peter
Gerty Sue
Eccles Diana
Altman Douglas G
Prospective study of Outcomes in Sporadic versus Hereditary breast cancer (POSH): study protocol
BMC Cancer
author_facet Ennis Sarah
Hammond Victoria
Simmonds Peter
Gerty Sue
Eccles Diana
Altman Douglas G
author_sort Ennis Sarah
title Prospective study of Outcomes in Sporadic versus Hereditary breast cancer (POSH): study protocol
title_short Prospective study of Outcomes in Sporadic versus Hereditary breast cancer (POSH): study protocol
title_full Prospective study of Outcomes in Sporadic versus Hereditary breast cancer (POSH): study protocol
title_fullStr Prospective study of Outcomes in Sporadic versus Hereditary breast cancer (POSH): study protocol
title_full_unstemmed Prospective study of Outcomes in Sporadic versus Hereditary breast cancer (POSH): study protocol
title_sort prospective study of outcomes in sporadic versus hereditary breast cancer (posh): study protocol
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2007-08-01
description <p>Abstract</p> <p>Background</p> <p>Young women presenting with breast cancer are more likely to have a genetic predisposition to the disease than breast cancer patients in general. A genetic predisposition is known to increase the risk of new primary breast (and other) cancers. It is unclear from the literature whether genetic status should be taken into consideration when planning adjuvant treatment in a young woman presenting with a first primary breast cancer. The primary aim of the POSH study is to establish whether genetic status influences the prognosis of primary breast cancer independently of known prognostic factors.</p> <p>Methods/design</p> <p>The study is a prospective cohort study recruiting 3,000 women aged 40 years or younger at breast cancer diagnosis; the recruiting period covers 1<sup>st </sup>June 2001 to 31<sup>st </sup>December 2007. Written informed consent is obtained at study entry. Family history and known epidemiological risk data are collected by questionnaire. Clinical information about diagnosis, treatment and clinical course is collected and blood is stored. Follow up data are collected annually after the first year. An additional recruitment category includes women aged 41 to 50 years who are found to be BRCA1 or BRCA2 gene carriers and were diagnosed with their first breast cancer during the study recruiting period.</p> <p>Discussion</p> <p>Power estimates were based on 10% of the cohort carrying a BRCA1 gene mutation. Preliminary BRCA1 and BRCA2 mutation analysis in a pilot set of study participants confirms we should have 97% power to detect a difference of 10% in event rates between gene carriers and sporadic young onset cases. Most of the recruited patients (>80%) receive an anthracycline containing adjuvant chemotherapy regimen making planned analyses more straightforward.</p>
url http://www.biomedcentral.com/1471-2407/7/160
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