Risk of Melanoma and Other Cancers in Melanoma-Prone Families

We evaluated the risk of developing melanoma over time in members of 23 melanoma-prone families. All 23 families had dysplastic nevi as well as melanoma. Forty-seven melanomas occurred prospectively, all in family members with dysplastic nevi. The prospective melanomas were markedly thinner than the...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of investigative dermatology 1993-03, Vol.100 (3), p.S350-S355
Hauptverfasser: Tucker, Margaret A., Fraser, Mary C., Goldstein, Alisa M., Elder, David E., Guerry, DuPont, Organic, Sara M.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page S355
container_issue 3
container_start_page S350
container_title Journal of investigative dermatology
container_volume 100
creator Tucker, Margaret A.
Fraser, Mary C.
Goldstein, Alisa M.
Elder, David E.
Guerry, DuPont
Organic, Sara M.
description We evaluated the risk of developing melanoma over time in members of 23 melanoma-prone families. All 23 families had dysplastic nevi as well as melanoma. Forty-seven melanomas occurred prospectively, all in family members with dysplastic nevi. The prospective melanomas were markedly thinner than the melanomas diagnosed prior to or at the time of the subject's entry into the study. The cumulative risk of melanoma by age 50 years among people with dysplastic nevi was 48.9±4.2%. Overall, the relative risk of a prospective melanoma among family members with previous melanoma was 229 (95% confidence interval 110–422). The risk varied by time interval and was 362 in the first 5 years, decreasing to 120 after 5 years. The risk of developing melanoma was 85 times increased (95% confidence interval 41–156) in family members with dysplastic nevi and also declined over time in this group. There was no significant excess of cancers other than melanoma. Close surveillance of these high-risk families has led to diagnosis of melanoma at an earlier developmental stage, which should result in a decrease in mortality over time.
doi_str_mv 10.1038/jid.1993.62
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_75618511</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022202X9390173F</els_id><sourcerecordid>75618511</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3112-44af80a8956da9e3c972fe1d1bc716f292682f4037efe018cbd62db8d2ec17073</originalsourceid><addsrcrecordid>eNptkEtLAzEUhYMoWqsr18IsxI1MzU1mkszChRRfUKmIgruQSW4wOg9NWsF_75SWrlzdxfk45_IRcgJ0ApSry4_gJlBVfCLYDhlByXgOspC7ZEQpYzmj7O2AHKb0QSmIolT7ZF8VBa0YH5Gr55A-s95nj9iYrm9NZjqXzRfvGLOp6SzGlIVum-ZPse8wuzVtaAKmI7LnTZPweHPH5PX25mV6n8_mdw_T61luOQDLi8J4RY2qSuFMhdxWknkEB7WVIDyrmFDMF5RL9EhB2doJ5mrlGFqQVPIxOV_3fsX-e4lpoduQLDbDU9gvk5alAFUCDODFGrSxTymi118xtCb-aqB6JUsPsvRKlhZsoE83tcu6RbdlN3aG_GyTm2RN4-MgJKQtVggupVph5RrDQcFPwKiTDTi4cyGiXWjXh3_n_wCUPoI8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>75618511</pqid></control><display><type>article</type><title>Risk of Melanoma and Other Cancers in Melanoma-Prone Families</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Tucker, Margaret A. ; Fraser, Mary C. ; Goldstein, Alisa M. ; Elder, David E. ; Guerry, DuPont ; Organic, Sara M.</creator><creatorcontrib>Tucker, Margaret A. ; Fraser, Mary C. ; Goldstein, Alisa M. ; Elder, David E. ; Guerry, DuPont ; Organic, Sara M.</creatorcontrib><description>We evaluated the risk of developing melanoma over time in members of 23 melanoma-prone families. All 23 families had dysplastic nevi as well as melanoma. Forty-seven melanomas occurred prospectively, all in family members with dysplastic nevi. The prospective melanomas were markedly thinner than the melanomas diagnosed prior to or at the time of the subject's entry into the study. The cumulative risk of melanoma by age 50 years among people with dysplastic nevi was 48.9±4.2%. Overall, the relative risk of a prospective melanoma among family members with previous melanoma was 229 (95% confidence interval 110–422). The risk varied by time interval and was 362 in the first 5 years, decreasing to 120 after 5 years. The risk of developing melanoma was 85 times increased (95% confidence interval 41–156) in family members with dysplastic nevi and also declined over time in this group. There was no significant excess of cancers other than melanoma. Close surveillance of these high-risk families has led to diagnosis of melanoma at an earlier developmental stage, which should result in a decrease in mortality over time.</description><identifier>ISSN: 0022-202X</identifier><identifier>EISSN: 1523-1747</identifier><identifier>DOI: 10.1038/jid.1993.62</identifier><identifier>PMID: 8440923</identifier><identifier>CODEN: JIDEAE</identifier><language>eng</language><publisher>Danvers, MA: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Biological and medical sciences ; Child ; Dermatology ; Disease Susceptibility - complications ; Dysplastic Nevus Syndrome - complications ; Dysplastic Nevus Syndrome - epidemiology ; Dysplastic Nevus Syndrome - pathology ; Family Health ; Female ; Genetic Predisposition to Disease ; Humans ; Male ; Medical sciences ; Melanoma - complications ; Melanoma - epidemiology ; Melanoma - genetics ; Melanoma - pathology ; Middle Aged ; Neoplasm Invasiveness ; Prospective Studies ; Retrospective Studies ; Risk Factors ; Tumors of the skin and soft tissue. Premalignant lesions</subject><ispartof>Journal of investigative dermatology, 1993-03, Vol.100 (3), p.S350-S355</ispartof><rights>1993 The Society for Investigative Dermatology, Inc</rights><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3112-44af80a8956da9e3c972fe1d1bc716f292682f4037efe018cbd62db8d2ec17073</citedby><cites>FETCH-LOGICAL-c3112-44af80a8956da9e3c972fe1d1bc716f292682f4037efe018cbd62db8d2ec17073</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=4637783$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8440923$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tucker, Margaret A.</creatorcontrib><creatorcontrib>Fraser, Mary C.</creatorcontrib><creatorcontrib>Goldstein, Alisa M.</creatorcontrib><creatorcontrib>Elder, David E.</creatorcontrib><creatorcontrib>Guerry, DuPont</creatorcontrib><creatorcontrib>Organic, Sara M.</creatorcontrib><title>Risk of Melanoma and Other Cancers in Melanoma-Prone Families</title><title>Journal of investigative dermatology</title><addtitle>J Invest Dermatol</addtitle><description>We evaluated the risk of developing melanoma over time in members of 23 melanoma-prone families. All 23 families had dysplastic nevi as well as melanoma. Forty-seven melanomas occurred prospectively, all in family members with dysplastic nevi. The prospective melanomas were markedly thinner than the melanomas diagnosed prior to or at the time of the subject's entry into the study. The cumulative risk of melanoma by age 50 years among people with dysplastic nevi was 48.9±4.2%. Overall, the relative risk of a prospective melanoma among family members with previous melanoma was 229 (95% confidence interval 110–422). The risk varied by time interval and was 362 in the first 5 years, decreasing to 120 after 5 years. The risk of developing melanoma was 85 times increased (95% confidence interval 41–156) in family members with dysplastic nevi and also declined over time in this group. There was no significant excess of cancers other than melanoma. Close surveillance of these high-risk families has led to diagnosis of melanoma at an earlier developmental stage, which should result in a decrease in mortality over time.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Dermatology</subject><subject>Disease Susceptibility - complications</subject><subject>Dysplastic Nevus Syndrome - complications</subject><subject>Dysplastic Nevus Syndrome - epidemiology</subject><subject>Dysplastic Nevus Syndrome - pathology</subject><subject>Family Health</subject><subject>Female</subject><subject>Genetic Predisposition to Disease</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Melanoma - complications</subject><subject>Melanoma - epidemiology</subject><subject>Melanoma - genetics</subject><subject>Melanoma - pathology</subject><subject>Middle Aged</subject><subject>Neoplasm Invasiveness</subject><subject>Prospective Studies</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><issn>0022-202X</issn><issn>1523-1747</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkEtLAzEUhYMoWqsr18IsxI1MzU1mkszChRRfUKmIgruQSW4wOg9NWsF_75SWrlzdxfk45_IRcgJ0ApSry4_gJlBVfCLYDhlByXgOspC7ZEQpYzmj7O2AHKb0QSmIolT7ZF8VBa0YH5Gr55A-s95nj9iYrm9NZjqXzRfvGLOp6SzGlIVum-ZPse8wuzVtaAKmI7LnTZPweHPH5PX25mV6n8_mdw_T61luOQDLi8J4RY2qSuFMhdxWknkEB7WVIDyrmFDMF5RL9EhB2doJ5mrlGFqQVPIxOV_3fsX-e4lpoduQLDbDU9gvk5alAFUCDODFGrSxTymi118xtCb-aqB6JUsPsvRKlhZsoE83tcu6RbdlN3aG_GyTm2RN4-MgJKQtVggupVph5RrDQcFPwKiTDTi4cyGiXWjXh3_n_wCUPoI8</recordid><startdate>199303</startdate><enddate>199303</enddate><creator>Tucker, Margaret A.</creator><creator>Fraser, Mary C.</creator><creator>Goldstein, Alisa M.</creator><creator>Elder, David E.</creator><creator>Guerry, DuPont</creator><creator>Organic, Sara M.</creator><general>Elsevier Inc</general><general>Nature Publishing</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199303</creationdate><title>Risk of Melanoma and Other Cancers in Melanoma-Prone Families</title><author>Tucker, Margaret A. ; Fraser, Mary C. ; Goldstein, Alisa M. ; Elder, David E. ; Guerry, DuPont ; Organic, Sara M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3112-44af80a8956da9e3c972fe1d1bc716f292682f4037efe018cbd62db8d2ec17073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Dermatology</topic><topic>Disease Susceptibility - complications</topic><topic>Dysplastic Nevus Syndrome - complications</topic><topic>Dysplastic Nevus Syndrome - epidemiology</topic><topic>Dysplastic Nevus Syndrome - pathology</topic><topic>Family Health</topic><topic>Female</topic><topic>Genetic Predisposition to Disease</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Melanoma - complications</topic><topic>Melanoma - epidemiology</topic><topic>Melanoma - genetics</topic><topic>Melanoma - pathology</topic><topic>Middle Aged</topic><topic>Neoplasm Invasiveness</topic><topic>Prospective Studies</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tucker, Margaret A.</creatorcontrib><creatorcontrib>Fraser, Mary C.</creatorcontrib><creatorcontrib>Goldstein, Alisa M.</creatorcontrib><creatorcontrib>Elder, David E.</creatorcontrib><creatorcontrib>Guerry, DuPont</creatorcontrib><creatorcontrib>Organic, Sara M.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of investigative dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tucker, Margaret A.</au><au>Fraser, Mary C.</au><au>Goldstein, Alisa M.</au><au>Elder, David E.</au><au>Guerry, DuPont</au><au>Organic, Sara M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk of Melanoma and Other Cancers in Melanoma-Prone Families</atitle><jtitle>Journal of investigative dermatology</jtitle><addtitle>J Invest Dermatol</addtitle><date>1993-03</date><risdate>1993</risdate><volume>100</volume><issue>3</issue><spage>S350</spage><epage>S355</epage><pages>S350-S355</pages><issn>0022-202X</issn><eissn>1523-1747</eissn><coden>JIDEAE</coden><abstract>We evaluated the risk of developing melanoma over time in members of 23 melanoma-prone families. All 23 families had dysplastic nevi as well as melanoma. Forty-seven melanomas occurred prospectively, all in family members with dysplastic nevi. The prospective melanomas were markedly thinner than the melanomas diagnosed prior to or at the time of the subject's entry into the study. The cumulative risk of melanoma by age 50 years among people with dysplastic nevi was 48.9±4.2%. Overall, the relative risk of a prospective melanoma among family members with previous melanoma was 229 (95% confidence interval 110–422). The risk varied by time interval and was 362 in the first 5 years, decreasing to 120 after 5 years. The risk of developing melanoma was 85 times increased (95% confidence interval 41–156) in family members with dysplastic nevi and also declined over time in this group. There was no significant excess of cancers other than melanoma. Close surveillance of these high-risk families has led to diagnosis of melanoma at an earlier developmental stage, which should result in a decrease in mortality over time.</abstract><cop>Danvers, MA</cop><pub>Elsevier Inc</pub><pmid>8440923</pmid><doi>10.1038/jid.1993.62</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0022-202X
ispartof Journal of investigative dermatology, 1993-03, Vol.100 (3), p.S350-S355
issn 0022-202X
1523-1747
language eng
recordid cdi_proquest_miscellaneous_75618511
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Adolescent
Adult
Biological and medical sciences
Child
Dermatology
Disease Susceptibility - complications
Dysplastic Nevus Syndrome - complications
Dysplastic Nevus Syndrome - epidemiology
Dysplastic Nevus Syndrome - pathology
Family Health
Female
Genetic Predisposition to Disease
Humans
Male
Medical sciences
Melanoma - complications
Melanoma - epidemiology
Melanoma - genetics
Melanoma - pathology
Middle Aged
Neoplasm Invasiveness
Prospective Studies
Retrospective Studies
Risk Factors
Tumors of the skin and soft tissue. Premalignant lesions
title Risk of Melanoma and Other Cancers in Melanoma-Prone Families
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T18%3A56%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Risk%20of%20Melanoma%20and%20Other%20Cancers%20in%20Melanoma-Prone%20Families&rft.jtitle=Journal%20of%20investigative%20dermatology&rft.au=Tucker,%20Margaret%20A.&rft.date=1993-03&rft.volume=100&rft.issue=3&rft.spage=S350&rft.epage=S355&rft.pages=S350-S355&rft.issn=0022-202X&rft.eissn=1523-1747&rft.coden=JIDEAE&rft_id=info:doi/10.1038/jid.1993.62&rft_dat=%3Cproquest_cross%3E75618511%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=75618511&rft_id=info:pmid/8440923&rft_els_id=S0022202X9390173F&rfr_iscdi=true