Skip to main content

SYSTEMATIC REVIEW article

Front. Public Health, 19 November 2024
Sec. Life-Course Epidemiology and Social Inequalities in Health
This article is part of the Research Topic The Impact of Advancing Global Oncology: Towards Equity in Precision Prevention and Medicine View all 4 articles

Social determinants of health and upper gastrointestinal cancer outcomes in the United States: a systematic review

  • 1Georgia Cancer Center at Augusta University, Augusta, GA, United States
  • 2Medical College of Georgia, Augusta University, Augusta, GA, United States
  • 3School of Computing, University of Georgia, Athens, GA, United States
  • 4School of Public Health, Augusta University, Augusta, GA, United States
  • 5Georgia Prevention Institute, Augusta University, Augusta, GA, United States

Introduction: Social determinants of health (SDOH) are the conditions in which individuals are born, grow, work, live, and age.

Methods: We examined the literature on the association between SDOH and survival of patients with gastrointestinal (GI) cancer [esophageal, duodenal and gastric cancer (GC)] in the United States from 2001 to 2022.

Results: From 38,654 studies across COCHRANE, EMBASE, SCOPUS, WEB OF SCIENCE, and PubMed, we identified 14 relevant studies focusing on GI cancer using the PRISMA flowchart. Eight of the 12 GC studies specifically focused on gastric adenocarcinoma (GAC), the most common histologic subtype. Uninsured patients had a significantly worse overall survival probability. For patients with GI cancer, the highest income level (i.e., in the highest quartile) was associated with improved survival. Being unmarried had a negative impact on overall survival. Overall, people with insurance, higher incomes, and who were married had better overall survival rates.

Discussion: Our findings suggest a clear association between SDOH and survival for patients with GI cancers. However, there is great variability in the factors studied and how these are measured and reported. A better understanding of SDOH is needed to design strategies with an aim to improve patient outcomes.

Systematic review registration: https://www.crd.york.ac.uk/prospero/, PROSPERO (CRD42022346854).

1 Introduction

It is projected that in 2040 there will be approximately 28.4 million new cases of cancer worldwide, representing a 47% increase from 2020 (1). Importantly, in high-income countries, the more vulnerable populations are often the most exposed (1). Predictions are that in 2024 there will be 353,820 new cases of gastrointestinal (GI) cancers diagnosed, and 174,320 individuals will die of GI cancers in the United States (US). Of these, esophageal cancer is anticipated to account for 22,370 new cases, gastric cancer for 26,890 cases, and small intestine cancers, including duodenal cancers, for 12,440 cases, all contributing significantly to the overall burden (2). Globally, the incidence of gastric cancer (GC) has decreased from 1990 to 2017, with this reduction largely attributed to economic development and rising Socio-demographic Index (SDI) levels. The lowest incidence rates were observed in southern sub-Saharan Africa (5.2 [5.0–5.4]), eastern sub-Saharan Africa (6.4 [5.9–6.8]), and high-income North America (6.5 [6.3–6.7]) (3).

The incidence of GC, particularly gastric adenocarcinoma (GAC), is higher in non-White racial and ethnic groups compared to the non-Hispanic White (NHW) population in the US (4). The highest incidence rates are observed among major racial and ethnic groups, notably non-Hispanic Black Americans, Hispanic Americans, and Asian Americans. Hispanic men and non-Hispanic Black (NHB) men have a 3.6-fold and 2.9-fold higher incidence of GAC, respectively, compared to NHW men. Among Asian American ethnic groups, the incidence of GAC is up to 14.5 times greater compared to NHW men, with similar trends observed women in these racial and ethnic populations (4, 5). Between 2000 and 2019, GC mortality declined significantly across populations at the national level in the United States. With the fastest declines being observed among both Asian populations (48.3%) and black populations (42.6%). Despite these declines, mortality rates remained statistically significant among minority populations at the county level (6). Disparities in GC mortality among racial and ethnic groups persist, with reports indicating that minority groups experience a two-fold higher mortality risk compared to other populations (7).

In 1998, the WHO launched a campaign for public health action on Social Determinants of Health (SDOH) (8), leading to the creation of the Commission on SDOH, which issued the first recommendations on measuring and addressing SDOH (9). SDOH are defined as conditions in which people are born, grow, work, live, and age, and include the wider set of forces and systems shaping the conditions of daily life (10). The Healthy People 2030 initiative divides SDOH into 5 domains: Economic Stability, Education Access and Quality, Health Care Access and Quality, Neighborhood and Built Environment, and Social and Community Context (11, 12).

There is growing evidence of the impact of SDOH on cancer outcomes (13), with a higher cancer mortality rate in the most underprivileged groups (14). Although prior studies have examined the association between SDOH and GI cancer survival, none of these used a comprehensive framework (as recommended by Healthy People 2030) (11). Because several SDOH components are highly correlated, studies using a comprehensive framework are needed. To address this gap, we performed a systematic review of the literature, examining the association between SDOH and GI cancer survival. The goal of this study is to consolidate the diverse existing literature on SDOH in GI cancer into a homogeneous classification framework. This approach aims to enhance understanding of the impact of SDOH on patients with GI cancers in order to guide future studies to better address healthcare disparities among these patients.

2 Materials and methods

This systematic review is registered in PROSPERO (CRD42022346854).1 It strictly follows the Preferred Reporting Items for Systematic Reviews and Meta-Analyses 2020 (PRISMA) statement (15) and aligns with the Cochrane Handbook for Systematic Reviews of Interventions (16).

A comprehensive search was performed in the COCHRANE, EMBASE, SCOPUS, WEB OF SCIENCE, and PubMed databases from 2002 to 2022. Additional manuscripts were searched in Google Scholar and in the references included. This 20-year time frame was selected to provide a balance of historical perspective and relatively recent data since social determinants have evolved over time. By limiting our search to this specific period, we aim to provide a concise and focused synthesis of literature that is both manageable and highly relevant to contemporary research questions (Supplementary Table 1).

Selected manuscripts reported US population-based observational studies on the effect of SDOH on GI cancer survival outcomes, aligned with the five Healthy People 2030 SDOH core domains (11). Studies examining colorectal cancer (CRC) were excluded due to its high incidence, since it might dominate the results. Instead, we focused on the less common GI cancers and will analyze CRC separately in a future analysis. Non-cancer studies without SDOH evaluation or outcomes related to cancer survival and general cancer studies without identifiable outcomes by cancer type were excluded. Duplicated publications, those published outside our specified cut-off date, non-English publications, revisions, letters to the editor, pre-clinical reports, and case series reports were also excluded. Eligible manuscripts identified based on the listed search criteria (Supplementary Table 1) were retrieved and imported to Rayyan software. Manuscripts were screened and duplicates removed. Two authors (BS and MS) assessed the relevance of the remaining manuscripts based on abstract and title, with disagreements resolved by consulting oncology experts (JC and AN). Manuscripts not meeting the eligibility criteria were excluded. Manuscripts addressing SDOH and cancer survival were initially selected (n = 758), and within this group, 20 studies specific to GI cancers were identified. In the second review stage, the full manuscripts were examined, and exclusion criteria applied (Supplementary Table 2). All references included after the abstract screening were independently assessed by two reviewers (RA and GD) for methodological quality and were evaluated for risk of bias assessment using the Joanna Briggs Institute (JBI) checklist, which comprises eight items and an overall assessment (Figure 1).

Figure 1
www.frontiersin.org

Figure 1. Risk of bias assessed by the Joanna Briggs institute critical appraisal tools for analytical cross-sectional studies.

A total of 14 eligible manuscripts were identified for this review (Figure 2). Eligible studies were uploaded to Nvivo software to enhance the rigor and depth of the qualitative analysis. Extracted data included first author, publication year, study location, database details, study type, patient characteristics (sample size, population sample, age group), aims, SDOH studied, associated factors, limitations and barriers, and results. Survival measures included overall survival (OS), cancer-specific survival (CSS) and progression-free survival (PFS).

Figure 2
www.frontiersin.org

Figure 2. Flowchart of the studies selection process.

We qualitatively synthesized data on the association between SDOH and GI cancer survival, considering each SDOH as an isolated variable. Study characteristics and SDOH data were extracted (Tables 1, 2), and significant results, including p values, were extracted (Tables 36). Statistically significant adjusted values, accounting for confounding factors such as age, sex, and ethnicity, were considered.

Table 1
www.frontiersin.org

Table 1. Population characteristics of included studies assessing SDOH for gastrointestinal (GI) cancer patients (n = 14).

Table 2
www.frontiersin.org

Table 2. SDOH according to the Healthy People 2030 framework assessed in gastrointestinal (GI) cancer patients of included manuscripts (n = 14).

Table 3
www.frontiersin.org

Table 3. Results of included studies assessing healthcare access and quality by tumor type (n = 11).

Table 4
www.frontiersin.org

Table 4. Results of included studies assessing economic stability by tumor type (n = 7).

Table 5
www.frontiersin.org

Table 5. Results of the included studies assessing education access and quality by cancer type (n = 4).

Table 6
www.frontiersin.org

Table 6. Results of included studies assessing social and community context by cancer type (n = 4).

3 Results

Table 1 summarizes the descriptive characteristics of the evidence included in our review. We identified studies in GC (n = 12), with eight studies focused on gastric adenocarcinoma (GAC) and four studies including other histologic subtypes (e.g., squamous cell carcinoma, mucinous carcinoma, signet ring cell carcinoma). Two studies focused on esophageal cancer (n = 2) and one on duodenal cancer (n = 1). One study originated from a single medical institution (Boston Medical Center) and one study was from a health system (multi-hospital healthcare system affiliated with the University of Tennessee Health Science Center). The remaining studies utilized national databases, including The Surveillance, Epidemiology, and End Results (SEER; n = 9) and The National Cancer Data Base (NCDB; n = 3).

Nine categories of SDOH were assessed across the 14 studies, using different measurement tools for the five main domains. Healthcare access and quality (n = 11), and economic stability (n = 7) were the most commonly analyzed domains. Within them, insurance status (n = 8) and income level (n = 5) were the most frequently assessed categories (Table 2).

3.1 Healthcare access and quality

Eleven studies analyzed Health Care Access and Quality (1727). The main categories assessed were insurance status (n = 8), access to treatment (n = 3), type of facility (n = 2), and hospital volume (n = 1; Table 3).

The correlation of insurance status with OS outcomes was explored in seven studies focused on GC and two studies on esophageal cancer. Uninsured patients had a worse OS probability. This trend was consistently observed across most of the studies evaluating insurance status (18, 21, 22, 2427). Fang et al. reported inferior OS for uninsured versus privately insured patients (p = 0.02), although this difference was not statistically significant when considering only CSS (23). Similar results were found for esophageal cancer patients that underwent esophagectomy when comparing privately insured with not privately insured patients (p = 0.002) (24). Medicaid coverage was an independent prognostic indicator of inferior OS among patients with GC (p-value = 0.001) (18) and locally advanced GC who underwent gastrectomy (p = 0.02), compared to those with private insurance (23). A survival disadvantage (statistical trend) was observed for patients with GC on Non-Federal Health Insurance (vs those on Medicare-Medicaid; p = 0.051) (21). Private insurance was associated with superior OS for patients with GC specifically in low-volume centers (1–99 surgeries over the 10-year observation period; p = 0.013). For patients with esophageal cancer treated with esophagectomy, inferior OS was evident for uninsured patients in both low- (p = 0.009), middle- (100–200 surgeries; p = 0.002), and high-volume (>200 surgeries) centers (p = 0.007) (25).

Among studies assessing the type of facility (24, 25), one study in esophageal cancer found that receiving treatment at a community center (p = 0.007) was associated with poor OS (24). Treatment of GC patients undergoing gastrectomy at academic institutions had better OS at low-volume centers (p = 0.011) (25).

Treatment access was evaluated by three studies in GC (17, 19, 20). There was a higher probability of not receiving cancer-directed therapy for patients living in high poverty areas (p = 0.0001) (17). A second study found that lower education level was associated with lack of treatment, which in turn was linked with inferior OS (p < 0.001) (20). Poor compliance with surgical treatment was significantly more common among single and widowed GC patients. Patients with poor compliance in turn demonstrated worse survival outcomes compared with those in the surgical compliance group (p < 0.0001) and those in the non-surgical group (p < 0.0001) (19).

3.2 Assessing economic stability

Seven studies (17, 18, 21, 2426, 28) analyzed economic stability by assessing income (n = 5) and poverty (n = 3) using different metrics (Table 4).

When income was used to measure Social Economic Stability (SES), a superior OS probability was identified for esophageal cancer patients in the highest quartiles of income (Q3 vs. Q1 p = 0.004; Q4 vs. Q1 p < 0.0001) (24).

For patients with GC, the highest income level (i.e., in the highest quartile) was associated with improved OS (p = 0.016) and CSS (p = 0.037) (18). There was an insignificant trend in the same direction for quartiles 2 and 3 compared to the lowest quartile. Higher median household income was also associated with higher OS rates (p = 0.0306) (28). Among lower and middle-volume centers, patients with the highest income had a better probability for OS (p < 0.001) (25). Using a different metric, a univariate analysis found a survival disadvantage for patients who resided in zip codes where >20% of the population lived in poverty (24.0 vs. 16.0 months; p = 0.006) (21).

No significant association was identified between living in high-poverty areas and survival outcomes in two studies analyzing GC patients undergoing surgical treatment (cancer-direct surgery, or surgery with curative intent) (17, 26). One found no correlation between income (above or below the median) and disease-specific survival (DSS; p = 0.859) in univariate analysis (26). In the second study, multivariate analysis revealed a non-statistical significant trend for the highest level of poverty associated with worse survival (p = 0.04) (17).

3.3 Assessing education access and quality

Four studies analyzed the education domain using education level quartiles (n = 2) or percent of population without a high school diploma (n = 2; Table 5) (18, 24, 25, 28). For patients with GC, both moderate and high education levels were significantly associated with superior OS (p = 0.001 and p = 0.005, respectively) and CSS probabilities (p < 0.001 and p = 0.004, respectively) (18). In another analysis, patients living in areas where a lower percent of the population did not have a high school education had OS probabilities (p = 0.0306) (28).

Among the studies that evaluated esophageal cancer OS outcomes, a higher level of education also had a positive impact (p = 0.009) (24), with better OS in low-volume hospitals with a lower percentage of patients who did not graduate from high school (p < 0.001) (25).

3.4 Assessing social and community context

Four studies analyzed marital status within the social and community context domain (Table 6) (18, 27, 29, 30). Being unmarried (including widowed/widower, single (never married) and separated/divorced) had a negative impact on OS (p < 0.001) (18, 29) and CSS (p = 0.027) among patients with GC (27). One study in patients with duodenal cancer also reported that unmarried status had an unfavorable correlation with OS and CSS (p < 0.001) (30).

4 Discussion

According to projected 2040 cancer burden statistics, the expected increase in cancer incidence correlates significantly with the Human Development Index (HDI), particularly in low and medium HDI countries (1). HDI dimensions overlap with SDOH, and our systematic review emphasizes the strong correlation of various SDOH domains in GC outcomes.

Past studies have shown a correlation between insurance status and stage at diagnosis of cancer (31). In our analysis, insurance status had a strong correlation with OS outcomes, with uninsured patients having a higher death risk compared to their insured counterparts. Interestingly, Medicaid-covered patients often experienced worse outcomes, possibly due to correlation with factors such as poverty, nutritional status, and lack of support systems among Medicaid beneficiaries (18, 23). Unfortunately, the unidimensional (or oligodimensional) evaluation of this metric does not allow proper evaluation of the whole universe of SDOH for these patients or the stage at diagnosis. The type of healthcare facilities where patients are treated also play a role, with academic institutions affiliated health facilities having the best OS (21, 25). The reasons for this are not explored in the studies analyzed, and may include more specialized and multidisciplinary care, access to clinical trials, and others. Socioeconomic factors such as poverty and lower education levels were linked to reduced access and adherence to treatment, resulting in inferior survival outcomes (17, 19, 20). Therefore, interventions that address disparities in health insurance coverage and access to specialized centers are key to improve outcomes across the whole spectrum of patients.

Economic stability influences GC survival, which can be attributed to its impact on healthcare access. Higher income level is associated with improved access to healthcare, preventive services, timely diagnosis, and treatment adherence (32). In our review, higher income levels were consistently associated with improved OS and CSS in both GC and esophageal cancer (18, 24). Understanding the correlation of economic stability with other SDOH may help target interventions for vulnerable populations where the impact may be greatest. Earlier studies reported associations between education and income, serving as indicators of SES and contributing to increasing the incidence of GC (33).

The association between education and GC survival may reflect the broader context of health behaviors and health literacy. Higher education levels are associated with better health-seeking behaviors (34). Advanced education consistently predicted better GC survival, showing superior OS and CSS. Notably, education remains significant even when considered alongside income in the same SES model (24). These findings align with the existing literature, indicating a strong correlation between education and health (18, 24, 25, 28). Improving health literacy in the general population and among patients with cancer should be prioritized by health authorities, health systems and healthcare providers to improve understanding of the disease and its treatment, eliminate stigmas, and provide resources to access the best possible care including clinical trials.

Several studies have suggested that social relationships have a considerable impact on mortality risk (35, 36). Marital status is widely used as a measure of social integration; however, an increasing number of studies document its contrasting effects, depending on the level of marital quality (3638). Essential indicators of social and community well-being, such as social inclusion, quality of relationships and social support, have not been evaluated in the context of GC. The studies reviewed here were constrained to assessing only marital status as the lone social and community SDOH among patients with GI cancer. Single individuals exhibited poorer OS and CSS compared to their married counterparts. These results highlight the supportive role of social relationships in navigating and coping with cancer (18, 27, 29, 30). Further research should explore the dynamics of social relationships and their impact on cancer care, including other relationships that may be of value to an individual (e.g., friends, other family members), the role of social support, and the impact of community interventions on patients’ well-being, which may help develop patient-centered care approaches.

A major strength of this study lies in its ability to address gaps resulting from the limited literature specifically examining the association between individual or a few SDOH and a specific cancer, such as GC. In contrast, most of the existing literature tends to study cancer as a whole (39, 40). This provides strength for larger cohorts but potentially overlooks or dismisses specific characteristics unique to certain cancers, such as GC.

Despite the strengths of our analysis, there are important limitations that should be noted. First, most studies used large national databases (SEER and NCDB). These databases are limited in data at an individual level, thus making generalizations that may not be applicable to individual patients. Further, these registries usually do not collect detailed information on SDOH. Second, the use of different definitions and classifications of SDOH and the use of different measurement tools results in difficulties in homogenizing the data. There are, for example, different approaches to analyze SES (above and below median vs. quartiles) or education (no high-school vs. other approaches). This should serve as a call for developing a more uniform and systematic approach to collecting data on SDOH both at individual institutions and in national databases.

5 Conclusion

Understanding SDOH in association with GI cancer survival requires exploring their underlying causes. Despite gaps in our knowledge of issues relating to the SDOH, as well as their reported heterogeneity, the impact of SDOH on cancer outcomes is clear. In order to address healthcare disparities in GC (and cancer in general), a comprehensive approach in collecting, reporting and analyzing SDOH is required. These factors should be included in outcomes analyses together with biologic characteristics and therapeutic interventions. A comprehensive approach would be better suited to understanding the correlation of all factors affecting outcomes in individual patients, and developing strategies to eliminate disparities. In the era of personalized medicine, we should not ignore that an important component of this personalization is the environment in which the patient lives.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary material, further inquiries can be directed to the corresponding authors.

Author contributions

BS: Conceptualization, Formal analysis, Investigation, Methodology, Project administration, Resources, Writing – original draft. RA: Data curation, Validation, Writing – review & editing. GD: Data curation, Validation, Writing – review & editing. MS: Data curation, Software, Validation, Writing – review & editing. GA: Visualization, Writing – review & editing. EB: Visualization, Writing – review & editing. M-HT: Writing – review & editing. AN: Writing – review & editing. JC: Conceptualization, Supervision, Writing – review & editing.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Acknowledgments

The authors would like to thank Rhea-Beth Markowitz for providing editorial assistance.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpubh.2024.1477028/full#supplementary-material

Footnotes

References

1. Sung, H, Ferlay, J, Siegel, RL, Laversanne, M, Soerjomataram, I, Jemal, A, et al. Global Cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. (2021) 71:209–49. doi: 10.3322/caac.21660

PubMed Abstract | Crossref Full Text | Google Scholar

2. Siegel, RL, Giaquinto, AN, and Jemal, A. Cancer statistics, 2024. CA Cancer J Clin. (2024) 74:12–49. doi: 10.3322/caac.21820

PubMed Abstract | Crossref Full Text | Google Scholar

3. Etemadi, A, Safiri, S, Bisignano, C, Shakeri, R, Amani, M, Fitzmaurice, C, et al. The global, regional, and national burden of stomach cancer in 195 countries, 1990-2017: a systematic analysis for the global burden of disease study 2017. Lancet Gastroenterol Hepatol. (2020) 5:42–54. doi: 10.1016/S2468-1253(19)30328-0

PubMed Abstract | Crossref Full Text | Google Scholar

4. Shah, SC, McKinley, M, Gupta, S, Peek, RM Jr, Martinez, ME, and Gomez, SL. Population-based analysis of differences in gastric Cancer incidence among races and ethnicities in individuals age 50 years and older. Gastroenterology. (2020) 159:1705–14.e2. doi: 10.1053/j.gastro.2020.07.049

PubMed Abstract | Crossref Full Text | Google Scholar

5. Mok, JW, Oh, YH, Magge, D, and Padmanabhan, S. Racial disparities of gastric cancer in the USA: an overview of epidemiology, global screening guidelines, and targeted screening in a heterogeneous population. Gastric Cancer. (2024) 27:426–38. doi: 10.1007/s10120-024-01475-9

PubMed Abstract | Crossref Full Text | Google Scholar

6. GBD US Health Disparities Collaborators . The burden of stomach cancer mortality by county, race, and ethnicity in the USA, 2000-2019: a systematic analysis of health disparities. Lancet Reg Health Am. (2023) 24:100547. doi: 10.1016/j.lana.2023.100547

Crossref Full Text | Google Scholar

7. Williams, PA, Kaleem, ZS, and Rajarshi, S. AACR Cancer Disparities Progress Report. Cancer Epidemiol Biomarkers Prev. (2022) 31:1249–50. doi: 10.1158/1055-9965.EPI-22-0542

Crossref Full Text | Google Scholar

8. Marmot, M, Friel, S, Bell, R, Houweling, TAJ, and Taylor, S. Closing the gap in a generation: health equity through action on the social determinants of health. Lancet. (2008) 372:1661–9. doi: 10.1016/S0140-6736(08)61690-6

Crossref Full Text | Google Scholar

9. Richard, Wilkinson. Social determinants of health: the solid facts. World Health Organization. Regional regional office for Europe. (1998). Available at: https://iris.who.int/handle/10665/108082 Accessed 4 Apr 2023.

Google Scholar

10. World Health Organization . Social Determinats of health. World health Organization. (2023). Available at: https://www.who.int/health-topics/social-determinants-of-health#tab=tab_1. Accessed 20 Jan 2023.

Google Scholar

11. Healthy People 2030 . Social determinants of health. Department of Health and Human Services, Office of Disease Prevention and Health Promotion (2023). Available at: https://health.gov/healthypeople/priority-areas/social-determinants-health. Accessed 20 Jan 2023.

Google Scholar

12. NEJM Catalyst . Social determinants of health (SDOH). NEJM Catalyst. (2017) 3. doi: 10.1056/CAT.17.0312(1)

Crossref Full Text | Google Scholar

13. Coughlin, SS. Social determinants of health and Cancer survivorship. J Environ Health Sci. (2021) 7:11–5. doi: 10.15436/2378-6841.21.3805

Crossref Full Text | Google Scholar

14. Singh, GK, and Jemal, A. Socioeconomic and racial/ethnic disparities in Cancer mortality, incidence, and survival in the United States, 1950-2014: over six decades of changing patterns and widening inequalities. J Environ Public Health. (2017) 2017:2819372. doi: 10.1155/2017/2819372

Crossref Full Text | Google Scholar

15. Page, MJ, McKenzie, JE, Bossuyt, PM, Boutron, I, Hoffmann, TC, Mulrow, CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. (2021) 372:71. doi: 10.1136/bmj.n71

Crossref Full Text | Google Scholar

16. Higgins, JPT, Thomas, J, and Chandler, J. Cochrane handbook for systematic reviews of interventions version. 2nd ed. Chichester (UK): John Wiley & Sons (2019).

Google Scholar

17. Nguyen, DK, and Maggard-Gibbons, M. Age, poverty, acculturation, and gastric cancer. Surgery. (2013) 154:444–52. doi: 10.1016/j.surg.2013.05.017

PubMed Abstract | Crossref Full Text | Google Scholar

18. Xu, J, and Du, S. Associations of education level with survival outcomes and treatment receipt in patients with gastric adenocarcinoma. Front Public Health. (2022) 10:868416. doi: 10.3389/fpubh.2022.868416

Crossref Full Text | Google Scholar

19. Liu, G, Xu, M, Gao, T, Xu, L, Zeng, P, Bo, H, et al. Surgical compliance and outcomes in gastric Cancer: a population-based cohort study. J Cancer. (2019) 10:779–88. doi: 10.7150/jca.29073

Crossref Full Text | Google Scholar

20. Liu, N, Molena, D, Stem, M, Blackford, AL, Sewell, DB, and Lidor, AO. Underutilization of treatment for regional gastric Cancer among the elderly in the USA. J Gastrointest Surg. (2018) 22:955–63. doi: 10.1007/s11605-018-3691-3

PubMed Abstract | Crossref Full Text | Google Scholar

21. Morgan, R, Cassidy, M, DeGeus, SWL, Tseng, J, McAneny, D, and Sachs, T. Presentation and survival of gastric Cancer patients at an urban academic safety-net hospital. J Gastrointest Surg. (2019) 23:239–46. doi: 10.1007/s11605-018-3898-3

PubMed Abstract | Crossref Full Text | Google Scholar

22. Rana, N, Gosain, R, Lemini, R, Wang, C, Gabriel, E, Mohammed, T, et al. Socio-demographic disparities in gastric adenocarcinoma: a population-based study. Cancers (Basel). (2020) 12:12. doi: 10.3390/cancers12010157

Crossref Full Text | Google Scholar

23. Fang, W, Hu, H, Jia, L, Zhang, J, Huang, C, and Hu, S. Survival disparities among non-elderly American adults with locally advanced gastric cancer undergoing gastrectomy by health insurance status. Am J Med Sci. (2022) 364:198–206. doi: 10.1016/j.amjms.2022.03.004

PubMed Abstract | Crossref Full Text | Google Scholar

24. Erhunmwunsee, L, Gulack, BC, Rushing, C, Niedzwiecki, D, Berry, MF, and Hartwig, MG. Socioeconomic status, not race, is associated with reduced survival in Esophagectomy patients. Ann Thorac Surg. (2017) 104:234–44. doi: 10.1016/j.athoracsur.2017.01.049

PubMed Abstract | Crossref Full Text | Google Scholar

25. Gabriel, E, Narayanan, S, Attwood, K, Hochwald, S, Kukar, M, and Nurkin, S. Disparities in major surgery for esophagogastric cancer among hospitals by case volume. J Gastrointest Oncol. (2018) 9:503–16. doi: 10.21037/jgo.2018.01.18

PubMed Abstract | Crossref Full Text | Google Scholar

26. Tsao, MW, Delozier, OM, Stiles, ZE, Magnotti, LJ, Behrman, SW, Deneve, JL, et al. The impact of race and socioeconomic status on the presentation, management and outcomes for gastric cancer patients: analysis from a metropolitan area in the Southeast United States. J Surg Oncol. (2020) 121:494–502. doi: 10.1002/jso.25827

PubMed Abstract | Crossref Full Text | Google Scholar

27. Qiu, M, Yang, D, and Xu, R. Impact of marital status on survival of gastric adenocarcinoma patients: results from the surveillance epidemiology and end results (SEER) database. Sci Rep. (2016) 6:21098. doi: 10.1038/srep21098

PubMed Abstract | Crossref Full Text | Google Scholar

28. Stessin, AM, and Sherr, DL. Demographic disparities in patterns of care and survival outcomes for patients with resected gastric adenocarcinoma. Cancer Epidemiol Biomarkers Prev. (2011) 20:223–33. doi: 10.1158/1055-9965.EPI-10-0158

PubMed Abstract | Crossref Full Text | Google Scholar

29. Jin, JJ, Wang, W, Dai, FX, Long, ZW, Cai, H, Liu, XW, et al. Marital status and survival in patients with gastric cancer. Cancer Med. (2016) 5:1821–9. doi: 10.1002/cam4.758

PubMed Abstract | Crossref Full Text | Google Scholar

30. Wang, N, Bu, Q, Liu, Q, Yang, J, He, H, Liu, J, et al. Effect of marital status on duodenal adenocarcinoma survival: a surveillance epidemiology and end results population analysis. Oncol Lett. (2019) 18:1904–14. doi: 10.3892/ol.2019.10475

PubMed Abstract | Crossref Full Text | Google Scholar

31. Zhao, J, Han, X, Nogueira, L, Fedewa, SA, Jemal, A, Halpern, MT, et al. Health insurance status and cancer stage at diagnosis and survival in the United States. CA Cancer J Clin. (2022) 72:542–60. doi: 10.3322/caac.21732

PubMed Abstract | Crossref Full Text | Google Scholar

32. McMaughan, DJ, Oloruntoba, O, and Smith, ML. Socioeconomic status and access to healthcare: interrelated drivers for healthy aging. Front Public Health. (2020) 8:231. doi: 10.3389/fpubh.2020.00231

PubMed Abstract | Crossref Full Text | Google Scholar

33. Uthman, OA, Jadidi, E, and Moradi, T. Socioeconomic position and incidence of gastric cancer: a systematic review and meta-analysis. J Epidemiol Community Health. (2013) 67:854–60. doi: 10.1136/jech-2012-201108

PubMed Abstract | Crossref Full Text | Google Scholar

34. Hahn, RA, and Truman, BI. Education improves public health and promotes health equity. Int J Health Serv. (2015) 45:657–78. doi: 10.1177/0020731415585986

PubMed Abstract | Crossref Full Text | Google Scholar

35. Valtorta, NK, Kanaan, M, Gilbody, S, Ronzi, S, and Hanratty, B. Loneliness and social isolation as risk factors for coronary heart disease and stroke: systematic review and meta-analysis of longitudinal observational studies. Heart. (2016) 102:1009–16. doi: 10.1136/heartjnl-2015-308790

PubMed Abstract | Crossref Full Text | Google Scholar

36. Holt-Lunstad, J, Smith, TB, and Layton, JB. Social relationships and mortality risk: a meta-analytic review. PLoS Med. (2010) 7:e1000316. doi: 10.1371/journal.pmed.1000316

PubMed Abstract | Crossref Full Text | Google Scholar

37. Robles, TF, Slatcher, RB, Trombello, JM, and McGinn, MM. Marital quality and health: a meta-analytic review. Psychol Bull. (2014) 140:140–87. doi: 10.1037/a0031859

Crossref Full Text | Google Scholar

38. Porter, LS, Keefe, FJ, Baucom, DH, Hurwitz, H, Moser, B, Patterson, E, et al. Partner-assisted emotional disclosure for patients with gastrointestinal cancer: results from a randomized controlled trial. Cancer. (2009) 115:4326–38. doi: 10.1002/cncr.24578

PubMed Abstract | Crossref Full Text | Google Scholar

39. Alcaraz, KI, Wiedt, TL, Daniels, EC, Yabroff, KR, Guerra, CE, and Wender, RC. Understanding and addressing social determinants to advance cancer health equity in the United States: a blueprint for practice, research, and policy. CA Cancer J Clin. (2020) 70:31–46. doi: 10.3322/caac.21586

PubMed Abstract | Crossref Full Text | Google Scholar

40. Tucker-Seeley, R, Abu-Khalaf, M, Bona, K, Shastri, S, Johnson, W, Phillips, J, et al. Social determinants of health and Cancer care: an ASCO policy statement. JCO Oncol Pract. (2024) 20:621–30. doi: 10.1200/OP.23.00810

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: cancer, gastrointestinal, gastric cancer, survival, social determinants, healthcare system

Citation: Santellano B, Agrawal R, Duchesne G, Sharara M, Agrawal G, Balas EA, Tsai M-H, Nayak A and Cortes JE (2024) Social determinants of health and upper gastrointestinal cancer outcomes in the United States: a systematic review. Front. Public Health. 12:1477028. doi: 10.3389/fpubh.2024.1477028

Received: 06 August 2024; Accepted: 04 November 2024;
Published: 19 November 2024.

Edited by:

Jaira Ferreira de Vasconcellos, James Madison University, United States

Reviewed by:

Nicholas Matovu, Queen’s University Belfast, United Kingdom
Hongqing An, Shandong Second Medical University, China

Copyright © 2024 Santellano, Agrawal, Duchesne, Sharara, Agrawal, Balas, Tsai, Nayak and Cortes. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Jorge E. Cortes, am9yZ2UuY29ydGVzQGF1Z3VzdGEuZWR1

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.