A Randomized Trial of Telephone-Based Smoking Cessation Treatment in the Lung Cancer Screening Setting

Author:

Taylor Kathryn L1ORCID,Williams Randi M1,Li Tengfei2ORCID,Luta George2ORCID,Smith Laney1,Davis Kimberly M1,Stanton Cassandra A3,Niaura Raymond4,Abrams David4,Lobo Tania1,Mandelblatt Jeanne1,Jayasekera Jinani1ORCID,Meza Rafael5ORCID,Jeon Jihyoun5ORCID,Cao Pianpian5ORCID,Anderson Eric D6,

Affiliation:

1. Cancer Prevention and Control Program, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center , Washington, DC, USA

2. Department of Biostatistics, Bioinformatics, and Biomathematics, Georgetown University Medical Center , Washington, DC, USA

3. Behavioral Health, Westat , Rockville, MD, USA

4. School of Global Public Health, New York University , New York, NY, USA

5. Department of Epidemiology, University of Michigan , Ann Arbor, MI, USA

6. Department of Pulmonary and Sleep Medicine, Georgetown University Medical Center , Washington, DC, USA

Abstract

Abstract Background Lung cancer mortality is reduced via low-dose computed tomography screening and treatment of early-stage disease. Evidence-based smoking cessation treatment in the lung screening setting can further reduce mortality. We report the results of a cessation trial from the National Cancer Institute’s Smoking Cessation at Lung Examination collaboration. Methods Eligible patients (n = 818) aged 50-80 years were randomly assigned (May 2017-January 2021) to the intensive vs minimal arms (8 vs 3 phone sessions plus 8 vs 2 weeks of nicotine patches, respectively). Bio-verified (primary) and self-reported 7-day abstinence rates were assessed at 3, 6, and 12 months post random assignment. Logistic regression analyses evaluated the effects of study arm. All statistical tests were 2-sided. Results Participants reported 48.0 (SD = 17.2) pack-years, and 51.6% were not ready to quit in less than 30 days. Self-reported 3-month quit rates were statistically significantly higher in the intensive vs minimal arm (14.3% vs 7.9%; odds ratio [OR] = 2.00, 95% confidence interval [CI] = 1.26 to 3.18). Bio-verified abstinence was lower but with similar relative differences between arms (9.1% vs 3.9%; OR = 2.70, 95% CI = 1.44 to 5.08). Compared with the minimal arm, the intensive arm was more effective among those with greater nicotine dependence (OR = 3.47, 95% CI = 1.55 to 7.76), normal screening results (OR = 2.58, 95% CI = 1.32 to 5.03), high engagement in counseling (OR = 3.03, 95% CI = 1.50 to 6.14), and patch use (OR = 2.81, 95% CI = 1.39 to 5.68). Abstinence rates did not differ statistically significantly between arms at 6 months (OR = 1.2, 95% CI = 0.68 to 2.11) or 12 months (OR = 1.4, 95% CI = 0.82 to 2.42). Conclusions Delivering intensive telephone counseling and nicotine replacement with lung screening is an effective strategy to increase short-term smoking cessation. Methods to maintain short-term effects are needed. Even with modest quit rates, integrating cessation treatment into lung screening programs may have a large impact on tobacco-related mortality.

Funder

National Cancer Institute at the National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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