Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2015 Oct 1.
Published in final edited form as: J Thorac Oncol. 2014 Oct;9(10):1459–1463. doi: 10.1097/JTO.0000000000000284

Socioeconomic status is associated with depressive severity among patients with advanced non-small cell lung cancer: Treatment setting and minority status do not make a difference

Christopher Fagundes 1, Desiree Jones 2, Elisabeth Vichaya 3, Charles Lu 4, Charles S Cleeland 3
PMCID: PMC4514021  NIHMSID: NIHMS709160  PMID: 25170640

Abstract

Introduction

Non-small cell lung cancer (NSCLC) is the leading cause of cancer-related morbidity and mortality. Unfortunately, patients with NSCLC have relatively poor survival rates compared with patients diagnosed with most other types of cancer. Accordingly, managing physical and mental health symptoms are important treatment goals. In the current investigation, we sought to determine whether individual socioeconomic status (SES; as indexed by level of education), racial/ethnic minority status, and hospital type (public vs. tertiary care center) were associated with NSCLC cancer patients’ depressive severity. Importantly, we investigated whether NSCLC patients’ individual SES was more or less prognostic of their depressive severity compared with minority status and the hospital context where they received treatment.

Methods

Patients scheduled for chemotherapy were assessed for depressed mood by the Beck Depression Inventory-II (BDI-II). Data were collected at baseline, and at approximately 6, 12, and 18 weeks.

Results

NSCLC patients with less education had more depressive severity than those with more education. Treatment setting and minority status were not associated with depressive severity. The interaction between education level and treatment setting predicting depressive severity was not significant suggesting that the association between education level and depressive severity did not differ by treatment setting.

Conclusion

Our study brings heightened awareness to the substantial, persistent SES differences that exist in depressive severity among late-stage NSCLC patients. Furthermore, these findings appear to persist regardless of minority status and whether the patient is treated at a public hospital or tertiary cancer center.

Keywords: Depression, quality of life, socioeconomic status, non-small cell lung cancer, medically underserved


Health disparities increase with each step down the socioeconomic status (SES) ladder. 1 Whether indexed by education, income, or job status, being low SES is associated with poor health.1 For most cancers, lower SES individuals are at greater risk for both incidence and mortality compared with those who are higher SES.2, 3 Much less is known about how SES impacts cancer patients’ mental and physical well-being.

Non-small cell lung cancer (NSCLC) is the leading cause of cancer-related morbidity and mortality.4 Unfortunately, patients with NSCLC have relatively poor survival rates compared with patients diagnosed with most other types of cancer. Accordingly, managing physical and mental health symptoms are important treatment goals.5 In order to improve NSCLC patients’ quality of life (QOL), it is imperative to identify factors associated with physical and mental well-being.

Recently, we demonstrated that lower SES individuals (as indexed by level of education) with advanced non-small cell lung cancer (NSCLC) had poorer physical well-being (i.e. pain, fatigue, disturbed sleep, shortness of breath, drowsiness) during chemotherapy compared with those who were higher SES.5 Likewise, NSCLC patients who were treated at public hospitals with good performance status were more likely to suffer from these symptoms compared with those treated at a tertiary care centers.5 Importantly, these findings persisted over 15 weeks of therapy.5

In the current investigation, we sought to determine whether SES, racial and ethnic minority status, and hospital type (pubic vs. tertiary care center) were associated with NSCLC cancer patients’ depressive severity over 15 weeks of therapy. Depression severity is an important aspect of mental well-being and one of the strongest predictors of QOL for cancer patients.6 Cancer patients’ depression is also a major contributor to their close family members’ well-being.7 Importantly, we investigated whether NSCLC patients’ individual SES was more or less prognostic of their depressive severity compared with the hospital context where they received treatment, and their status as a racial or ethnic minority.

Study Participants

Advanced stage (IIIB-IV) NSCLC patients who were scheduled for chemotherapy were recruited for this study between January 2004 and December 2008. They were recruited from thoracic medical oncology clinics of a tertiary cancer center in Houston, Texas and from the general oncology clinics of 3 public hospitals (2 in Houston, 1 in Miami, Florida) providing care for medically underserved (non-insured/underinsured and/or low-income) patients.8 The study was approved by the institutional review boards of the participating institutions. All patients gave informed consent to participate. The study time period was limited to the first 18 weeks of treatment based on a standard chemotherapy protocol that included 6, 3-week cycles of treatment.

Of 234 eligible patients approached to participate in the study, 189 consented to participate. Four withdrew before baseline assessment, such that 185 were included in the final analysis. Of these, 102 were recruited from the tertiary cancer center and 83 from the public hospitals. All 185 patients contributed data at baseline, 140 at 6 weeks, 107 at 12 weeks, and 79 at 18 weeks from the start of the study (Figure. 1).

Figure 1.

Figure 1

Flow of participants through the study. NSCLC indicates Non Small Cell Lung Cancer.

Measures

The Beck Depression Inventory II (BDI-II)9 is a widely used instrument for measuring the intensity of depression. It contains 21 items that assess various aspects of depression. Each item is rated on a 4-point scale, resulting in a maximum attainable score of 63. A higher total score indicates more-severe depressive severity. The BDI-II has high clinical sensitivity with a reliability coefficient of 0.92 and predictive validity of 0.91.9 Assessments were obtained at baseline and at 6, 12, and 18 weeks from initiation of chemotherapy using the BDI-II’s standard cut points.9 The BDI-II has been found to be a reliable measure of depression across race/ethnicity and gender10, 11.

Comorbidities

The Charlson index is the most widely used comorbidity index. Originally developed for predicting mortality in breast cancer patients, it has now been widely used with both cancer and noncancer populations.12

Demographic and clinical variables

Participants answered questions about their age, race, highest level of education, marital status, and gender. Following participants’ authorization, electronic medical records were reviewed to obtain initial treatment date. Educational level was used to assess the women in our sample as has been done in previous studies using cancer populations that included older adult women because it was difficult to know if the women in our same sample worked outside the home.13 In addition, education is less vulnerable to fluctuations in current income and job status.1416 Participants reported number of years of formal schooling they had received to indicate level of education.

Analytic Method

Education was modeled as a continuous variable based on prior work showing that the association between SES and health is monotonic (i.e., the association between SES and health shows a gradient increase).17, 18 Descriptive statistics, including means, standard deviations (SD) and percentages were used to describe patient demographics and clinical characteristics. Using mixed models regression, we addressed the question of whether SES (as indexed by level of education), minority status, and hospital type were associated with depressive severity across visits. We utilized restricted information maximum likelihood (REML) estimation to fit all models. REML is superior to listwise deletion for handling attrition.19 It performs well when data are missing at random and improves nonrandom circumstances over ignoring cases entirely.20 We employed an unstructured within-subjects covariance matrix and examined the model residuals to confirm that they were distributed normally. We included education, visit, minority status, time since treatment, marital status, comorbidities, sex, age, and stage in the model. Age and depressive severity were time-varying. All other variables were time invariant.

In ancillary analyses, we adjusted for cancer treatment rather than cancer stage (stage and treatment type are highly related and were not entered simultaneously to avoid multicollinearity); none of the results presented below changed. We also created a variable indicating if and when a patient dropped out at any time before the end of the study; we included this variable in ancillary analyses to ensure it did not bias the results.

Results

Preliminary Analyses

Patient demographic and clinical characteristics by treatment site (tertiary vs. public) are presented in Table 1. A higher proportion of patients at the tertiary center had stage IV disease. Patients at the tertiary center were more likely to be married, have attended college, be employed, or be retired. Individuals who were lost to attrition did not significantly differ on any of the study variables compared with those who completed both visits. Those who were less educated were more likely to be treated at a public hospital compared with a tertiary cancer center (r = −.42, p = .001). Across all visits and groups, 67.1% experienced minimal depressive severity, 18.8% experienced mild depressive severity, 9.0% experienced moderate depressive severity, and 5.2% experienced severe depressive severity.

Table 1.

Sample Characteristics by Treatment Site

Characteristic Tertiary (n = 102) Public (n = 83) P
No. (%) No. (%)
Age
 Mean (years) 61.3 58 .012
 Standard Deviation 9.4 8.1
Gender
 Men 67 (65.7) 49 (59.0) .352
 Women 35 (34.3) 34 (41.0)
Marital status
 Married 84 (82.4) 32 (38.6) <.001
 Unmarried 18 (17.6) 51 (61.4)
Education level
 Mean (years) 13.6 10.7 <.001
 Standard Deviation 3.1 3.3
Job status
 Employed outside the home 24 (24.0) 13 (15.7) <.001
 Homemaker 8 (8.0) 3 (3.6)
 Retired 43 (43.0) 13 (15.7)
 Medical leave or disability 23 (23.0) 32 (38.6)
 Unemployed/other 2 (2.0) 22 (26.5)
Ethnicity
 Asian 0 (0.0) 1 (1.2) <.001
 Black Non-Hispanic 7 (6.9) 38 (45.8)
 Hispanic 1 (1.0) 25 (30.1)
 White Non-Hispanic 94 (92.2) 19 (22.9)
Cancer stage
 IIIB 7 (6.9) 29 (34.9) <.001
 IV 95 (93.1) 54 (65.1)
Previous treatment
 Chemotherapy 27 (26.5) 18 (21.7) .538
 Surgery 19 (18.6) 3 (3.6) .002
 Radiation 37 (36.3) 16 (19.3) .016
 Treatment naïve 59 (57.8) 29 (34.9) .008
Charlson comorbidity score
 0 to 1 69 (68.3) 64 (81.0) .054
 2+ 32 (31.7) 15 (19.0)

Analyses

As can be seen in Table 2, participants with more education had less depressive severity than those with less education. The interaction between education and time was not significant (b = −.01, p = .61) demonstrating that the association between education and depressive severity did not differ across visits. Treatment setting was not associated with depressive severity. Likewise, treatment setting did not interact with visit (b = −.01, p = .25). Those who were members of a racial/ethnic minority group did not experience more depressive severity than those who were not. To estimate the magnitude that depressive severity differed by level of education between participants lower and higher in educational level, we used the covariate-adjusted means at 1 standard deviation above and below the mean level of education. Participants with less education (−1 SD) had 42.5% more depressive severity than those with more education (+1 SD).

Table 2.

Summary of Mixed Models Analysis Predicting Depression Severity

Variable Depression Severity
B SE p 95% CI
Visit −.019 .02 .42 −.06 .03
Time Since Treatment .000 .00 .29 −.00 .00
Race (0=nonwhite, 1=white) .07 .017 .69 −.27, .41
Stage −.09 .15 .56 −.40, .21
Comorbidities −.02 .05 .65 −.12, .08
Married .08 .14 .58 −.20, .35
Age −.01 .01 .41 −.02, .01
Sex (Male=0, Female=1) −.01 .12 .94 −.25, .24
Education Level −.07 .03 .04 −.13, −.01
Treatment Site (1=Tertiary, 2=Public) .18 .18 .30 −.16, .53

In ancillary analyses, we tested for the interaction between education level and treatment setting predicting depressive severity and it was not significant (b = .01, p = .66). Finally, we adjusted for drop out by including a covariate that modeled number of time points completed. Educational level was still associated depressive severity (b = −.07, p = .04), while treatment setting was not (b = .22, p = .22).

Discussion

Higher SES (as indexed by education) NSCLC patients had less depressive severity than those who were lower SES. This association persisted irrespective of whether or not the patients were members of an ethnic or racial minority group. It also persisted regardless of whether the patients were treated at a public hospital or a tertiary cancer center. In fact, NSCLC patients treated at tertiary cancer centers were no less likely to experience elevated levels of depressive severity than those treated at public hospitals.

Previous studies have reported that medically underserved cancer patients are more likely to suffer from depression compared with others.21, 22 However, this is the first study, to our knowledge, to compare the impact of patients’ individual SES relative to their treatment context. This is particularly important given our prior work that demonstrated that treatment context (i.e. public vs. tertiary cancer center) was a major factor associated with NSCLC patients’ physical well-being as indexed by a composite symptom burden index.5

There are several factors that may explain the association between SES and depressive severity among NSCLC patients. As previously reported, those who are low SES suffer from more physical symptoms compared with those who are higher SES.5 Indeed, physical symptoms can enhance depressive severity.23 Furthermore, lower SES individuals do not benefit from same quality of social support as higher SES individuals because their support network has many competing demands.13 High quality social support is one of the most effective ways to buffer against stress and depression during a stressful life event.24, 25

Depression is a risk factor for mortality among NSCLC patients such that those who were depressed had twice the risk of death compared to non-depressed patients.26 Recent work demonstrated that interventions aimed at improving depressive severity and symptom control among those with NSCLC may also promote longer survival.27 These interventions may be particularly beneficial for low SES individuals.

This study has several limitations. First, it included patients from a single tertiary center; thus, generalization of our results to other tertiary centers is not warranted. Second, it did not include patients from community care settings. It would be interesting for future studies to use income and job status in addition to education to evaluate SES. Finally, this study included patients with advanced NSCLC only; thus, results may not be generalizable to patients with other types of cancer or less advanced disease. Future studies to assess patients’ depression should include longitudinal designs and incorporate patients from multiple public, community, and tertiary care centers.

Our study brings heightened awareness to the substantial, persistent SES differences that exist in depressive severity among late-stage NSCLC patients. Clinicians in all treatment facilities should screen for depression and institute early and appropriate management. These interventions may improve quality of life and even impact survival time.2731

Acknowledgments

FUNDING SOURCES

This work was supported by the National Cancer Institute at The National Institutes of Health (grant number NIH/NCI R01 CA026582 to Charles S. Cleeland), the Hawn Foundation, and the University Cancer Foundation.

The authors thank Jeanie F. Woodruff, ELS, Department of Symptom Research at MD Anderson for editorial services, and Gary M. Mobley and Katherine R. Gilmore at MD Anderson for data management.

Footnotes

The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Cancer Institute or the National Institutes of Health.

CONFLICT OF INTEREST DISCLOSURES

The authors made no disclosures.

References

  • 1.Adler N, Rehkopf D. US disparities in health: descriptions, causes, and mechanisms. Public Health. 2008;29:235. doi: 10.1146/annurev.publhealth.29.020907.090852. [DOI] [PubMed] [Google Scholar]
  • 2.Stowe R, Peek M, Perez N, Yetman D, Cutchin M, Goodwin J. Herpesvirus reactivation and socioeconomic position: a community-based study. Journal of Epidemiology and Community Health. 2010;64:666. doi: 10.1136/jech.2008.078808. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Ward E, Jemal A, Cokkinides V, et al. Cancer disparities by race/ethnicity and socioeconomic status. CA: A Cancer Journal for Clinicians. 2004;54:78–93. doi: 10.3322/canjclin.54.2.78. [DOI] [PubMed] [Google Scholar]
  • 4.Cancer Facts and Figures. 2011 Available from : http://www.cancer.org/acs/groups/content/@epidemiologysurveilance/documents/document/acspc-029771.pdf.
  • 5.Cleeland CS, Mendoza TR, Wang XS, et al. Levels of symptom burden during chemotherapy for advanced lung cancer: differences between public hospitals and a tertiary cancer center. J Clin Oncol. 2011;29:2859–2865. doi: 10.1200/JCO.2010.33.4425. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Visser M, Smets E. Fatigue, depression and quality of life in cancer patients: how are they related? Supportive Care in Cancer. 1998;6:101–108. doi: 10.1007/s005200050142. [DOI] [PubMed] [Google Scholar]
  • 7.Kurtz ME, Kurtz J, Given CW, Given B. Relationship of caregiver reactions and depression to cancer patients’ symptoms, functional states and depression—a longitudinal view. Social Science & Medicine. 1995;40:837–846. doi: 10.1016/0277-9536(94)00249-s. [DOI] [PubMed] [Google Scholar]
  • 8.U.S. Department of Health and Human Services, Health Resources and Sevices Administration. Shortage designation: Medically underserved areas and populations. Available from : http://bhpr.hrsa.gov/shortage/muaguide.htm.
  • 9.Beck AT, Brown G, Steer RA. Beck Depression Inventory II Manual. San Antonio, TX: 1996. [Google Scholar]
  • 10.Osman A, Downs WR, Barrios FX, Kopper BA, Gutierrez PM, Chiros CE. Factor structure and psychometric characteristics of the Beck Depression Inventory-II. Journal of Psychopathology and Behavioral Assessment. 1997;19:359–376. [Google Scholar]
  • 11.Whisman MA, Judd CM, Whiteford NT, Gelhorn HL. Measurement Invariance of the Beck Depression Inventory–Second Edition (BDI-II) Across Gender, Race, and Ethnicity in College Students. Assessment. 2013;20:419–428. doi: 10.1177/1073191112460273. [DOI] [PubMed] [Google Scholar]
  • 12.Dobnig H, Pilz S, Scharnagl H, et al. Independent association of low serum 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D levels with all-cause and cardiovascular mortality. Archives of Internal Medicine. 2008;168:1340–1349. doi: 10.1001/archinte.168.12.1340. [DOI] [PubMed] [Google Scholar]
  • 13.Collins NL. Working models of attachment: Implications for explanation, emotion, and behavior. Journal of Personality and Social Psychology. 1996;71:810. doi: 10.1037//0022-3514.71.4.810. [DOI] [PubMed] [Google Scholar]
  • 14.Marmot M, Fuhrer R, Ettner S, Marks N, Bumpass L, Ryff C. Contribution of psychosocial factors to socioeconomic differences in health. Milbank Quarterly. 1998;76:403–448. doi: 10.1111/1468-0009.00097. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Gorman B, Sivaganesan A. The role of social support and integration for understanding socioeconomic disparities in self-rated health and hypertension. Social Science & Medicine. 2007;65:958–975. doi: 10.1016/j.socscimed.2007.04.017. [DOI] [PubMed] [Google Scholar]
  • 16.Winkleby M, Jatulis D, Frank E, Fortmann S. Socioeconomic status and health: how education, income, and occupation contribute to risk factors for cardiovascular disease. American Journal of Public Health. 1992;82:816. doi: 10.2105/ajph.82.6.816. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Adler N, Boyce T, Chesney M, et al. Socioeconomic status and health. American Psychologist. 1994;49:15–24. doi: 10.1037//0003-066x.49.1.15. [DOI] [PubMed] [Google Scholar]
  • 18.Gallo L, Bogart L, Vranceanu A, Matthews K. Socioeconomic status, resources, psychological experiences, and emotional responses: A test of the reserve capacity model. Journal of Personality and Social Psychology. 2005;88:386–399. doi: 10.1037/0022-3514.88.2.386. [DOI] [PubMed] [Google Scholar]
  • 19.Jeličič H, Phelps E, Lerner RM. Use of missing data methods in longitudinal studies: The persistence of bad practices in developmental psychology. Developmental Psychology. 2009;45:1195–1199. doi: 10.1037/a0015665. [DOI] [PubMed] [Google Scholar]
  • 20.Schafer JL, Graham JW. Missing data: Our view of the state of the art. Psychological Methods. 2002;7:147–177. [PubMed] [Google Scholar]
  • 21.Luckett T, Goldstein D, Butow PN, et al. Psychological morbidity and quality of life of ethnic minority patients with cancer: a systematic review and meta-analysis. Lancet Oncol. 2011;12:1240–1248. doi: 10.1016/S1470-2045(11)70212-1. [DOI] [PubMed] [Google Scholar]
  • 22.Simon AE, Wardle J. Socioeconomic disparities in psychosocial wellbeing in cancer patients. European Journal of Cancer. 2008;44:572–578. doi: 10.1016/j.ejca.2007.12.013. [DOI] [PubMed] [Google Scholar]
  • 23.Fishbain DA, Cutler R, Rosomoff HL, Rosomoff RS. Chronic pain-associated depression: antecedent or consequence of chronic pain? A review. The Clinical journal of pain. 1997;13:116–137. doi: 10.1097/00002508-199706000-00006. [DOI] [PubMed] [Google Scholar]
  • 24.Cohen S, Wills TA. Stress, social support, and the buffering hypothesis. Psychological bulletin. 1985;98:310. [PubMed] [Google Scholar]
  • 25.Stice E, Ragan J, Randall P. Prospective relations between social support and depression: differential direction of effects for parent and peer support? Journal of Abnormal Psychology. 2004;113:155. doi: 10.1037/0021-843X.113.1.155. [DOI] [PubMed] [Google Scholar]
  • 26.Chen ML, Chen MC, Yu CT. Depressive symptoms during the first chemotherapy cycle predict mortality in patients with advanced non-small cell lung cancer. Support Care Cancer. 2011;19:1705–1711. doi: 10.1007/s00520-010-1005-8. [DOI] [PubMed] [Google Scholar]
  • 27.Temel JS, Greer JA, Muzikansky A, et al. Early palliative care for patients with metastatic non-small-cell lung cancer. N Engl J Med. 2010;363:733–742. doi: 10.1056/NEJMoa1000678. [DOI] [PubMed] [Google Scholar]
  • 28.Bakitas M, Lyons KD, Hegel MT, et al. Effects of a palliative care intervention on clinical outcomes in patients with advanced cancer: the Project ENABLE II randomized controlled trial. JAMA. 2009;302:741–749. doi: 10.1001/jama.2009.1198. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Giese-Davis J, Collie K, Rancourt KM, Neri E, Kraemer HC, Spiegel D. Decrease in depression symptoms is associated with longer survival in patients with metastatic breast cancer: a secondary analysis. J Clin Oncol. 2011;29:413–420. doi: 10.1200/JCO.2010.28.4455. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Hopwood P, Stephens RJ. Depression in patients with lung cancer: prevalence and risk factors derived from quality-of-life data. J Clin Oncol. 2000;18:893–903. doi: 10.1200/JCO.2000.18.4.893. [DOI] [PubMed] [Google Scholar]
  • 31.Carlson LEWA, Mitchell AJ. Screening for distress and umnet needs in patients with cancer: review and recommendations. J Clin Oncol. 2012;30(11):1160–77. doi: 10.1200/JCO.2011.39.5509. [DOI] [PubMed] [Google Scholar]

RESOURCES