Introduction There is increasing attention on the cancer burden for adults with intellectual and developmental disabilities (IDD). Emerging evidence suggests there are differences in cancer experiences and outcomes for individuals living with IDD, from risk through survivorship. These differences may be attributed to features of the IDD, such as cognitive deficits and communication, as well as social determinants of health-like lower education levels and ableism. However, there is no comprehensive overview of the literature quantifying these potential disparities and describing the influencing factors. In this paper, we describe a scoping review protocol to systematically review published literature on cancer for adults with IDD. The purpose of this review is to identify differences in cancer risk, stage at diagnosis, treatment and survival along the cancer continuum for adults with IDD and outline potential contributing factors creating these disparities.
Methods and analysis We will follow Arksey and O’Malley’s expanded framework for scoping reviews to conduct this review. We will systematically search electronic databases for peer-reviewed, published journal articles to identify appropriate studies in collaboration with a health science librarian. Two reviewers will independently review titles and abstracts followed by a full-text review to determine whether it meets inclusion criteria. A data chart for collecting and sorting information will be developed in consultation with the team. Results will be collated and reported following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) extension for scoping reviews: PRISMA-Scoping Reviews. Extracted information will be summarised quantitatively and qualitatively to meet review objectives.
Ethics and dissemination This scoping review will employ a methodology to identify literature related to cancer outcomes and experiences for adults with IDD. Results will be disseminated to relevant stakeholders who care for and support individuals with IDD at local, provincial and national levels and through publishing findings. By highlighting the disparities in the cancer system and gaps in the research, this scoping review can provide direction for future action.
- intellectual and developmental disabilities
- health equity
- cancer outcomes
- health disparities
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Strengths and limitations of this study
This will be the first scoping review to systematically search outcomes for individuals with intellectual and developmental disabilities (IDD) along the cancer continuum from risk to survivorship/end-of-life.
This review will map and describe the factors including social determinants of health that influence cancer outcomes and experiences of adults with IDD.
As this is a scoping review, quality assessment and grading will not be performed, minimising the ability to provide clinical recommendations to improve cancer care for persons with IDD.
Studies published in English and French will be included.
There is greater attention and focus on the burden of cancer among individuals with intellectual and developmental disabilities (IDD). IDD, including Down syndrome, cerebral palsy and autism spectrum disorder, are life-long disorders originating before the age of 18 and affect 1%–3% of the population. IDD diagnoses range from mild to profound impairment with features such as diminished communication, difficulty processing information and problem solving, as well as challenges with activities of daily living.1 2 Significant improvements in life expectancy,3 4 the recognition that cancer is a leading cause of death in persons with IDD5 6 and the possibility that significant limitations in intellectual functioning may make it challenging for persons with IDD to access and navigate a cancer setting1 2 7 are influencing this shift in focus.
Disparities in cancer outcomes persist within universal healthcare systems across the cancer control spectrum, from prevention to survivorship and end-of-life care. Many of the factors influencing these disparities are not connected to the cancer itself, but to a person’s social and economic context that shape their ability to access cancer care. Groups most vulnerable to these disparities are ones that experience discrimination and underlying levels of economic, social and geographic disadvantage.8 Cancer risk factors, screening rates, stage at diagnosis, receipt of guideline-recommended treatment, symptom management and cancer mortality vary by age, sex, immigration status, sexual orientation, socioeconomic position, geographic location, rurality and in indigenous populations.9–22 International, national and local cancer agencies have directed efforts to addressing barriers that lead to poorer outcomes and experiences for vulnerable populations.23–27 To make clinical care and delivery of support services more responsive to the needs of the vulnerable groups, there is an imperative to improve understanding of disparities within the cancer system. While this is an emerging area of research, there has been a lack of focus on the needs of adults with IDD, leaving many unanswered questions.28 29
Adults with IDD may be at greater risk of worse outcomes along the cancer continuum for a number of reasons.29 30 Potential pathways are related to features of IDD, that is, cognitive deficits and difficulties with communication and are influenced by the social determinants of health that shape one’s economic and material reality.31 In particular, determinants such as provider bias and ableism; lower levels of employment, education and social support; lack of access to suitable transportation; a lack of provider knowledge and organisation of the health system that hinders access to services have been suggested as mechanisms leading to poorer outcomes.32–37 Existing literature reviews focusing on cancer and IDD to inform provider and system-level interventions are narrative in nature,28 29 38 analyse a handful of studies on a particular cancer type38 39 or do not highlight modifiable barriers to improve cancer care, limiting actionable content.28 29 39 This review seeks to address this gap and provide an overview of the literature on cancer outcomes among adults with IDD and the factors that influence them over the cancer continuum, from risk and prevention to end-of-life/survivorship.
The primary objectives of this scoping review are to systematically map and examine the evidence base comparing cancer outcomes for adults with IDD to those without, to explore the literature describing cancer care experiences for adults with IDD. It will focus primarily on cancer incidence, screening, staging, treatment and prognosis. Our goals are to direct future research efforts by identifying literature gaps and limitations, and highlight relevant social determinants of health influence cancer outcomes for individuals with IDD. It is our hope that this review will expand the wider body of research examining cancer disparities for vulnerable populations.
Methods and analysis
A scoping methodology approach will be used to explore the literature describing cancer outcomes for individuals with IDD. Scoping reviews can examine broad questions that aim to describe research activity in an area and its evidence base.40–42 We will follow the expanded Arksey and O’Malley (2005) framework for scoping reviews.40–42We will follow the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) extension for reporting scoping reviews: PRISMA-Scoping Reviews checklist.43
Identifying the research question
The scoping review will answer the questions:
What are the effects of living with an IDD on adult cancer risk, screening, stage at diagnosis, treatment and survival relative to those without IDD?
What factors related to features of IDD may contribute to differences in cancer care experiences and outcomes for individuals with IDD compared with those without?
What social determinants of health may contribute to differences in cancer care experiences and outcomes for individuals with IDD compared with those without?
The research team developed these questions and initial protocol in an iterative process and will revise the protocol as needed throughout the review process.
Search strategy and information sources
The primary search strategy was developed for Medline by the research team in collaboration with a health sciences librarian (JL). We will execute a similar search in Embase, Cochrane, CINAHL, Scopus and PsycINFO. The search will employ the following Medical Subject Headings (MeSH) headings for IDD and cancer, respectively, and will be linked with Boolean operator OR within a category and using the Boolean operator AND between IDD and cancer:
IDD: [exp intellectual disability/], [exp Developmental Disabilities/]; [exp Child Development Disorders, Pervasive/].
Cancer: exp [neoplasms/].
Preliminary searches in Medline and Embase identified 749 and 1916 potential citations, respectively. We have elected to complete a sensitive strategy given the lack of specificity in cancer-related MeSH headings for our research objectives. A copy of the search strategy has been included as a online supplementary file. We will restrict the study to those articles published in 2000 or later to best approximate the risk of cancer and cancer-related outcomes in adults living with IDD currently, given changes in IDD definitions and increased life expectancy over time.4 We will also review reference lists of relevant review articles and perform a cited reference search of included studies.
Study selection will follow two stages. The first will be an initial review of titles and abstracts by two reviewers. The initial review will be done independently, with reviewers discussing results once screening is complete. Resolving disagreement will be attempted first by the two reviewers, but if necessary a third member of the research team will be consulted to reach consensus. Once the initial decision on which articles to include, we will begin the second stage of conducting a full-text review. Two reviewers will assess the articles to determine whether it meets the inclusion criteria. Those articles where there is uncertainty will be reviewed by a third member of the team to determine its eligibility. Table 1 outlines the inclusion/exclusion criteria following the population, concept and context categories for scoping reviews.44 Due to expertise within the team, we will include studies in both English and French.
Charting the data
A data chart will be developed in consultation with the research team. This chart will facilitate the collection and sorting of information from selected studies. Key areas that will be included in this chart will include: description of study population (eg, age, sex, socioeconomic status and comorbidity), definition of IDD, IDD diagnosis, context of IDD care (eg, institution and community), which milestone along the cancer continuum is explored in the study, cancers included (eg, lung, breast and melanoma), sources of information (eg, hospital records and cancer registry), study time frame, study location and sample size. For studies where the study population is not adults with IDD and is their caregiver or healthcare provider, this information will be noted. Cancer incidence, prevalence, screening rates, stage at diagnosis, treatment (eg, chemotherapy, radiation and surgery), survival from diagnosis or other relevant timepoints, palliation, follow-up care during remission, recurrence rates and quality of life measures will be quantified and measures of comparison to the general cancer population extracted where possible. Major themes from qualitative studies will be extracted and summarised across studies. Where possible we will summarise quantitative and qualitative data within and across IDD diagnoses as well as within and across countries. The data chart will be piloted by two reviewers, with differences in charting to be resolved by a third member of the research team. After initial pilot, results will be shared with the research team to determine whether the data chart satisfactorily captures information to respond to research questions. Revisions will be incorporated if determined necessary.
Collating, summarising and reporting the results
Results will be summarised both quantitatively and qualitatively to provide a description of collected data. Descriptive statistics indicating frequencies and central measures of tendency will be used to report the number of studies reporting outcomes or care experiences at each stage of the cancer continuum, as well as the type of contributing characteristic(s) such as biological, social or economic factors will also be reported. The descriptive statistics will be reported in tables. A narrative synthesis of the findings will also be reported.
We will engage with relevant stakeholders, including individuals within the IDD community such as individuals with IDD, their family members and service providers, as well as community organisations. to determine suitable approaches for dissemination and additional knowledge translation activities.
Patient and public involvement
Patients and the public were not involved in the development of this protocol.
This protocol outlines a rigorous method to systematically search and map the literature on cancer outcomes and care for individuals with IDD. To the best of the research team’s knowledge, this is the first review that attempts to explore this area in any great detail. Significantly, this scoping review has the potential to highlight gaps and limitations in the existing body of research, and as such can provide direction for future inquiry.
Contributors MS and AM conceived of and developed the protocol. JL, AM and MS conceived of the search strategy. MS, AM, HO-K and CK provided feedback to inform the protocol’s theoretical foundation. AM executed the search. MS, JL, HO-K, SS, JH, CK, DD, MK, KD and AM contributed to the development of the inclusion/exclusion criteria and to the final manuscript.
Funding This project was funded through an unrestricted Research Start-Up Funds grant from the Office of the Vice President (Research & International) at the University of Manitoba (Mahar).
Competing interests None declared.
Patient consent for publication Not required.
Provenance and peer review Not commissioned; externally peer reviewed.