Smoking Cessation: An Integral Part of Lung Cancer Treatment

Lung cancer is the leading cause of cancer death in the United States [1]. Two or 3 out of every 100 men and 1 or 2 out of every 100 women, who are now 60 years old, will get lung cancer sometime during the next 10 years [1]. Cigarette smoking is responsible for an estimated 90% of all lung cancers [2]. The estimates for the prevalence of smoking at the time of lung cancer diagnosis have ranged from 24 to 60%, compared with 12–29% among the general US population [3,4,5,6,7]. Up to 83% of all smokers continue to smoke after a diagnosis of lung cancer [5,8,9]. Parsons et al. [10] found in a review of 10 studies that people who continue to smoke after a diagnosis of early stage lung cancer almost double their risk of dying. Despite a growing body of evidence that smoking cessation after a lung cancer diagnosis is linked to more effective treatment and a better prognosis, the belief prevails that treating tobacco dependence is useless [11].

Survival rates for lung cancer are improving every year; currently the expected 5-year survival for non-small cell lung cancer (NSCLC) is 60–75% for stage I and 36–60% for stage II disease [12]. New anticancer agents, including angiogenesis and epidermal growth factor receptor inhibitors, have the potential to increase the number of lung cancer survivors [13]. As lung cancer patients experience longer survival times they are more likely to benefit from the quality of life (QOL) improvements that abstinence from smoking can provide [14,15]. In the past, smoking cessation has not been considered an integral part of the treatment of cancer but, with improved cancer treatments and survival rates, smoking cessation among cancer patients has become increasingly important [16]. There is a pressing need to clarify the role of smoking cessation in the care of lung cancer patients. This paper will report on the benefits of smoking cessation for lung cancer patients and the elements of effective smoking cessation treatment, with consideration of tailoring to the needs of lung cancer patients.

Smoking cessation programs for lung cancer patients have long been thought to have more cost than benefit. Slatore et al. [15] developed a decision analysis model to evaluate the cost effectiveness of a smoking cessation intervention initiated immediately before surgical lung resection. The smoking cessation program was found to be cost-effective at both 1 and 5 years postsurgery. Smoking cessation for lung cancer patients yields both immediate and long-term benefits. There are significant positive effects of smoking cessation on the health of lung cancer patients: decreased risk of disease, increased survival time, decreased postoperative complications, increased efficacy of chemotherapy, decreased radiation therapy complications, and improved QOL.

The immediate benefits of cessation include improved oxygenation, lowered blood pressure, improved smell, taste, circulation and breathing, increased energy, and improved immune response [17]. Smoking cessation is associated with improved cognitive function, psychological well-being, and self-esteem [18,19]. Lung cancer patients report after successful smoking cessation all of the same benefits plus decreased fatigue and shortness of breath, increased activity level, and improved performance status, appetite, sleep, and mood [18,20,21]. These benefits are of special import because patients with lung cancer have a greater symptom burden than patients with other cancers [22].

Decreased Risk of Disease

Patients with pulmonary neoplasms have an increased risk of developing a second tumor of the lung, either at the same time or at a later time. The second tumor can represent an independent primary or a recurrence/metastasis [23]. Smoking cessation can decrease the risk of synchronous multiple primary lung cancer tumors [24], metachronous lung cancers in small cell lung cancer survivors [25], and second primary tumors [25,26,27,28,29].

Nicotine induces polycyclic aromatic hydrocarbons (PAHs), products of incomplete combustion, which are some of the major lung carcinogens found in tobacco smoke [30]. PAHs are also potent inducers of hepatic enzymes [31]. Many drugs are substrates for hepatic CYP1A2, and their metabolism can be induced in smokers, resulting in a clinically significant decrease in pharmacologic effects. Thus, smokers may require higher doses of drugs that are CYP1A2 substrates. It is important to recognize that these pharmacokinetic drug interactions are caused by the PAHs in tobacco smoke, not the nicotine. Pharmacodynamic drug interactions with tobacco smoke are largely due to nicotine. Because it activates the sympathetic nervous system, nicotine can counter the pharmacologic actions of certain drugs [32]. Nicotine replacement therapy does not contribute to the pharmacokinetic drug interactions discussed in this article [32].

Nicotine itself is not carcinogenic, but it has been shown that, in vivo, nicotine can induce the proliferation of lung cancer cell lines, promote angiogenesis, and promote resistance to apoptosis (cell death) induced by chemotherapeutic agents [33]. These events are mediated through the nicotinic acetylcholine receptors (nAChRs) on lung cancer cells which impact on the efficacy of cisplatin, a frequently used chemotherapeutic agent [33]. Nicotine can contribute to the progression of lung cancers because nicotine can promote anchorage-independent growth in NSCLCs and induce morphological changes characteristic of a migratory, invasive phenotype in NSCLCs [34].

Tucker [25] found that, compared to the general population, the risk of all second cancers among NSCLC patients was increased 3.5 times. Among those who received chest irradiation, second lung cancer risk was increased 13-fold in comparison to a 7-fold increase among nonirradiated patients. The risk was highest among current smokers; an interaction was present between chest irradiation and continued smoking (RR = 21), and a 19-fold risk increase was found among current smokers treated with alkylating agents. A synergism between chest radiation therapy and smoking in the development of second lung cancers was also found [25].

Gritz et al. [35] studied smoking behavior in 840 adults with stage I NSCLC; at the time of diagnosis, 60% of the patients were smokers. Two years after diagnosis, 40% of the smokers had quit smoking. According to this study, smoking cessation at the time of diagnosis of lung cancer may reduce the rate of development of metachronous tumors. Richardson et al. [26] found that the relative risk of developing a second lung cancer following curative-intent therapy for squamous cell lung cancer was lower for those who had stopped smoking.

Increased Survival Time

Smoking cessation after a diagnosis of lung cancer has been linked to increased survival time [36,37]. In a review of smoking cessation after diagnosis of a primary lung tumor, Parsons et al. [10] showed that the associated increase in risk of continuing to smoke is modest at around 20%; the adjusted estimates, however, suggested a more than doubling of the risk of death from continued smoking. Fox et al. [7] found that, among NSCLC patients diagnosed with early-stage disease, current smokers had a poorer prognosis for survival after radiation therapy. In their sample of 237 patients treated with definitive radiation or chemoradiation, 2-year overall survival was calculated from the time of initiation of treatment. Among those with stage I/II disease, current smokers had a 2-year survival rate of 41% and a median survival of 13.7 months while nonsmokers had a 2-year survival rate of 56% and a median survival of 27.9 months (p = 0.01). In a study of 5,229 patients with NSCLC and squamous cell lung cancer, the median survival times among those who had never smoked, former smokers, and current smokers with NSCLC were 1.4, 1.3, and 1.1 years, respectively (p < 0.01). The relative risk per 10 years of smoking abstinence was 0.85, demonstrating a direct biological effect of smoking on survival [38].

In a 2003 retrospective review (covering a 10-year period) of studies using a concurrent chemoradiotherapy regimen for patients with limited small cell lung cancer, those who continued to smoke during chemoradiotherapy had poorer survival rates than those who did not [39]. Tammemagi et al. [40] found that current smoking at diagnosis was an important independent predictor of shortened lung cancer survival after adjusting for the baseline covariates age, gender, illicit drug use, adverse symptoms, histology, and stage. The relative risk for smoking (current vs. former/never) was 1.37 (95% CI 1.18–1.59; p < 0.001).

In 2010, Parsons et al. [10] conducted a systematic review with meta-analysis on evidence that smoking cessation after diagnosis of a primary lung tumor affects prognosis. The review revealed evidence that smoking cessation after diagnosis of early-stage lung cancer improves prognostic outcomes and most of the gain is likely due to reduced cancer progression.

Decreased Postoperative Complications

Nonsmokers are at decreased risk of postoperative complications compared with smokers [41]. Yildizeli et al. [42] assessed operative morbidity and mortality on NSCLC patients that underwent a sleeve lobotomy. Current smoking had a significant effect on the development of postoperative complications including infection, bronchopleural fistula [42], and morbidity and mortality [43].

In a 2005 prospective study of patients with primary or secondary lung cancer who were undergoing anatomical lung resection, the 4 groups studied were: nonsmokers (21%), past quitters of >2 months’ duration (62%), recent quitters of <2 months’ duration (13%), and ongoing smokers (4%). Overall pulmonary complications occurred in 8, 19, 23, and 23% of patients in these groups, respectively, with a significant difference between nonsmokers and all smokers (p < 0.03) [44]. The risk of pneumonia was significantly lower in nonsmokers (3%) compared to all smokers (average 11%; p < 0.05), with no difference detected among subgroups of smokers (p < 0.17). When comparing recent quitters with ongoing smokers, no differences in pulmonary complications of pneumonia were found (p < 0.67). A smoking history of >60 pack-years (OR 2.54; 95% CI 1.28–5.04; p < 0.0008) was independently associated with overall pulmonary complications. In patients undergoing thoracotomy for primary lung cancer or metastatic cancer to the lung, there was no evidence of an increase in pulmonary complications among those who quit smoking within 2 months of having undergone surgery [44].

Improved Response to Chemotherapy and Radiation

Both chemotherapy and radiation treatment are likely to produce fewer complications and less morbidity among nonsmokers than smokers [5,45]. Smoking can have detrimental effects on the efficacy of chemotherapy including chemoresistance, chemoinsensitivity, and altered chemotherapeutic levels [5]. Smoking can significantly affect the pharmacokinetics and toxicity profile of some drugs (e.g. irinotecan) [46]. NSCLC patients with constitutional symptoms (i.e. fever, anorexia, and weight loss) and more pack-years of smoking are less likely to respond to chemotherapy [47].

As previously mentioned, some elements of cigarette smoke are known to affect drug metabolizing CYP enzymes and therefore affect treatment outcome. Nicotine in tobacco smoke can decrease the efficacy of certain drugs because of an increase in the metabolism of the drugs through the induction of hepatic enzymes [31]. Van der Bol et al. [46] found that smoking significantly lowers both the exposure to irinotecan and treatment-induced neutropenia, indicating a potential risk of treatment failure. Shepherd et al. [48] found that twice the normal dose of erlotinib was required to produce the necessary circulating levels of the drug in smokers compared to never-smokers. In a survival analysis, treatment with erlotinib (p < 0.001) and never having smoked (p < 0.01) were associated with longer progression-free survival. The interaction between smoking status and treatment was significantly predictive of a differential effect on survival [49]. Studies have suggested that exposure to nicotine might negatively impact on the apoptotic potential of chemotherapeutic agents, including cisplatin [33].

Lung cancer patients who smoke have a 20% greater chance of experiencing radiation pneumonitis [50]. The number of packages per year of cigarette smoking is significantly positively associated with infection in patients with NSCLC during radiotherapy [51]. Fox et al. [7] found that, among NSCLC patients diagnosed with early stage disease, current smokers had a poorer prognosis for survival after radiation therapy.

Improved QOL

The cessation of smoking after a lung cancer diagnosis has been consistently linked to an increase in QOL [7,20,26,27,28,29,52]. Garces et al. [20] found that persistent cigarette smoking after a lung cancer diagnosis negatively impacted QOL scores. The adjusted mean total Lung Cancer Symptom Scale (LCSS) scores for never-smokers and persistent smokers were 17.6 and 28.7, respectively (p < 0.0001), with higher scores indicating greater severity of symptoms. Myrdal et al. [53] found that patients who smoked after surgery experienced impaired QOL compared with nonsmokers, and they had significantly lower scores for mental health and vitality than former smokers who stopped smoking at the time of surgery or before and than those who had never smoked.

Performance status is an important factor in QOL. In a recent study, records were reviewed for 206 patients with NSCLC; those who quit smoking after the diagnosis maintained a better performance status at 6 and 12 months, regardless of disease stage, age, race, sex, therapy types, and comorbidities, than those who continued to smoke. Those who quit smoking maintained a better performance status at 0–6 months (OR 7.09; 95% CI 1.99–25.3) and at 0–12 months (OR 6.99; 95% CI 1.76–27.7) than those who continued smoking [21].

Although the benefits of cessation are extensive, they are not generally known to lung cancer patients and their clinicians. The specific benefits of smoking cessation (both immediate and long-term) that relate to lung cancer symptom distress need to be incorporated into smoking cessation interventions. Tobacco dependence should be treated at the time of diagnosis of lung cancer, during treatment, and posttreatment.

Given the critical negative health effects of smoking on lung cancer survival and the major health benefits of smoking cessation, it is important that cancer care providers adopt the role of tobacco cessation treatment providers. The following section presents the clinical practice guidelines for treating tobacco dependence with a specific focus on the cancer care providers’ role.

Current guidelines for treatment of tobacco dependence have been published by the US Public Health Service in 2000 and updated in 2008 [54]. The guidelines recommend use of the ‘5 A’s’: clinicians should ask all patients about tobacco use, advise smokers to quit, assess willingness to make a quitting attempt, assist patients with quitting smoking, and arrange follow-up (table 1).

In addition to counseling, all smokers attempting cessation should receive pharmacotherapy [55]. First-line, FDA-approved medications for smoking cessation include nicotine replacement therapies (NRT), bupropion sustained release (SR), and varenicline (Chantix) (table 2). An excellent resource that provides accurate, up-to-date pharmacotherapy information for smoking cessation treatment, including dosing, precautions, side effects, and costs is: ‘Rx for Change’, sponsored by the University of California, San Francisco School of Pharmacy (http://rxforchange.ucsf.edu). Rx for Change for Cancer Care Providers is a brief curriculum designed specifically for treating tobacco dependence in cancer patients and survivors.

• Nicotine Replacement Therapy. NRT is based on the principle that nicotine is the dependence-producing constituent of cigarette smoking and that smoking cessation can be achieved by replacing nicotine without the toxins in cigarette smoke [56]. The goal is to relieve the symptoms of withdrawal, which allows the patient to focus on conditioning factors when attempting to stop smoking. NRT products are currently available over the counter and are the first-line medication choice of many smokers attempting to quit on their own. Because NRT has been deemed safe and effective and major side effects are very rare, they should be recommended to all smokers including cancer patients, except for those few for whom they are medically contraindicated. These include patients with underlying cardiovascular disease: recent myocardial infarctions, life-threatening arrhythmias, and severe angina. NRT is not recommended for smokeless tobacco users or individuals smoking fewer than 10 cigarettes per day [54]. Patient education and follow-up is important for successful cessation. Dose tapering is not required when discontinuing treatment.

• Bupropion (SR). Bupropion SR is a norepinephrine and dopamine re-uptake blocker and is also commonly used as an antidepressant. Its clinical effects are a decreased craving for cigarettes and symptoms of nicotine withdrawal [54]. Clinical trials have demonstrated bupropion’s efficacy as a smoking cessation adjunct in populations of individuals who have a history of major depressive disorder, as well as those who do not [57]. Bupropion SR can be safely used with NRT. However, it should be avoided in patients with an increased risk for seizures. The possibility of age-related slower drug clearance mandates a modification of the standard bupropion dosing protocol: 150 mg/day for the first week; if no adverse effects occur, increase to 300 mg for the second week; if no adverse effects occur, maintain this dosage for 12 weeks [58].

• Varenicline (Chantix). Varenicline is a partial nicotinic agonist; it binds to the nicotinic receptors, thereby preventing nicotine binding. This partial agonist activity induces receptor stimulation and reduces withdrawal symptoms during cessation. Varenicline blocks the dopaminergic stimulation responsible for the reinforcement and reward associated with smoking [59]. This action reduces the craving for cigarettes. The effectiveness of varenicline in smoking cessation was demonstrated in 6 clinical trials. Five of the 6 studies were randomized, controlled, clinical trials in which varenicline was shown to be superior to the placebo in helping people quit smoking. In 2 of the 5 placebo-controlled studies, varenicline-treated patients were more successful in giving up smoking than patients treated with bupropion [60,61,62].

There have been case reports of neuropsychiatric symptoms (behavior changes, agitation, depressed mood, and suicidal ideation or behavior) and reports of worsening of preexisting psychiatric illness. These reports are rare in comparison to the total number of patients using the medication [63]. Clinicians need to closely monitor for neuropsychiatric symptoms while patients are using varenicline and bupropion as smoking cessation aids [64].

• Combination Pharmacotherapy. Data from randomized, controlled trials suggest that certain combinations of first-line cessation medications are efficacious in promoting long-term abstinence. As such, the 2008 Clinical Practice Guideline considers the following regimens to be appropriate first-line therapy in patients attempting to quit smoking [54]:

– Combination NRT. Combination NRT according to Rx for Change [65] involves the use of a long-acting formulation (patch) in combination with a short-acting formulation (gum, lozenge, inhaler, or nasal spray). The long-acting formulation, which delivers relatively constant levels of the drug, is used to prevent the onset of severe withdrawal symptoms, and the short-acting formulation, which delivers nicotine at a faster rate, is used as needed to control withdrawal symptoms that may occur during potential relapse situations (e.g. after meals, when under stress, or when around other smokers). A recent meta-analysis found that the nicotine patch in combination with a short-acting NRT formulation (gum, inhaler, or nasal spray) was significantly more effective than single-agent NRT. The odds of long-term (≥6 months) cessation were 1.4 with combination therapy compared to monotherapy (95% CI 1.1–1.6) [65,66].

– NRT and Bupropion SR. Combination therapy with bupropion SR and NRT has been evaluated in 3 long-term controlled trials. Patients receiving combination therapy in standard dosages were significantly more likely to quit than were patients randomized to the nicotine patch alone. The odds of long term (≥6 months) abstinence were 1.3 with the combination therapy compared to the nicotine patch monotherapy (95% CI 1.0–1.8) [54].

Patients with cancer may have higher levels of nicotine dependence, higher levels of co-morbidity, or more difficulty quitting, as well as poorer health and physical functioning, and more stress and emotional distress, suggesting the need for more intense or tailored programs [67,68]. Given the impact of smoking on treatment (surgery, radiation, and chemotherapy), a patient’s smoking status should be considered as part of the treatment decisions. Systematic advice received from multiple providers is more effective than advice from a single provider [54]. A stepped care approach may be useful for patients experiencing difficulty with quitting [52]. Schnoll et al. [69] highlighted the need for motivational smoking cessation interventions for cancer patients. They investigated the difference between cancer patients who enroll in smoking cessation programs and those that do not. Decliners were significantly more likely to have head and neck cancer (vs. lung cancer) and report a lower readiness to quit smoking. There are few randomized clinical trials investigating tobacco dependence treatment for lung cancer patients [70].

Tobacco dependence is a chronic disease and relapse is intrinsic to this disease. Lung cancer patients who smoke are, more often than not, highly dependent smokers. For the highly dependent smoker, tailored intensive interventions that combine behavioral interventions with pharmacologic cessation aides may be helpful [5]. Combination pharmacotherapy has also been found to be effective with highly dependent smokers [71]. Intensive interventions, however, may not be appropriate for all lung cancer patients, so other innovative interventions need to be considered. The use of telephone counseling has been shown to be effective among the general population and is now available in every state throughout the US (1-800-Quit-Now) [72]. Evidence has shown that proactive counseling helps motivated smokers stay abstinent and that 3 or more calls increase the odds of quitting compared with standard self-help or brief health care provider advice [73].

Other literature that can inform tailored cessation counseling for lung cancer patients includes studies that have targeted older smokers. The mean age of lung cancer patients is 70 years [74]. Hall et al. [58] purport that treatment for older smokers needs to conceptualize tobacco dependence as a chronic disease; most smokers have multiple quitting attempts and relapse is the norm [75,76]. Hall et al. achieved abstinence rates with older smokers of more than 55% at 24, 52, 64, and 104 weeks using bupropion and extended cognitive behavioral treatment.

Only 3 smoking cessation intervention studies have been conducted with diagnosed lung cancer patients [45,77,78]. In 1997, a smoking cessation intervention was evaluated among patients with lung cancer during hospitalization. Upon admission, 87% of the subjects expressed intent to quit smoking in the next month. The intervention included only 15 subjects and consisted of 3 daily 20- to 30-min visits and 5 weekly follow-up phone calls. At 6 weeks postintervention, 14 (93%) subjects reported making at least 1 quitting attempt and 40% were confirmed abstinent. The finding suggested that a more intensive intervention can succeed and would be of interest to lung cancer patients [55]. Browning et al. [77] evaluated the effectiveness of a smoking cessation intervention that included face-to-face and phone follow-up behavioral interventions with 14 patients with lung cancer. The number of subjects using NRT was not noted and only 3 subjects used bupropion. Cox et al. [45] found that nicotine dependence treatment is effective for patients with a lung cancer diagnosis and that the majority of lung cancer patients were motivated to quit smoking. The 6-month tobacco abstinence rate was 22% for the lung cancer patients compared with 14% for the control patients (p = 0.024). The intervention involved a brief consultation with a cessation counselor and a treatment plan individualized to the patient’s needs. Data on the type of recommended interventions and whether patients adhered to these recommendations were not entered into the database. None of the interventions studied in the literature met the US Public Health Service Guidelines recommendation for a combination of both behavioral and pharmacologic treatment [54].

There are several additional features based on the 2008 guidelines for smoking cessation [54] to consider when treating tobacco dependence in patients with lung cancer.

• Motivation. Improving one’s health may not be the most effective motivational factor; however, providing information about the short-term and long-term benefits of smoking cessation during lung cancer treatment is essential. Evidence suggests that the majority of lung cancer patients are motivated to stop smoking [45]. Although a diagnosis of lung cancer is assumed to be a strong motivator, lung cancer patients who smoke are at various stages of readiness to quit. For the lung cancer patient the time of diagnosis provides a window of opportunity where receptivity to a smoking cessation attempt may be increased. However, if this opportunity is not realized at the time of diagnosis the health care provider needs to continue to ask and assess for readiness throughout the course of treatment. Previous attempts at smoking cessation can be framed as opportunities to discover effective strategies for successful cessation. Tone and manner should convey a concern for the patient’s well-being as well as a commitment to help him or her quit, when the patient is ready. The message is: ‘It’s important that you quit as soon as possible, and I can help you.’ For those patients willing to quit, extended treatment has been found to be the most effective with older smokers and is essential for lung cancer patients; smoking cessation should be an integral part of the entire course of lung cancer treatment [58].

• Stigma and Self-Blame. Anecdotal evidence suggests that stigma is an important factor in the care of lung cancer patients [79]. Whether they smoked or not, lung cancer patients reported stigmatization from clinicians, as well as family members and friends, because the disease is strongly associated with smoking [79]. Smokers have become a marginalized part of society [80]. Current and former smokers have identified several factors that contribute to perceptions of LCS including: perceptions of smoking as a choice, not an addiction; discrimination perpetrated against smokers through no-smoking policies, and perceptions that smokers are less educated [80]. Recently, with the development of the lung cancer stigma scale, there is empirical evidence that lung cancer patients experience significant levels of perceived stigma whether or not they are current or past smokers. Stigma had a strong significant correlation with increased depression and diminished QOL[Cataldo et al., unpubl. data]. Education about coping strategies to deal with self-blame and stigma needs to be incorporated into the smoking cessation intervention.

• Mood Management. As a result of a lung cancer diagnosis, patients often experience increased psychological distress, increased feelings of burden, stress, and stigmatization [81,82,83,84]. Lung cancer patients experience more psychological distress than other cancer patients, making mood management an essential aspect of treatment. It is important to evaluate and treat the patient for mood disorders and assist patients in the identification of effective coping strategies. Coping strategies are an essential part of smoking cessation for lung cancer patients.

• Smoke-Free Homes. Considerable evidence suggests that having a smoke-free home may be associated with increased successful quitting [85,86,87]. Smokers who adopt a smoke-free home are almost 5 times more likely to quit for ≥90 days [87]. It is important to explain the impact of second-hand smoke on the health of pets and others and to encourage a contract for a smoke-free environment to be signed by the patient and their significant circle.

• Social Support. Little perceived social support has been found to predict smoking relapse [88,89,90]. It is important to include in the intervention management a current support network and to identify those supporting cessation and smoking. Bottoroff et al. [81] investigated continued family smoking after lung cancer diagnosis and found that clinicians need to focus on collective behavior in the family setting to understand processes that influence health behavior changes. It is important to assist patients in finding ways to elicit positive support and handle negative support. Research suggests that partner involvement in smoking cessation may encourage long-term abstinence. Park et al. [91] found that interventions to enhance partner support showed the most promise when implemented with live-in, married, and equivalent-to-married partners. They concluded that such interventions should focus on enhancing supportive behaviors, while minimizing behaviors critical of smoking. A strong predictor of relapse is having another smoker in the home [87]. Lung cancer patients often live with a smoker; treating a dyad or more than 1 smoker in a home may increase the chances of smoking abstinence success.

The lung cancer experience is unique in many ways (with issues of self-blame and stigma, anticipated short survival time, and increased symptom burden and distress), the lung cancer patient who smokes is highly dependent on tobacco while faced with an urgent life crisis; research is needed to develop effective and tailored smoking cessation interventions.Given the prevalence of lung cancer patients who smoke and the significant benefits of smoking cessation, cancer care providers need to offer full support and tobacco dependence treatment that is tailored to patients’ specific needs. Intensive and extended tobacco cessation programs, including counseling with behavioral therapy and the use of nicotine replacement and combined pharmacology with extended follow-up, are highly efficacious, cost-effective, and a critical component of quality lung cancer care.

This research was supported by California Tobacco-Related Disease Research Program (TRDRP) grants 16RT-0149 and 17RT-0077, National Institute of Drug Addiction grant K23-DA018691, and National Institute of Nursing Research grant NR011934-01.

The content is solely the responsibility of the authors and does not represent the official views of the California TRDRP or NIDA. No Human Subject issues are involved, and there is no review board application.