Risk of second primary in situ and invasive melanoma in a Dutch population-based cohort: 1989-2008
Summary Background Patients with melanoma are at increased risk of developing a subsequent melanoma. Objectives To estimate the risks of developing a second primary in situ or invasive cutaneous melanoma after a first melanoma, between 1989 and 2008. Methods Patients were followed until diagnosis...
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Veröffentlicht in: | British journal of dermatology (1951) 2012-12, Vol.167 (6), p.1321-1330 |
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container_title | British journal of dermatology (1951) |
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creator | van der Leest, R.J.T. Liu, L. Coebergh, J.W.W. Neumann, H.A.M. Mooi, W.J. Nijsten, T. de Vries, E. |
description | Summary
Background Patients with melanoma are at increased risk of developing a subsequent melanoma.
Objectives To estimate the risks of developing a second primary in situ or invasive cutaneous melanoma after a first melanoma, between 1989 and 2008.
Methods Patients were followed until diagnosis of a second melanoma, date of death or end of study. Cumulative risks, standardized incidence ratio (SIR, observed second melanomas divided by background age‐, calendar‐ and sex‐specific incidence rates of melanoma, as recorded in the Netherlands Cancer Registry) and absolute excess risk (AER, observed minus expected per 10 000 person‐years) of second melanomas were calculated.
Results In total, 10 765 patients with in situ melanoma and 46 700 with invasive melanoma were included. The cumulative risks of a second invasive melanoma after a first in situ or invasive melanoma at 20 years of follow‐up were 6·2% and 5·0%, respectively. The relative risk of developing any melanoma (in situ or invasive) after any first melanoma (measured as SIR) varied from 12·4‐fold [invasive after invasive melanoma; 95% confidence interval (CI) = 11·6–13·2] to 26·4‐fold (in situ after in situ melanoma; 95% CI = 22·6–30·7) increase compared with the general population. SIRs and AERs remained elevated up to 20 years after the first melanoma.
Conclusions This study shows significantly increased long‐term risks (both relative and absolute) of developing a second invasive melanoma after a first melanoma (invasive and in situ), and might serve as a basis for follow‐up guidelines. |
doi_str_mv | 10.1111/j.1365-2133.2012.11123.x |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1220570237</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1220570237</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4663-7295f047eef980991737ef421606a57286ea9c12abbb841ffabad189b2d70d8b3</originalsourceid><addsrcrecordid>eNqNkV-P1CAUxYnRuOPoVzAkxsSXjhdoofhgsu7o-mej0Wj0jVAKWWbbMkK7zn576c44Jj7JC-Te3z2cnIsQJrAi-TzfrAjjVUEJYysKhM5Vyla7O2hxbNxFCwAQBUjOTtCDlDYAhEEF99EJpaKSlPIFar74dIWDw8maMLR4G32v4w32A05-nLDONT9c6-SvLe5tp4fQ67mr8XoazSXehu3U6dGHoWh0si024TLE8QUmspYFBagfontOd8k-OtxL9O3N669nb4uLT-fvzk4vClNyzgpBZeWgFNY6WYOURDBhXUkJB64rQWtutTSE6qZp6pI4pxvdklo2tBXQ1g1bomd73W0MPyebRtX7ZGyXPdswJUUohUoAZSKjT_5BN2GKQ3anKMtZliXkCJeo3lMmhpSideqQjiKg5j2ojZrjVnPcat6Dut2D2uXRx4cPpqa37XHwT_AZeHoAdDK6c1EPxqe_HBclKauZe7nnfvnO3vy3AfXq_fr2mQWKvYBPo90dBXS8UjwnXKnvH8_z1Lr6_EGu1Q_2G5TLrzY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2311144021</pqid></control><display><type>article</type><title>Risk of second primary in situ and invasive melanoma in a Dutch population-based cohort: 1989-2008</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>van der Leest, R.J.T. ; Liu, L. ; Coebergh, J.W.W. ; Neumann, H.A.M. ; Mooi, W.J. ; Nijsten, T. ; de Vries, E.</creator><creatorcontrib>van der Leest, R.J.T. ; Liu, L. ; Coebergh, J.W.W. ; Neumann, H.A.M. ; Mooi, W.J. ; Nijsten, T. ; de Vries, E.</creatorcontrib><description>Summary
Background Patients with melanoma are at increased risk of developing a subsequent melanoma.
Objectives To estimate the risks of developing a second primary in situ or invasive cutaneous melanoma after a first melanoma, between 1989 and 2008.
Methods Patients were followed until diagnosis of a second melanoma, date of death or end of study. Cumulative risks, standardized incidence ratio (SIR, observed second melanomas divided by background age‐, calendar‐ and sex‐specific incidence rates of melanoma, as recorded in the Netherlands Cancer Registry) and absolute excess risk (AER, observed minus expected per 10 000 person‐years) of second melanomas were calculated.
Results In total, 10 765 patients with in situ melanoma and 46 700 with invasive melanoma were included. The cumulative risks of a second invasive melanoma after a first in situ or invasive melanoma at 20 years of follow‐up were 6·2% and 5·0%, respectively. The relative risk of developing any melanoma (in situ or invasive) after any first melanoma (measured as SIR) varied from 12·4‐fold [invasive after invasive melanoma; 95% confidence interval (CI) = 11·6–13·2] to 26·4‐fold (in situ after in situ melanoma; 95% CI = 22·6–30·7) increase compared with the general population. SIRs and AERs remained elevated up to 20 years after the first melanoma.
Conclusions This study shows significantly increased long‐term risks (both relative and absolute) of developing a second invasive melanoma after a first melanoma (invasive and in situ), and might serve as a basis for follow‐up guidelines.</description><identifier>ISSN: 0007-0963</identifier><identifier>EISSN: 1365-2133</identifier><identifier>DOI: 10.1111/j.1365-2133.2012.11123.x</identifier><identifier>PMID: 22759226</identifier><identifier>CODEN: BJDEAZ</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Biological and medical sciences ; Cohort Studies ; Dermatology ; Female ; Follow-Up Studies ; Health risk assessment ; Humans ; Invasiveness ; Male ; Medical sciences ; Melanoma ; Melanoma - epidemiology ; Melanoma - etiology ; Melanoma - mortality ; Middle Aged ; Neoplasms, Second Primary - epidemiology ; Neoplasms, Second Primary - etiology ; Neoplasms, Second Primary - mortality ; Netherlands - epidemiology ; Risk assessment ; Risk Factors ; Skin Neoplasms - epidemiology ; Skin Neoplasms - etiology ; Skin Neoplasms - mortality ; Tumors of the skin and soft tissue. Premalignant lesions</subject><ispartof>British journal of dermatology (1951), 2012-12, Vol.167 (6), p.1321-1330</ispartof><rights>2012 The Authors. BJD © 2012 British Association of Dermatologists</rights><rights>2014 INIST-CNRS</rights><rights>2012 The Authors. BJD © 2012 British Association of Dermatologists.</rights><rights>Copyright Blackwell Publishing Ltd. Dec 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4663-7295f047eef980991737ef421606a57286ea9c12abbb841ffabad189b2d70d8b3</citedby><cites>FETCH-LOGICAL-c4663-7295f047eef980991737ef421606a57286ea9c12abbb841ffabad189b2d70d8b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2133.2012.11123.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2133.2012.11123.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26741456$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22759226$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van der Leest, R.J.T.</creatorcontrib><creatorcontrib>Liu, L.</creatorcontrib><creatorcontrib>Coebergh, J.W.W.</creatorcontrib><creatorcontrib>Neumann, H.A.M.</creatorcontrib><creatorcontrib>Mooi, W.J.</creatorcontrib><creatorcontrib>Nijsten, T.</creatorcontrib><creatorcontrib>de Vries, E.</creatorcontrib><title>Risk of second primary in situ and invasive melanoma in a Dutch population-based cohort: 1989-2008</title><title>British journal of dermatology (1951)</title><addtitle>Br J Dermatol</addtitle><description>Summary
Background Patients with melanoma are at increased risk of developing a subsequent melanoma.
Objectives To estimate the risks of developing a second primary in situ or invasive cutaneous melanoma after a first melanoma, between 1989 and 2008.
Methods Patients were followed until diagnosis of a second melanoma, date of death or end of study. Cumulative risks, standardized incidence ratio (SIR, observed second melanomas divided by background age‐, calendar‐ and sex‐specific incidence rates of melanoma, as recorded in the Netherlands Cancer Registry) and absolute excess risk (AER, observed minus expected per 10 000 person‐years) of second melanomas were calculated.
Results In total, 10 765 patients with in situ melanoma and 46 700 with invasive melanoma were included. The cumulative risks of a second invasive melanoma after a first in situ or invasive melanoma at 20 years of follow‐up were 6·2% and 5·0%, respectively. The relative risk of developing any melanoma (in situ or invasive) after any first melanoma (measured as SIR) varied from 12·4‐fold [invasive after invasive melanoma; 95% confidence interval (CI) = 11·6–13·2] to 26·4‐fold (in situ after in situ melanoma; 95% CI = 22·6–30·7) increase compared with the general population. SIRs and AERs remained elevated up to 20 years after the first melanoma.
Conclusions This study shows significantly increased long‐term risks (both relative and absolute) of developing a second invasive melanoma after a first melanoma (invasive and in situ), and might serve as a basis for follow‐up guidelines.</description><subject>Biological and medical sciences</subject><subject>Cohort Studies</subject><subject>Dermatology</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Invasiveness</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Melanoma</subject><subject>Melanoma - epidemiology</subject><subject>Melanoma - etiology</subject><subject>Melanoma - mortality</subject><subject>Middle Aged</subject><subject>Neoplasms, Second Primary - epidemiology</subject><subject>Neoplasms, Second Primary - etiology</subject><subject>Neoplasms, Second Primary - mortality</subject><subject>Netherlands - epidemiology</subject><subject>Risk assessment</subject><subject>Risk Factors</subject><subject>Skin Neoplasms - epidemiology</subject><subject>Skin Neoplasms - etiology</subject><subject>Skin Neoplasms - mortality</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><issn>0007-0963</issn><issn>1365-2133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkV-P1CAUxYnRuOPoVzAkxsSXjhdoofhgsu7o-mej0Wj0jVAKWWbbMkK7zn576c44Jj7JC-Te3z2cnIsQJrAi-TzfrAjjVUEJYysKhM5Vyla7O2hxbNxFCwAQBUjOTtCDlDYAhEEF99EJpaKSlPIFar74dIWDw8maMLR4G32v4w32A05-nLDONT9c6-SvLe5tp4fQ67mr8XoazSXehu3U6dGHoWh0si024TLE8QUmspYFBagfontOd8k-OtxL9O3N669nb4uLT-fvzk4vClNyzgpBZeWgFNY6WYOURDBhXUkJB64rQWtutTSE6qZp6pI4pxvdklo2tBXQ1g1bomd73W0MPyebRtX7ZGyXPdswJUUohUoAZSKjT_5BN2GKQ3anKMtZliXkCJeo3lMmhpSideqQjiKg5j2ojZrjVnPcat6Dut2D2uXRx4cPpqa37XHwT_AZeHoAdDK6c1EPxqe_HBclKauZe7nnfvnO3vy3AfXq_fr2mQWKvYBPo90dBXS8UjwnXKnvH8_z1Lr6_EGu1Q_2G5TLrzY</recordid><startdate>201212</startdate><enddate>201212</enddate><creator>van der Leest, R.J.T.</creator><creator>Liu, L.</creator><creator>Coebergh, J.W.W.</creator><creator>Neumann, H.A.M.</creator><creator>Mooi, W.J.</creator><creator>Nijsten, T.</creator><creator>de Vries, E.</creator><general>Blackwell Publishing Ltd</general><general>Wiley-Blackwell</general><general>Oxford University Press</general><scope>BSCLL</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>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>201212</creationdate><title>Risk of second primary in situ and invasive melanoma in a Dutch population-based cohort: 1989-2008</title><author>van der Leest, R.J.T. ; Liu, L. ; Coebergh, J.W.W. ; Neumann, H.A.M. ; Mooi, W.J. ; Nijsten, T. ; de Vries, E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4663-7295f047eef980991737ef421606a57286ea9c12abbb841ffabad189b2d70d8b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Biological and medical sciences</topic><topic>Cohort Studies</topic><topic>Dermatology</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Health risk assessment</topic><topic>Humans</topic><topic>Invasiveness</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Melanoma</topic><topic>Melanoma - epidemiology</topic><topic>Melanoma - etiology</topic><topic>Melanoma - mortality</topic><topic>Middle Aged</topic><topic>Neoplasms, Second Primary - epidemiology</topic><topic>Neoplasms, Second Primary - etiology</topic><topic>Neoplasms, Second Primary - mortality</topic><topic>Netherlands - epidemiology</topic><topic>Risk assessment</topic><topic>Risk Factors</topic><topic>Skin Neoplasms - epidemiology</topic><topic>Skin Neoplasms - etiology</topic><topic>Skin Neoplasms - mortality</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van der Leest, R.J.T.</creatorcontrib><creatorcontrib>Liu, L.</creatorcontrib><creatorcontrib>Coebergh, J.W.W.</creatorcontrib><creatorcontrib>Neumann, H.A.M.</creatorcontrib><creatorcontrib>Mooi, W.J.</creatorcontrib><creatorcontrib>Nijsten, T.</creatorcontrib><creatorcontrib>de Vries, E.</creatorcontrib><collection>Istex</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>British journal of dermatology (1951)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van der Leest, R.J.T.</au><au>Liu, L.</au><au>Coebergh, J.W.W.</au><au>Neumann, H.A.M.</au><au>Mooi, W.J.</au><au>Nijsten, T.</au><au>de Vries, E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk of second primary in situ and invasive melanoma in a Dutch population-based cohort: 1989-2008</atitle><jtitle>British journal of dermatology (1951)</jtitle><addtitle>Br J Dermatol</addtitle><date>2012-12</date><risdate>2012</risdate><volume>167</volume><issue>6</issue><spage>1321</spage><epage>1330</epage><pages>1321-1330</pages><issn>0007-0963</issn><eissn>1365-2133</eissn><coden>BJDEAZ</coden><abstract>Summary
Background Patients with melanoma are at increased risk of developing a subsequent melanoma.
Objectives To estimate the risks of developing a second primary in situ or invasive cutaneous melanoma after a first melanoma, between 1989 and 2008.
Methods Patients were followed until diagnosis of a second melanoma, date of death or end of study. Cumulative risks, standardized incidence ratio (SIR, observed second melanomas divided by background age‐, calendar‐ and sex‐specific incidence rates of melanoma, as recorded in the Netherlands Cancer Registry) and absolute excess risk (AER, observed minus expected per 10 000 person‐years) of second melanomas were calculated.
Results In total, 10 765 patients with in situ melanoma and 46 700 with invasive melanoma were included. The cumulative risks of a second invasive melanoma after a first in situ or invasive melanoma at 20 years of follow‐up were 6·2% and 5·0%, respectively. The relative risk of developing any melanoma (in situ or invasive) after any first melanoma (measured as SIR) varied from 12·4‐fold [invasive after invasive melanoma; 95% confidence interval (CI) = 11·6–13·2] to 26·4‐fold (in situ after in situ melanoma; 95% CI = 22·6–30·7) increase compared with the general population. SIRs and AERs remained elevated up to 20 years after the first melanoma.
Conclusions This study shows significantly increased long‐term risks (both relative and absolute) of developing a second invasive melanoma after a first melanoma (invasive and in situ), and might serve as a basis for follow‐up guidelines.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>22759226</pmid><doi>10.1111/j.1365-2133.2012.11123.x</doi><tpages>10</tpages></addata></record> |
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subjects | Biological and medical sciences Cohort Studies Dermatology Female Follow-Up Studies Health risk assessment Humans Invasiveness Male Medical sciences Melanoma Melanoma - epidemiology Melanoma - etiology Melanoma - mortality Middle Aged Neoplasms, Second Primary - epidemiology Neoplasms, Second Primary - etiology Neoplasms, Second Primary - mortality Netherlands - epidemiology Risk assessment Risk Factors Skin Neoplasms - epidemiology Skin Neoplasms - etiology Skin Neoplasms - mortality Tumors of the skin and soft tissue. Premalignant lesions |
title | Risk of second primary in situ and invasive melanoma in a Dutch population-based cohort: 1989-2008 |
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