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Duke Comprehensive Cancer Center [C. M. M., I. M. L., P. L.], Duke Department of Community and Family Medicine [C. M. M., B. K. R.], H. P. Lee Moffit Cancer Center and Research Institute [G. B.], Center for Clinical Health Policy Research, Duke University Medical Center [G. S., S. D.], Cecil G. Sheps Center for Health Services Research, University of North Carolina at Chapel Hill [J. A.], Chapel Hill, North Carolina, and Division of Cancer Control and Population Sciences, National Cancer Institute, NIH, Bethesda, Maryland 20892 [B. K. R.]
Purpose: Markers of genetic susceptibility to tobacco-related cancers couldpersonalize harms of smoking and motivate cessation. Our objective was to assess whether a multicomponent intervention that included feedback about genetic susceptibility to lung cancer increased risk perceptions and rates of smoking cessation compared with a standard cessation intervention.
Experimental Design: Our design was a two-arm trial with eligible smokers randomized in a 1:2 ratio to Enhanced Usual Care or Biomarker Feedback (BF). Surveys were conducted at baseline, 6, and 12 months later. The setting was an inner city community health clinic. African-American patients who were current smokers (n = 557) were identified by chart abstraction and provider referral. All smokers received a self-help manual and, if appropriate, nicotine patches. Smokers in the BF arm also were offered a blood test for genotyping the GST3 gene (GSTM1), sent a test result booklet, and called up to four times by a health educator. Prevalent abstinence was assessed by self-report of having smoked no cigarettes in the prior 7 days at the 6- and 12-month follow-ups and sustained abstinence, i.e., not smoking at either follow-up or in-between.
Results: Smoking cessation was greater for the BF arm than the Enhanced Usual Care arm (19% versus 10%, respectively; P < 0.006) at 6 months but not at 12 months.
Conclusions: Smokers agreed to genetic feedback as part of a multicomponent cessation program. Although the program increased short-term cessation rates compared with standard intervention, genetic feedback of susceptibility may not benefit smokers with high baseline risk perceptions.
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