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. Author manuscript; available in PMC: 2018 Apr 2.
Published in final edited form as: J Psychosoc Oncol. 2015;33(6):703–723. doi: 10.1080/07347332.2015.1082171

Incorporating a Smoking Cessation Intervention into Lung Cancer Screening Programs: Preliminary Studies

CHARLOTTE J HAGERMAN 1, CATHERINE A TOMKO 2, CASSANDRA A STANTON 3, JENNA A KRAMER 4, DAVID B ABRAMS 5, ERIC D ANDERSON 6, KATHRYN L TAYLOR 7
PMCID: PMC5880211  NIHMSID: NIHMS950923  PMID: 26600242

Abstract

Two preliminary studies assessed whether telephone counseling (TC) is a feasible smoking cessation intervention following lung cancer screening. Seven older smokers undergoing lung cancer screening (pack years = 61.5) completed three TC sessions, which incorporated the screening result as motivation to quit. Participation (87.5%) and retention (85.7%) rates were good, and four smokers quit smoking (three of whom received abnormal results). We conducted four focus groups with 16 current and former older smokers (pack years = 55). Most believed that an abnormal scan would motivate them to quit and expressed interest in TC. TC may be feasible and potentially efficacious within lung screening programs.

Keywords: focus groups, lung cancer screening, smoking cessation, telephone counseling, teachable moment

INTRODUCTION

Lung cancer is the leading cause of cancer-related death and smoking accounts for almost 90% of lung cancers (American Cancer Society, 2014; U.S. Department of Health and Human Services, 2014). The National Lung Screening Trial (NLST) reported that lung cancer mortality was reduced by 20% due to the detection and treatment of early stage disease (Aberle, Adams, Berg, Black, Clapp, & Fagerstrom, 2011). As a result, the U.S. Preventive Services Task Force recommended screening of individuals at high risk for lung cancer with mandated insurance coverage beginning in 2015 (U.S. Department of Health and Human Services, 2015; U.S. Preventive Services Task Force, 2013). The Centers for Medicare and Medicaid Services (CMS) has also proposed coverage of lung cancer screening among 65- to 74-year-old individuals (Centers for Medicare & Medicaid Services (CMS), 2015).

It is estimated that over 8 million people in the United States meet the criteria to undergo screening and that screening could prevent 12,000 deaths annually (Ma, Ward, Smith, & Jemal, 2013). Cost-effectiveness models suggest that screening plus concurrent smoking cessation programs represent an unprecedented opportunity to save even more lives than with screening alone, and that cessation will be essential to realizing the full benefit of screening (McMahon, Kong, Bouzan, Weinstein, Cipriano, & Tramontano, 2011; Villanti, Jiang, Abrams, & Pyenson, 2013). The USPSTF, CMS, and other organizations recommend that smoking cessation be offered in conjunction with screening. However, there are no clinical guidelines or evidence-based cessation protocols with demonstrated effectiveness in this setting.

The critical ‘teachable moment’ that can occur after a health event such as cancer screening has been shown to enhance both intention to quit and cessation (Anderson, Yip, Henschke, Yankelevitz, Ostroff, & Burns, 2009; Ashraf, Saghir, Dirksen, Pedersen, Thomsen, & Dossing, 2014; McBride, Emmons, & Lipkus, 2003; Ostroff, Shuk, Krebs, Lu, Burkhalter, & Cortez-Weir, 2001; Styn, Land, Perkins, Wilson, Romkes, & Weissfeld, 2009; Taylor, Cox, Zincke, Mehta, McGuire, & Gelmann, 2007; Townsend, Clark, Jett, Patten, Schroeder, & Nirelli, 2005; van der Aalst, van Klaveren, van den Bergh, Willemsen, & de Koning, 2011). Results from our previous observational study suggested that an abnormal screening result was significantly associated with becoming more motivated to quit, while a normal screening result was associated with less motivation (Taylor et al., 2007). Among NLST participants, we have also found that the likelihood of quitting following an abnormal result increased with the severity of the result, in the absence of a cessation intervention (Tammemagi, Berg, Riley, Cunningham, & Taylor, 2014).

One of the unanswered questions in this area is whether offering a cessation intervention can capitalize on the momentum created by undergoing lung cancer screening. Three randomized trials have used cessation interventions with lung screening participants and showed promising overall cessation rates: a pilot telephone counseling (TC) trial reported 22% cessation at 6 months, a comparison between a standard brochure and a tailored web-based intervention reported 12% to 15% cessation at 2 years, and standard versus Internet-based self-help reported 5% to 10% at 1 year (Clark, Cox, Jett, Patten, Schroeder, & Nirelli, 2004; Ferketich, Otterson, King, Hall, Browning, & Wewers, 2012; van der Aalst, van den Bergh, Willemsen, de Koning, & van Klaveren, 2010; van der Aalst, de Koning, van den Bergh, Willemsen, & van Klaveren, 2012). Although very encouraging, these trials found no significant differences between intervention and control arms (Clark et al., 2004; Ferketich et al., 2012; van der Aalst et al., 2010; van der Aalst et al., 2012).

In the present study, we developed a telephone-based cessation intervention in which we specifically leveraged the screening result to enhance motivation to quit, a strategy that previous trials have not employed. Incorporation of an individual’s screening result into a cessation intervention attempts to enhance intention to quit by providing an individualized, motivational cessation intervention that is feasible to implement within lung screening programs. This intervention was designed to be evidence-based, brief, scalable, and testable in a randomized trial. Thus, if found to be effective, it can be readily implemented in a cost-efficient manner.

Finally, we conducted a qualitative focus group study with individuals eligible for lung cancer screening to further assess feasibility, attitudes toward lung cancer screening, and interest in an associated smoking cessation intervention.

PILOT STUDY OF TELEPHONE COUNSELING: MATERIALS AND METHODS

Participants

Eligibility criteria included: 1) status as a current smoker; 2) ≥ 30 pack-year smoking history (number of years smoked multiplied by packs per day smoked), and 3) enrollment in the Georgetown University Medical Center (GUMC) lung cancer screening program. Participants were included regardless of their readiness to quit.

Procedures

The nurse navigator for the lung screening program recruited current smokers when they registered for screening. The screening cost to participants was $75 (if not covered by insurance). The research assistant later called to conduct the baseline telephone interview (T0) prior to the screening appointment, and then mailed the consent form for participants to return. One week after participants had received their screening results, we conducted the second assessment (T1), followed by three brief TC calls approximately one week apart. One week after the third counseling call (approximately one-month post-receipt of the screening results), we conducted the final telephone assessment (T2).

Measures

Demographic and Clinical Characteristics

We assessed age, sex, race, education, marital status, comorbidities, family history of lung cancer at baseline, and screening-related comorbidities at the one-month assessment.

Smoking History and Smoking Status

At baseline, we assessed smoking history, smoking status in the past 30 days (including cigarettes per day (cpd) and number of days smoked), other tobacco use (including pipes, cigars, tiparillos, e-cigarettes, and snus), and the number of quit attempts for ≥ 24 hours since the prior assessment. At each assessment, we assessed nicotine dependence with a single item from the Fagerstrom Test for Nicotine Dependence (Heatherton et al., 1991): time to first cigarette (“less than 5 minutes of waking” to “more than 8 hours after waking”). This question has previously been used as a single-item measure of nicotine dependence (Baker, Piper, McCarthy, Bolt, Smith, & Kim, 2007). Also at each assessment, participants completed the readiness to quit ladder (Biener & Abrams, 1991; Burgess, van, Noorbaloochi, Clothier, Taylor, & Sherman, 2014; Sachs, Wild, Thomas, Hammal, & Finegan, 2012; Webb Hooper, Baker, & Robinson, 2014), from “I enjoy smoking so much that I will not consider quitting no matter what happens” to “I have already cut down and set a quit date.”

Lung Cancer Screening Results

We obtained the screening results and follow-up recommendations from the electronic medical record prior to conducting the T1 assessment. Results were classified as 1) normal, no follow-up required, 2) abnormal findings, not suspicious for lung cancer, or 3) abnormal findings, suspicious for lung cancer.

Perceived Risk and Worry

At each assessment, we measured participants’ perceived risk of developing lung cancer compared to others of the same gender and smoking status. The five response categories ranged from “I am at much less risk than others,” to “I am at much greater risk than others.” We also assessed perceived worry about developing lung cancer on a four-point scale, from “not at all worried” to “extremely worried.”

Biochemical Verification of Cessation

Participants who self-reported quitting during the study were mailed a NicAlert saliva cotinine test kit (Cooke, Bullen, Whittaker, McRobbie, Chen, & Walker, 2008) if they were not using any form of NRT (N = 2) or were scheduled to undergo a carbon monoxide breath test to coincide with a medical appointment (N = 1). One participant who self-reported quitting at the T1 assessment was lost to follow-up and did not complete biochemical verification. Participants were given a $15 gift card for completing the test.

Telephone Counseling Intervention

The TC intervention followed the U.S. Department of Health and Human Services’ Guidelines for Treating Tobacco Use and Dependence (Fiore, Jaen, Baker, Bailey, Benowitz, & Curry, 2009). It was based on Project Ascend protocol (Graham & Papandonatos, 2008) and modified to incorporate discussion of participants’ lung screening results. The intervention was also shortened from eight to three sessions to promote feasibility and portability to other lung screening settings. Each session was designed to be brief (10 to 15 minutes) and to use motivational interviewing techniques (Rollnick & Miller, 1995). Motivational interviewing is a client-centered style of counseling which seeks to resolve ambivalence toward change. It encourages the counselor to listen empathically, facilitate talk of change, and respond to any resistance to change (Rollnick & Miller, 1995). In the current telephone counseling intervention, the counselor used these strategies to help participants identify the barriers and benefits of quitting, to facilitate changes in smoking habits, and to encourage participants to discuss NRT, Chantix® (varenicline), and Zyban® (bupropion) with their physician. For participants who reported quitting, calls focused on their reasons for quitting, identified triggers and potential causes of relapse, and discussed ways to recover should the participant slip or relapse. Discussion of lung screening results was incorporated into all counseling calls. Counselors asked participants to discuss the emotional impact of the screening result, any impact that the result had on their smoking, and to elaborate on future smoking plans in light of the results.

At the end of each call, counselors offered smoking cessation resources to participants and tracked requests for information. Resources included: the American Legacy Foundation’s BecomeAnEx booklet and website (American Legacy Foundation, 2014), the national telephone quitline number (1–800-QUIT-NOW), encouragement to speak with their physicians about NRT and prescription medicines, the Centers for Disease Control’s text message cessation program, and a list of phone numbers for local in-person cessation groups.

Counselor Training

The smoking cessation counselor was certified as a tobacco treatment specialist through accredited programs (Association for the Treatment of Tobacco Use and Dependence [ATTUD], 2014).

PILOT STUDY OF TELEPHONE COUNSELING: RESULTS

Participation Rates

We enrolled 7 of 8 (87.5%) eligible participants over a 5 month period at the GUMC lung screening program. All seven participants completed the baseline assessment (T0), the post-screening assessment (T1), and two counseling calls. Six participants (85.7%) completed all three counseling calls and the 1-month assessment (T2).

Demographic Characteristics

Participants ranged from 49 to 73 years old (M = 63, SD = 8.6), four were female, five were white, four had a college degree or more education, three were married, five were retired, and all seven had health insurance.

Tobacco Use

We have provided detailed tobacco use and screening information for each participant at each assessment, showing how participants changed over time (Table 1). Pack years ranged from 33 to 112 (M = 61.5, SD = 26.9). At baseline, five participants smoked 2 to 10 CPD, and five smoked their first cigarette ≥15 minutes after waking. At the T2 assessment, three participants reported continued smoking and three reported that they had quit (with biochemical verification of quit status). One additional participant reported having quit at the T1 assessment, but was lost to follow-up and did not complete biochemical verification.

TABLE 1.

Tobacco Use and Screening Information for Each Participant at each Assessment

Assessment Number of
TC sessions
completed
Screening
result
Smoking Cessation Outcomes Perceived Risk
Outcomes


Number of
Quit
Attempts
(at least
24 hours)
Number of
days
smoked
(out of 30)
Cigarettes
per day
Time to
first
cigarette
Intention
to quit
Resources
requested
during
counseling
calls
Final
smoking
status
Risk of
developing
lung cancer
Worry
about
developing
lung cancer
Subject 1 Baseline (pre-screen; T0) 3 sessions Abnormal, suspicious for lung cancer Missing 20–27 days 2–5 per day Within 5 min Ready to quit in 6 months 1–800-QUIT-NOW quitline, list of in-person cessation groups Quit during study (Verified with NicAlert) At the same risk as others Somewhat worried
One-week post receipt of screening results(T1) Quit Smoking 3–5 days 6–10 per day Former smoker Former smoker At the same risk as others Very worried
One-month post-receipt of screening results (T2) Quit Smoking 0 days 0 per day Former smoker Already quit/worried about relapsing At the same risk as others Very worried
Subject 2 Baseline 2 sessions Abnormal, suspicious for lung cancer 1 28–30 days 6–10 per day 30 min to 1 hour Ready to quit in 30 days None requested Quit during study (as of T1 assessment) Not verified-lost to follow-up At the same risk as others Somewhat worried
Post-receipt of results Quit Smoking 0 days 0 per day Former smoker Former smoker At the same risk as others Somewhat worried
One-month Lost to follow up Lost to follow-up Lost to follow-up Lost to follow-up Lost to follow-up Lost to follow-up Lost to follow-up
Subject 3 Baseline 3 sessions Normal 6 20–27 days 2–5 per day 1–2 hours Already cut down/set a quit date None requested Current smoker At the same risk as others Very worried
Post-receipt of results 15 10–19 days 2–5 per day 1–2 hours Ready to quit–6 mos At the same risk as others Somewhat worried
One-month 3 20–27 days 6–10 per day 30 minutes to 1 hour Already cut down/set a quit date At less risk than others Not at all worried
Subject 4 Baseline 3 sessions Normal 0 28–30 days 20 (1 pack) per day 15–29 minutes Often thinks about quitting but no plans 1–800-QUIT-NOW quitline Quit during study (verified with NicAlert) At the same risk as others Very worried
Post-receipt of results Quit Smoking 0 days 0 per day Former smoker Former smoker At higher risk than others Somewhat worried
One-month Quit Smoking 0 days 0 per day Former smoker Quit and 100% confident can stay quit At less risk than others Not at all worried
Subject 5 Baseline 3 sessions Not suspicious for lung cancer, but other finding present 0 28–30 days 6–10 per day 6–14 minutes Often thinks about quitting but no plans None requested Current smoker Refused Not at all worried
Post-receipt of results 0 28–30 days 6–10 per day 30 minutes to 1 hour Often thinks about quitting but no plans Refused Not at all worried
One-month 0 10–19 days 6–10 per day 1–2 hours Ready to quit in 6 months At the same risk as others Not at all worried
Subject 6 Baseline 3 sessions Abnormal, suspicious for lung cancer 2 28–30 days 11–20 per day 15–29 minutes Sometimes thinks about quitting but no plans BecomeAnEx website, BecomeAnEx booklet, 1–800-QUIT-NOW quitline Quit during study (verified with CO monitor) At the same risk as others Somewhat worried
Post-receipt of results 0 28–30 days 2–5 per day More than 8 hours Ready to quit in 6 months At the same risk as others Somewhat worried
One-month 0 0 days 0 per day Former smoker Refused At the same risk as others Somewhat worried
Subject 7 Baseline 3 sessions Not suspicious for lung cancer, but other finding present 0 28–30 days 6–10 per day 15–29 minutes Often thinks about quitting but no plans BecomeAnEx booklet Current smoker At the same risk as others Somewhat worried
Post-receipt of results 0 28–30 days 6–10 per day 30 minutes to 1 hour Often thinks about quitting but no plans At the same risk as others Very worried
One-month 0 28–30 days 6–10 per day 1–2 hours Ready to quit in 6 months At the same risk as others Somewhat worried

Lung Cancer Screening Results and Change in Smoking Status

Of the two participants with normal results (i.e., there were no nodules or other abnormal findings), one quit smoking and one continued smoking. Both of the participants who had results not suspicious for lung cancer but with another abnormality (e.g., COPD) continued smoking. However, they both became more ready to quit by the end of the study and also increased the time before the first cigarette of the day (Table 1). Finally, the three participants with results that were suspicious for lung cancer (nodule ≥ 4 mm) all reported quitting during the course of the study (two with biochemical verification).

Lung Cancer Screening Results, Lung Cancer Worry, and Perceived Risk

Of the two participants with normal results, both reported decreased worry and perceived risk, from the T0 to the T2 assessment. Considering the four participants who had abnormal results (combining results that were suspicious and not suspicious for lung cancer) and who had complete data, none reported a change in perceived risk from T0 to T2, three reported no change in lung cancer worry from T0 to T2, and one participant reported increased worry.

FOCUS GROUP STUDY: MATERIALS AND METHODS

Participants

Eligible participants were current and former smokers (quit within the past 15 years) with at least a 30 pack-year smoking history.

Procedures

We conducted four focus groups, which included 16 participants we recruited through Craigslist, the GUMC lung cancer screening program, and the GUMC Minority Health & Health Disparities Research Center. Prior to the focus groups, participants completed the consent form, a brief questionnaire, and consented to audiotaping the meeting. We addressed 1) participants’ smoking history and prior cessation attempts; 2) interest in various cessation methods; 3) awareness of and attitudes toward CT lung cancer screening; and 4) feedback on potential smoking cessation interventions within a lung cancer screening program. Each participant received a $20 gift card.

Measures

The brief questionnaire assessed demographic information, lung screening history, pack-years, current smoking status, prior cessation methods, and interest in using cessation methods in the future. The survey also assessed current smokers’ readiness to quit and former smokers’ confidence in staying quit using the contemplation ladder (Apodaca, Abrantes, Ramsey, & Brown, 2007; Biener & Abrams, 1991).

Qualitative Analyses

To analyze participants’ responses in the focus groups, three investigators developed themes based on mutual agreement and then determined the presence of the themes in the transcripts. The themes from the discussions included smoking history, the impact of lung cancer screening and its results, and feasible cessation interventions.

FOCUS GROUP STUDY: RESULTS

Demographics

The 16 participants included 11 women and 5 men, aged 47 to 71 years (M = 62.5, SD = 5.9). Ten participants were African American, 4 were currently married, 9 were college graduates, 6 were employed full- or part-time, and 15 had health insurance.

Smoking Status

The five former smokers had an average of 52.2 pack years (SD = 42.1) and had been quit for an average of 9.8 years (SD = 7.8). The 11 current smokers had an average of 55.7 pack years (SD = 52.5). Among the current smokers, in the past 30 days, seven smoked every day or almost every day, while four smoked some days. Four of the current smokers were smoking < 1 pack per day (ppd), four were smoking one ppd, and three were smoking > 1 ppd.

Intention to Quit

Among the 10 current smokers with complete data, 2 reported “having cut back and setting a quit date,” 6 reported that they “often think about quitting but have no specific plans to quit,” and 2 reported “sometimes” or “rarely thinking about quitting.”

Lung Screening History

Seven of the 16 participants had previously been screened, and six had discussed lung screening with a doctor. Regarding plans for screening, 10 participants said that they definitely would be screened and 3 said that they probably would be screened within the next year.

Focus Group Discussion

Table 2 presents the major themes that were addressed and exemplar responses. Nine participants endorsed the “teachable moment” of lung screening, believing that an abnormal screening result would motivate them (and other smokers) to quit. Some participants suggested that quitting would be much easier after receiving an abnormal result. In fact, two of the former smokers explained that receiving an abnormal screening result was the reason they had quit smoking. However, three participants acknowledged that an abnormal result could cause a person to accept his/her fate and continue to smoke. Regarding a normal result, only two participants believed that it would give them permission to continue smoking.

TABLE 2.

Discussion Topics and Quotes from 4 Focus Groups (N = 16)

Discussion Topics Themes Examples of Participant Responses
The Effect of Abnormal Screening Results on Smoking Abnormal screening results motivate smokers to quit. “It was always in the back of my mind that it’s going to be somebody else and not me until I saw that x-ray. That really brought it home.”
“I would be frantic. I would just probably pass out and die then. It would make me want to stop, yes.”
“I always felt that people, when they’re confronted with a bad x-ray, that to me is easy [to quit]…What’s hard is to quit when you’re not looking in the face of evidence.”
“… I contracted double pneumonia and during the process of hospitalization they did an x-ray of my lung and they found a [benign] golf ball-sized blot on my lung… That really freaked me out. And I’ve never touched a cigarette [since].”
“I mean, suddenly it just hit me cold and I suddenly realized that I could die… it was an infection related to the double pneumonia—it wasn’t a cancer or whatever, but the idea that it could have been a malignant tumor just freaked me out. And that basically is how I stopped.”
Abnormal screening results encourage continued smoking. “Well yeah, if it’s a positive result a person is going to realize ‘I’m going to die.’ And they could continue smoking because they’re going to die anyway.”
The Effect of Normal Screening Results on Smoking Normal screening results give permission to smoke. “I remember getting results and they were good and I remember thinking, good, I can still smoke.”
“If the tests come out normal, can I cheat fate a little longer.”
Normal screening results do not give permission to smoke “I don’t think of it that way, anyway, like I got a clean scan and now I have a license to smoke. That’s just not a particular connection.”
Interest in Nicotine Replacement Therapy and Other Cessation Medications Hope to quit without using these aids. “The medicine and all that, the medicine’s no good to me because you have to go here first (pointing to head) and condition yourself.”
“The side-effects [of Chantix] alone are scary enough. Thoughts of suicide.”
“I’m hoping to have a moment of clarity one morning when I wake up… [and say], ‘I’m not smoking anymore.”’
Would be interested in using these aids. “I did acupuncture as well and the acupuncturist was extremely effective. So much so that it was actually disconcerting.”
“If I had somebody, or a text message, who would keep me on the sort of awareness path of a constant reminded and sort of make me realize how weak and ineffectual I am.”
“The scan is the first step. So then the second step that I would consider is a counseling program and/or, as part of that counseling program, they could discuss some of these alternative methods like herbal therapies or homeopathic medicines.”
“… Chantix really works. I was amazed. I wasn’t even tempted for a cigarette.”
Interest in Telephone Counseling Counseling would help me (and others) quit smoking. “… individual counseling, whether face-to-face or by telephone is something that could keep someone engaged with the process of wanting to quit.”
“I think individual counseling would keep people engaged. Like a career counselor or a life coach or whatever, making sure you’re aware of the risk and making sure you’re on track.”
“I’m just thinking about if someone called me once a week… Just knowing that there’s someone that cares… It’s just that personal touch of someone out there saying ‘hey, keep it up.”’
Counseling may not be for everyone. “I don’t think anyone can talk to me to get me to stop.”

Participants also discussed preferences for cessation interventions. Five participants endorsed nicotine replacement therapy (NRT) and medications to help smokers quit (specifically Chantix). However, others did not endorse these cessation methods due to concerns about side effects, as well as the belief that smoking is also a psychological addiction and therefore not amenable to pharmacotherapy. In fact, many participants hoped to “just quit.” However, one current smoker admitted that his willpower would never be that strong. Among the five participants who directly spoke about TC, four believed that it would be useful in helping them quit. However, one participant did not think counseling in general would be effective for him.

DISCUSSION

These pilot studies provide preliminary evidence that a telephone-based smoking cessation intervention may be feasible and potentially efficacious when delivered in conjunction with a lung cancer screening program. Protocol adherence was very good in the TC study, including adherence to the counseling calls and to biochemical verification. Several focus group participants indicated that counseling might help them to quit and that an abnormal screening result would motivate them to quit smoking. However, TC was not endorsed by all participants and thus further work is necessary to determine additional cessation interventions that are also feasible within this setting.

In addition to the question of feasibility, these findings support previous research which provides evidence for lung cancer screening as a teachable moment for smokers (Anderson et al., 2009; Ashraf et al., 2014; McBride et al., 2003; McMahon et al., 2011; Ostroff et al., 2011; Senore, Giordano, Bellisario, Di, & Segnan, 2012; Slatore, Baumann, Pappas, & Humphrey, 2014; Taylor et al., 2007; Villanti et al., 2013). We found that the three smokers whose screening results were suspicious for lung cancer quit during the course of the study. Among the four other participants who received a normal result or a minor abnormality, only one quit smoking. Prior studies have shown that abnormal results in particular may directly increase smoking cessation (Anderson et al., 2009; Ashraf et al., 2014; McBride et al., 2003; Styn et al., 2009; Tammemagi et al., 2014). This study is unique in that it pairs the teachable moment with TC to capitalize on this critical time with an empirically supported cessation method.

One challenge facing cessation interventions following lung cancer screening is that a portion of smokers are not ready to quit at the time of screening. However, several studies of smoking cessation in smokers who do not intend to quit in settings other than lung cancer screening have demonstrated abstinence rates from 10% to 15% (Cox, Clark, Jett, Patten, Schroeder, & Nirelli, 2003; Hepper, Drage, Davies, Rupp, LaMothe, & Schoenfelder, 1980; Loss, Hall, & Speers, 1979). Furthermore, previous research also shows that TC in particular works for older smokers who may not be ready to quit initially (American Lung Association, 2012; Bach, Mirkin, Oliver, Azzoli, Berry, & Brawley, 2012; Jaklitsch, Jacobson, Austin, Field, Jett, & Keshavjee, 2012; van der Aalst et al., 2011; Wender, Fontham, Barrera, Colditz, Church, & Ettinger, 2013; Wood, Eapen, Ettinger, Hou, Jackman, & Kazerooni, 2012). These results are reflected in the TC pilot, which included patients with varying degrees of interest in quitting, yet had promising cessation results.

The TC pilot revealed several opportunities to identify participants’ unique patterns of smoking, their level of nicotine dependence, their risk perceptions, self-efficacy, and outcome expectancies. Based on the assessments and the motivational interviewing intervention framework (Rollnick & Miller, 1995), TC provides ample opportunities to increase motivation, to set goals, encourage adherence to pharmacotherapy, and refer for additional cessation assistance (e.g., with a primary care physician).

Although promising, these studies are limited by small sample sizes as well as the lack of a control group in the TC pilot. As the next step in this research, we are conducting a randomized trial in which lung screening participants are randomly assigned to receive TC vs. a minimal treatment intervention. In an effort to improve the impact of the TC intervention, we have modified it in the ongoing study by starting the TC intervention within 1–2 days of receipt of the screening results, and by increasing the TC calls to six, which may be particularly useful for those who are not initially ready to quit. In the event that the TC arm demonstrates an improved cessation rate over the minimal treatment arm, this intervention can be incorporated into lung screening programs with relatively minimal requirements.

Clinical Implications

It is important to note that quitting smoking can greatly improve even a long-term smoker’s health, increasing life expectancy by as much as four years among 55- to 64-year-olds who quit versus continue smoking (Jha, Ramasundarahettige, Landsman, Rostron, Thun, & Anderson, 2013). Given that continued smoking remains the single biggest cause of premature death and chronic disease burden, especially among low income populations (U.S. Department of Health and Human Services, 2014), providing evidence-based smoking cessation counseling is a requirement for lung cancer screening programs (Centers for Medicare & Medicaid Services, 2015). Further, capitalizing on the teachable moment of lung screening may be critical to enhancing its impact and cost effectiveness. The challenge for determining the optimal intervention protocol for use in this unique screening setting is to conduct the appropriate demonstration studies, followed with large-scale randomized clinical trials for efficacy, and then implementation-dissemination trials for generalizability and scalability. These studies are especially important given the increased rates of screening that are likely to occur due to the mandated insurance coverage beginning in 2015 (U.S. Department of Health and Human Services, 2015; U.S. Preventive Services Task Force, 2013) and the coverage for 65- to 74-year-old individuals (U.S. Department of Health and Human Services, 2015) for individuals at high risk for lung cancer.

Acknowledgments

The authors thank the participants for their time spent participating in this study and thank Susan Marx for her administrative support.

FUNDING

This was an investigator-initiated study funded by the Prevent Cancer Foundation. Additional support was provided by the Lombardi Comprehensive Cancer Center Support Grant P30 CA 051008. The funders played no role in the design, conduct or analysis of the study, nor in the interpretation and reporting of the study findings.

Contributor Information

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

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

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

JENNA A. KRAMER, Division of Pulmonary, Critical Care, & Sleep Medicine, Medstar Georgetown University Hospital, Washington, DC, USA.

DAVID B. ABRAMS, The Schroeder Institute for Tobacco Research and Policy Studies at Legacy Foundation, Washington, DC, USA; Johns Hopkins Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA; and Department of Oncology, Georgetown University Medical Center, Washington, DC, USA.

ERIC D. ANDERSON, Division of Pulmonary, Critical Care, & Sleep Medicine, Medstar Georgetown University Hospital, Washington, DC, USA.

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

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