Oral Leukoplakia and Risk of Progression to Oral Cancer: A Population-Based Cohort Study

Abstract Background The optimal clinical management of oral precancer remains uncertain. We investigated the natural history of oral leukoplakia, the most common oral precancerous lesion, to estimate the relative and absolute risks of progression to cancer, the predictive accuracy of a clinician’s d...

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Veröffentlicht in:JNCI : Journal of the National Cancer Institute 2020-10, Vol.112 (10), p.1047-1054
Hauptverfasser: Chaturvedi, Anil K, Udaltsova, Natalia, Engels, Eric A, Katzel, Jed A, Yanik, Elizabeth L, Katki, Hormuzd A, Lingen, Mark W, Silverberg, Michael J
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container_issue 10
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container_title JNCI : Journal of the National Cancer Institute
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creator Chaturvedi, Anil K
Udaltsova, Natalia
Engels, Eric A
Katzel, Jed A
Yanik, Elizabeth L
Katki, Hormuzd A
Lingen, Mark W
Silverberg, Michael J
description Abstract Background The optimal clinical management of oral precancer remains uncertain. We investigated the natural history of oral leukoplakia, the most common oral precancerous lesion, to estimate the relative and absolute risks of progression to cancer, the predictive accuracy of a clinician’s decision to biopsy a leukoplakia vis-à-vis progression, and histopathologic predictors of progression. Methods We conducted a retrospective cohort study (1996–2012) of patients with oral leukoplakia (n = 4886), identified using electronic medical records within Kaiser Permanente Northern California. Among patients with leukoplakia who received a biopsy (n = 1888), we conducted a case-cohort study to investigate histopathologic predictors of progression. Analyses included indirect standardization and unweighted or weighted Cox regression. Results Compared with the overall Kaiser Permanente Northern California population, oral cancer incidence was substantially elevated in oral leukoplakia patients (standardized incidence ratio = 40.8, 95% confidence interval [CI] = 34.8 to 47.6; n = 161 cancers over 22 582 person-years). Biopsied leukoplakias had a higher oral cancer risk compared with those that were not biopsied (adjusted hazard ratio = 2.38, 95% CI = 1.73 to 3.28). However, to identify a prevalent or incident oral cancer, the biopsy decision had low sensitivity (59.6%), low specificity (62.1%), and moderate positive–predictive value (5.1%). Risk of progression to oral cancer statistically significantly increased with the grade of dysplasia; 5-year competing risk-adjusted absolute risks were: leukoplakia overall = 3.3%, 95% CI = 2.7% to 3.9%; no dysplasia = 2.2%, 95% CI = 1.5% to 3.1%; mild-dysplasia = 11.9%, 95% CI = 7.1% to 18.1%; moderate-dysplasia = 8.7%, 95% CI = 3.2% to 17.9%; and severe dysplasia = 32.2%, 95% CI = 8.1%–60.0%. Yet 39.6% of cancers arose from biopsied leukoplakias without dysplasia. Conclusions The modest accuracy of the decision to biopsy a leukoplakia vis-à-vis presence or eventual development of oral cancer highlights the need for routine biopsy of all leukoplakias regardless of visual or clinical impression. Leukoplakia patients, particularly those with dysplasia, need to be closely monitored for signs of early cancer.
doi_str_mv 10.1093/jnci/djz238
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We investigated the natural history of oral leukoplakia, the most common oral precancerous lesion, to estimate the relative and absolute risks of progression to cancer, the predictive accuracy of a clinician’s decision to biopsy a leukoplakia vis-à-vis progression, and histopathologic predictors of progression. Methods We conducted a retrospective cohort study (1996–2012) of patients with oral leukoplakia (n = 4886), identified using electronic medical records within Kaiser Permanente Northern California. Among patients with leukoplakia who received a biopsy (n = 1888), we conducted a case-cohort study to investigate histopathologic predictors of progression. Analyses included indirect standardization and unweighted or weighted Cox regression. Results Compared with the overall Kaiser Permanente Northern California population, oral cancer incidence was substantially elevated in oral leukoplakia patients (standardized incidence ratio = 40.8, 95% confidence interval [CI] = 34.8 to 47.6; n = 161 cancers over 22 582 person-years). Biopsied leukoplakias had a higher oral cancer risk compared with those that were not biopsied (adjusted hazard ratio = 2.38, 95% CI = 1.73 to 3.28). However, to identify a prevalent or incident oral cancer, the biopsy decision had low sensitivity (59.6%), low specificity (62.1%), and moderate positive–predictive value (5.1%). Risk of progression to oral cancer statistically significantly increased with the grade of dysplasia; 5-year competing risk-adjusted absolute risks were: leukoplakia overall = 3.3%, 95% CI = 2.7% to 3.9%; no dysplasia = 2.2%, 95% CI = 1.5% to 3.1%; mild-dysplasia = 11.9%, 95% CI = 7.1% to 18.1%; moderate-dysplasia = 8.7%, 95% CI = 3.2% to 17.9%; and severe dysplasia = 32.2%, 95% CI = 8.1%–60.0%. Yet 39.6% of cancers arose from biopsied leukoplakias without dysplasia. Conclusions The modest accuracy of the decision to biopsy a leukoplakia vis-à-vis presence or eventual development of oral cancer highlights the need for routine biopsy of all leukoplakias regardless of visual or clinical impression. Leukoplakia patients, particularly those with dysplasia, need to be closely monitored for signs of early cancer.</description><identifier>ISSN: 0027-8874</identifier><identifier>EISSN: 1460-2105</identifier><identifier>DOI: 10.1093/jnci/djz238</identifier><identifier>PMID: 31860085</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Adult ; Aged ; Biopsy ; California - epidemiology ; Cancer ; Cohort analysis ; Cohort Studies ; Confidence intervals ; Disease Progression ; Dysplasia ; Electronic health records ; Electronic medical records ; Female ; Health risks ; Humans ; Leukokeratosis ; Leukoplakia, Oral - epidemiology ; Leukoplakia, Oral - pathology ; Male ; Middle Aged ; Mouth Neoplasms - epidemiology ; Mouth Neoplasms - pathology ; Oral cancer ; Patients ; Population studies ; Population-based studies ; Precancerous Conditions - epidemiology ; Precancerous Conditions - pathology ; Regression analysis ; Retrospective Studies ; Risk ; Risk assessment ; Standardization ; Statistical analysis</subject><ispartof>JNCI : Journal of the National Cancer Institute, 2020-10, Vol.112 (10), p.1047-1054</ispartof><rights>Published by Oxford University Press 2019. This work is written by US Government employees and is in the public domain in the US. 2019</rights><rights>Published by Oxford University Press 2019. This work is written by US Government employees and is in the public domain in the US.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c506t-819dd87765c016fab8a497599a1747b91f0b3372eb0f34165f3d31991816fcc03</citedby><cites>FETCH-LOGICAL-c506t-819dd87765c016fab8a497599a1747b91f0b3372eb0f34165f3d31991816fcc03</cites><orcidid>0000-0001-9322-1395</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,1585,27926,27927</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31860085$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chaturvedi, Anil K</creatorcontrib><creatorcontrib>Udaltsova, Natalia</creatorcontrib><creatorcontrib>Engels, Eric A</creatorcontrib><creatorcontrib>Katzel, Jed A</creatorcontrib><creatorcontrib>Yanik, Elizabeth L</creatorcontrib><creatorcontrib>Katki, Hormuzd A</creatorcontrib><creatorcontrib>Lingen, Mark W</creatorcontrib><creatorcontrib>Silverberg, Michael J</creatorcontrib><title>Oral Leukoplakia and Risk of Progression to Oral Cancer: A Population-Based Cohort Study</title><title>JNCI : Journal of the National Cancer Institute</title><addtitle>J Natl Cancer Inst</addtitle><description>Abstract Background The optimal clinical management of oral precancer remains uncertain. We investigated the natural history of oral leukoplakia, the most common oral precancerous lesion, to estimate the relative and absolute risks of progression to cancer, the predictive accuracy of a clinician’s decision to biopsy a leukoplakia vis-à-vis progression, and histopathologic predictors of progression. Methods We conducted a retrospective cohort study (1996–2012) of patients with oral leukoplakia (n = 4886), identified using electronic medical records within Kaiser Permanente Northern California. Among patients with leukoplakia who received a biopsy (n = 1888), we conducted a case-cohort study to investigate histopathologic predictors of progression. Analyses included indirect standardization and unweighted or weighted Cox regression. Results Compared with the overall Kaiser Permanente Northern California population, oral cancer incidence was substantially elevated in oral leukoplakia patients (standardized incidence ratio = 40.8, 95% confidence interval [CI] = 34.8 to 47.6; n = 161 cancers over 22 582 person-years). Biopsied leukoplakias had a higher oral cancer risk compared with those that were not biopsied (adjusted hazard ratio = 2.38, 95% CI = 1.73 to 3.28). However, to identify a prevalent or incident oral cancer, the biopsy decision had low sensitivity (59.6%), low specificity (62.1%), and moderate positive–predictive value (5.1%). Risk of progression to oral cancer statistically significantly increased with the grade of dysplasia; 5-year competing risk-adjusted absolute risks were: leukoplakia overall = 3.3%, 95% CI = 2.7% to 3.9%; no dysplasia = 2.2%, 95% CI = 1.5% to 3.1%; mild-dysplasia = 11.9%, 95% CI = 7.1% to 18.1%; moderate-dysplasia = 8.7%, 95% CI = 3.2% to 17.9%; and severe dysplasia = 32.2%, 95% CI = 8.1%–60.0%. Yet 39.6% of cancers arose from biopsied leukoplakias without dysplasia. Conclusions The modest accuracy of the decision to biopsy a leukoplakia vis-à-vis presence or eventual development of oral cancer highlights the need for routine biopsy of all leukoplakias regardless of visual or clinical impression. Leukoplakia patients, particularly those with dysplasia, need to be closely monitored for signs of early cancer.</description><subject>Adult</subject><subject>Aged</subject><subject>Biopsy</subject><subject>California - epidemiology</subject><subject>Cancer</subject><subject>Cohort analysis</subject><subject>Cohort Studies</subject><subject>Confidence intervals</subject><subject>Disease Progression</subject><subject>Dysplasia</subject><subject>Electronic health records</subject><subject>Electronic medical records</subject><subject>Female</subject><subject>Health risks</subject><subject>Humans</subject><subject>Leukokeratosis</subject><subject>Leukoplakia, Oral - epidemiology</subject><subject>Leukoplakia, Oral - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mouth Neoplasms - epidemiology</subject><subject>Mouth Neoplasms - pathology</subject><subject>Oral cancer</subject><subject>Patients</subject><subject>Population studies</subject><subject>Population-based studies</subject><subject>Precancerous Conditions - epidemiology</subject><subject>Precancerous Conditions - pathology</subject><subject>Regression analysis</subject><subject>Retrospective Studies</subject><subject>Risk</subject><subject>Risk assessment</subject><subject>Standardization</subject><subject>Statistical analysis</subject><issn>0027-8874</issn><issn>1460-2105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUtLJDEUhcOgjD3qyr0EBBmQ0jwqLxeCNr6gQXFGcBdSqZRWd3WlTKoGnF9v2lZRF97NXZyPc8_lALCF0T5Gih5MW1sflNP_hMofYIRzjjKCEVsBI4SIyKQU-Rr4FeMUpVEk_wnWKJYcIclG4O4qmAZO3DDzXWNmtYGmLeFNHWfQV_A6-PvgYqx9C3sPX9ixaa0Lh_AYXvtuaEyfxOzERFfCsX_woYd_-qF82gCrlWmi23zd6-D27PTv-CKbXJ1fjo8nmWWI95nEqiylEJxZhHllCmlyJZhSBotcFApXqKBUEFegiuaYs4qWFCuFZaKtRXQdHC19u6GYu9K6tk8pdRfquQlP2ptaf1ba-kHf-39aMM4pw8ng96tB8I-Di72e19G6pjGt80PUhBIliOJicWvnCzr1Q2jTe5rkgmMmSU4StbekbPAxBle9h8FILxrTi8b0srFEb3_M_86-VZSA3SXgh-5bp2e75J7L</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Chaturvedi, Anil K</creator><creator>Udaltsova, Natalia</creator><creator>Engels, Eric A</creator><creator>Katzel, Jed A</creator><creator>Yanik, Elizabeth L</creator><creator>Katki, Hormuzd A</creator><creator>Lingen, Mark W</creator><creator>Silverberg, Michael J</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><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>7TO</scope><scope>7U7</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9322-1395</orcidid></search><sort><creationdate>20201001</creationdate><title>Oral Leukoplakia and Risk of Progression to Oral Cancer: A Population-Based Cohort Study</title><author>Chaturvedi, Anil K ; 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Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>JNCI : Journal of the National Cancer Institute</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chaturvedi, Anil K</au><au>Udaltsova, Natalia</au><au>Engels, Eric A</au><au>Katzel, Jed A</au><au>Yanik, Elizabeth L</au><au>Katki, Hormuzd A</au><au>Lingen, Mark W</au><au>Silverberg, Michael J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oral Leukoplakia and Risk of Progression to Oral Cancer: A Population-Based Cohort Study</atitle><jtitle>JNCI : Journal of the National Cancer Institute</jtitle><addtitle>J Natl Cancer Inst</addtitle><date>2020-10-01</date><risdate>2020</risdate><volume>112</volume><issue>10</issue><spage>1047</spage><epage>1054</epage><pages>1047-1054</pages><issn>0027-8874</issn><eissn>1460-2105</eissn><abstract>Abstract Background The optimal clinical management of oral precancer remains uncertain. We investigated the natural history of oral leukoplakia, the most common oral precancerous lesion, to estimate the relative and absolute risks of progression to cancer, the predictive accuracy of a clinician’s decision to biopsy a leukoplakia vis-à-vis progression, and histopathologic predictors of progression. Methods We conducted a retrospective cohort study (1996–2012) of patients with oral leukoplakia (n = 4886), identified using electronic medical records within Kaiser Permanente Northern California. Among patients with leukoplakia who received a biopsy (n = 1888), we conducted a case-cohort study to investigate histopathologic predictors of progression. Analyses included indirect standardization and unweighted or weighted Cox regression. Results Compared with the overall Kaiser Permanente Northern California population, oral cancer incidence was substantially elevated in oral leukoplakia patients (standardized incidence ratio = 40.8, 95% confidence interval [CI] = 34.8 to 47.6; n = 161 cancers over 22 582 person-years). Biopsied leukoplakias had a higher oral cancer risk compared with those that were not biopsied (adjusted hazard ratio = 2.38, 95% CI = 1.73 to 3.28). However, to identify a prevalent or incident oral cancer, the biopsy decision had low sensitivity (59.6%), low specificity (62.1%), and moderate positive–predictive value (5.1%). Risk of progression to oral cancer statistically significantly increased with the grade of dysplasia; 5-year competing risk-adjusted absolute risks were: leukoplakia overall = 3.3%, 95% CI = 2.7% to 3.9%; no dysplasia = 2.2%, 95% CI = 1.5% to 3.1%; mild-dysplasia = 11.9%, 95% CI = 7.1% to 18.1%; moderate-dysplasia = 8.7%, 95% CI = 3.2% to 17.9%; and severe dysplasia = 32.2%, 95% CI = 8.1%–60.0%. Yet 39.6% of cancers arose from biopsied leukoplakias without dysplasia. Conclusions The modest accuracy of the decision to biopsy a leukoplakia vis-à-vis presence or eventual development of oral cancer highlights the need for routine biopsy of all leukoplakias regardless of visual or clinical impression. Leukoplakia patients, particularly those with dysplasia, need to be closely monitored for signs of early cancer.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>31860085</pmid><doi>10.1093/jnci/djz238</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-9322-1395</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
Biopsy
California - epidemiology
Cancer
Cohort analysis
Cohort Studies
Confidence intervals
Disease Progression
Dysplasia
Electronic health records
Electronic medical records
Female
Health risks
Humans
Leukokeratosis
Leukoplakia, Oral - epidemiology
Leukoplakia, Oral - pathology
Male
Middle Aged
Mouth Neoplasms - epidemiology
Mouth Neoplasms - pathology
Oral cancer
Patients
Population studies
Population-based studies
Precancerous Conditions - epidemiology
Precancerous Conditions - pathology
Regression analysis
Retrospective Studies
Risk
Risk assessment
Standardization
Statistical analysis
title Oral Leukoplakia and Risk of Progression to Oral Cancer: A Population-Based Cohort Study
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