Abstract
Background
Intervention-generated inequalities are unintended variations in outcome that result from the organisation and delivery of health interventions. Socioeconomic inequalities in treatment may occur for some common cancers. Although the incidence and outcome of lung cancer varies with socioeconomic position (SEP), it is not known whether socioeconomic inequalities in treatment occur and how these might affect mortality. We conducted a systematic review and meta-analysis of existing research on socioeconomic inequalities in receipt of treatment for lung cancer.Methods and Findings
MEDLINE, EMBASE, and Scopus were searched up to September 2012 for cohort studies of participants with a primary diagnosis of lung cancer (ICD10 C33 or C34), where the outcome was receipt of treatment (rates or odds of receiving treatment) and where the outcome was reported by a measure of SEP. Forty-six papers met the inclusion criteria, and 23 of these papers were included in meta-analysis. Socioeconomic inequalities in receipt of lung cancer treatment were observed. Lower SEP was associated with a reduced likelihood of receiving any treatment (odds ratio [OR] = 0.79 [95% CI 0.73 to 0.86], p<0.001), surgery (OR = 0.68 [CI 0.63 to 0.75], p<0.001) and chemotherapy (OR = 0.82 [95% CI 0.72 to 0.93], p = 0.003), but not radiotherapy (OR = 0.99 [95% CI 0.86 to 1.14], p = 0.89), for lung cancer. The association remained when stage was taken into account for receipt of surgery, and was found in both universal and non-universal health care systems.Conclusions
Patients with lung cancer living in more socioeconomically deprived circumstances are less likely to receive any type of treatment, surgery, and chemotherapy. These inequalities cannot be accounted for by socioeconomic differences in stage at presentation or by differences in health care system. Further investigation is required to determine the patient, tumour, clinician, and system factors that may contribute to socioeconomic inequalities in receipt of lung cancer treatment.Please see later in the article for the Editors' Summary
Editors' Summary
Background
Lung cancer is the most commonly occurring cancer worldwide and the commonest cause of cancer-related death. Like all cancers, lung cancer occurs when cells begin to grow uncontrollably because of changes in their genes. The most common trigger for these changes in lung cancer is exposure to cigarette smoke. Most cases of lung cancer are non-small cell lung cancer, the treatment for which depends on the “stage” of the disease when it is detected. Stage I tumors, which are confined to the lung, can be removed surgically. Stage II tumors, which have spread to nearby lymph nodes, are usually treated with surgery plus chemotherapy or radiotherapy. For more advanced tumors, which have spread throughout the chest (stage III) or throughout the body (stage IV), surgery generally does not help to slow tumor growth and the cancer is treated with chemotherapy and radiotherapy. Small cell lung cancer, the other main type of lung cancer, is nearly always treated with chemotherapy and radiotherapy but sometimes with surgery as well. Overall, because most lung cancers are not detected until they are quite advanced, less than 10% of people diagnosed with lung cancer survive for 5 years.Why Was This Study Done?
As with many other cancers, socioeconomic inequalities have been reported for both the incidence of and the survival from lung cancer in several countries. It is thought that the incidence of lung cancer is higher among people of lower socioeconomic position than among wealthier people, in part because smoking rates are higher in poorer populations. Similarly, it has been suggested that survival is worse among poorer people because they tend to present with more advanced disease, which has a worse prognosis (predicted outcome) than early disease. But do socioeconomic inequalities in treatment exist for lung cancer and, if they do, could these inequalities contribute to the poor survival rates among populations of lower socioeconomic position? In this systematic review and meta-analysis, the researchers investigate the first of these questions. A systematic review uses predefined criteria to identify all the research on a given topic; a meta-analysis is a statistical approach that combines the results of several studies.What Did the Researchers Do and Find?
The researchers identified 46 published papers that studied people with lung cancer in whom receipt of treatment was reported in terms of an indicator of socioeconomic position, such as a measure of income or deprivation. Twenty-three of these papers were suitable for inclusion in a meta-analysis. Lower socioeconomic position was associated with a reduced likelihood of receiving any treatment. Specifically, the odds ratio (chance) of people in the lowest socioeconomic group receiving any treatment was 0.79 compared to people in the highest socioeconomic group. Lower socioeconomic position was also associated with a reduced chance of receiving surgery (OR = 0.68) and chemotherapy (OR = 0.82), but not radiotherapy. The association between socioeconomic position and surgery remained after taking cancer stage into account. That is, when receipt of surgery was examined in early-stage patients only, low socioeconomic position remained associated with reduced likelihood of surgery. Notably, the association between socioeconomic position and receipt of treatment was similar in studies undertaken in countries where health care is free at the point of service for everyone (for example, the UK) and in countries with primarily private insurance health care systems (for example, the US).What Do These Findings Mean?
These findings suggest that patients in more socioeconomically deprived circumstances are less likely to receive any type of treatment, surgery, and chemotherapy (but not radiotherapy) for lung cancer than people who are less socioeconomically deprived. Importantly, these inequalities cannot be explained by socioeconomic differences in stage at presentation or by differences in health care system. The accuracy of these findings may be affected by several factors. For example, it is possible that only studies that found an association between socioeconomic position and receipt of treatment have been published (publication bias). Moreover, the studies identified did not include information regarding patient preferences, which could help explain at least some of the differences. Nevertheless, these results do suggest that socioeconomic inequalities in receipt of treatment may exacerbate socioeconomic inequalities in the incidence of lung cancer and may contribute to the observed poorer outcomes in lower socioeconomic position groups. Further research is needed to determine the system and patient factors that contribute to socioeconomic inequalities in lung cancer treatment before clear recommendations for changes to policy and practice can be made.Additional Information
Please access these Web sites via the online version of this summary at http://dx.doi.org/10.1371/journal.pmed.1001376.- The US National Cancer Institute provides information about all aspects of lung cancer for patients and health care professionals (in English and Spanish); a monograph entitled Area Socioeconomic Variations in U. S. Cancer Incidence, Mortality, Stage, Treatment, and Survival, 19751999 is available
- Cancer Research UK also provides detailed information about lung cancer and links to other resources, such as a policy statement on socioeconomic inequalities in cancer and a monograph detailing cancer and health inequalities in the UK
- The UK National Health Service Choices website has a page on lung cancer that includes personal stories about diagnosis and treatment
- MedlinePlus provides links to other US sources of information about lung cancer (in English and Spanish)
Figures
Citation: Forrest
LF, Adams J, Wareham H, Rubin G, White M (2013) Socioeconomic
Inequalities in Lung Cancer Treatment: Systematic Review and
Meta-Analysis. PLoS Med 10(2):
e1001376.
doi:10.1371/journal.pmed.1001376
Academic Editor: Colin D. Mathers, World Health Organization, Switzerland
Received: July 26, 2012; Accepted: December 14, 2012; Published: February 5, 2013
Copyright: © 2013 Forrest et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: LF (ESRC studentship ES/I020926/1) and HW are PhD students funded by ESRC as members of Fuse, the Centre for Translational Research in Public Health (www.fuse.ac.uk). JA, MW, and GR are funded in part as a staff member (JA), director (MW), and senior investigator (GR) of Fuse. Fuse is a UK Clinical Research Collaboration (UKCRC) Public Health Research Centre of Excellence. Funding for Fuse from the British Heart Foundation, Cancer Research UK, Economic and Social Research Council, Medical Research Council, the National Institute for Health Research, under the auspices of the UK Clinical Research Collaboration, is gratefully acknowledged. The views expressed in this paper do not necessarily represent those of the funders or UKCRC. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: GR is a member of several advisory groups for the Department of Health's National Awareness and Early Diagnosis Initiative. All other authors have declared that no competing interests exist.
Abbreviations: CI, confidence interval; NSCLC, non-small cell lung cancer; OR, odds ratio; SCLC, small cell lung cancer; SEER, National Cancer Institute's Surveillance, Epidemiology and End Results; SEP, socioeconomic position; UHCS, universal health care system
Academic Editor: Colin D. Mathers, World Health Organization, Switzerland
Received: July 26, 2012; Accepted: December 14, 2012; Published: February 5, 2013
Copyright: © 2013 Forrest et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: LF (ESRC studentship ES/I020926/1) and HW are PhD students funded by ESRC as members of Fuse, the Centre for Translational Research in Public Health (www.fuse.ac.uk). JA, MW, and GR are funded in part as a staff member (JA), director (MW), and senior investigator (GR) of Fuse. Fuse is a UK Clinical Research Collaboration (UKCRC) Public Health Research Centre of Excellence. Funding for Fuse from the British Heart Foundation, Cancer Research UK, Economic and Social Research Council, Medical Research Council, the National Institute for Health Research, under the auspices of the UK Clinical Research Collaboration, is gratefully acknowledged. The views expressed in this paper do not necessarily represent those of the funders or UKCRC. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: GR is a member of several advisory groups for the Department of Health's National Awareness and Early Diagnosis Initiative. All other authors have declared that no competing interests exist.
Abbreviations: CI, confidence interval; NSCLC, non-small cell lung cancer; OR, odds ratio; SCLC, small cell lung cancer; SEER, National Cancer Institute's Surveillance, Epidemiology and End Results; SEP, socioeconomic position; UHCS, universal health care system
Introduction
Lung cancer is the most commonly occurring cancer worldwide. In the USA and the UK it is the second most incident cancer [1],[2], as well as the most common cause of cancer mortality [2],[3]. Survival differs internationally. In the UK, fewer than 10% of those diagnosed with lung cancer survive for 5 years [3],[4], with higher survival rates found in Nordic countries [4],[5], the USA [2],[5], Australia, and Canada [4].Lung cancers are classified into small cell (SCLC) and non-small cell (NSCLC) lung cancers. NSCLC is more common than SCLC and has a better survival rate [6]. National Institute for Health and Clinical Excellence (NICE) guidelines recommend radical surgery for stage I or II NSCLC [6]. Chemotherapy and radiotherapy are recommended for later-stage NSCLC patients and are the treatments of choice for SCLC [6]. Treatment intervention with surgery, chemotherapy, or radiotherapy has been shown to improve lung cancer survival [6].
Socioeconomic inequalities in incidence of, and survival from, the majority of cancers have been reported [1],[3],[7]. A recent non-systematic review revealed socioeconomic inequalities in receipt of treatment for colorectal cancer [8], and it has been suggested that socioeconomic differences in access to treatment might at least partially explain socioeconomic differences in survival [9]. Unintended variations in outcome that result from the way that health interventions are organised and delivered have been described as intervention-generated inequalities [10].
Incidence of lung cancer is higher [1],[11], and survival poorer [7], in the most deprived patient groups. However, it is not known whether socioeconomic inequalities in receipt of treatment exist for lung cancer and, if so, what contribution they make to overall socioeconomic inequalities in outcome. In order to explore the first of these questions, we undertook a systematic review and meta-analysis of cohort studies examining the association between socioeconomic position (SEP) and receipt of lung cancer treatment.
Methods
A protocol (see Text S2) was developed and systematic methods were used to identify relevant studies, assess study eligibility for inclusion, and evaluate study quality. The review is reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines [12] (see Text S1 for PRISMA checklist).Literature Search
The online databases of MEDLINE and EMBASE were searched up to September 2012 (see Table S1 for full search strategies). No language restriction was applied. A search of Scopus uncovered no further papers. Additional studies were identified by reviewing the reference lists of all included studies and by using a forward citation search to identify more recent studies that had cited included studies. EndNote X5 software was used to manage the references.Study Eligibility
Studies that met the following criteria were included in the review: primary, cohort studies of participants with a primary diagnosis of lung cancer (ICD10 C33 or C34) reported separately from other cancers; published in a peer-reviewed journal; where at least one reported outcome was receipt of treatment (measured by rates or odds of receiving treatment); and where receipt of this outcome was reported by a measure of SEP. Any curative or palliative treatment for lung cancer including surgery, chemotherapy, and radiotherapy was included.Studies where SEP was included as a descriptive variable or confounder, but where outcomes for receipt of treatment by SEP were not presented, were not eligible for inclusion, but the authors were contacted to determine whether relevant data were available that might allow for inclusion in the review.
Studies where multivariable analysis was conducted (and included control for a minimum of age and sex as confounders); receipt of treatment was compared to not receiving treatment; odds ratios (ORs) and 95% confidence intervals (CIs) of receipt of treatment in low compared to high SEP were calculated; and SEP was not further stratified by another variable, were considered suitable for inclusion in meta-analysis.
Acceptable measures of SEP were: area-based indices of deprivation (e.g., Index of Multiple Deprivation [IMD], Townsend Score, Carstairs Index); and area or individual measures of income, poverty, or education level.
Multiple papers using the same or overlapping study data were included. Sensitivity analyses were conducted including all eligible papers and using different combinations of included papers, but only data from the better quality or more detailed paper in each overlapping study group were included in the final meta-analyses. Sensitivity meta-analyses are included in the supplemental material.
Study Selection and Data Extraction
Studies obtained from the database searches were independently assessed by two researchers (LFF and HW) in three phases: title, abstract, and full paper screening. Any disagreements at any of the screening stages were resolved by discussion between the two researchers in the first instance and with a third reviewer (JA) if agreement could not be reached. Data extraction was carried out by LFF using an Access database pro-forma developed for this purpose, and double-checked by HW.There is evidence to suggest that health insurance status is an important factor relating to access to lung cancer care in countries such as the USA that rely on insurance-based health care systems [13]. Insurance status is less relevant and rarely measured in most other countries. Therefore, three analytical categories were developed a priori: studies conducted in a universal health care system (UHCS), free at the point of access (similar to the UK); studies conducted in countries with primarily private insurance health care systems (non-UHCS, similar to the USA) [14]; and studies conducted in countries with social insurance health care systems (similar to many European countries). No studies were identified that fell into the third category.
Study Quality
A study quality tool, adapted from existing quality tools [15],[16], was used to divide studies into six quality categories, with 1 being the lowest, and 6 the highest, quality (see Text S3). Quality assessment was carried out by LFF and checked by HW.Cohort studies reporting only univariable analysis are of lower quality in terms of their ability to control for confounding. Only studies conducting multivariable analysis (quality scores 3–6) were included in the meta-analysis. All studies that met the inclusion criteria were analysed in the narrative synthesis.
Statistical Analysis
Trends in receipt of treatment across SEP groups were described in the narrative analysis of all studies that met the inclusion criteria.Meta-analysis of eligible studies was undertaken using Cochrane Collaboration Review Manager 5.1. Natural logs of the ORs and their standard errors (SEs) were calculated for use in forest plots. Random-effects meta-analysis of the odds of treatment in the lowest compared to the highest SEP group was conducted. Where a study reported the most deprived class as the comparator, reverse ORs were calculated. Studies that presented a single OR as either an OR for a one unit increase in deprivation score or incremental quintile increase in income were not included.
Subgroup analyses by treatment type and health care system were conducted. In meta-analyses where a “substantial” percentage [17] of the variability appeared to be due to the heterogeneity of the studies rather than to chance, further subgroup analyses by stage, histology, and quality score were conducted, where appropriate, in order to examine potential sources of heterogeneity. A funnel plot was used to assess potential publication bias.
Results
Included Papers/Studies
A total of 46 papers met the inclusion criteria and were included in the review (see the PRISMA flow diagram [Figure 1]). Twenty-eight papers were from UHCS countries (Tables 1 and 2). Of these, 19 UK papers examined 13 study populations, although as these included national and regional populations from different sources, there was some further population overlap. One UK paper also compared treatment in Scotland and Canada [18]. A further nine papers from Canada (2), Sweden (1), Australia (1), Italy (1), France (1), and New Zealand (3) were included. The three New Zealand papers all examined the same population.CI, confidence interval; SEP, socioeconomic position.
doi:10.1371/journal.pmed.1001376.g001
doi:10.1371/journal.pmed.1001376.t001
doi:10.1371/journal.pmed.1001376.t002
doi:10.1371/journal.pmed.1001376.t003
doi:10.1371/journal.pmed.1001376.t004
In terms of quality, the non-UHCS studies that carried out multivariable analyses had better control for confounding than did UHCS studies, as they tended to stratify by stage and histology. However, half of the non-UHCS papers used a Medicare-only population aged over 65, and so were more restrictive in population terms than the UHCS studies.
Twenty-nine papers met the criteria for meta-analysis—19 from UHCSs and 10 from non-UHCSs. However, six studies that examined receipt of treatment in low compared to high SEP presented the results as a single OR and so could not be included in the meta-analyses. Seventeen studies were included in the final meta-analyses and a further six in the sensitivity meta-analyses.
Surgery
Thirty-one papers (29 study populations) included receipt of surgery as an outcome—18 UHCS papers (15 study populations) and 13 non-UHCS papers (14 study populations) (Tables 5 and 6). Of the papers that reported measures of significance (CIs or p-values), 20 out of 27 (74%) reported that lower SEP was significantly associated with lower likelihood of surgery when comparing the lowest with the highest SEP group, although three of these 20 papers did not find a significant trend across groups.doi:10.1371/journal.pmed.1001376.t005
doi:10.1371/journal.pmed.1001376.t006
CI, confidence interval; non-UHCS, non-universal health care system; NSCLC, non-small cell lung cancer; OR, odds ratio; SE, standard error; SEP, socioeconomic position; UHCS, universal health care system.
doi:10.1371/journal.pmed.1001376.g002
Chemotherapy
Twenty-three papers included chemotherapy as an outcome—14 UHCS papers (12 populations) and nine non-UHCS papers (10 populations) (Tables 7 and 8). Of the 21 papers that reported measures of significance, 15 (71%) reported that lower SEP was significantly associated with lower likelihood of receipt of chemotherapy.doi:10.1371/journal.pmed.1001376.t007
doi:10.1371/journal.pmed.1001376.t008
CI, confidence interval; non-UHCS, non-universal health care system; OR, odds ratio; SE, standard error; SEP, socioeconomic position; UHCS, universal health care system.
doi:10.1371/journal.pmed.1001376.g003
Radiotherapy
Eighteen papers (18 populations) examined receipt of radiotherapy for lung cancer—12 in UHCS settings (11 populations) and six in non-UHCS settings (seven populations) (Tables 9 and 10). Only one UHCS study found an association between SEP and receipt of radiotherapy. The non-UHCS studies had very heterogeneous outcomes.doi:10.1371/journal.pmed.1001376.t009
doi:10.1371/journal.pmed.1001376.t010
CI, confidence interval; non-UHCS, non-universal health care system; OR, odds ratio; SE, standard error; SEP, socioeconomic position; UHCS, universal health care system.
doi:10.1371/journal.pmed.1001376.g004
Treatment Type not Specified
Seven papers (eight study populations) examined receipt of unspecified treatment, and three papers considered receipt of unspecified curative treatment in three populations (Tables 11–13). In the meta-analysis of five non-overlapping studies, low SEP was associated with a lower likelihood of receiving unspecified treatment (OR = 0.78 [95% CI 0.74 to 0.83], p<0.001, I2 = 0) (Figure 5). This was also seen when studies with overlapping populations were included (OR = 0.80 [95% CI 0.77 to 0.84], p<0.001, I2 = 17%) (Figure S5).CI, confidence interval; OR, odds ratio; SE, standard error; SEP, socioeconomic position.
doi:10.1371/journal.pmed.1001376.g005
doi:10.1371/journal.pmed.1001376.t011
doi:10.1371/journal.pmed.1001376.t012
doi:10.1371/journal.pmed.1001376.t013
Discussion
Principal Findings
To our knowledge, this is the first systematic review and meta-analysis examining socioeconomic inequalities in receipt of lung cancer treatment. It shows an association between low SEP and reduced likelihood of receipt of any type of treatment, surgery, and chemotherapy. The results were generally consistent across different health care systems.Interpretation of Results
Surgery is suitable only for patients with early-stage NSCLC, and it has been suggested that patients with cancer in a lower SEP are more likely to present later and with later-stage disease [20]. This may help explain why socioeconomic inequalities in receipt of surgery are observed in some studies. However, presentation with later-stage cancer in lower SEP patients has not been consistently observed [19]. In this review, when receipt of treatment was examined in studies of early-stage patients only (from non-UHCS studies), low SEP remained associated with reduced likelihood of surgery. Thus, the association between SEP and receipt of surgery appears to be independent of stage. Similar results were seen for NSCLC studies in both health care systems.Receipt of treatment may also be influenced by clinical suitability for treatment, and socioeconomic differences in the number of co-morbidities present may explain socioeconomic inequalities in treatment. In the three UHCS studies that took co-morbidity into account, SEP was not associated with receipt of surgery [21],[22] or of any treatment [23] when the trend across SEP groups was examined, suggesting that co-morbidity may be a potential mediator of socioeconomic inequalities in treatment in UHCSs. However, most of the non-UHCS studies did include co-morbidity as a confounder, and socioeconomic inequalities in treatment were still observed, suggesting that there may be differences between health care systems here.
Strengths and Weaknesses of the Review and of the Available Evidence
This is one of the first equity reviews published [24],[25], the first systematic review of the literature on intervention-generated inequalities in lung cancer treatment to our knowledge, and the first cancer equity review to include a meta-analysis. Extensive searches were carried out to identify studies. However, it is possible that not all relevant studies were obtained.The included studies reported observational data only. The suitability of meta-analysis for observational studies has been questioned, as it may produce precise but spurious results [26]. Examining the possible sources of heterogeneity by conducting sensitivity analyses across different sub-groups may be less prone to bias than calculating an overall summary effect [26]. Here, although an overall summary effect OR was calculated, heterogeneity was taken into account. Separate analyses by type of treatment were carried out, with further stratification by stage and histology. Universal and non-UHCSs were examined separately and random effects rather than fixed effects meta-analyses were conducted. These precautions did not change the overall pattern of results seen.
Significant heterogeneity remained in some cases, which could be considered a limitation, although this is not surprising because of the characteristics of the studies included. For studies examining receipt of chemotherapy and radiotherapy it was generally not possible to differentiate between curative and palliative treatment and, if patterns of care differ for these by SEP, this might explain the high degree of heterogeneity seen. However, although there is some suggestion that heterogeneity can be considered high at >50% [17], when confidence intervals were calculated these were wide, so it was difficult to be confident about the degree of heterogeneity present [27].
Results for receipt of radiotherapy differed in the non-UHCS sub-group compared to overall but, as only two studies were included in this sub-group, it is difficult to be sure that different patterns of receipt of radiotherapy by SEP are due to differences in health care system.
Many of the non-UHCS studies used overlapping population sub-groups from the SEER database. There was also population overlap between some UHCS datasets. We attempted to include only substantially non-overlapping datasets within the final meta-analyses to ensure independence of results. A judgement had to be made as to which was the best-quality and most appropriate paper to include, but sensitivity analyses using different inclusion combinations (Figure S8) did not change the overall findings, nor did including all suitable studies regardless of population overlap (Figures S1, S3, S4, S5, S7).
Included papers contained data for patients diagnosed between 1978 and 2008. As treatment guidance has changed over time, older studies may be less applicable to current clinical practice. However, the majority of included studies were published within the last five years, and sensitivity analyses excluding studies published prior to 2000 did not change the overall findings.
Various measures of SEP were used, and these were categorised differently—an acknowledged problem in equity reviews [28]. All but one study measured SEP at the area level. This is a further limitation, as area-based measures of SEP are unlikely to be accurate markers of individual-level circumstances and access to resources [29]. Area-based measures of SEP can be calculated using address, making them easy to add to disease registers, such as those used in many of the studies synthesised here. However, the reliance on area-based markers of SEP may underestimate the strength of the true association between SEP and receipt of treatment.
Not all studies reported details of stage and histology—both of which influence treatment type—and very few UHCS studies took co-morbidity into account. Thus, the ORs used in the meta-analyses were not consistently adjusted for the same covariates. However, we attempted to take these factors into account in the quality scores and by conducting subgroup sensitivity analyses. Examining only high-quality studies did not alter our findings nor did sensitivity analyses, although consequent reduction in numbers did result in loss of significance in some analyses, potentially due to lack of power to detect differences.
In order to conduct meta-analysis it is necessary to compare the odds of treatment in the lowest-SEP group with the odds in the highest, which simplifies what may be a complex relationship across SEP groups. However, studies that reported a change in odds ratios across the SEP categories, and thus explored trends in receipt of treatment, generally supported the overall findings of the review.
A number of existing tools suitable for assessing cohort study quality were considered [15],[16]. However, none of these tools was entirely appropriate for the type of studies included and, as has been done in previous reviews [13],[30], we devised a unique tool, adapting and utilising aspects of other available tools. This approach has the benefit of producing a quality tool that is highly specific for the type of studies examined.
As with any systematic review, we are unable to exclude the possibility of publication bias. Studies reporting null findings are less likely to be published or, if they are published, not to report numerical outcomes [17]. A funnel plot to assess potential publication bias did not show obvious bias (Figure S9). However, a number of papers recovered in the search included SEP in the description of the study population but did not report receipt of treatment by SEP [31]–[34]. Study authors were contacted and asked to provide further information, but only one supplied the requested data [34]. It is likely that SEP was not significantly associated with receipt of treatment in the other studies, but this was not always clearly reported. However, publication bias is thought to be less important than other sources of bias, such as confounding, in meta-analyses of observational studies [26].
Implications for Policy and Practice
Socioeconomic inequalities in receipt of treatment may exacerbate socioeconomic inequalities in incidence of lung cancer, which is strongly associated with higher smoking rates in more deprived populations, so may further contribute to the poorer outcomes in lower SEP groups.Socioeconomic inequalities in treatment may be due to differences in access to care. Within a non-UHCS it might be expected that socioeconomic differences in receipt of treatment would be observed due to income-related differences in health insurance status. Patients with lung cancer in the USA who do not have insurance have been shown to have more limited access to care [13]. However, as socioeconomic inequalities in receipt of lung cancer treatment were also observed in UHCSs that do not depend on ability to pay and in non-UHCS studies where insurance type was taken into account, this would suggest that other system factors may be contributing to this inequality. The extent to which receipt of treatment is influenced by factors such as patient choice is not known.
Variability at the patient, tumour, system, and individual clinician levels needs to be investigated before clear recommendations for changes to policy and practice can be made.
Future Research
This review has demonstrated a clear association between lower SEP and reduced likelihood of receiving surgery, chemotherapy, and any type of unspecified treatment for lung cancer. The reasons for these inequalities need to be more thoroughly investigated. Better-quality UHCS studies, including statistical control for co-morbidity and stratification by stage and histology—so that only those patients eligible for a particular treatment are included in the population-denominator—are required. It would also be useful to be able to distinguish between curative and palliative intent of treatment. In non-UHCS, studies in younger populations, examining a range of insurance providers, are required.Further investigation into the system and patient factors that might contribute to socioeconomic inequalities in receipt of lung cancer care is necessary, to help develop interventions that ensure equitable receipt of appropriate treatment. This should include a quantitative exploration of inequalities at each stage of the care pathway as well as qualitative work exploring reasons for inequality. Inequalities in receipt of treatment may contribute to inequalities in cancer survival and so cohort survival analyses are warranted in order to investigate intervention-generated inequalities in lung cancer outcomes.
No comments:
Post a Comment