grant

Influence of Menthol Cigarette Smoking on Lung Cancer Screening Eligibility in a National Prospective Study

Organization RUTGERS BIOMEDICAL AND HEALTH SCIENCESLocation Newark, UNITED STATESPosted 1 Aug 2025Deadline 31 Jul 2027
NIHUS FederalResearch GrantFY202521+ years oldAdultAdult HumanAdvanced CancerAdvanced Malignant NeoplasmAfrican AmericanAfrican American groupAfrican American individualAfrican American peopleAfrican American populationAfrican AmericansAfro AmericanAfroamericanAgeAmerican maleAmerican manAmerican menAssessment instrumentAssessment toolBiological MarkersCT screeningCancer CauseCancer Causing AgentsCancer DetectionCancer EtiologyCancersCarcinogen exposureCarcinogensCessation of lifeCigaretteConsumptionDataData SetDeathDeath CertificatesDevelopmentDiagnosisDistantEarly DiagnosisEconomic IncomeEconomical IncomeEligibilityEligibility DeterminationEthnic OriginEthnicityExposure toFaceFemaleGeneralized GrowthGeographyGrowthGuidelinesHealth Care SystemsHeterogeneityHigh-Risk CancerHispanicIncomeIndividualInequityLinkLow incomeMalignant NeoplasmsMalignant TumorMalignant Tumor of the LungMalignant neoplasm of lungMarketingMeasuresMentholNicotine DependenceOncogensOutcomePatternPersonsPopulationProbabilityPrognosisProspective StudiesProtocol ScreeningPulmonary CancerPulmonary malignant NeoplasmRaceRacesRecommendationRecordsResearchRiskRisk AssessmentRisk EstimateSmokeSmokingSmoking HistorySurvey InstrumentSurveysSurvival RateTimeTissue GrowthTobaccoTobacco ConsumptionTobacco useToxicant exposureU.S. MalesU.S. Preventative Services Task ForceU.S. Preventative Task ForceU.S. Preventive Services Task ForceU.S. Preventive Task ForceUS MenUS Preventative Services Task ForceUS Preventative Task ForceUS Preventive Health Services Task ForceUS Preventive Services Task ForceUS Preventive Task ForceUS maleUSPSTFUnited States Preventative Services Task ForceUnited States Preventative Task ForceUnited States Preventive Services Task ForceUnited States Preventive Task ForceVital StatisticsVulnerable PopulationsWomanadulthoodagedagesbio-markersbiologic markerbiomarkercancer registrycancer riskcigarette smokecigarette smokingcigarette useclinical diagnosiscohortcomputed tomography screeningdata harmonizationdata registrydeath riskdevelopmentaldifferences due to racedifferences in racediffers by racediffers in raceearly detectionearly screeningexposure to nicotinefacesfacialharmonized dataincomeslow dose computed tomographylow dose computerized tomographylow-dose CTlung cancerlung cancer early detectionlung cancer screeningmales in Americamales in the U.S.males in the USmales in the USAmales in the United Statesmalignancymarginalized groupmarginalized individualmarginalized peoplemarginalized populationmeetingmeetingsmen in Americamen in the U.S.men in the USmen in the USAmen in the United Statesmortalitymortality riskneoplasm registryneoplasm/cancernicotine addictionnicotine dependentnicotine exposureoncogenic agentontogenypack/yearpopulation surveypreferencerace based differencesrace differencesrace related differencesracialracial backgroundracial differenceracial originracially differentrecommended screeningresponsescreeningscreening guidelinesscreening recommendationsscreeningssecondary analysissexsmoking exposuresmoking initiationsmoking-related diseasesmoking-related disordersuccesstobacco product usetoxic exposureuptakevulnerable groupvulnerable individualvulnerable people
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Full Description

PROJECT SUMMARY/ABSTRACT
Lung cancer is the leading cause of cancer death among US men and women and accounted for more than

125,000 deaths in 2023—more than 20% of all cancer deaths. An important strategy to reduce mortality is lung

cancer screening by low-dose computed tomography (LDCT), which has been estimated to reduce lung cancer

mortality by up to 20%. In 2013, the US Preventive Services Task Force (USPSTF) began recommending LDCT

lung cancer screening for people aged 55–80 years with a 30 pack-year history of smoking who currently smoke

or had quit within 15 years; in 2021, these criteria were revised to include adults aged 50–80 with a 20 pack-

year smoking history. Although uptake has been slow, there have been favorable shifts in diagnoses towards

earlier stages. Still, nearly half of lung cancers today are diagnosed at distant stages, and inequities in lung

cancer screening and mortality persist for several groups such as African Americans, women, and people with

lower income, many of whom smoke menthol vs non-menthol cigarettes and at increasing rates. Menthol in

cigarettes is associated with increased smoking initiation, propensity to progress to regular smoking, increased

nicotine dependence, and decreased cessation success. Paradoxically, people who smoke menthol cigarettes

have comparable levels of nicotine and carcinogen exposure biomarkers yet consume fewer cigarettes per day

than people who smoke non-menthol cigarettes. Prior studies have concluded that menthol cigarette type need

not be considered when estimating risk for lung cancer. However, these studies predated growth in the menthol

cigarette market and the introduction of LDCT lung cancer screening, for which eligibility is determined largely

by cigarettes smoked per day. This raises new questions about the potential indirect impact of menthol cigarette

smoking on lung cancer screening and outcomes: if people who smoke menthol consume fewer cigarettes per

day, are they less likely to meet screening eligibility criteria, despite having the same exposure to carcinogens?

If true, people who smoke menthol face greater risk for later-stage diagnosis, and subsequently, mortality. This

application will utilize the Tobacco Use Supplement to the Current Population Survey (TUS-CPS) and the

Tobacco Longitudinal Mortality Study (TLMS) to evaluate the influence of menthol in cigarettes on lung cancer

screening eligibility and outcomes. Under Aim 1, we will compare lung cancer screening eligibility for people who

smoke menthol vs nonmenthol cigarettes, hypothesizing that menthol smoking will be associated with decreased

probability of meeting screening eligibility criteria. We will also examine changes over time and differences by

race/ethnicity, sex, and income through stratified analyses. Under Aim 2 we will evaluate lung cancer screening

eligibility and menthol smoking exposure among individuals who have died of lung cancer using a case-case

approach. We hypothesize that adjusted odds of menthol smoking will be higher for ineligible vs eligible cases

and will evaluate heterogeneity by time (< 2013 vs after), race/ethnicity, sex, and income. We will also investigate

the reasons for ineligibility among those not eligible (e.g., pack-years vs age) and if this differs by menthol status.

Grant Number: 1R21CA301405-01
NIH Institute/Center: NIH

Principal Investigator: Michelle Bover Manderski

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