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JNCI Cancer Spectrum logoLink to JNCI Cancer Spectrum
. 2021 Jan 23;5(1):pkaa123. doi: 10.1093/jncics/pkaa123

Factors Associated With Health-Related Quality of Life Among Cancer Survivors in the United States

Xuesong Han 1,, L Ashley Robinson 1,2,3, Roxanne E Jensen 4, Tenbroeck G Smith 5, K Robin Yabroff 1
PMCID: PMC7883550  PMID: 33615136

Abstract

Background

With increasing prevalence of cancer survivors in the United States, health-related quality of life (HRQOL) has become a major priority. We describe HRQOL in a nationally representative sample of cancer survivors and examine associations with key sociodemographic, clinical, and lifestyle characteristics.

Methods

Cancer survivors, defined as individuals ever diagnosed with cancer (N = 877), were identified from the 2016 Medical Expenditure Panel Survey-Experiences with Cancer Survivorship Supplement, a nationally representative survey. Physical and mental health domains of HRQOL were measured by the Global Physical Health (GPH) and Global Mental Health (GMH) subscales of the Patient-Reported Outcomes Measurement Information System Global-10. Multivariable linear regression was used to examine associations of sociodemographic, clinical, and lifestyle factors with GPH and GMH scores. All statistical tests were 2-sided.

Results

Cancer survivors’ mean GPH (49.28, SD = 8.79) and mean GMH (51.67, SD = 8.38) were similar to general population means (50, SD = 10). Higher family income was associated with better GPH and GMH scores, whereas a greater number of comorbidities and lower physical activity were statistically significantly associated with worse GPH and GMH. Survivors last treated 5 years ago and longer had better GPH than those treated during the past year, and current smokers had worse GMH than nonsmokers (all β > 3 and all P <.001).

Conclusions

Cancer survivors in the United States have generally good HRQOL, with similar physical and mental health scores to the general US population. However, comorbidities, poor health behaviors, and recent treatment may be risk factors for worse HRQOL. Multimorbidity management and healthy behavior promotion may play a key role in maximizing HRQOL for cancer survivors.


There were 16.9 million cancer survivors in the United States in 2019 (1). More than two-thirds are long-term survivors, having lived 5 or more years since their cancer diagnoses (2). Cancer survivors often experience long-term and late effects of treatment, leading to impaired health-related quality of life (HRQOL) (3‐7). Survivors prioritize optimizing HRQOL as a goal in their long-term care and life decisions (8,9). Oncology research increasingly uses HRQOL as an important outcome in observational studies, interventions, and health surveillance (10,11). Oncology practice increasingly uses patient-reported outcomes to identify cancer patients’ needs related to symptoms, psychosocial needs, and HRQOL (10,11).

Previous research among selected populations of cancer survivors suggests that poor HRQOL is associated with low socioeconomic status, lack of private insurance, comorbid conditions, and intensive treatment (3,5,12‐16). Poor HRQOL is also associated with lifestyle factors such as obesity and physical inactivity (6,13,17‐19). Few studies (4,6,7) have examined HRQOL among nationally representative, population-based samples of cancer survivors, but they were based on older data before 2011. Advances in treatment may result in different symptoms and late effects from traditional therapies (20‐23). Moreover, a number of efforts have been implemented to improve care of cancer survivors, including survivorship care plans highlighting discussions of late and long-term effects of treatment, the need for follow-up care, lifestyle recommendations, and emotional and social needs (24,25). Thus, a current evaluation of the HRQOL for US cancer survivors is needed.

The Medical Expenditure Panel Survey (MEPS) has been collecting data on health status and health care use and expenditures among a nationally representative sample of the noninstitutionalized US population since 1996 (26). In 2016, a supplemental questionnaire designed to measure patient experiences with cancer was fielded to eligible MEPS participants self-reporting a history of cancer; it is referred to as the MEPS Experiences with Cancer Survivorship Supplement (MEPS-ECSS) (27). The MEPS-ECSS provides a nationally representative sample of cancer survivors who have provided HRQOL information using the Patient-Reported Outcomes Measurement Information System (PROMIS) measures of physical and mental health, making it well suited to investigate HRQOL among cancer survivors. Using information from the MEPS-ECSS, we examined HRQOL and its association with key sociodemographic, clinical, and lifestyle factors among cancer survivors.

Methods

Sample Population

Adult cancer survivors were identified from the 2016 MEPS-ECSS conducted by the Agency for Healthcare Research and Quality (26,27). The ECSS used a mailed questionnaire to collect data about cancer survivorship, health-care access, ability to participate in usual activities and work, health insurance, and quality of life. The response rate for 2016 MEPS was 46.0%, and the response rate for the ECSS was 81.2%, yielding an overall response rate of 37.4% (26). Because the MEPS data are deidentified and publicly accessible, the study does not constitute human participant research and an institutional review board approval was not required.

From the 1236 cancer survivors, after excluding individuals diagnosed solely with nonmelanoma skin cancer or skin cancer of unknown type (n = 267), who did not answer all HRQOL questions (n = 72), or who were uninsured (n = 20), due to small number and its high correlation with age, our analytic sample included 877 cancer survivors ages 18 years and older (Supplementary Figure 1, available online).

Outcome Variables

The MEPS-ECSS included 8 questions (Supplementary Table 1, available online) from the PROMIS Global Health 10, excluding the 2 questions on general health and satisfaction with social roles that do not contribute to scale scores (28). Four of the 8 items (physical health, physical function, fatigue, and pain interference) reflect different aspects of physical health and contribute to a Global Physical Health (GPH) score, and another 4 items (quality of life, mental health, social support, and emotional problems) reflect different aspects of mental health and contribute to a Global Mental Health (GMH) score (28). Higher scores represent better HRQOL. The PROMIS Global Health has been validated for use in research and clinical settings (28‐30).

The GPH and GMH were our primary outcomes. Raw scores for GPH and GMH were converted into T-scores (Supplementary Table 2, available online; T-score distributions of both GPH and GMH are standardized such that 50 represents the mean for the US general population with a SD of 10) (31) and analyzed as continuous variables. A difference of 3.0-5.0 points is considered a meaningful difference (32). Ratings of 2 items measuring pain and fatigue (common symptoms in cancer survivors) were dichotomized and examined as secondary outcomes. For cancer pain interference, a score of 4 or higher on a 10-point scale indicated moderate or severe interference (33); for fatigue, we dichotomized the 5-point scale responses of “moderate,” “severe,” or “very severe” vs “mild” or “none” based on distribution (Supplementary Figure 2, available online) and for consistency with the pain dichotomization.

Sociodemographic, Clinical, and Lifestyle Characteristics

Self-reported independent variables were selected based on a priori knowledge on risk factors of HRQOL, including age (18-54 years, 55-64 years, 65-74 years, 75+ years), sex, race and ethnicity (non-Hispanic White or other), marital status (married or widowed, divorced, separated, or never married), education level (less than high school graduate, high school graduate, some college or more), family income level (low [<139% federal poverty level (FPL)], middle [139%-400% FPL], high [400%+ FPL]), health insurance coverage (any private, public only), and employment status (employed, retired, unable to work because of illness or disability or having a job to return to, not working for other reasons). As widely used by previous studies (34‐36), comorbidities were measured using MEPS priority conditions, including arthritis, asthma, diabetes, emphysema, heart disease (angina, coronary heart disease, heart attack, other heart conditions or diseases), high cholesterol, hypertension, and stroke. The total numbers of comorbidities were also categorized for each respondent (0, 1, 2, 3, or 4+). Cancer types were grouped in the following categories: female breast, prostate, colorectal, cervical, melanoma, uterine, and other (including bladder, lung, lymphoma, and other less common cancer types). They were combined with sex and regrouped into female breast cancer only, prostate cancer only, female other, and male other to obtain stable estimation in modeling based on the sex differences in HRQOL (4,13) and distribution of cancer types in both sexes. Years since last treatment were categorized as less than 1, 1 to less than 5, 5 or longer, and never treated or missing. Weight status was categorized as normal weight (body mass index [BMI] = 18.5-24.9 kg/m2), overweight (BMI = 25-29.9 kg/m2), obese (BMI = 30+ kg/m2), or other (BMI <18.5 kg/m2 or unknown). Meeting physical activity guidelines (yes or no/unknown) was defined as currently spending 0.5 hour or more in moderate to vigorous physical activity at least 5 times per week, per the American Cancer Society physical activity guidelines for cancer survivors (37). Cigarette smoking status was measured as currently smoking (yes or no/unknown).

Statistical Analyses

Sample characteristics were summarized with descriptive statistics. Sample weights were used to estimate the size of the survivor population in the United States in each category. The distributions of the GPH and GMH raw scores and T-scores were calculated for the total sample (Supplementary Figure 2, available online). Generalized linear regression models were fitted to examine the associations of sociodemographic, clinical, and lifestyle factors with GPH and GMH T-scores; logistic regressions were used for pain and fatigue. Bivariable and multivariable regression models were fitted. Sex and cancer type were combined into 1 variable in multivariable models, employment status was excluded from multivariable models due to high collinearity with age, and number of comorbid conditions and exact comorbid conditions were included in the multivariable models alternatively. P values for each level of independent variables were presented to indicate the HRQOL variation across different groups defined by each specific characteristic factor. A P value of less than .05 with parameter estimate of 3.0 or greater was considered a statistically significant and clinically meaningful difference. All statistical tests were 2-sided. Analyses were conducted with SAS 9.4 (Cary, NC). All analyses incorporated weighting to account for the complex survey design and survey nonresponse.

Results

Among the 877 cancer survivors, which represent 13.4 million survivors nationally, the majority were 65 years or older (59.9%), female (60.5%), non-Hispanic White (81.6%), married (58.3%), with at least high school education (86.4%), with any private insurance (66.0%), and not employed (65.0%) (Table 1). Nearly 90% had at least 1 comorbidity, and about one-half had 3 or more comorbidities. The most common comorbidities were hypertension, arthritis, and high cholesterol. Female breast cancer and prostate cancer were the most common types of cancer reported. A total of 43% were treated for their cancer within the past 5 years. Most survivors were overweight or obese (65.8%), did not meet physical activity guidelines (56.9%), and were not current smokers (89.1%), representing 8.9 million, 7.6 million, and 11.9 million survivors in the nation, respectively (Table 1).

Table 1.

Characteristics and HRQOL of cancer survivors, MEPS 2016

Characteristic Sample, No. Weighted % Weighted No. (million) GPH T-score
Mean (SD)
GMH T-score
Mean (SD)
Total 877 100.0 13.4 49.28 (8.79) 51.67 (8.38)
Sociodemographic factors
 Age group, y
  18-54 186 19.9 2.7 48.49 (8.98) 49.74 (8.66)
  55-64 170 20.1 2.7 51.51 (8.48) 53.08 (8.36)
  65-74 252 29.4 3.9 49.31 (8.95) 51.21 (8.40)
  ≥75 269 30.5 4.1 48.29 (8.55) 52.47 (8.01)
 Sex
  Male 337 39.5 5.3 50.06 (8.09) 51.84 (7.53)
  Female 540 60.5 8.1 48.77 (9.24) 51.57 (8.95)
 Race/ethnicity
  Non-Hispanic White only 594 81.6 10.9 49.75 (8.56) 52.30 (8.22)
  All other race/ethnicities 283 18.4 2.5 47.21 (9.74) 48.93 (8.81)
 Current marital status
  Married 473 58.3 7.8 50.37 (7.98) 52.86 (7.95)
  Not marrieda 404 41.7 5.6 47.74 (9.74) 50.03 (8.81)
 Educational attainment
  Less than high school graduate 159 13.6 1.8 43.48 (9.63) 46.73 (8.85)
   High school graduate 254 28.2 3.8 47.76 (8.44) 50.02 (8.14)
  Some college or more 462 58.2 7.8 51.34 (8.26) 53.58 (7.95)
 Family income as percent of poverty line
  Low income <139% 224 19.3 2.6 44.39 (9.55) 47.48 ± 9.78
  Middle income 139%-400% 323 34.0 4.5 47.18 (9.06) 49.77 ± 8.12
  High income >400% 330 46.7 6.2 52.83 (7.26) 54.80 ± 7.21
 Health insurance coverageb
  Any private 518 66.0 8.8 51.44 (7.88) 53.42 ± 7.85
  Public only 359 34.0 4.5 45.08 (9.61) 48.30 ± 8.86
 Employment status
  Employed 276 35.0 4.7 54.07 (7.15) 54.89 (7.43)
  Retired 312 37.5 5.0 49.96 (7.35) 53.27 (6.96)
  Unable to work because ill/disabled 150 13.9 1.9 38.64 (7.75) 42.60 (7.47)
  Not working for other reasons 139 13.7 1.8 45.96 (10.31) 48.32 (10.13)
Clinical factors
 No. of comorbid conditionsc
  0 88 10.4 1.4 55.00 (7.35) 55.53 (7.23)
  1 166 18.1 2.4 54.48 (7.11) 54.39 (7.36)
  2 167 21.3 2.9 50.81 (8.14) 53.45 (7.51)
  3 188 20.5 2.7 49.20 (7.67) 51.89 (7.76)
  ≥4 268 29.7 4.0 43.05 (8.81) 47.24 (9.15)
 Comorbid conditionc
  Arthritis 504 58.3 7.8 46.75 (8.71) 50.15 (8.73)
  Asthma 111 11.4 1.5 44.73 (11.18) 47.11 (10.18)
   Diabetes 184 19.3 2.6 43.28 (9.48) 47.29 (8.55)
   Emphysema 66 7.7 1.0 41.51 (8.12) 44.37 (8.12)
   Heart disease 300 36.3 4.8 46.11 (9.02) 50.19 (9.16)
   High cholesterol 488 56.0 7.5 47.98 (8.67) 50.85 (8.44)
   Hypertension 550 59.6 8.0 47.12 (8.99) 50.14 (8.46)
   Stroke 100 10.7 1.4 41.92 (7.65) 45.51 (9.23)
 Cancer type
   Female breast 224 25.5 3.4 49.95 (9.94) 52.41 (9.27)
   Prostate 155 16.8 2.2 51.38 (9.11) 54.29 (8.59)
   Colorectal 83 9.0 1.2 47.76 (10.63) 50.28 (9.32)
   Melanoma 69 9.9 1.3 50.39 (10.53) 54.04 (8.81)
   Cervical 69 7.1 0.9 47.75 (10.05) 49.31 (9.67)
   Uterus 56 6.6 0.9 49.17 (8.73) 52.64 (10.49)
   Other 275 31.1 4.2 47.58 (10.83) 49.62 (10.32)
 Years since last cancer treatment
   <1 209 23.9 3.2 46.31 (8.44) 49.88 (8.09)
   1 to <5 173 19.1 2.6 48.67 (8.02) 50.74 (7.19)
   ≥5 379 44.5 5.9 50.89 (9.10) 52.79 (8.82)
   Never treated/missing 116 12.5 1.7 50.17 (8.74) 52.60 (8.97)
 Lifestyle factors
  BMI, kg/m2
   18.5 to 24.9 242 28.5 3.8 51.78 (8.80) 53.13 (8.56)
   25 to 29.9 283 32.3 4.3 51.25 (7.63) 53.41 (8.14)
   ≥30 304 33.5 4.5 46.00 (8.84) 49.29 (8.16)
   <18.5 or unknown 48 5.8 0.8 44.93 (9.54) 48.66 (7.02)
 Meeting physical activity guidelinesd
   Yes 336 43.1 5.8 53.63 (7.65) 54.99 (7.52)
   No/unknown 511 56.9 7.6 45.98 (8.63) 49.17 (8.42)
 Current smoker
   Yes 104 10.9 1.5 43.88 (8.86) 43.73 (8.26)
   No/unknown 773 89.1 11.9 49.94 (8.62) 52.65 (8.04)
a

Not married includes widowed, divorced, separated, or never married.

b

Public insurance includes Medicare, Medicaid, and/or other public hospital or physician coverage. TRICARE/CHAMPVA was treated as private coverage, as were employer-based, union-based, and other private insurance.

c

Comorbid conditions include arthritis, asthma, diabetes, emphysema, heart disease (angina, coronary heart disease, heart attack, other heart condition/disease), high cholesterol, hypertension, and stroke.

d

Meeting physical activity guidelines defined as currently spending one-half hour or more in moderate to vigorous physical activity at least 5 times per week.

BMI = body mass index; GMH = global mental health; GPH = global physical health; HRQOL = health-related quality of life; MEPS = Medical Expenditure Panel Survey.

The GPH and GMH T-scores of survivors in our sample (mean [SD] = 49.28 [8.79] and 51.67 [8.38], respectively) were similar to scores in the general population (ie, within 3 points of the general population means of 50) (Table 1). T-scores (mean [SD]) in subpopulations of cancer survivors indicated the worst physical HRQOL in those unemployed due to illness or disability (38.64 [7.75]) and those with comorbid emphysema (41.51 [8.12]) or stroke (41.92 [7.65]) and the worst mental HRQOL in those unemployed due to illness or disability (42.60 [7.47]) and current smokers (43.73 [8.26]). Employed survivors, those without comorbidity, and those meeting physical activity guidelines had the best HRQOL in both domains (all mean T-scores ≥53).

Table 2 shows associations of socioeconomic, clinical, and lifestyle factors with HRQOL from bivariate and multivariable models. In the bivariable models, most independent variables had statistically significant associations with GPH and GMH. In multivariable models, high family income was statistically significantly associated with better GPH (β = 3.60) and GMH (β = 3.44), having 2 or more comorbidities (β = −4.50, −4.89, and −9.80 for 2, 3, and 4+ comorbidities, respectively) and not meeting physical activity guidelines (β = −4.42) were associated with worse GPH, and having 3 or more comorbidities (β = −3.30 and −7.08 for 3 and 4+ comorbidities, respectively) and not meeting physical activity guidelines (β = −3.38) were associated with worse GMH (all P <.001). Moreover, survivors last treated 5 years or longer ago had better GPH than those treated during the past year (β = 3.37); older age was associated with better GMH (β = 4.81) and currently smoking was associated with worse GMH (β = −4.99) (Table 2, all P <.001). When including exact comorbid conditions instead of the number of comorbid conditions in the multivariable models, we found that emphysema and stroke were associated with poorer GPH (β = −4.10 and β = −4.07, respectively) and GMH (β = −3.73 and β = −3.55, respectively). Moreover, arthritis (β = −4.07) and diabetes (β = −3.72) were associated with poorer GPH (Table 3, all P <.001).

Table 2.

Factors associated with HRQOL among cancer survivors, MEPS 2016a multivariable model

Characteristic Global physical health
Global mental health
Bivariate model
Multivariable model
Bivariate model
Multivariable model
β (SE) P β (SE) P β (SE) P β (SE) P
Sociodemographic factors
 Age group, y
  18-54 Ref Ref Ref Ref
   55-64 3.02 (0.78) <.001 2.66 (0.66) <.001 3.34 (0.84) <.001 2.79 (0.75) <.001
   65-74 0.81 (0.63) .20 2.99 (0.51) <.001 1.47 (0.48) .003 2.69 (0.44) <.001
   ≥75 −0.21 (0.51) .69 3.24 (0.51) <.001 2.73 (0.49) <.001 4.81 (0.47) <.001
 Sex
   Male Ref Ref
   Female −1.29 (0.45) .005 −0.27 (0.42) 0.52
 Race/ethnicity
   Non-Hispanic White only Ref Ref Ref Ref
   All other race/ethnicities −2.53 (0.47) <.001 −1.76 (0.53) .001 −3.37 (0.43) <.001 −2.41 (0.39) <.001
 Current marital status
   Married Ref Ref Ref Ref
   Not marrieda −2.63 (0.50) <.001 1.02 (0.48) .04 −2.83 (0.52) <.001 −0.10 (0.57) .86
 Educational attainment
   Less than high school graduate Ref Ref Ref Ref
   High school graduate 4.28 (0.58) <.001 1.00 (0.52) .06 3.29 (0.66) <.001 0.73 (0.55) .19
   Some college or more 7.86 (0.59) <.001 1.82 (0.54) <.001 6.86 (0.67) <.001 1.88 (0.58) .002
 Family income as percent of poverty line
   Low income ≤138% Ref Ref Ref Ref
   Middle income 139%-400% 2.79 (0.62) <.001 1.11 (0.58) .06 2.29 (0.73) .002 0.97 (0.57) .09
   High income >400% 8.44 (0.54) <.001 3.60 (0.60) <.001 7.32 (0.74) <.001 3.44 (0.68) <.001
 Health insurance coveragec
   Any private Ref Ref Ref Ref
   Public only −6.35 (0.52) <.001 −2.70 (0.43) <.001 −5.12 (0.41) <.001 −1.68 (0.37) <.001
 Employment status
   Employed Ref Ref
   Retired −4.10 (0.50) <.001 −1.62 (0.48) .001
   Unable to work because ill/disabled −15.42 (0.60) <.001 −12.29 (0.62) <.001
   Not working for other reasons −8.10 (0.81) <.001 −6.58 (0.62) <.001
Clinical factors
 No. of comorbid conditionsd
  0 Ref Ref Ref Ref
  1 −0.52 (0.84) .54 −0.72 (0.72) .32 −1.14 (0.79) 0.15 −1.33 (0.83) .11
  2 −4.19 (0.74) <.001 −4.50 (0.65) <.001 −2.08 (0.74) .006 −2.87 (0.78) <.001
  3 −5.80 (0.65) <.001 −4.89 (0.58) <.001 −3.64 (0.87) <.001 −3.30 (0.81) <0.001
  ≥4 −11.95 (0.69) <.001 −9.80 (0.70) <.001 −8.29 (0.75) <.001 −7.08 (.77) <.001
 Comorbid conditiond
  Arthritis −6.07 (0.50) <.001 −3.67 (0.45) <.001
  Asthma −5.14 (0.67) <.001 −5.16 (0.60) <.001
  Diabetes −7.42 (0.62) <.001 −5.43 (0.36) <.001
  Emphysema −8.42 (0.75) <.001 −7.92 (0.66) <.001
  Heart disease −4.98 (0.50) <.001 −2.33 (0.44) <.001
  High cholesterol −2.95 (0.41) <.001 −1.87 (0.39) <.001
  Hypertension −5.34 (0.51) <.001 −3.80 (0.44) <.001
  Stroke −8.23 (0.59) <.001 −6.90 (0.47) <.001
 Cancer type
  Female breast only Ref Ref Ref Ref
  Prostate only 1.52 (0.64) .02 1.29 (0.40) .002 1.63 (0.56) .004 1.13 (0.43) .009
  Female other −2.51 (0.51) <.001 −0.54 (0.40) .18 −1.66 (0.48) <.001 0.44 (0.40) .28
  Male other −1.31 (0.71) .06 −0.96 (0.59) .10 −2.18 (0.56) .001 −1.69 (0.54) .002
 Years since last cancer treatment
  <1 Ref Ref Ref Ref
  1 to <5 2.36 (0.63) <.001 1.56 (0.52) .003 0.86 (0.55) .12 0.11 (0.43) .81
  ≥5 4.58 (0.55) <.001 3.37 (0.44) <.001 2.92 (0.53) <.001 1.86 (0.43) <.001
  Never treated/missing 3.86 (0.73) <.001 3.95 (0.74) <.001 2.72 (1.01) .008 2.42 (1.00) .01
Lifestyle factors
 BMI, kg/m2
  18.5-24.9 Ref Ref Ref Ref
  25-29.9 −0.53 (0.58) .36 −0.61 (0.50) .22 0.28 (0.62) .65 0.10 (0.53) .85
  ≥30 −5.78 (0.63) <.001 −2.88 (0.46) <.001 −3.85 (0.44) <.001 −1.47 (0.39) <.001
 Meeting physical activity guidelinese
  Yes Ref Ref Ref Ref
  No/unknown −7.65 (0.40) <.001 −4.42 (0.34) <.001 −5.81 (0.37) <.001 −3.38 (0.32) <.001
 Current smoker
  No/unknown Ref Ref Ref Ref
  Yes −6.06 (0.61) <.001 −2.08 (0.67) .002 −8.92 (0.42) <.0001 −4.99 (0.48) <.001
a

Results from linear regression models. In multivariable models, sex and cancer type were combined into 1one variable, employment status was excluded due to high collinearity with age, and number of comorbid conditions and exact comorbid conditions were included in models alternatively. — = inapplicable as the variable was not included in the multivariable models; BMI = body mass index; HRQOL = health-related quality of life; MEPS = Medical Expenditure Panel Survey.

b

Not married includes widowed, divorced, separated, or never married.

c

Public insurance includes Medicare, Medicaid, and/or other public hospital or physician coverage. TRICARE/CHAMPVA was treated as private coverage, as were employer-based, union-based, and other private insurance.

d

Comorbid conditions include arthritis, asthma, diabetes, emphysema, heart disease (angina, coronary heart disease, heart attack, other heart condition or disease), high cholesterol, hypertension, and stroke.

e

Meeting physical activity guidelines defined by currently spending one-half hour or more in moderate to vigorous physical activity at least 5 times per week based on the American Cancer Society guideline.

Table 3.

Adjusted associations of comorbid conditions with HRQOL among cancer survivors, MEPS 2016a

Comorbid condition Global physical health
Global mental health
β (SE) P β (SE) P
Arthritis −4.07 (0.41) <.001 −2.74 (0.40) <.001
Asthma −1.49 (0.63) .02 −2.05 (0.50) <.001
Diabetes −3.72 (0.56) <.001 −2.82 (0.36) <.001
Emphysema −4.10 (0.83) <.001 −3.73 (0.60) <.001
Heart disease −2.10 (0.36) <.001 −0.39 (0.42) .35
High cholesterol 0.12 (0.39) .75 0.14 (0.39) .72
Hypertension −1.59 (0.44) <.001 −1.42 (0.47) .003
Stroke −4.07 (0.60) <.001 −3.55 (0.45) <.001
a

Multivariable linear regression models were adjusted for current age group, race or ethnicity, current marital status, education, family income, health insurance, cancer type, years since diagnosis, body weight status, meeting physical activity guidelines, and current smoking status. HRQOL = health-related quality of life; MEPS = Medical Expenditure Panel Survey.

Cancer survivors treated 5 years or longer ago were statistically significantly less likely to report moderate or higher pain (odds ratio [OR] = 0.61, 95% confidence interval = 0.38 to 0.97) or fatigue (OR = 0.49, confidence interval = 0.32 to 0.75) compared with those treated during the past year. Survivors with 2 or more comorbidities (ORs > 2; P <.05) were more likely to report such symptoms (Supplementary Tables 3 and 4, available online).

Discussion

In this study, we analyzed sociodemographic, clinical, and lifestyle information from a cancer survivor questionnaire nested within a contemporary nationally representative survey. Higher family income, older age, and longer time since last treatment were associated with better HRQOL in physical and/or mental domains, whereas comorbidities, especially emphysema and stroke, and unhealthy lifestyle factors such as not meeting physical activity guidelines and smoking were statistically significantly associated with poorer HRQOL. Our findings highlight the importance of multimorbidity management and healthy behavior promotion for cancer survivors and providers who serve this growing population.

We found the number and type of comorbidities were strongly associated with survivors’ HRQOL in both physical and mental health domains, consistent with recent findings (4). Having 3 or more comorbid conditions or having emphysema or stroke was associated with the poorest HRQOL scores. Comorbid conditions could develop independently as survivors age or might be late effects of cancer treatments (3,38). Medicare claims data showed that the common comorbid chronic conditions among elderly cancer patients include cardiovascular illness, metabolic illness, mental health problems, and musculoskeletal conditions (39), largely consistent with our data in cancer survivors. These comorbidities can cause pain and/or fatigue, 2 common symptoms that cancer survivors suffer from with detrimental effects to their physical, social, and emotional function (3,4,40‐42). This suggests that those providing care to cancer survivors with comorbid conditions should be especially vigilant for debilitating cancer-related and other symptoms that may be impairing their health, functioning, and quality of life. Moreover, provider discussion and treatment of such symptoms may support improved quality of life and other health outcomes for survivors.

Lifestyle factors, including physical activity and smoking, showed strong associations with HRQOL in our study, consistent with previous research (13,17,18,43,44). In this nationally representative sample of cancer survivors, over one-half did not meet physical activity guidelines, and 10% were current smokers, representing 7.6 million and 1.5 million survivors in the nation respectively, suggesting the need for intervention. Improving healthy behaviors such as weight management, increasing physical activity, and smoking cessation are effective strategies to improve well-being, especially for cancer survivors (45-47). Physical activity can alleviate side effects and lasting effects of cancer treatments such as fatigue, insomnia, sexual dysfunction, metabolic syndrome, bone loss, and cognitive dysfunction (3). However, lasting behavior change can be challenging without professional intervention. In a recent study, less than 40% cancer survivors reported ever discussing lifestyle or health recommendations in detail with any provider at any time since cancer diagnosis (48). The Affordable Care Act has implemented multiple provisions to improve access to clinical preventive services by removing cost barriers and funding health promotion programs in workplaces and communities (49). Moreover, by increasing health insurance coverage options (50-52), professional assistance for changing unhealthy behaviors (eg, obesity counseling, and smoking cessation counseling and medications) may be more accessible and affordable. Efforts are warranted to increase providers’ awareness of health behavior services covered by health insurance to which patients and survivors can be referred and to increase provider-patient discussion of health behaviors, which could potentially improve healthy behaviors among survivors and lead to better HRQOL.

This study’s strengths include a recent, large, nationally representative sample of cancer survivors; PROMIS Global Health scores, a well-tested and validated HRQOL measure; and examination of key risk factors for poor HRQOL. This study shares limitations of many survey-based studies: the data are cross-sectional, limiting our ability to make causal inferences from the results; information about behaviors and cancer types of associated factors are self-reported and may be subject to recall errors; and the overall MEPS-ECSS response rate was relatively low. Although we used MEPS sample weights in all analyses, and they incorporate adjustments for survey nonresponse and reduce potential survey nonresponse bias, these weights cannot eliminate it entirely. Survey sample weights reflect the assumption that nonrespondents are similar to respondents within all weighting classes. However, survey nonrespondents may differ from respondents in unmeasured ways. Nonetheless, the overall MEPS-ECSS response rate is consistent with other national and state surveys in the United States. We were unable to adjust for other clinical factors that may affect HRQOL, such as cancer stage, specific cancer treatments, and other comorbidities not systematically queried in the MEPS. Given small numbers of unknown values, we combined the unknowns with the “no” category of meeting physical activity guidelines and smoking, which may lead to an underestimation of the detrimental effects of unhealthy behaviors on HRQOL. Also, because the PROMIS questionnaire was only administered among cancer survivors and not all MEPS participants, we were not able to compare HRQOL and its associations with various factors between cancer survivors and individuals without a cancer history. Future studies are warranted to investigate the synergistic effects of cancer history, comorbidities, and lifestyle behaviors on HRQOL to inform tailored approaches for improving quality of life.

In conclusion, using a recent nationally representative survey of cancer survivors, we found that survivors with low family income, those with 3 or more comorbidities, and the recently treated were more likely to report poor HRQOL. These sociodemographic and clinical characteristics can be used to identify survivors at risk of poor HRQOL in clinical and public health settings. Moreover, poor HRQOL was strongly associated with greater comorbidity burden and unhealthy lifestyle behaviors, including not meeting physical activity guidelines and smoking, suggesting that multimorbidity management and healthy behavior promotion may play a key role in optimizing HRQOL for cancer survivors.

Funding

The research was supported by the Intramural Research Department of the American Cancer Society.

Notes

Role of the funder: Study authors were employees of the Intramural Research Department of the American Cancer Society or the National Cancer Institute. No specific funding was provided for this research.

Disclosures: None of the authors have relevant financial interests, activities, relationships, or affiliations to this paper. Dr Xuesong Han received funding from AstraZeneca for an unrelated project.

Disclaimers: The article was prepared as part of one of the author's (REJ) official duties as employees of the US Federal Government. The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the National Cancer Institute.

Author contributions: All authors conceived and designed the study. XH and LR analyzed data and drafted the manuscript. All authors critically revised the manuscript and provided final approval of the version to be submitted.

Data Availability

Data are publicly accessible at https://meps.ahrq.gov/mepsweb/data_stats/download_data_files.jsp

Supplementary Material

pkaa123_Supplementary_Data

References

  • 1. American Cancer Society. Cancer Treatment and Survivorship Facts and Figures 2019-2021 Atlanta, GA: American Cancer Society; 2019.
  • 2. National Cancer Institute. Cancer Stat Facts: Cancer of Any Site https://seer.cancer.gov/statfacts/html/all.html. Published 2019. Accessed August 17, 2019.
  • 3. Shapiro CL.  Cancer survivorship. N Engl J Med. 2018;379(25):2438–2450. [DOI] [PubMed] [Google Scholar]
  • 4. Huang IC, Hudson MM, Robison LL, et al.  Differential impact of symptom prevalence and chronic conditions on quality of life in cancer survivors and non-cancer individuals: a population study. Cancer Epidemiol Biomarkers Prev. 2017;26(7):1124–1132. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Quinn GP, Goncalves V, Sehovic I, et al.  Quality of life in adolescent and young adult cancer patients: a systematic review of the literature. Patient Relat Outcome Meas. 2015;6:19–51. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Richardson LC, Wingo PA, Zack MM, et al.  Health-related quality of life in cancer survivors between ages 20 and 64 years. Cancer. 2008;112(6):1380–1389. [DOI] [PubMed] [Google Scholar]
  • 7. Weaver KE, Forsythe LP, Reeve BB, et al.  Mental and physical health-related quality of life among U.S. cancer survivors: population estimates from the 2010 National Health Interview Survey. Cancer Epidemiol Biomarkers Prev. 2012;21(11):2108–2117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Smith TG, Dunn ME, Levin KY, et al.  Cancer survivor perspectives on sharing patient-generated health data with central cancer registries. Qual Life Res. 2019;28(11):2957–2967. [DOI] [PubMed] [Google Scholar]
  • 9. Tapi Nzali MD, Bringay S, Lavergne C, et al.  What patients can tell us: topic analysis for social media on breast cancer. JMIR Med Inform. 2017;5(3):e23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Alfano CM, Leach CR, Smith TG, et al.  Equitably improving outcomes for cancer survivors and supporting caregivers: a blueprint for care delivery, research, education, and policy. CA A Cancer J Clin. 2019;69(1):35–49. [DOI] [PubMed] [Google Scholar]
  • 11. Cella D, Stone AA.  Health-related quality of life measurement in oncology: advances and opportunities. Am Psychol. 2015;70(2):175–185. [DOI] [PubMed] [Google Scholar]
  • 12. Huang CY, Wang MJ, Lin YH, et al.  Depressive symptoms and health-related quality of life among prostate cancer survivors. Cancer Nurs. 2018;41(1):E1–E8. [DOI] [PubMed] [Google Scholar]
  • 13. Bours MJL, Linden BWA, Winkels RM, et al.  Candidate predictors of health-related quality of life of colorectal cancer survivors: a systematic review. Oncologist. 2016;21(4):433–452. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. Shin H, Bartlett R, De Gagne JC.  Health-related quality of life among survivors of cancer in adolescence: an integrative literature review. J Pediatr Nurs. 2019;44:97–106. [DOI] [PubMed] [Google Scholar]
  • 15. Rao D, Debb S, Blitz D, et al.  Racial/ethnic differences in the health-related quality of life of cancer patients. J Pain Symptom Manage. 2008;36(5):488–496. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. Sharma N, Purkayastha A.  Factors affecting quality of life in breast cancer patients: a descriptive and cross-sectional study with review of literature. J Mid-Life Health. 2017;8(2):75–83. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. Connor AE, Baumgartner RN, Pinkston CM, et al.  Obesity, ethnicity, and quality of life among breast cancer survivors and women without breast cancer: the long-term quality of life follow-up study. Cancer Causes Control. 2016;27(1):115–124. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18. Gopalakrishna A, Longo TA, Fantony JJ, et al.  Lifestyle factors and health-related quality of life in bladder cancer survivors: a systematic review. J Cancer Surviv. 2016;10(5):874–882. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Rodriguez JL, Hawkins NA, Berkowitz Z, et al.  Factors associated with health-related quality of life among colorectal cancer survivors. Am J Prev Med. 2015;49(6):S518–S527. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20. Chow EJ, Antal Z, Constine LS, et al.  New agents, emerging late effects, and the development of precision survivorship. J Clin Oncol. 2018;36(21):2231–2240. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. Krzyszczyk P, Acevedo A, Davidoff EJ, et al.  The growing role of precision and personalized medicine for cancer treatment. Technology.  2018;06(3-4):79–100. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. van den Bulk J, Verdegaal EM, de Miranda NF.  Cancer immunotherapy: broadening the scope of targetable tumours. Open Biol. 2018;8(6):180037. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23. Smith L, Venella K.  Cytokine release syndrome: inpatient care for side effects of CAR T-cell therapy. Clin J Oncol Nurs. 2017;21(2):29–34. [DOI] [PubMed] [Google Scholar]
  • 24. Chawla N, Blanch-Hartigan D, Virgo KS, et al.  Quality of patient-provider communication among cancer survivors: findings from a nationally representative sample. J Oncol Pract. 2016;12(12):e964–e973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Hill RE, Wakefield CE, Cohn RJ, et al.  Survivorship care plans in cancer: a meta-analysis and systematic review of care plan outcomes. Oncologist. 2020;25(2):e351–e372. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26. Agency for Healthcare Research and Quality. Medical Expenditure Panel Survey https://meps.ahrq.gov/mepsweb/index.jsp. Accessed August 17, 2019. [PubMed]
  • 27. Yabroff KR, Dowling E, Rodriguez J, et al.  The Medical Expenditure Panel Survey (MEPS) experiences with cancer survivorship supplement. J Cancer Surviv. 2012;6(4):407–419. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28. Hays RD, Bjorner JB, Revicki DA, et al.  Development of physical and mental health summary scores from the patient-reported outcomes measurement information system (PROMIS) global items. Qual Life Res. 2009;18(7):873–880. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. Barile JP, Reeve BB, Smith AW, et al.  Monitoring population health for Healthy People 2020: evaluation of the NIH PROMIS® Global Health, CDC Healthy Days, and Satisfaction With Life instruments. Qual Life Res. 2013;22(6):1201–1211. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Schalet BD, Rothrock NE, Hays RD, et al.  Linking physical and mental health summary scores from the veterans RAND 12-Item Health Survey (VR-12) to the PROMIS((R)) Global Health Scale. J Gen Intern Med. 2015;30(10):1524–1530. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. Patient-Reported Outcomes Measurement Information System. A brief guide to the PROMIS Global health instrument. https://www.healthmeasures.net/images/PROMIS/manuals/PROMIS_Global_Scoring_Manual.pdf. Published 2017. Accessed September 11, 2020.
  • 32. Yost KJ, Eton DT, Garcia SF, et al.  Minimally important differences were estimated for six Patient-Reported Outcomes Measurement Information System-Cancer Scales in advanced-stage cancer patients. J Clin Epidemiol. 2011;64(5):507–516. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33. Paul SM, Zelman DC, Smith M, et al.  Categorizing the severity of cancer pain: further exploration of the establishment of cutpoints. Pain. 2005;113(1-2):37–44. [DOI] [PubMed] [Google Scholar]
  • 34. Guy GP Jr, Yabroff KR, Ekwueme DU, et al.  Economic burden of chronic conditions among survivors of cancer in the United States. J Clin Oncol. 2017;35(18):2053–2061. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35. Kaul S, Avila JC, Jupiter D, et al.  Modifiable health-related factors (smoking, physical activity and body mass index) and health care use and costs among adult cancer survivors. J Cancer Res Clin Oncol. 2017;143(12):2469–2480. [DOI] [PubMed] [Google Scholar]
  • 36. Wang SY, Hsu SH, Gross CP, et al.  Association between time since cancer diagnosis and health-related quality of life: a population-level analysis. Value Health. 2016;19(5):631–638. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. Rock CL, Doyle C, Demark-Wahnefried W, et al.  Nutrition and physical activity guidelines for cancer survivors. CA Cancer J Clin. 2012;62(4):243–274. [DOI] [PubMed] [Google Scholar]
  • 38. Sarfati D, Koczwara B, Jackson C.  The impact of comorbidity on cancer and its treatment. CA Cancer J Clin. 2016;66(4):337–350. [DOI] [PubMed] [Google Scholar]
  • 39. Edwards BK, Noone AM, Mariotto AB, et al.  Annual report to the nation on the status of cancer, 1975-2010, featuring prevalence of comorbidity and impact on survival among persons with lung, colorectal, breast, or prostate cancer. Cancer. 2014;120(9):1290–1314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40. Jiang C, Wang H, Wang Q, et al.  Prevalence of chronic pain and high-impact chronic pain in cancer survivors in the United States. JAMA Oncol. 2019;5(8):1224. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41. Watson A, van Kessel K.  Cancer survivors' experiences and explanations of postcancer fatigue: an analysis of online blogs. Cancer Nurs. 2018;41(2):117–123. [DOI] [PubMed] [Google Scholar]
  • 42. Smith TG, Troeschel AN, Castro KM, et al.  Perceptions of patients with breast and colon cancer of the management of cancer-related pain, fatigue, and emotional distress in community oncology. J Clin Oncol. 2019;37(19):1666–1676. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43. Duncan MJ, Kline CE, Vandelanotte C, et al.  Cross-sectional associations between multiple lifestyle behaviors and health-related quality of life in the 10,000 steps cohort. PLoS One. 2014;9(4):e94184. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44. Dube SR, Liu J, Fan AZ, et al.  Assessment of age-related differences in smoking status and health-related quality of life (HRQoL): findings from the 2016 Behavioral Risk Factor Surveillance System. J Commun Psychol. 2019;47(1):93–103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45. Ligibel JA, Alfano CM, Courneya KS, et al.  American Society of Clinical Oncology position statement on obesity and cancer. J Clin Oncol. 2014;32(31):3568–3574. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46. Burke S, Wurz A, Bradshaw A, et al.  Physical activity and quality of life in cancer survivors: a meta-synthesis of qualitative research. Cancers (Basel). 2017;9(12):53. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47. Ramaswamy AT, Toll BA, Chagpar AB, et al.  Smoking, cessation, and cessation counseling in patients with cancer: a population-based analysis. Cancer. 2016;122(8):1247–1253. [DOI] [PubMed] [Google Scholar]
  • 48. Rai A, Chawla N, Han X, et al.  Has the quality of patient-provider communication about survivorship care improved?  J Oncol Pract. 2019;15(11):e916–e924. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49. Koh HK, Sebelius KG.  Promoting prevention through the Affordable Care Act. N Engl J Med. 2010;363(14):1296–1299. [DOI] [PubMed] [Google Scholar]
  • 50. Davidoff AJ, Guy GP Jr, Hu X, et al.  Changes in health insurance coverage associated with the Affordable Care Act among adults with and without a cancer history: population-based national estimates. Med Care. 2018;56(3):220–227. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51. Han X, Yabroff KR, Ward E, et al.  Comparison of insurance status and diagnosis stage among patients with newly diagnosed cancer before vs after implementation of the patient protection and Affordable Care Act. JAMA Oncol. 2018;4(12):1713–1720. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52. Jemal A, Lin CC, Davidoff AJ, et al.  Changes in insurance coverage and stage at diagnosis among nonelderly patients with cancer after the Affordable Care Act. J Clin Oncol. 2017;35(35):3906–3915. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

pkaa123_Supplementary_Data

Data Availability Statement

Data are publicly accessible at https://meps.ahrq.gov/mepsweb/data_stats/download_data_files.jsp


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