Perceived Life Expectancy Is Associated with Colorectal Cancer Screening in England

Colorectal cancer (CRC) is the third most common cancer in men and the second most common cancer in women worldwide, with an estimated 1.4 million cases and 693,300 deaths in 2012 [1]. The highest incidence rates are in developed countries, many of which have screening tests available through opportunistic or organized programs [2]. In the UK, the National Health Service (NHS) provides CRC screening without charge using the fecal occult blood test (FOBt), which is mailed biennially to the home addresses of all men and women aged 60–74 years. Although the NHS Bowel Cancer Screening Programme was one of the first organized CRC screening programs worldwide, the UK lags behind other countries internationally in CRC outcomes, making effective screening an important public health priority [3]. However, screening uptake is low, with just over 50% of eligible adults participating in any biennial screening round. In other countries where FOBt screening is offered, uptake also tends to be low [2]. Because routine screening improves CRC outcomes and reduces mortality in the population [4, 5], a better understanding of the causes of low uptake is needed to inform system-level interventions to increase participation.

A potentially salient factor in explaining cancer screening uptake that has been previously overlooked is perceived life expectancy (PLE). Participation in cancer screening represents an investment in future health. Screening participants undergo the immediate burden of completing a screening test in the hope of protecting their future health and survival through a negative result or an early diagnosis of cancer. This perspective on health, as a form of human capital that depreciates with time and can be invested in through behaviors such as cancer screening, forms the basis of the theory of health as human capital [6‐8]. PLE estimates are informed by knowledge that people have readily at hand that may not always be queried about in study questionnaires, such as a more complete range of personal health and risk behaviors. PLE is predictive of actual mortality in American adults aged 50 and over in the US Health and Retirement Study across 2- and 8-year follow-up periods [9, 10]. The utility of PLE for predicting future behavior and actual mortality risk has been advocated for in the economic literature [11].

It is important to understand the nature of any potential association between PLE and CRC screening uptake, as the American College of Physicians does not recommend cancer screening for adults who have a remaining life expectancy of less than 10 years [12]. PLE could therefore be a useful factor that people may take into account when making informed decisions about cancer screening, but little is known about the degree to which it influences these decisions. Previously, PLE has been positively associated with uptake of mammography screening for breast cancer in the European Survey of Health, Ageing, and Retirement (SHARE), where women who expected to live longer were more likely to take up screening than those with low expectations of their future longevity [13]. The prospective association between PLE and participation in CRC screening through a nationally organized screening program is unknown.

We aimed to investigate the prospective association between perceived life expectancy, indexed as an individual’s own estimate of their chance of living another 10–15 years in 2008/2009, and participation in CRC screening through England’s NHS Bowel Cancer Screening Programme from 2010 to 2012/2013. We hypothesized that participation in CRC screening, a form of future health investment, would be higher among those with higher self-perceived remaining life expectancy.

Table 1 shows the baseline characteristics of participants. Grouping the PLE responses, 6% of participants (243/3975) estimated their chance of living another 10–15 years as 0–24%, 8% (312/3975) estimated a 25–49% chance, 44% (1737/3975) estimated a 50–74% chance, and 42% (1683/3975) estimated a 75–100% chance. The mean age at baseline was 62.6 years (SD 4.1). Just over half of participants were female (55%; 2174/3975). Nearly one third had post-secondary degree education (29%; 1152/3975) and 22% had no educational qualifications (885/3975). Only 2% of the sample was not white (88/3975). Most participants were married or living as married (77%; 3071/3975). On average, the age of mother currently or at death was 78 years (SD 12), and the age of father currently or at death was 72 years (SD 13). Smoking status, self-rated health, and chronic disease diagnoses are also shown in Table 1.

Table 1 also shows the baseline characteristics of participants according to FOBt uptake status over the follow-up. Just over two thirds of participants (71%; 2817/3975) reported completing at least one FOBt over the follow-up. FOBt uptake greatly differed across PLE categories, with 52% (126/243) of participants who estimated a 0–24% PLE having completed the test compared to 76% (1272/1683) of those who estimated a 75–100% PLE (p < 0.0001). Most other covariates were, as predicted, significantly positively associated with FOBt uptake over the study follow-up period, including having an older age of either mother or father currently or at death and having a higher score on the numeracy assessment (Table 1). Adjusted analyses are therefore essential to examine the independent prospective association between PLE and FOBt uptake. Having a previous cancer diagnosis was not associated with FOBt uptake over the follow-up.

In the fully adjusted model (Table 2), PLE was associated with FOBt uptake in a statistically significant linear dose-response fashion (p _trend < 0.0001), with the following ORs predicting FOBt uptake (yes vs. no): OR = 1.32 (95% CI 0.93–1.88) for 25–49%, OR = 1.52 (95% CI 1.14–2.03) for 50–74%, and OR = 1.74 (95% CI 1.29–2.34) for 75–100%, all vs. 0–24% (Table 2). Older age was negatively associated with FOBt uptake (OR = 0.96; 95% CI 0.95–0.98 per year), as was having no educational qualifications (OR = 0.79; 95% CI 0.64–0.98 vs. degree level education), being single (OR = 0.72; 95% CI 0.61–0.84 vs. married or living as married), being a current smoker (OR = 0.52; 95% CI 0.42–0.65), and having poor self-rated health (OR = 0.64; 95% CI 0.44–0.92; Table 2). Being female was positively associated with FOBt uptake (OR = 1.30; 95% CI 1.12–1.51), as was having better numeracy (OR = 1.06; 95% CI 1.00–1.13 per point out of 6; Table 2). In the model adjusted for continuous ELSA Mortality Risk Index score and covariates, the relationship between PLE and FOBt screening became slightly stronger than in the previous ORs: OR = 1.35 (95% CI 0.93–1.88) for 25–49%, OR = 1.56 (95% CI 1.18–2.08) for 50–74%, and OR = 1.81 (95% CI 1.35–2.43) for 75–100%, all vs. 0–24% (Table 2). Independently of PLE and covariates, higher 10-year mortality risk according to the Index was associated with lower odds of participating in FOBt screening (OR = 0.91; 95% CI 0.88–0.94 per point increase; Table 2).

Table 3 shows the mean PLE estimates across each scoring point on the ELSA Mortality Risk Index. The continuous PLE estimates decreased linearly as ELSA Index scores increased, with a correlation of moderate strength (Pearson’s r = −0.27; p < 0.0001). In this study, the ELSA Index scores ranged from 1 point (lowest mortality risk, corresponding to a 10-year mortality rate of 3% in the development study) to 18 points (highest mortality risk, corresponding to a 10-year mortality rate of 95% in the development study). In those who scored 1 point on the ELSA Index, the mean self-reported chance of living another 10–15 years was 73.6% (SD 17.9%). In those who scored 12 or more points on the ELSA Index, the mean self-reported chance of living another 10–15 years was 46.4% (SD 27.4%).

The main results were not affected in the sensitivity analyses excluding from the fully adjusted model each of the 54 participants who reported completing the FOBt outside the national screening program (OR = 1.31; 95% CI 0.92–1.87 for 25–49%, OR = 1.48; 95% CI 1.11–1.97 for 50–74%, OR = 1.69; 95% CI 1.26–2.29 for 75–100%, all vs. 0–24%) and the 151 participants who reported completing FOBt screening prior to the study period (OR = 1.40; 95% CI 0.97–2.03 for 25–49%, OR = 1.53; 95% CI 1.13–2.06 for 50–74%, OR = 1.76; 95% CI 1.29–2.40 for 75–100%, all vs. 0–24%). Restricting the analysis to those whose PLE estimates ranged from 10 to 11 years, rather than 10 to 15 years, as in the full sample, resulted in a slightly stronger magnitude of association between PLE and screening uptake (not shown).

In this population-based cohort study of English men and women who were age-eligible for nationally organized FOBt-based CRC screening, perceived life expectancy at baseline was a strong positive predictor of FOBt uptake over the 4-year study follow-up. Three quarters of men and women who rated their chances of living another 10 to 15 years as 75–100% at baseline completed at least one FOBt over the follow-up, compared to half of those who rated their chances as 0–24%. This finding was independent of sociodemographic factors, numeracy skills, self-rated health, and other risk factors for mortality, including smoking status and chronic disease diagnoses. It was also independent of score on a validated index of 10-year mortality risk for older adults, indicating that perceived and objectively estimated mortality risk might make unique contributions to predicting CRC screening behavior. Our finding has particular salience for two issues in CRC screening: the fact that CRC screening is not recommended for adults with an actual life expectancy of less than 10 years, and persistent socioeconomic inequalities in CRC screening uptake.

Based on increasing evidence for the lack of benefit of CRC screening in older adults with a low life expectancy, the American College of Physicians does not recommend screening in adults with less than 10 years of remaining actual life expectancy [12]. In this group, the benefits of early diagnosis are minimal and considered to be outweighed by the potential harms of screening including unnecessary diagnostic procedures and overtreatment. In the USA, recent studies have found that participation in cancer screening is common among this group [20‐22], sparking the development of strategies to tailor screening guidelines to account for differential life expectancies within age strata [23, 24]. Uptake of screening among adults with low life expectancy is thought to occur partly because there is generally high public enthusiasm for cancer screening at older ages and also because the contraindication of screening can be difficult for physicians to communicate to patients with high mortality risk [25‐28]. Information about the time frame that elapses before screening confers a mortality benefit is not communicated to the public as part of the screening invitations in the UK, and it does currently not form part of the guidelines for CRC screening given by the US Centers for Disease Control and Prevention, the US Preventive Services Task Force, or the American Cancer Society [28‐30].

Better public communication about the aims of screening may help to optimize uptake, as our study indicates that people may take into account their expectations of the future when making decisions about screening. This is good news, although a substantial proportion of adults who perceived their own life expectancy as low—less than a 25% chance of living another 10–15 years—still participated in CRC screening. Assuming a reasonable level of accuracy in their life expectancy estimations, the reasons why these adults complete screening despite their low expectations of future survival require further investigation. Conversely, many people with high expectations of their future survival did not complete CRC screening and consequently may be missing out on the benefits of screening intended for this group. These findings are concerning, as PLE showed good concordance with objectively estimated 10-year mortality risk in this study and was predictive of actual mortality risk in a national sample of older American adults. In the HRS, older adults who survived over a 2-year follow-up had, on average, a 50-point higher estimate of 15–25-year PLE than those who died [10]. In a longer 8-year follow-up, those who died reported a 56% chance of 15–25-year survival at baseline, on average, compared with a 65% average chance reported by those who survived [11].

The potential impact of life expectancy perceptions on socioeconomic inequalities in CRC screening uptake is also important to consider. Inequalities in screening uptake based on several socioeconomic indicators have been demonstrated in several country contexts [31, 32]. Adults with low educational attainment and who have experienced economic hardship have, on average, lower expectations for their remaining life expectancy than those who are better off [33]. Having higher perceived life expectancy is thought to increase one’s sense of control over their own life and events in the future (the “horizon hypothesis”) [34], which could in turn increase the likelihood of participating in cancer screening [35]. Low perceptions of personal life expectancy, if more frequent among adults of low socioeconomic status, might have the adverse effect of contributing to inequalities in CRC screening uptake and eventually to cancer outcomes, including mortality. Further work is needed to examine the accuracy of life expectancy perceptions across socioeconomic groups, in order to establish the degree to which lowered expectations of the future may present a barrier to cancer screening that could be targeted and modified by public communication strategies.

Our results are consistent with those from the European SHARE study, which found that PLE was positively associated with mammography uptake in women [13]. In our study, “ever” FOBt uptake over the follow-up from 2010 to 2012/2013 was 71%, consistent with NHS records for ever uptake of 70.1% in the general eligible population of over 60,000 men and women in the southern region of England over a similar time period [36]. Overall, uptake was negatively associated with age in our study. When screening was initially available to 60–69-year-olds from 2006 to 2010, age was positively associated with uptake, likely because older adults would have received more biennial screening invitations than younger adults within this age range [36]. Adults aged 70–74 years were then invited from 2010 as part of an age extension. In the period from 2006 to 2012, NHS records show that uptake peaks in the middle of the 60–74 age range [36]. Our results also show this trend when broken down by age at follow-up, with uptake at 64% among 60-year-olds, 75% among 69-year-olds, and 50% among 74-year-olds. Our results for the other predictors of FOBt uptake, which were being female, having higher education, being married, not smoking, having better numeracy skills, and better self-rated health, are consistent with previous research [31, 32, 36‐39].

A limitation of this study is that FOBt uptake was assessed through self-report. However, uptake rates were consistent with those observed in the general screening-eligible population over a similar time period [36]. Self-reported screening uptake in a similar sample, in the context of England’s NHS Bowel Cancer Screening Programme, was recently highly concordant with NHS records (94.2% agreement, κ = 0.74) [15]. History of colonoscopy or sigmoidoscopy or completion of a physician-recommended FOBt was not assessed in the study interview. These scenarios, respectively, would have made participants ineligible for the program or may have overridden any effects of PLE on screening behavior. We expect that this would apply to the minority of study participants. We did not have data on the total number of FOBt screening kits that a person had completed in the past. Some people in the sample may have completed screening prior to the study period, as the screening program was implemented in small areas in 2006 and rolled out nationwide during the period 2006 to 2010 [40]. The reverse relationship of screening participation on PLE is uncertain and may depend on the time elapsed between a screening episode and the PLE assessment. The PLE estimates in this study may represent, to a degree, the aggregate of health-related behaviors and events that people experienced over their lives. When considered in this way, there may be bidirectional relationships between PLE and health-related behaviors, a question that requires further investigation.

Measurement error may have been introduced if participants’ PLE estimates changed between the study baseline and the actual time of cancer screening. If this occurred and was non-differential across the study population, then odds ratios for PLE and FOBt screening will be biased towards the null, underestimating the magnitude of the true association. If certain subgroups were more likely to decrease or increase in PLE than others, the odds ratios may be biased downwards or upwards. If PLE estimates were relatively accurate, then they would, to a degree, represent the same underlying construct as objectively estimated mortality risk (i.e., actual mortality risk). The PLE estimates showed good concordance with 10-year mortality risk according to the validated and reliable ELSA Mortality Risk Index [17]. While our results indicate that there is overlap between self-perceived and objectively estimated mortality risk, they predicted FOBt uptake independently of one another, indicating that they might make unique contributions to predicting behavior. We hypothesize that inaccuracies in PLE estimates would be greatest among those older adults with low educational attainment, low socioeconomic status, or poor literacy or numeracy skills or who have experienced aging-related cognitive decline. Further work with follow-up mortality data is needed to identify which adults had incorrectly low or high perceptions of their remaining life expectancy. The two scenarios may have different implications for cancer screening and potentially other health behaviors as well. This is an important area for future work.

In summary, this is the first longitudinal analysis of perceived life expectancy and CRC screening uptake in the context of an organized, publicly available screening program. We found that men and women who rated their chance of living another 10 to 15 years as 75–100% at baseline were significantly more likely to complete at least one FOBt for CRC screening than those who rated their chance as 0–25%. A substantial proportion of adults with low expectations of survival participated in CRC screening, despite this screening test not being recommended for adults with low remaining life expectancy. If PLE estimations are reasonably accurate among this group, they might be subject to greater harm than benefit from screening. At the same time, one quarter of adults with high expectations of their own life expectancy appeared to be missing out on the benefits of screening intended for this group. It appears that CRC screening may not be optimized to the greatest possible benefit for either group. A better understanding of how people develop their mental models of PLE might help identify those who are at risk of overly fatalistic attitudes towards their futures and potentially at risk of declining important health services such as cancer screening.

While we do not recommend that PLE be used as a basis for decision making about screening, further research should investigate whether public communication about the role of actual life expectancy in conferring the benefits of cancer screening might help to improve decision making. Any potential communication strategies would have to be carefully designed and implemented to avoid any public misunderstanding. Mortality risk calculators that are validated, accurate, and suitably brief could be useful tools to aid in shared clinical decision making with respect to cancer screening, although their potential to foster fatalistic attitudes about life expectancy must be carefully considered. Finally, if the accuracy of life expectancy perceptions differs across population subgroups, the implications of public communication for social equity in uptake of screening will require careful consideration.