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
Hauptverfasser: van der Leest, R.J.T., Liu, L., Coebergh, J.W.W., Neumann, H.A.M., Mooi, W.J., Nijsten, T., de Vries, E.
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container_end_page 1330
container_issue 6
container_start_page 1321
container_title British journal of dermatology (1951)
container_volume 167
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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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. 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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. 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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 &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; 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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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Wiley Online Library Journals Frontfile Complete
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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