- Research article
- Open Access
- Open Peer Review
Lifestyle behaviors, obesity, and perceived health among men with and without a diagnosis of prostate cancer: A population-based, cross-sectional study
© Rogers et al; licensee BioMed Central Ltd. 2008
- Received: 03 May 2007
- Accepted: 22 January 2008
- Published: 22 January 2008
A better understanding of how prostate cancer survivors differ from men without prostate cancer and whether these potential differences vary across demographic subgroups will help to focus and prioritize future public health interventions for improving the health and well-being of prostate cancer survivors. Therefore, our study aims were to compare lifestyle behaviors, body mass index (BMI), and perceived health in men with and without a diagnosis of prostate cancer in a national, population-based sample and to explore whether these comparisons differ for demographic subgroups.
In a cross-sectional study, men aged ≥ 40 were identified from the Behavioral Risk Factor Surveillance System (BRFSS) 2002 data (n = 63,662). Respondents reporting history of prostate cancer (n = 2,524) were compared with non prostate cancer controls (n = 61,138) with regard to daily fruit and vegetable servings (FVPD), smoking, alcohol, sedentary behavior, BMI, and perceived health. Multivariable logistic regression calculated adjusted odds ratios (OR) and 95% confidence intervals (CI) for the entire sample and for age, race, education, and urbanicity subgroups.
Men with prostate cancer did not differ from men without prostate cancer with regard to smoking, alcohol, sedentary behavior, and obesity but were more likely to consume ≥ 5 FVPD (OR, 95% CI: 1.30, 1.09–1.56) and report poor or fair health (OR, 95% CI: 1.62, 1.33–1.97). Subgroup analyses demonstrated attenuation of the higher likelihood of ≥ 5 FVPD among prostate cancer survivors in rural respondents (OR, 95% CI: 0.98, 0.72–1.33). Poorer perceived health was greatest if ≤ 65 years of age (OR, 95% CI: 2.54, 1.79–3.60) and nonsignificant if black (OR, 95% CI: 1.41, 0.70–2.82). Smoking and alcohol which were not significant for the sample as a whole, demonstrated significant associations in certain subgroups.
Although efforts to enhance perceived health and healthy lifestyle behaviors among prostate cancer survivors are warranted, demographic subgroups such as prostate cancer survivors ≤ 65 and rural populations may require more aggressive interventions.
- Prostate Cancer
- Cancer Survivor
- Sedentary Behavior
- Lifestyle Behavior
- Behavioral Risk Factor Surveillance System
Prostate cancer is the most common cancer in the US affecting over 200,000 men annually . Over the past 20 years, the survival rate for prostate cancer across all stages has increased to nearly 100%  resulting in over 1.8 million prostate cancer survivors nationally . Attention to lifestyle behaviors is an important aspect of quality cancer care for survivors . Cancer survivors are at increased risk for recurrence, secondary cancers, and other chronic diseases such as cardiovascular disease, arthritis, and hypertension that may be attenuated by healthy lifestyle choices [4, 5]. Prostate cancer survivors, specifically, may be more apt to die from comorbidities rather than their cancer diagnosis [6, 7].
In addition to the potential beneficial impact on comorbidities, healthy lifestyle behaviors may provide other benefits for prostate cancer survivors. Physical activity improves quality of life among prostate cancer survivors , reduces treatment related fatigue [8, 9], and may slow prostate cancer progression with the potential to reduce mortality [10, 11]. A healthy diet may improve physical functioning  and slow progression of early stage disease . Although the benefits of smoking cessation among prostate cancer survivors has not been specifically studied, smoking has been associated with an increased risk of developing prostate cancer  and with poorer treatment response and survival in cancers other than prostate (e.g., lung, head and neck) [14–16]. Lastly, the benefits of reduced alcohol intake are inadequately studied , but higher alcohol intake has been associated with reduced survival in cancers other than prostate (e.g., breast) [18, 19].
Although making healthy lifestyle choices is important for cancer survivors, the prevalence of healthy behaviors is less than optimal with prostate cancer survivors being less likely than other cancer survivors (e.g., breast, colorectal) to make healthy changes in their diet and/or physical activity after cancer diagnosis [20–24]. Although inconsistent, the few studies comparing cancer survivors of any type with participants without a cancer diagnosis suggest differences in lifestyle behaviors (e.g., diet, physical activity, smoking, and alcohol) depending on cancer type and age subgroups [3, 21, 24–28]. The only U.S. study to date comparing prostate cancer survivors specifically with noncancer controls with regard to lifestyle behaviors, noted that prostate cancer survivors reported lower smoking rates (11.1% versus 23.6%) and more frequent moderate-heavy alcohol use (22.3% versus 18.9%) . This study did not adjust for demographic factors or assess diet, body mass index (BMI), and perceived health when assessing differences based on cancer type. Because demographic differences are suspected to occur due to psychosocial, cultural, and economic reasons [29–32], it is fortunate that an Australian population-based study performed such adjustments and confirmed the greater probability of moderate alcohol intake in prostate cancer survivors when compared with non-cancer controls . Although this study did not find differences for other health-related behaviors (including diet and BMI), no assessment of perceived health was reported. Because cancer survivors are at increased risk for poorer perceived health and knowledge of etiolologic factors is inadequate , perceived health is of particular importance. A better understanding of how prostate cancer survivors differ from men without prostate cancer and whether these potential differences vary across demographic subgroups will help to focus and prioritize future public health interventions for improving the health and well-being of prostate cancer survivors.
Therefore, our primary study aim was to compare differences in lifestyle behaviors, BMI, and perceived health for men with and without a diagnosis of prostate cancer using a national population-based sample. Our secondary study aim was to explore whether these potential differences in lifestyle, BMI, and perceived health varied across demographic subgroups of age, race, education, and urbanicity. The secondary study aim is particularly important because demographic factors other than age have not been adequately evaluated in related studies.
Study design and participants
Study participants were men, ≥ 40 years of age (n = 63,662) identified from the Behavioral Risk Factor Surveillance System (BRFSS) 2002 data. Details of the BRFSS design [34, 35] including its reliability and validity  have been described elsewhere, and are briefly described here. The BRFSS is an ongoing national population-based cross-sectional survey conducted in the United States annually since its initiation in 1984. The Centers for Disease Control and Prevention (CDC) collaborates with 54 reporting areas which include all the states, three territories, and the District of Columbia. Trained interviewers use a structured telephone survey of health-related behaviors from noninstitutionalized participants aged 18+ who are identified by the random-digit dialing method. The self-reported information includes demographic data, and other lifestyle factors related to chronic diseases, injuries, and preventable infectious diseases. The BRFSS is approved by the Centers for Disease Control and Prevention Institutional Review Board prior to collection of data.
For this study, the main classification variable was a self-reported history of prostate cancer as measured by the following BRFSS question: 'Have you ever been told by a doctor, nurse, or other health professional that you had prostate cancer?' According to CDC protocol, only male participants aged 40+ years old were asked to respond. In our study, men who answered 'yes' were defined as prostate cancer survivors (n = 2,524), while those who answered 'no' were defined as non prostate cancer controls (n = 61,138).
The lifestyle behaviors, BMI, and perceived health were defined as follows. Based on self-report, fruit and vegetable intake was dichotomized as less than five servings per day versus five or more servings per day. Cigarette smoking was dichotomized as current versus nonsmoker. Respondents who reported smoking every day or some days and ≥ 100 cigarettes in their lifetime were classified as current smokers while nonsmokers included both former smokers (i.e., smoked ≥ 100 cigarettes in their lifetime but did not currently smoke) and never smokers. At risk for binge alcohol use was defined as having five or more drinks on one occasion in the past 30 days. Men at risk for heavy alcohol consumption (yes/no) were defined as having an average of more than 2 drinks per day during the preceding month. To assess sedentary behavior (yes/no), respondents reported whether or not they had participated in any leisure-time exercise during the past month, such as running, calisthenics, golf, gardening, or walking. Self-reported weight and height were used to calculate body mass index (BMI; weight [kg]/height [m2]) which was then classified into three categories of less than 25 (healthy), 25 to 30 (overweight), more than 30 (obese) for reporting of estimated prevalence percentages. Perceived health was assessed with the following question: "Would you say that in general your health is poor, fair, good, very good, or excellent?" Perceived health was categorized into three levels (i.e., poor/fair, good, and very good/excellent) for analysis.
Because of known associations with lifestyle behaviors in other populations, several potential confounding demographic factors were assessed [37–40]. Self reported age in years was categorized by decade for estimated prevalence percentage reporting only (i.e., the continuous age variable was used in logistic regression analyses). Race was dichotomized into 'black' if the respondent self-reported race as Black or African American, and 'non-black' if White, Asian, Native Hawaiian, or otherPacificIslander, AmericanIndianorAlaskanNative, or otherrace was reported. Education was defined as less than 12 years, 12 years, or more than 12 years of education. Urbanicity was classified as rural versus urban residence based on the Metropolitan Statistical Area (MSA) coding (i.e., rural residence was defined as counties that are not part of a metropolitan statistical area and urban residence was defined as counties in a metropolitan statistical area).
The weighted 2002 data provided by the CDC were used for all data analyses using SAS statistical software (version 9.1; SAS Institute Inc., Cary, NC, USA). SAS PROC SURVEY routines were used to allow for appropriate weighting procedures necessary to account for the complex sampling strategy and adjust for factors such as non-telephone coverage, non-response, and probability of selection. All of the study measures had minimal missing information (0.1% to 2.0%). Because the annual income had 11% missing data, education level (<1% missing) was chosen as the measure of socioeconomic status. Weighted prevalence estimates of lifestyle behaviors, BMI, perceived health, and demographic factors for prostate cancer survivors and non prostate cancer controls were calculated with differences examined with chi-square test for categorical variables and t-test for continuous variables.
To achieve the primary study aim, the relationships between a history of prostate cancer diagnosis and lifestyle behaviors, BMI, and perceived health were examined among all respondents with unadjusted and adjusted prevalence odds ratios (OR) and 95% confidence intervals (CI) calculated using multivariable logistic regression. Adjustment was made for race, age in years (continuous), education, and urbanicity because these variables have demonstrated the potential for confounding due to an association with lifestyle factors and/or prostate cancer in other populations [13, 21, 24, 37–40]. Because adjustment for additional factors [i.e., health status, whether or not the respondent had a personal doctor, whether or not the respondent had health insurance, geographic region in the U.S. (i.e., west, northeast, south, midwest), and body mass index] did not alter the odds ratios, we have reported only the ORs adjusted for race, age, education, and urbanicity.
To achieve the secondary study aim, the associations between a prostate cancer diagnosis and lifestyle behaviors, BMI, and perceived health were assessed with multivariable logistic regression calculation of adjusted ORs for demographic subgroups. Each demographic characteristic (i.e., age, race, education, and urbanicity) was dichotomized. Only two subgroups were considered for each characteristic to facilitate adequate stratum specific sample sizes. For the subgroup analyses, the ORs were adjusted for the other three demographic characteristics. Specifically, ORs for the age subgroups (i.e., ≤ 65 and > 65 years of age), were adjusted for race, education and urbanicity. Similarly, ORs for race subgroups were adjusted for age, education, and urbanicity; ORs for education subgroups were adjusted for age, race, and urbanicity; and ORs for urbanicity were adjusted for age, race, and education. To test for significant differences in the ORs across demographic strata, each model was repeated with an inclusion of the demographic factor and the appropriate interaction term (i.e., demographic variable*prostate cancer diagnosis).
Weighted prevalence estimates of demographic factors, lifestyle behaviors, body mass index, and perceived health among prostate cancer survivors and noncancer controls, Behavioral Risk Factor Surveillance System, 2002.
Prostate cancer survivors Percent†
Noncancer controls Percent†
40 – 49
50 – 59
60 – 69
70 – 79
80 – 89
Mean ± SD
71.7 ± 9.8
55.4 ± 11.7
< 12 yrs
> 12 yrs
Fruit and vegetable servings
≥ 5 per day
< 5 per day
Binge alcohol use
Not at risk
Heavy alcohol consumption
Not at risk
Body mass index
< 25 (normal)
25 to 30 (overweight)
> 30 (obese)
Mean ± SD
26.9 ± 8.8
27.8 ± 9.4
Adjusted prevalence odds ratio (OR) and 95% confidence interval (CI) for the associations between prostate cancer diagnosis and lifestyle behaviors, body mass index, and perceived health.
Unadjusted OR (95% CI)
*Adjusted OR (95% CI)
Fruit and vegetable servings
≥ 5 per day
1.75 (1.49 – 2.08)
1.30 (1.09 – 1.56)
< 5 per day
0.44 (0.35 – 0.54)
0.86 (0.68 – 1.08)
Binge alcohol use
0.35 (0.26 – 0.47)
0.81 (0.59 – 1.11)
Not at risk
Heavy alcohol consumption
0.57 (0.38 – 0.86)
0.79 (0.50 – 1.24)
Not at risk
1.05 (0.90 – 1.23)
0.91 (0.77 – 1.09)
Body mass index
25 – 30
0.98 (0.82 – 1.16)
1.13 (0.95 – 1.35)
0.64 (0.52 – 0.78)
0.87 (0.70 – 1.08)
2.68 (2.25 – 3.19)
1.62 (1.33 – 1.97)
1.64 (1.37 – 1.95)
1.30 (1.07 – 1.57)
Adjusted prevalence odds ratio (OR) and 95% confidence interval (CI) for the associations between prostate cancer diagnosis and lifestyle behaviors, body mass index, and perceived health, stratified by age, race, education, and urbanicity.
≥ 5 per day
(0.95 – 1.85)
(1.10 – 1.64)
(0.89 – 2.99)
(1.06 – 1.54)
(0.99 – 1.89)
(1.03 – 1.56)
(1.14 – 1.72)
(0.72 – 1.33)
< 5 per day
(0.47 – 0.92)
(0.64 – 1.21)
(0.43 – 1.66)
(0.67 – 1.10)
(0.70 – 1.32)
(0.51 – 1.03)
(0.59 – 1.08)
(0.78 – 1.45)
Binge alcohol use
(0.39 – 0.79)
(0.51 – 1.28)
(0.16 – 1.02)
(0.61 – 1.18)
(0.67 – 1.40)
(0.43 – 1.14)
(0.53 – 1.13)
(0.62 – 1.50)
Not at risk
Heavy alcohol consumption
(0.34 – 1.22)
(0.46 – 1.45)
(0.06 – 1.02)
(0.52 – 1.32)
(0.36 – 1.27)
(0.45 – 1.51)
(0.49 – 1.38)
(0.30 – 1.27)
Not at risk
(0.72 – 1.43)
(0.77 – 1.13)
(0.34 – 0.95)
(0.81 – 1.16)
(0.61 – 0.99)
(0.82 – 1.29)
(0.68 – 1.05)
(0.89 – 1.50)
Body mass index
25 – 30
(0.88 – 1.75)
(0.91 – 1.37)
(0.96 – 3.26)
(0.91 – 1.32)
(0.92 – 1.74)
(0.85 – 1.29)
(0.94 – 1.44)
(0.80 – 1.35)
(0.78 – 1.66)
(0.59 – 1.00)
(0.69 – 2.45)
(0.66 – 1.05)
(0.63 – 1.28)
(0.65 – 1.11)
(0.66 – 1.12)
(0.65 – 1.22)
(1.79 – 3.60)
(1.29 – 2.01)
(0.70 – 2.82)
(1.35 – 2.03)
(1.20 – 2.43)
(1.02 – 1.65)
(1.31 – 2.10)
(1.08 – 1.94)
(1.32 – 2.50)
(0.92 – 1.45)
(0.85 – 3.31)
(1.03 – 1.54)
(0.76 – 1.61)
(1.13 – 1.74)
(1.07 – 1.68)
(0.82 – 1.54)
Based on a national, population-based survey, men with a history of prostate cancer do not differ from those without a history of prostate cancer with regard to smoking status, binge and heavy alcohol use, sedentary behavior, and obesity. Prostate cancer survivors may, however, be more apt to consume fruits and vegetables and report poorer perceived health. Demographic characteristics may influence the prevalence of lifestyle behaviors, BMI, and poorer perceived health for prostate cancer survivors compared to those without a history of prostate cancer.
Our study is strengthened by its use of a national, population-based survey and its focus on an understudied cancer survivor population. Our approach was unique in its comparison of prostate cancer survivors with a control population without a prostate cancer diagnosis with regard to lifestyle behaviors, BMI and perceived health. Prior studies have compared lifestyle behaviors among survivors with different cancer types [3, 12, 20–22] and/or among cancer survivors (all types combined, breast cancer survivors only, or testicular cancer only) and noncancer controls [21, 26–28]. However, few studies have used national level population-based surveys [3, 21, 24, 28], only two studies have specifically compared the behaviors of prostate cancer survivors with non-prostate cancer controls [24, 28], only one has included comparison of diet and BMI , and no prior study has performed a comparison of perceived health. Furthermore, age influences lifestyle behavior prevalence among cancer survivors [21, 24] but no prior study has assessed the potential influence of race, education, and urbanicity on the prevalence of health behaviors, BMI, and perceived health among prostate cancer survivors when compared with controls.
With regard to lifestyle behaviors, the higher fruit and vegetable consummation reported by prostate cancer survivors is consistent with prior studies and may be partially explained by the fact that a cancer diagnosis may cause an individual to adopt healthier behaviors [25, 41]. However, the cross-sectional study design and lack of information on time since diagnosis in the BRFSS data precludes proof of this potential cause and effect relationship. The cross-sectional design also introduces the possibility of survival bias. Because obesity has been associated with increased prostate cancer recurrence and mortality [42–44] and may play a role in the increased prostate cancer risk in black men , survival bias could bias the prevalence odds ratios to reflect better diet and activity behaviors among the prostate cancer survivors. Therefore, the significant reduction in prevalence of consuming < 5 daily servings of fruits and vegetables and sedentary behavior (especially among black men) is consistent with the association between obesity and prostate cancer risk. This finding is also consistent with a recent study demonstrating that a lifestyle intervention including diet, exercise, and stress management may reduce prostate cancer progression .
The most prevalent poor lifestyle behavior was inadequate fruit and vegetable intake followed by sedentary behavior. Because the 2002 BRFSS dataset utilized for this study categorized fruit and vegetable intake according to the recommendations at that time of ≥ 5 servings per day, it would be expected that compliance with the more recent recommendation of ≥ 9 fruit and vegetable servings daily  would be even lower. Smoking and binge/heavy alcohol use, although present, were less frequent. Our finding that 69.3% of prostate cancer survivors reported eating < 5 daily servings of fruits and vegetables is consistent with that reported by Demark-Wahnefried  (65%) but slightly higher than that reported by Coups  (i.e., 39.8%). The prevalence of smoking and alcohol was also consistent with prior studies [20, 21, 24]. Because we did not assess regular physical activity but only sedentary behavior, comparison with prior studies is difficult. Nevertheless, our results are consistent with prior reports of regular exercise among 29.3%  to 62%  of prostate cancer survivors.
Although measurement bias may exist because lifestyle behaviors and prostate cancer diagnosis were self-reported, it is reassuring that our lifestyle prevalence rates were consistent with other studies and prostate cancer diagnosis leads to sufficient physician attention and treatment that it is less likely that the diagnosis would be unknown or forgotten. If respondents had been asked to recall lifestyle exposures prior to cancer diagnosis, those with cancer might over or underestimate the behaviors. However, respondents were asked about current behavior suggesting that self-report would be expected to be similar in both the prostate cancer survivors and the comparison group and, therefore, would not significantly influence the reported associations. Also, residual confounding may exist when analyzing nonrandomized, observational study using public domain data with predetermined variables and data collection procedures as with the BRFSS data, but adjustment for surrogate markers for health-related confounders did not significantly change the odds ratios and the increased generalizability achieved with a national sample outweighs this potential risk. Additional caution is advised due to the possibility of statistical associations by chance alone when multiple comparisons are performed (as in Table 3) and reduced precision of the odds ratios due to the large age difference between those with and without a prostate cancer diagnosis. Moreover, our analyses are limited by the lack of information about primary cancer diagnoses other than prostate cancer. It is feasible that the patients without a prostate cancer diagnosis had a cancer diagnosis of another type and/or the prostate cancer patients had more than one cancer diagnoses. Because of the increased risk of second primary cancers after prostate cancer treatment , it is possible that differences reported for the prostate cancer patients are primarily related to greater overall cancer burden rather than prostate cancer specifically. Nevertheless, confirmation of our study results in populations with documentation of prostate cancer diagnosis based on other sources besides self-report (e.g., cancer registries) and follow-up studies testing the hypotheses generated by our study are warranted. Such studies should assess the potential confounding or moderating effect of other cancer diagnoses on associations reported.
The suboptimal practice of healthful lifestyle behaviors is especially concerning among cancer survivors because they often report poorer health [24, 33], a finding also noted for the prostate cancer survivors in our study. This lower perceived health may be related to a negative psychological impact of a cancer diagnosis and/or higher prevalence of chronic comorbid disease other than cancer [4, 5]. Prostate cancer survivors who make healthier lifestyle choices report better quality of life, suggesting that addressing these inadequacies may be a model for improving poor perceived health .
Our results suggest that efforts to enhance perceived health and healthy lifestyle behaviors among prostate cancer survivors are warranted. Certain demographic subgroups may warrant more aggressive interventions such as addressing the higher odds for poorer perceived health in prostate cancer survivors ≤ 65 and lower odds for fruits and vegetable intake in rural populations. Moreover, examining the reasons for the reduced at risk alcohol consumption in black respondents and less prevalent sedentary behavior in respondents with ≤ 12 years of education, may suggest cultural influences that could be used in other lifestyle interventions or sources of measurement error in certain subgroups (e.g., less educated individuals may report occupational physical activity even when self-reported leisure activity is requested). Prospective, cohort studies are needed to assess the changes in lifestyle behaviors, BMI, and perceived health that occur after a prostate cancer diagnosis. These studies should include diverse study populations with regard to age, race, education, and geographic location to confirm potential differences across demographic strata with regard to lifestyle behaviors, BMI, and perceived health. Outcome measures should be designed to explore the potential reasons for differences across demographic strata [e.g., socio-cultural, social cognitive (e.g., readiness for change)]. Discovering these reasons will guide the design of effective behavior change interventions to improve lifestyle behaviors which in turn has the potential to improve the quality of life, health, and survival of prostate cancer survivors.
Dr. Courneya is supported by the Canada Research Chairs Program and a Research Team Grant from the National Cancer Institute of Canada (NCIC) with funds from the Canadian Cancer Society (CCS) and the NCIC/CCS Sociobehavioral Cancer Research Network.
- ACS: Cancer Facts and Figures 2007. 2007, Atlanta, GA , American Cancer SocietyGoogle Scholar
- NCI: Cancer Survivorship Research: Cancer Control & Population. 2003, National Cancer InstituteGoogle Scholar
- Ko C, Chaudhry S: The need for a multidisciplinary approach to cancer care. J Surg Res. 2002, 105 (1): 53-57. 10.1006/jsre.2002.6449.View ArticlePubMedGoogle Scholar
- Aziz NM: Cancer survivorship research: challenge and opportunity. J Nutr. 2002, 132 (11 Suppl): 3494S-3503S.PubMedGoogle Scholar
- Yabroff KR, Lawrence WF, Clauser S, Davis WW, Brown ML: Burden of illness in cancer survivors: findings from a population-based national sample. J Natl Cancer Inst. 2004, 96 (17): 1322-1330.View ArticlePubMedGoogle Scholar
- Fowler JE, Terrell FL, Renfroe DL: Co-morbidities and survival of men with localized prostate cancer treated with surgery or radiation therapy. J Urol. 1996, 156 (5): 1714-1718. 10.1016/S0022-5347(01)65489-2.View ArticlePubMedGoogle Scholar
- Yao SL, Dipaola RS: An evidence-based approach to prostate cancer follow-up. Semin Oncol. 2003, 30 (3): 390-400. 10.1016/S0093-7754(03)00099-X.View ArticlePubMedGoogle Scholar
- Segal RJ, Reid RD, Courneya KS, Malone SC, Parliament MB, Scott CG, Venner PM, Quinney HA, Jones LW, D'Angelo ME, Wells GA: Resistance exercise in men receiving androgen deprivation therapy for prostate cancer. J Clin Oncol. 2003, 21 (9): 1653-1659. 10.1200/JCO.2003.09.534.View ArticlePubMedGoogle Scholar
- Windsor PM, Nicol KF, Potter J: A randomized, controlled trial of aerobic exercise for treatment-related fatigue in men receiving radical external beam radiotherapy for localized prostate carcinoma. Cancer. 2004, 101 (3): 550-557. 10.1002/cncr.20378.View ArticlePubMedGoogle Scholar
- Giovannucci EL, Liu Y, Leitzmann MF, Stampfer MJ, Willett WC: A prospective study of physical activity and incident and fatal prostate cancer. Arch Intern Med. 2005, 165 (9): 1005-1010. 10.1001/archinte.165.9.1005.View ArticlePubMedGoogle Scholar
- Ornish D, Weidner G, Fair WR, Marlin R, Pettengill EB, Raisin CJ, Dunn-Emke S, Crutchfield L, Jacobs FN, Barnard RJ, Aronson WJ, McCormac P, McKnight DJ, Fein JD, Dnistrian AM, Weinstein J, Ngo TH, Mendell NR, Carroll PR: Intensive lifestyle changes may affect the progression of prostate cancer. J Urol. 2005, 174 (3): 1065-9; discussion 1069-70. 10.1097/01.ju.0000169487.49018.73.View ArticlePubMedGoogle Scholar
- Demark-Wahnefried W, Clipp EC, Morey MC, Pieper CF, Sloane R, Snyder DC, Cohen HJ: Physical function and associations with diet and exercise: Results of a cross-sectional survey among elders with breast or prostate cancer. Int J Behav Nutr Phys Act. 2004, 1 (1): 16-10.1186/1479-5868-1-16.View ArticlePubMedPubMed CentralGoogle Scholar
- Lund Nilsen TI, Johnsen R, Vatten LJ: Socio-economic and lifestyle factors associated with the risk of prostate cancer. Br J Cancer. 2000, 82 (7): 1358-1363. 10.1054/bjoc.1999.1105.View ArticlePubMedGoogle Scholar
- Browman GP, Wong G, Hodson I, Sathya J, Russell R, McAlpine L, Skingley P, Levine MN: Influence of cigarette smoking on the efficacy of radiation therapy in head and neck cancer. N Engl J Med. 1993, 328 (3): 159-163. 10.1056/NEJM199301213280302.View ArticlePubMedGoogle Scholar
- Kawahara M, Ushijima S, Kamimori T, Kodama N, Ogawara M, Matsui K, Masuda N, Takada M, Sobue T, Furuse K: Second primary tumours in more than 2-year disease-free survivors of small-cell lung cancer in Japan: the role of smoking cessation. Br J Cancer. 1998, 78 (3): 409-412.View ArticlePubMedPubMed CentralGoogle Scholar
- Do KA, Johnson MM, Doherty DA, Lee JJ, Wu XF, Dong Q, Hong WK, Khuri FR, Fu KK, Spitz MR: Second primary tumors in patients with upper aerodigestive tract cancers: joint effects of smoking and alcohol (United States). Cancer Causes Control. 2003, 14 (2): 131-138. 10.1023/A:1023060315781.View ArticlePubMedGoogle Scholar
- Kuhn KG, Boesen E, Ross L, Johansen C: Evaluation and outcome of behavioural changes in the rehabilitation of cancer patients: a review. Eur J Cancer. 2005, 41 (2): 216-224. 10.1016/j.ejca.2004.09.018.View ArticlePubMedGoogle Scholar
- Hebert JR, Hurley TG, Ma Y: The effect of dietary exposures on recurrence and mortality in early stage breast cancer. Breast Cancer Res Treat. 1998, 51 (1): 17-28. 10.1023/A:1006056915001.View ArticlePubMedGoogle Scholar
- McDonald PA, Williams R, Dawkins F, Adams-Campbell LL: Breast cancer survival in African American women: is alcohol consumption a prognostic indicator?. Cancer Causes Control. 2002, 13 (6): 543-549. 10.1023/A:1016337102256.View ArticlePubMedGoogle Scholar
- Demark-Wahnefried W, Peterson B, McBride C, Lipkus I, Clipp E: Current health behaviors and readiness to pursue life-style changes among men and women diagnosed with early stage prostate and breast carcinomas. Cancer. 2000, 88 (3): 674-684. 10.1002/(SICI)1097-0142(20000201)88:3<674::AID-CNCR26>3.0.CO;2-R.View ArticlePubMedGoogle Scholar
- Coups EJ, Ostroff JS: A population-based estimate of the prevalence of behavioral risk factors among adult cancer survivors and noncancer controls. Prev Med. 2005, 40 (6): 702-711. 10.1016/j.ypmed.2004.09.011.View ArticlePubMedGoogle Scholar
- Patterson RE, Neuhouser ML, Hedderson MM, Schwartz SM, Standish LJ, Bowen DJ: Changes in diet, physical activity, and supplement use among adults diagnosed with cancer. J Am Diet Assoc. 2003, 103 (3): 323-328.PubMedGoogle Scholar
- Maskarinec G, Murphy S, Shumay DM, Kakai H: Dietary changes among cancer survivors. Eur J Cancer Care. 2001, 10 (1): 12-20. 10.1046/j.1365-2354.2001.00245.x.View ArticleGoogle Scholar
- Bellizzi KM, Rowland JH, Jeffery DD, McNeel T: Health behaviors of cancer survivors: examining opportunities for cancer control intervention. J Clin Oncol. 2005, 23 (34): 8884-8893. 10.1200/JCO.2005.02.2343.View ArticlePubMedGoogle Scholar
- Satia JA, Campbell MK, Galanko JA, James A, Carr C, Sandler RS: Longitudinal changes in lifestyle behaviors and health status in colon cancer survivors. Cancer Epidemiol Biomarkers Prev. 2004, 13 (6): 1022-1031.PubMedGoogle Scholar
- Thorsen L, Nystad W, Dahl O, Klepp O, Bremnes RM, Wist E, Fossa SD: The level of physical activity in long-term survivors of testicular cancer. Eur J Cancer. 2003, 39 (9): 1216-1221. 10.1016/S0959-8049(03)00151-5.View ArticlePubMedGoogle Scholar
- Blanchard CM, Cokkinides V, Courneya KS, Nehl EJ, Stein K, Baker F: A comparison of physical activity of posttreatment breast cancer survivors and noncancer controls. Behav Med. 2003, 28 (4): 140-149.View ArticlePubMedGoogle Scholar
- Eakin EG, Youlden DR, Baade PD, Lawler SP, Reeves MM, Heyworth JS, Fritschi L: Health behaviors of cancer survivors: data from an Australian population-based survey. Cancer Causes Control. 2007, 18 (8): 881-894. 10.1007/s10552-007-9033-5.View ArticlePubMedGoogle Scholar
- Deshmukh-Taskar P, Nicklas TA, Yang SJ, Berenson GS: Does food group consumption vary by differences in socioeconomic, demographic, and lifestyle factors in young adults? The Bogalusa Heart Study. J Am Diet Assoc. 2007, 107 (2): 223-234. 10.1016/j.jada.2006.11.004.View ArticlePubMedPubMed CentralGoogle Scholar
- Hart S, Morrison C: Effect of age, family status, and physical activity on selected dietary components of TAC pilots. Mil Med. 1992, 157 (8): 397-401.PubMedGoogle Scholar
- Park CL, Gaffey AE: Relationships between psychosocial factors and health behavior change in cancer survivors: an integrative review. Ann Behav Med. 2007, 34 (2): 115-134.View ArticlePubMedGoogle Scholar
- Watters JL, Satia JA, Galanko JA: Associations of psychosocial factors with fruit and vegetable intake among African-Americans. Public Health Nutr. 2007, 10 (7): 701-711. 10.1017/S1368980007662284.View ArticlePubMedGoogle Scholar
- Nord C, Mykletun A, Thorsen L, Bjoro T, Fossa SD: Self-reported health and use of health care services in long-term cancer survivors. Int J Cancer. 2005, 114 (2): 307-316. 10.1002/ijc.20713.View ArticlePubMedGoogle Scholar
- Mokdad AH, Stroup DF, Giles WH: Public health surveillance for behavioral risk factors in a changing environment. Recommendations from the Behavioral Risk Factor Surveillance Team. MMWR Recomm Rep. 2003, 52 (RR-9): 1-12.PubMedGoogle Scholar
- Iachan R, Schulman J, Collins S, Powell-Griner E, Nelson DE: Methods for combining state BRFSS survey data for national estimation. Proceedings of the Section on Survey Reseasrch Methos, American Statistical Association. 1999, 711-714.Google Scholar
- Nelson DE, Holtzman D, Bolen J, Stanwyck CA, Mack KA: Reliability and validity of measures from the Behavioral Risk Factor Surveillance System (BRFSS). Soz Praventivmed. 2001, 46 Suppl 1: S3-42.PubMedGoogle Scholar
- Trost SG, Owen N, Bauman AE, Sallis JF, Brown W: Correlates of adults' participation in physical activity: review and update. Med Sci Sports Exerc. 2002, 34 (12): 1996-2001. 10.1097/00005768-200212000-00020.View ArticlePubMedGoogle Scholar
- Allison PJ: Factors associated with smoking and alcohol consumption following treatment for head and neck cancer. Oral Oncol. 2001, 37 (6): 513-520. 10.1016/S1368-8375(01)00015-X.View ArticlePubMedGoogle Scholar
- Kuntsche E, Rehm J, Gmel G: Characteristics of binge drinkers in Europe. Soc Sci Med. 2004, 59 (1): 113-127. 10.1016/j.socscimed.2003.10.009.View ArticlePubMedGoogle Scholar
- Payette H, Shatenstein B: Determinants of healthy eating in community-dwelling elderly people. Can J Public Health. 2005, 96 Suppl 3: S27-31, S30-5.PubMedGoogle Scholar
- Demark-Wahnefried W, Aziz NM, Rowland JH, Pinto BM: Riding the crest of the teachable moment: promoting long-term health after the diagnosis of cancer. J Clin Oncol. 2005, 23 (24): 5814-5830. 10.1200/JCO.2005.01.230.View ArticlePubMedPubMed CentralGoogle Scholar
- Amling CL, Riffenburgh RH, Sun L, Moul JW, Lance RS, Kusuda L, Sexton WJ, Soderdahl DW, Donahue TF, Foley JP, Chung AK, McLeod DG: Pathologic variables and recurrence rates as related to obesity and race in men with prostate cancer undergoing radical prostatectomy. J Clin Oncol. 2004, 22 (3): 439-445. 10.1200/JCO.2004.03.132.View ArticlePubMedGoogle Scholar
- Amling CL: Relationship between obesity and prostate cancer. Curr Opin Urol. 2005, 15 (3): 167-171. 10.1097/01.mou.0000165550.94663.fb.View ArticlePubMedGoogle Scholar
- Freedland SJ, Aronson WJ, Kane CJ, Presti JC, Amling CL, Elashoff D, Terris MK: Impact of obesity on biochemical control after radical prostatectomy for clinically localized prostate cancer: a report by the Shared Equal Access Regional Cancer Hospital database study group. J Clin Oncol. 2004, 22 (3): 446-453. 10.1200/JCO.2004.04.181.View ArticlePubMedGoogle Scholar
- USDHHS, USDA: Dietary guidelines for Americans, 2005. 2005, Washington, DC , U.S. Department of Health & Human Services, U.S. Department of AgricultureGoogle Scholar
- Moon K, Stukenborg GJ, Keim J, Theodorescu D: Cancer incidence after localized therapy for prostate cancer. Cancer. 2006, 107 (5): 991-998. 10.1002/cncr.22083.View ArticlePubMedGoogle Scholar
- Daubenmier JJ, Weidner G, Marlin R, Crutchfield L, Dunn-Emke S, Chi C, Gao B, Carroll P, Ornish D: Lifestyle and health-related quality of life of men with prostate cancer managed with active surveillance. Urology. 2006, 67 (1): 125-130. 10.1016/j.urology.2005.07.056.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2458/8/23/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.