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. Author manuscript; available in PMC: 2020 Jun 1.
Published in final edited form as: J Community Health. 2019 Jun;44(3):552–560. doi: 10.1007/s10900-019-00622-z

Smoking and Smoking Cessation Among Persons with Tobacco- and Non-tobacco-Associated Cancers

M Shayne Gallaway 1, Bin Huang 2,3, Quan Chen 3, Thomas C Tucker 3,4, Jaclyn K McDowell 3, Eric Durbin 3,5, Sherri L Stewart 1, Eric Tai 1
PMCID: PMC6504566  NIHMSID: NIHMS1014065  PMID: 30767102

Abstract

Purpose

To examine smoking and use of smoking cessation aids among tobacco-associated cancer (TAC) or non-tobacco-associated cancer (nTAC) survivors. Understanding when and if specific types of cessation resources are used can help with planning interventions to more effectively decrease smoking among all cancer survivors, but there is a lack of research on smoking cessation modalities used among cancer survivors.

Methods

Kentucky Cancer Registry data on incident lung, colorectal, pancreatic, breast, ovarian, and prostate cancer cases diagnosed 2007–2011, were linked with health administrative claims data (Medicaid, Medicare, private insurers) to examine the prevalence of smoking and use of smoking cessation aids 1 year prior and 1 year following the cancer diagnosis. TACs included colorectal, pancreatic, and lung cancers; nTAC included breast, ovarian, and prostate cancers.

Results

There were 10,033 TAC and 13,670 nTAC survivors. Smoking before diagnosis was significantly higher among TAC survivors (p < 0.0001). Among TAC survivors, smoking before diagnosis was significantly higher among persons who: were males (83%), aged 45–64 (83%), of unknown marital status (84%), had very low education (78%), had public insurance (89%), Medicaid (85%) or were uninsured (84%). Smoking cessation counseling and pharmacotherapy were more common among TAC than nTAC survivors (p < 0.01 and p = 0.05, respectively).

Discussion

While smoking cessation counseling and pharmacotherapy were higher among TAC survivors, reducing smoking among all cancer survivors remains a priority, given cancer survivors are at increased risk for subsequent chronic diseases, including cancer. Tobacco cessation among all cancer survivors (not just those with TAC) can help improve prognosis, quality of life and reduce the risk of further disease. Health care providers can recommend for individual, group and telephone counseling and/or pharmacotherapy recommendations. These could also be included in survivorship care plans.

Keywords: Smoking, Smoking cessation, Tobacco-associated cancers, Health administrative claims, Linkage, Registry

Introduction

Tobacco use is the leading preventable cause of cancer and cancer deaths [51]. Cigarette smoking is causally linked to 12 cancers, including: oral cavity and pharynx; larynx; esophagus; lung, bronchus, and trachea; stomach; kidney and renal pelvis; pancreas; liver; urinary bladder; uterine cervix; colon and rectum; and acute myeloid leukemia [51]. While not conclusive, research also suggests a possible causal relationship between cigarette smoking and breast and prostate cancer mortality [9, 51]. Each year in the United States, approximately 660,000 people are diagnosed with a cancer associated with tobacco use [26]. In 2016, there were more than 15 million cancer survivors in the United States [36]. Despite evidence that continued smoking places all cancer survivors (regardless of whether their initial cancer was associated with tobacco) at increased risk for a new or recurrent cancer diagnosis, many continue to smoke [30]. Previous studies have shown that the prevalence of smoking among cancer survivors is similar to that of the general population [12, 19, 20, 49, 53].

Cigarette smoking is harmful for all people, including those previously diagnosed with cancers [30, 33, 34, 39] and continued smoking negatively affects cancer treatment [6, 15, 24, 35]. Screening for tobacco use at the time of a cancer diagnosis is important for assessing risks of multiple cancers and developing treatment and survivor care plans to enhance the length and health-related quality of life. Patient smoking history can also help to link patients with cessation resources.

Tobacco cessation treatments are effective among smokers with cancer [21, 29, 48]. The Centers for Disease Control and Prevention’s (CDC) National Comprehensive Cancer Control Program (NCCCP) supports increasing knowledge and availability of evidence-based tobacco cessation services among cancer survivors [11, 16]. Individual, group, and telephone cessation counseling and seven FDA-approved cessation medications have been found to be safe and effective when used as directed [7, 27, 31, 4346, 51]. Cessation counseling and pharmacotherapy are even more effective when they are combined than when either is used alone [44]. Understanding when and if specific types of cessation resources are used can help with planning interventions to more effectively decrease smoking among all cancer survivors, but there is a lack of research on smoking cessation modalities used among cancer survivors [53].

The purpose of this study was to examine the prevalence of smoking and the use of cessation aids among persons diagnosed with what have been causally deemed tobacco-associated cancers (TAC) and non-tobacco-associated cancers (nTAC) [51] using data from the Kentucky Cancer Registry (KCR).

Methods

Data

The Kentucky Cancer Registry (KCR) conducted a data link-age to augment its cancer incidence data with health claims data. The intent was to improve data quality of the registry data and inform the quality of care and outcomes research, while also providing an empirical basis to assess adherence to evidence-based quality-of-life measures and patterns of care among cancer survivors in Kentucky. Probabilistic data linkage combined with a manual review process were used to conduct the data linkage between the KCR data for lung, colorectal, pancreatic, breast, ovarian, and prostate cancer patients diagnosed in 2007–2011 and health administrative claims including: Medicare [Surveillance, Epidemiology and End Results (SEER)-Medicare, 2000–2013], Medicaid (Kentucky Family Health Service, 2000–2015), Humana and State Employee Insurance (Humana-Comprehensive Health Insights, 2007–2015), and Anthem (HealthCore, 2006–2015).

Only the most common cancers were linked to ensure proper linkage, completeness of data, and limit errors. The six cancers included account for the majority of cancer deaths in Kentucky and the United States [50]. To reduce biases introduced from data linkage, only the first primary invasive cancer cases diagnosed in 2007–2011 were included. Only cases with continuous enrollment coverage in health administrative claims data for 12 months before and 12 months after date of diagnosis were included. Registry cases captured through autopsy or death certificate only were excluded. We categorized the six included cancers according to the U.S. Surgeon General’s report on smoking [51]: TACs included those with sufficient evidence to infer a causal relationship with smoking (i.e., lung, colorectal, and pancreatic cancers). NTACs included those with suggestive, inadequate or no causal evidence with smoking (i.e., breast, prostate cancers).

Smoking Status

Smoking cessation (counseling (individual or group) or pharmacotherapy) were based on claims within 1 year before or 1 year after cancer diagnosis. Cases were classified with a history of smoking before the cancer diagnosis if documentation of personal history of tobacco use (ICD-9V15.82) or tobacco use disorder (ICD-9 305.1) was identified in linked records for the 12 months before the cancer diagnosis. Cases were classified with use of smoking cessation treatments before and after the cancer diagnosis if documentation of smoking cessation counseling (health-care common procedure coding system [HCPCS]: 99406, 99407, G0375, G0376) or pharmacotherapy (i.e., nicotine replacement therapy, bupropion, varenicline) was identified in linked records for the 12 months before, or 12 months after diagnosis (or during the month of diagnosis). Smoking status was initially pulled from KCR records and augmented with health administrative claims data. If smoking status in the KCR data was either “Non Smoker” or “Unknown,” but it was “Yes” for history of smoking or smoking cessation treatment information in the claims data, then the final smoking status was classified as “Smoker.”

Demographic Variables

Stratified by TAC and nTAC, the following demographic characteristics were examined: sex, age, race/ethnicity (white non-Hispanic, black non-Hispanic, Hispanic, other), education (percentage with high school education at county level, categorized by quantiles: very low, low, moderate, high), marital status [married (or living with a partner), previously married (divorced, separated, widowed), never married, unknown], poverty (percentage below poverty line at county level, categorized by quantiles: low, moderate, high, very high), Appalachian status (included or not included based upon Appalachian Region Commission https://www.arc.gov/appalachian_region/CountiesinAppalachia.asp), and insurance (uninsured, private, Medicaid, Medicare, other public, unknown).

Statistical Analysis

The prevalence of smoking at the time of cancer diagnosis and the use of smoking cessation aids (before and after cancer diagnosis) were estimated for TAC and nTAC survivors. Chi square test statistics were conducted with a threshold of p < 0.05 used as a measure of significant difference across relevant strata for cancer cases with a valid smoking status. All analyses were completed using SAS 9.4 (SAS Institute, Cary, NC).

Results

Cancer Survivor Characteristics

From 2007 to 2011, there were 10,033 TAC and 13,670 nTAC cancer survivors identified from the KCR and included in the dataset. Sixty-four percent of TAC and 40% of nTAC survivors smoked in the 12 months before their cancer diagnosis (Table 1). A history of smoking was most common among TAC survivors (lung [84%], pancreas [48%], colorectal [44%]). Among nTAC survivors, those with prostate cancer had the highest prevalence of a history of smoking (43%). Smoking history was unknown for 15% of TAC and 28% of nTAC survivors.

Table 1.

Smoking history among tobacco- and non-tobacco-associated cancer survivors

Total
Smoking historya
Yes
No
Unknown
n n % n % n %
Tobacco-associated cancersb 10,033 6453c 64.3 2030 20.2 1550 15.4
  Lung 5096 4287 84.1 242 4.7 567 11.1
  Colorectal 4563 1986 43.5 1697 37.2 880 19.3
  Pancreas 374 180 48.1 91 24.3 103 27.5
Non-tobacco-associated cancers 13,670 5468 40.0 4437 32.5 3765 27.5
  Prostrate 7342 3188 43.4 1631 22.2 2523 34.4
  Breast 5916 2148 36.3 2625 44.4 1143 19.3
  Ovary 412 132 32.0 181 43.9 99 24.0
a

Personal history of tobacco use (ICD-9 V15.82) or tobacco use disorder (ICD-9 305.1) identified in linked records for the 12 months before the cancer diagnosis

b

Tobacco-associated cancer for this study is defined as those cancers causally linked to tobacco and for which complete registry and claims data were available. Non-tobacco-associated cancers are defined for this study as those for which complete registry and claims data were available. The six cancers listed account for the majority of cancer deaths in the United States

c

Significant within-group difference between tobacco- and non-tobacco-associated cancer groups

A history of smoking in the 12 months prior to a cancer diagnosis was significantly higher among TAC survivors compared to nTAC survivors (p < 0.0001, not shown). Significant between groups differences were observed. Among TAC survivors, pre-diagnosis smoking was significantly higher among males (83%, Table 2). It was also higher among those aged 45–64 (83%), with unknown marital status (84%), with very low education (78%), with Medicaid (85%), with public insurance (other than Medicaid or Medicare, 89%), and uninsured (84%). Among nTAC survivors, pre-diagnosis smoking was significantly higher among males (66%), and those: who were aged 45–64 (60%), had unknown marital status (77%), were non-Hispanic black (62%) or other (63%) race/ethnicity, had very low education (58%), had low (57%) or very high (58%) poverty level, and those who had an unknown insurance (84%).

Table 2.

Smoking history (prior to cancer diagnosis)a and demographic characteristics for tobacco-and non-tobacco-associated cancer survivors

Tobacco-associated cancer (TAC)
Non-tobacco-associated cancer (nTAC)
History of smoking
History of smoking
No
Yes
p No
Yes
p
n % n % n % n %
Overall 2030 23.9 6453 76.1 4437 44.8 5468 55.2
Sex < 0.001 < 0.001
  Male 716 17.0 3507 83.0 1631 33.8 3188 66.2
  Female 1314 30.8 2946 69.2 2806 55.2 2280 44.8
Age < 0.001 < 0.001
  < 25 b b 13 92.9 b
  25–44 48 34.0 93 66.0 135 53.4 118 46.6
  45–64 355 17.2 1709 82.8 981 40.5 1439 59.5
  65 + 1625 25.9 4647 74.1 3308 45.8 3910 54.2
Marital status 0.003 < 0.001
  Married 1058 23.1 3530 76.9 2727 45.5 3260 54.5
  Previously married 769 25.1 2295 74.9 1282 45.5 1533 54.5
  Never married 170 27.0 459 73.0 330 48.2 355 0.0
  Unknown 33 16.3 169 83.7 98 23.4 320 76.6
Race/ethnicity 0.254 < 0.001
  White, non-hispanic 1881 24.0 5967 76.0 4071 45.4 4892 54.6
  Black, non-hispanic 97 21.4 357 78.6 255 38.5 407 61.5
  Hispanic 7 31.8 15 68.2 20 54.1 17 45.9
  Other 45 28.3 114 71.7 91 37.4 152 62.6
Education 0.044 < 0.001
  Very Low 461 21.7 1663 78.3 1024 42.3 1397 57.7
  Low 492 24.2 1537 75.8 1124 45.6 1339 54.4
  Moderate 857 25.0 2576 75.0 1663 43.9 2124 56.1
  High 220 24.5 677 75.5 626 50.7 608 49.3
Poverty 0.161 < 0.001
  Low 499 22.8 1692 77.2 1039 43.5 1348 56.5
  Moderate 605 24.9 1824 75.1 1159 43.9 1481 56.1
  High 461 25.1 1379 74.9 1240 49.4 1271 50.6
  Very high 465 23.0 1558 77.0 999 42.2 1368 57.8
Appalachian status 0.465 0.166
  Appalachian 618 23.4 2020 76.6 1195 43.7 1541 56.3
  Non-appalachian 1412 24.2 4433 75.8 3242 45.2 3927 54.8
Insurance < 0.001 < 0.001
  Uninsured 5 15.6 27 84.4 10 45.5 12 54.5
  Private 329 28.4 828 71.6 1016 51.1 971 48.9
  Medicaid 79 14.6 463 85.4 133 28.7 330 71.3
  Medicare 1600 24.1 5032 75.9 3223 44.9 3949 55.1
  Other public 9 11.4 70 88.6 25 33.8 49 66.2
  Unknown 8 19.5 33 80.5 30 16.3 154 83.7
a

Personal history of tobacco use (ICD-9 V15.82) or tobacco use disorder (ICD-9 305.1) identified in linked records for the 12 months before the cancer diagnosis

b

Cell count suppressed due to insufficient sample size (n < 5), per Kentucky Cancer Registry guidelines

Use of Smoking Cessation Aids Among Cancer Survivors

Smoking cessation counseling before and/or after a cancer diagnosis was significantly more common among TAC survivors (4.8%) compared to nTAC survivors (2.2%) (p < 0.01, Table 3). Among TAC survivors, lung cancer survivors were most likely to have documentation of any smoking cessation counseling (not shown). Among nTAC survivors, breast cancer survivors were most likely to have documentation of any smoking cessation counseling (not shown). Smoking cessation counseling differed significantly between TAC and nTAC survivors by insurance status (p = 0.01, Table 4).

Table 3.

Use of smoking cessation counseling or pharmacotherapy (before and/or after diagnosis) among tobacco- and non-tobacco-associated cancer survivors with a history of smoking

Smoking cessationa Tobacco-associated
cancer (TAC)
Non-tobacco-
associated cancer
(nTAC)

n

%

n

%
Counseling
 None 6146 95.2 5348 97.8
 Any 307 4.8d 120 2.2
 Pre-diagnosisb 146 2.3d 49 0.9
 Post-diagnosisc 197 3.1d 81 1.5
 Pre + post-diagnosis 36 0.6 10 0.2
Pharmacotherapy
 None 6241 96.7 5322 97.3
 Any 212 3.3d 146 2.7
 Pre-diagnosisb 104 1.6 103 1.9
 Post-diagnosisc 156 2.4d 103 1.9
 Pre + post-diagnosis 48 0.7 60 1.1
a

Documentation of smoking cessation counseling (HCPS: 99406, 99407, G0375, G0376)

b

Twelve months before cancer diagnosis

c

Twelve months after diagnosis (or during the month of diagnosis)

d

Significant within-group difference between tobacco- and non-tobacco-associated cancer groups

Table 4.

Any use of smoking cessation counseling or pharmacology (prior to or after diagnosis) among tobacco-associated cancer (TAC) and non-tobacco-associated cancer (nTAC) survivors with a history of smoking

Smoking cessation (before or after diagnosis)a
Counseling
Pharmacotherapy
TAC
nTAC
p TAC
nTAC
p
n % n % n % n %
Overall 307 100 120 100 212 100 146 100
Sex 0.333 0.226
  Male 135 44.0 59 49.2 89 42.0 52 35.6
  Female 172 56.0 61 50.8 123 58.0 94 64.4
Age 0.505 0.001
  < 25 b b b b
  25–44 b b b 17 11.6
  45–64 111 36.2 35 29.2 108 50.9 73 50.0
  65 + 190 61.9 83 69.2 99 46.7 56 38.4
Marital status 0.136 0.089
  Married 149 48.5 53 44.2 98 46.2 78 53.4
  Previously married 120 39.1 43 35.8 88 41.5 46 31.5
  Never married 26 8.5 13 10.8 21 9.9 13 8.9
  Unknown 12 3.9 11 9.2 5 2.4 9 6.2
Race/ethnicity 0.551 0.736
  White, non-hispanic 291 94.8 111 92.5 201 94.8 136 93.2
  Black, non-hispanic 12 3.9 6 5.0 7 3.3 8 5.5
  Hispanic b b b b
  Other b b b b
Education 0.951 0.117
  Very low 102 33.2 37 30.8 59 27.8 45 30.8
  Low 71 23.1 27 22.5 62 29.2 32 21.9
  Moderate 107 34.9 45 37.5 81 38.2 54 37.0
  High 27 8.8 11 9.2 10 4.7 15 10.3
Poverty 0.245 0.377
  Low 67 21.8 32 26.7 53 25.0 31 21.2
  Moderate 76 24.8 26 21.7 46 21.7 40 27.4
  High 79 25.7 22 18.3 64 30.2 36 24.7
  Very high 85 27.7 40 33.3 49 23.1 39 26.7
Appalachian status 0.500 0.956
  Appalachian 107 34.9 46 38.3 72 34.0 50 34.2
  Non-appalachian 200 65.1 74 61.7 140 66.0 96 65.8
Insurance 0.009 0.019
  Uninsured b b b b
  Private 28 9.1 22 18.3 32 15.1 34 23.3
  Medicaid 17 5.5 4 3.3 31 14.6 27 18.5
  Medicare 257 83.7 89 74.2 145 68.4 78 53.4
  Other public b b b b
  Unknown b 5 4.2 b 6 4.1
a

Documentation of smoking cessation counseling (HCPS: 99406, 99407, G0375, G0376)

b

Cell count suppressed due to insufficient sample size (n < 5), per Kentucky Cancer Registry guidelines

Smoking cessation pharmacotherapy before and/or after a cancer diagnosis was significantly more common among TAC survivors (3.3%) compared to nTAC survivors (2.7%) (p = 0.05, Table 3). Among TAC survivors, those with lung and pancreas cancers were most likely to have documentation of any smoking cessation pharmacotherapy (not shown). Among nTAC survivors, those with breast cancer were most likely to have documentation of any smoking cessation pharmacotherapy (not shown). Use of smoking cessation pharmacology differed significantly between TAC and Ntac survivors by age (p = 0.001) and insurance status (p = 0.02, Table 4).

Discussion

We found that the prevalence of smoking cessation counseling or pharmacotherapy used before and/or after a cancer diagnosis was more common among TAC survivors compared to nTAC survivors. In general, the prevalence of smoking has been shown to decline after a cancer diagnosis [56], but longer-term cancer survivors who have quit smoking may relapse [2, 3, 53]. In this study, we also found the use of smoking cessation counseling or pharmacotherapy differed significantly by insurance status, and less than 1% of uninsured survivors reported using either of these. Patients who receive advice about cessation from their health care providers are more likely to quit tobacco use. However, previous research has demonstrated that health professionals may miss opportunities to advise cancer survivors about smoking cessation and/or assist them with cessation [17, 40, 52, 55], or may not consider tobacco cessation treatment delivery as a core health care service [23]. Smoking cessation is beneficial for prognosis and quality of life among all cancer survivors, regardless of whether they were diagnosed with a TAC or nTAC [30, 33, 34, 39]. In 2015, less than half of current and former cancer survivor smokers (participating in the National Health Interview Survey [NHIS]) reported using cessation counseling and/or medication when trying to quit [22]. Previous population studies have found that the majority of quit attempts tend to be unassisted [1, 8, 18]. Health care providers can assist all cancer survivors by providing them with local counseling and/or pharmacotherapy resources.

The prevalence of smoking in the year before a cancer diagnosis was significantly higher among TAC survivors compared to nTAC survivors. This was largely driven by the pre-diagnosis prevalence of smoking among lung cancer survivors. The prevalence of smoking in this study was similar to the prevalence reported in previous studies [4, 5, 15, 37, 38, 41, 42, 54]. Current smoking status at the time of a cancer diagnosis has been shown to increase mortality for a number of cancer sites [54]. As has been observed in this study and others [4, 5, 15, 37, 38, 41, 42, 54] the prevalence of smoking status can vary widely among persons diagnosed with different cancers. Approximately one-third of cancer deaths are attributable to cigarette smoking in the United States, but even higher rates have been reported in the South where nearly 40% of cancer deaths in men are caused by smoking [32]. States with a high prevalence of smokers also have a high prevalence of TAC cases [47]. However, information about smoking status is not always available in cancer registry data, making a direct inference of this association in population-based data challenging. In this study, using the KCR linked with medical claims data, we were able to determine that the prevalence of smoking in the year prior to a diagnosis was significantly higher among TAC cases compared to nTAC cases. Several central cancer registries have linked with health administrative claims data, but were mostly limited to single claims sources, such as Medicaid, Medicare or private insurance groups, and most linkages are not done to augment smoking information collected from medical records. The KCR was able to link over 80% of cases with claims from Medicaid, Medicare and private insurers. The substantial coverage of linked cancer cases provided the unique opportunity to augment smoking information i collected from medical records and investigate smoking cessation counseling or pharmacotherapy at the population level.

A history of smoking was significantly more common among TAC survivors who were middle- to retirement-aged males with public or no insurance. A similar pattern was observed among nTAC survivors. Though few comparable studies have reported demographic characteristics specifically for smokers diagnosed with TACs, smoking continues to be more prevalent among poor and less educated populations [28]. This is consistent with the patterns observed in our dataset. In a study that specifically assessed the prevalence of persistent smoking after a TAC diagnosis [53], there was evidence of increased smoking among TAC survivors who were poor, uninsured, and less educated following their cancer diagnosis. Increasing the availability and use of tobacco cessation services for cancer survivors is of paramount importance in reducing TAC deaths. A TAC diagnosis can be a valuable teachable moment to facilitate quitting [25]. Providers can ask survivors whether they use tobacco products, encourage those who do to quit, and access their willingness to quit. They could also talk with survivors about the risks of tobacco use after a cancer diagnosis. Cessation counseling could occur during active cancer treatment and/ or after treatment has been completed. Patients who receive advice about cessation from their health care providers are more likely to quit tobacco use. Health care providers can recommend individual, group and telephone counseling, or one of seven FDA-approved cessation medications found to be safe and effective [44, 51]. Recommended tobacco cessation counseling services and medications would be beneficial if included in survivorship care plans, and would provide patients a written record of services available that they can access any time following a diagnosis. Community-based programs such as CDC’s Tobacco Control Program and National Comprehensive Cancer Control Program (NCCCP) can assist healthcare providers in this area (Centers for Disease Control and Prevention & Office of Smoking and Health [[10]; Comprehensive Cancer Control National Partnership, [11, 16]). Specifically the NCCCP helps identify the prevalence of cancer survivors who are current smokers, assists providers with completion and distribution of survivorship care plans, and educates providers and community health workers about counseling patients to live healthy lifestyles following a cancer diagnosis [14].

This study is subject to at least five limitations. First, augmenting the KCR with medical claims enabled positively identifying smoking status for the majority of the population; however, smoking status was unknown for 22% of survivors. Second, the medical claims data on smoking cessation counseling or pharmacotherapy may be not be a complete representation of the true number of quit attempts or use of cessation aids. We could not account for the majority of smoking quit attempts that are unassisted (i.e., no counseling or pharmacotherapy) [8]. Third, the small sample size of survivors with documented smoking cessation aids limited analyses of disparities in use of these products among specific populations. Fourth, the KCR claims-linked data consists of only six cancer sites, thus limiting the extent to which we could explore smoking and smoking-related characteristics among other cancers caused by smoking. Finally, approximating smoking history and smoking cessation using medical claims data has inherent limitations. The use of ICD-9 codes to identify smoking status has been shown to be reliable [57], but the absence of an ICD-9 code may not equate to a lack of smoking history. Similarly, the existence of relevant smoking cessation counseling and pharmacotherapy codes may not accurately reflect whether a survivor adhered to a treatment or filled a prescription [13].

Reducing smoking among all cancer survivors remains a priority, given that cancer survivors are at increased risk for subsequent chronic diseases, including cancer. Tobacco cessation among all cancer survivors can help improve prognosis, quality of life, and reduce the risk of further disease.

Acknowledgements

None.

Funding Funds to support this work were received from the Centers for Disease Control and Prevention [National Center for Chronic Disease Prevention and Health Promotion (U48DP0085014–01 SIP = 14–017)], and Markey Cancer Center Support Grant [Division of Cancer Prevention, National Cancer Institute (NCI P30 CA177558)].

Footnotes

Compliance with Ethical Standards

Conflict of Interest None.

References

  • 1.Babb S (2017). Quitting smoking among adults—United States, 2000–2015. Morbidity and Mortality Weekly Report, 65(52), 1457–1464. [DOI] [PubMed] [Google Scholar]
  • 2.Bellizzi K, Rowland J, Jeffery D, & McNeel T (2005). Health behaviors of cancer survivors: examining opportunities for cancer control intervention. Journal of Clinical Oncology, 23(34), 8884–8893. [DOI] [PubMed] [Google Scholar]
  • 3.Berg CJ, Thomas A, Mertens A, Schauer G, Pinsker E, Ahluwalia J, & Khuri F (2013). Correlates of continued smoking versus cessation among survivors of smoking-related cancers. Psycho-oncology, 22(4), 799–806. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Berube S, Lemieux J, Moore L, Maunsell E, & Brisson J (2014). Smoking at time of diagnosis and breast cancer-specific survival: new findings and systematic review with meta-analysis. Breast Cancer Research, 16(2), R42 10.1186/bcr3646. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Brand RE, Greer JB, Zolotarevsky E, Brand R, Du H, Simeone D, et al. (2009). Pancreatic cancer patients who smoke and drink are diagnosed at younger ages. Clinical Gastroenterology and Hepatology, 7(9), 1007–1012. 10.1016/j.cgh.2009.06.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Browman G, Browman GP, Wong G, Hodson I, Sathya J, Russell R, et al. (1993). Influence of cigarette smoking on the efficacy of radiation therapy in head and neck cancer. The New England Journal of Medicine, 328(3), 159–163. [DOI] [PubMed] [Google Scholar]
  • 7.Cahill K, Stead L, & Lancaster T (1996). Nicotine receptor partial agonists for smoking cessation. Cochrane Database of Systematic Reviews, The Cochrane Library; 10.1002/14651858.CD006103.pub6. [DOI] [PubMed] [Google Scholar]
  • 8.Caraballo RS, Shafer PR, Patel D, Davis KC, & McAfee TA (2017). Quit methods used by US adult cigarette smokers, 2014–2016. Preventing Chronic Disease, 14(E32), 1–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Carter BD, Abnet CC, Feskanich D, Freedman ND, Hartge P, Lewis CE, et al. (2015). Smoking and mortality–beyond established causes. N Engl J Med, 372(7), 631–640. 10.1056/NEJMsa1407211. [DOI] [PubMed] [Google Scholar]
  • 10.Centers for Disease Control and Prevention, & Office of Smoking and Health. (2018). National Tobacco Control Program Retrieved from https://www.cdc.gov/tobacco/stateandcommunity/tobacco_control_programs/ntcp/index.htm.
  • 11.Comprehensive Cancer Control National Partnership. (2016). Increase availability of tobacco cessation services for cancer survivors Retrieved from http://www.cccnationalpartners.org/increase-availability-tobacco-cessation-services-cancer-survivors.
  • 12.Cox L, Africano N, Tercyak K, & Taylor K (2003). Nicotine dependence treatment for patients with cancer. Cancer, 98(3), 632–644. [DOI] [PubMed] [Google Scholar]
  • 13.Crystal S, Akincigil A, Bilder S, & Walkup JT (2007). Studying prescription drug use and outcomes with medicaid claims data: strengths, limitations, and strategies. Medical Care, 45(10 Supl 2), S58–S65. 10.1097/MLR.0b013e31805371bf. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Department of Health and Human Services, & Centers for Disease Control and Prevention. (2015). Increasing the implementation of evidence-based cancer survivorship interventions to increase quality and duration of life among cancer patients Retrieved from https://www.grants.gov/view-opportunity.html?oppId=274757.
  • 15.Des Rochers C, Dische S, & Saunders MI (1992). The problem of cigarette smoking in radiotherapy for cancer in the head and neck. Clinical Oncology, 4(4), 214–216. [DOI] [PubMed] [Google Scholar]
  • 16.Division of Cancer Prevention and Control Centers for Disease Control and Prevention. (2017, March 7th, 2017). National comprehensive cancer control program (NCCCP) Retrieved from https://www.cdc.gov/cancer/ncccp/.
  • 17.Earle CC, & Neville B (2004). Under use of necessary care among cancer survivors. Cancer, 101(8), 1712–1719. [DOI] [PubMed] [Google Scholar]
  • 18.Edwards SA, Bondy S, Callaghan R, & Mann R (2014). Prevalence of unassisted quit attempts in population-based studies: A systematic review of the literature. Addictive Behaviors, 39(3), 512–519. [DOI] [PubMed] [Google Scholar]
  • 19.Emmons K, Li F, Whitton J, Mertens A, Hutchinson R, Diller L, & Robison L (2002). Predictors of smoking initiation and cessation among childhood cancer survivors: a report from the childhood cancer survivor study. Journal of Clinical Oncology, 20(6), 1608–1616. [DOI] [PubMed] [Google Scholar]
  • 20.Fairley T (2009). Health behaviors and quality of life of cancer survivors in Massachusetts, 2006: Data use for comprehensive cancer control. Preventing chronic disease 7(1), A09. [PMC free article] [PubMed] [Google Scholar]
  • 21.Fiore MC, Jaen CR, Baker TB, Bailey WC, Benowitz NL, Curry SJ, et al. (2008). Treating tobacco use and dependence: 2008 Update. Clinical Practice Guideline Rockville: U.S. Department of Health and Human Services, Public Health Service. [Google Scholar]
  • 22.Gallaway MS, Glover-Kudon R, Momin B, Puckett M, Lunsford NB, Ragan KR, et al. (2018). Smoking cessation attitudes and practices among Cancer Survivors–United States, 2015. J Cancer Surviv 10.1007/s11764-018-0728-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Goldstein AO, Ripley-Moffitt CE, Pathman DE, & Patsakham KM (2013). Tobacco use treatment at the U.S. National Cancer Institute’s designated cancer centers. Nicotine & Tobacco Research, 15(1), 52–58. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Gritz E (2005). Smoking, the missing drug interaction in clinical trials: ignoring the obvious. Cancer Epidemiology, Biomarkers & Prevention, 14(10), 2287–2293. [DOI] [PubMed] [Google Scholar]
  • 25.Gritz ER, Fingeret M, Vidrine D, Lazev A, Mehta N, & Reece G (2006). Successes and failures of the teachable moment. Cancer, 106(1), 17–27. [DOI] [PubMed] [Google Scholar]
  • 26.Henley SJ, Thomas C, Sharapova S, Momin B, Massetti G, Winn D, et al. (2016). Vital Signs: disparities in tobacco-related cancer incidence and mortality—United States, 2004–2013. MMWR. Morbidity and Mortality Weekly Report, 65(44), 1212–1218. [DOI] [PubMed] [Google Scholar]
  • 27.Hughes JR, & Callas PW (2010). Definition of a quit attempt: a replication test. Nicotine & Tobacco Research, 12(11), 1176–1179. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Jamal A, Homa D, Oconnor E, Babb S, Caraballo R, Singh T, et al. (2015). Current cigarette smoking among adults—United States, 2005–2014. MMWR. Morbidity and Mortality Weekly Report, 64(44), 1233–1240. [DOI] [PubMed] [Google Scholar]
  • 29.Kawahara M, Ushijima S, Kamimori T, Kodama N, Ogawara M, Matsui K, et al. (1998). Second primary tumours in more than 2-year disease-free survivors of small-cell lung cancer in Japan: the role of smoking cessation. British Journal of Cancer, 78(3), 409–412. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Klosky JL, Tyc V, Garces Webb D, Buscemi J, Klesges R, & Hudson M (2007). Emerging issues in smoking among adolescent and adult cancer survivors. Cancer, 110(11), 2408–2419. [DOI] [PubMed] [Google Scholar]
  • 31.Lancaster T, & Stead L (1996). Individual behavioural counselling for smoking cessation. Cochrane Database of Systematic Reviews, The Cochrane Library; 10.1002/14651858.CD001292.pub2. [DOI] [PubMed] [Google Scholar]
  • 32.Lortet-Tieulent J, Goding Sauer A, Siegel RL, Miller KD, Islami F, Fedewa SA, et al. (2016). State-level cancer mortality attributable to cigarette smoking in the United States. JAMA Internal Medicine, 176(12), 1792–1798. 10.1001/jamainternmed.2016.6530. [DOI] [PubMed] [Google Scholar]
  • 33.Mackenbach JP (2001). Determinants of levels and changes of physical functioning in chronically ill persons: Results from the GLOBE Study. Journal of Epidemiology and Community Health, 55(9), 631–638. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Mariotto A (2007). Multiple cancer prevalence: a growing challenge in long-term survivorship. Cancer Epidemiology, Biomarkers & Prevention, 16(3), 566–571. [DOI] [PubMed] [Google Scholar]
  • 35.Mason DP, Subramanian S, Nowicki E, Grab J, Murthy S, Rice T, & Blackstone E (2009). Impact of smoking cessation before resection of lung cancer: a society of thoracic surgeons general thoracic surgery database study. The Annals of Thoracic Surgery, 88(2), 362–371. [DOI] [PubMed] [Google Scholar]
  • 36.National Cancer Institute, National Institute of Health, & Department of Health and Human Services. (January 2017). Cancer Trends Progress Report Retrieved from https://progressreport.cancer.gov.
  • 37.Passarelli MN, Newcomb PA, Hampton JM, Trentham-Dietz A, Titus LJ, Egan KM, et al. (2016). Cigarette smoking before and after breast cancer diagnosis: mortality from breast cancer and smoking-related diseases. Journal of Clinical Oncology, 34(12), 1315–1322. 10.1200/JCO.2015.63.9328. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Polednak AP (2006). Obtaining smoking histories for population-based studies on multiple primary cancers: Connecticut, 2002. International Journal of Cancer, 119(1), 233–235. 10.1002/ijc.21786. [DOI] [PubMed] [Google Scholar]
  • 39.Richardson GE (1993). Smoking cessation after successful treatment of small-cell lung cancer is associated with fewer smoking-related second primary cancers. Annals of Internal Medicine, 119(5), 383–390. [DOI] [PubMed] [Google Scholar]
  • 40.Sabatino S (2007). Provider counseling about health behaviors among cancer survivors in the United States. Journal of Clinical Oncology, 25(15), 2100–2106. [DOI] [PubMed] [Google Scholar]
  • 41.Sharp L, McDevitt J, Brown C, & Comber H (2017). Smoking at diagnosis significantly decreases 5-year cancer-specific survival in a population-based cohort of 18,166 colon cancer patients. Alimentary Pharmacology and Therapeutics, 45(6), 788–800. 10.1111/apt.13944. [DOI] [PubMed] [Google Scholar]
  • 42.Shiels MS, Gibson T, Sampson J, Albanes D, Andreotti G, Freeman LB, et al. (2014). Cigarette smoking prior to first cancer and risk of second smoking-associated cancers among survivors of bladder, kidney, head and neck, and stage I lung cancers. Journal of Clinical Oncology, 32(35), 3989–3995. 10.1200/JCO.2014.56.8220. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Silagy C (1994). Nicotine replacement therapies in smoking cessation. Biomedicine & Pharmacotherapy, 48(8–9), 407–408. [Google Scholar]
  • 44.Siu AL (2015). Behavioral and pharmacotherapy interventions for tobacco smoking cessation in adults, including pregnant women: U.S. Preventive Services Task Force recommendation statement. Annals of Internal Medicine, 163(8), 622–634. [DOI] [PubMed] [Google Scholar]
  • 45.Stead L (2010). Group behaviour therapy programmes for smoking cessation. Canadian Journal of Dental Hygiene, 44(2), 84. [Google Scholar]
  • 46.Stead L, & Young T (2005). Cochrane Column. International Journal of Epidemiology, 34(5), 1001–1003. [Google Scholar]
  • 47.Stewart SL, Cardinez CJ, Richardson LC, Norman L, Kaufmann R, Pechacek TF, et al. (2008). Surveillance for cancers associated with tobacco use—United States, 1999–2004. MMWR Surveill Summ, 57(8), 1–33. [PubMed] [Google Scholar]
  • 48.Tucker MA (1997). Second primary cancers related to smoking and treatment of small-cell lung cancer. Lung Cancer Working Cadre. Journal of the National Cancer Institute, 89(23), 1782–1788. [DOI] [PubMed] [Google Scholar]
  • 49.Tyc VL (2005). A comparison of tobacco-related risk factors between adolescents with and without cancer. Journal of Pediatric Psychology, 30(4), 359–370. [DOI] [PubMed] [Google Scholar]
  • 50.U.S. Cancer Statistics Working Group. (2017). U.S. Cancer Statistics Publication Criteria Retrieved from https://www.cdc.gov/cancer/npcr/uscs/technical_notes/criteria.htm.
  • 51.U.S. Department of Health and Human Services. (2014). The health consequences of smoking: 50 years of progress: A report of the surgeon general Retrieved from Atlanta, Georgia: https://www.surgeongeneral.gov/library/reports/50-years-of-progress/index.html. [Google Scholar]
  • 52.Underwood JM, Townsend J, Stewart SL, Buchannan N, Ekwueme DU, Hawkins NA, et al. (2012). Surveillance of demographic characteristics and health behaviors among adult cancer survivors—behavioral risk factor surveillance system, United States, 2009. Morbidity and Mortality Weekly Report, 61(1), 1–23. [PubMed] [Google Scholar]
  • 53.Underwood JM, Townsend J, Tai E, White A, Davis S, & Fairley T (2012). Persistent cigarette smoking and other tobacco use after a tobacco-related cancer diagnosis. Journal of Cancer Survivorship, 6(3), 333–344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Warren GW, Kasza KA, Reid ME, Cummings KM, & Marshall JR (2013). Smoking at diagnosis and survival in cancer patients. International Journal of Cancer, 132(2), 401–410. 10.1002/ijc.27617. [DOI] [PubMed] [Google Scholar]
  • 55.Weaver KE, Danhauer SC, Tooze JA, Blackstock AW, Spangler J, Thomas L, & Sutfin EL (2012). Smoking cessation counseling beliefs and behaviors of outpatient oncology providers. The Oncologist, 17(3), 455–462. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Westmaas JL, Newton CC, Stevens VL, Flanders WD, Gapstur SM, & Jacobs EJ (2015). Does a recent cancer diagnosis predict smoking cessation? An analysis from a large prospective US cohort. Journal of Clinical Oncology, 33(15), 1647–1652. 10.1200/JCO.2014.58.3088. [DOI] [PubMed] [Google Scholar]
  • 57.Wiley LK, Shah A, Xu H, & Bush WS (2013). ICD-9 tobacco use codes are effective identifiers of smoking status. Journal of the American Medical Informatics Association, 20(4), 652–658. 10.1136/amiajnl-2012-001557. [DOI] [PMC free article] [PubMed] [Google Scholar]

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