Fiona Crawford-Williams1,2*
Sonja March1,2
Michael J. Ireland1,2
Arlen Rowe1,2Belinda Goodwin1,2Melissa K. Hyde3,4
Suzanne K. Chambers1,3,4,5,6Joanne F. Aitken1,3,4,7Jeff Dunn1,3,8,9
- 1Institute for Resilient Regions, University of Southern Queensland, Springfield Central, QLD, Australia
- 2School of Psychology and Counselling, University of Southern Queensland, Springfield Central, QLD, Australia
- 3Cancer Research Centre, Cancer Council Queensland, Fortitude Valley, QLD, Australia
- 4Menzies Health Institute Queensland, Griffith University, Southport, QLD, Australia
- 5Prostate Cancer Foundation of Australia, St Leonards, NSW, Australia
- 6Exercise Medicine Research Institute, Edith Cowan University, Perth, WA, Australia
- 7School of Public Health and Social Work, Queensland University of Technology, Brisbane, QLD, Australia
- 8School of Social Science, University of Queensland, Brisbane, QLD, Australia
- 9School of Medicine, Griffith University, Brisbane, QLD, Australia
Background: In Australia, cancer survival is significantly lower in non-metropolitan compared to metropolitan areas. Our objective was to evaluate the evidence on geographical variations in the clinical management and treatment of colorectal cancer (CRC).
Methods: A systematic review of published and gray literature was conducted. Five databases (CINAHL, PubMed, Embase, ProQuest, and Informit) were searched for articles published in English from 1990 to 2018. Studies were included if they assessed differences in clinical management according to geographical location; focused on CRC patients; and were conducted in Australia. Included studies were critically appraised using a modified Newcastle–Ottawa Scale. PRISMA systematic review reporting methods were applied.
Results: 17 articles met inclusion criteria. All were of high (53%) or moderate (47%) quality. The evidence available may suggest that patients in non-metropolitan areas are more likely to experience delays in surgery and are less likely to receive chemotherapy for stage III colon cancer and adjuvant radiotherapy for rectal cancer.
Conclusion: The present review found limited information on clinical management across geographic regions in Australia and the synthesis highlights significant issues both for data collection and reporting at the population level, and for future research in the area of geographic variation. Where geographical disparities exist, these may be due to a combination of patient and system factors reflective of location. It is recommended that population-level data regarding clinical management of CRC be routinely collected to better understand geographical variations and inform future guidelines and policy.
Introduction
Australia and New Zealand have the highest incidence rates of colorectal cancer (CRC) in the world, and it is the second leading cause of cancer death in Australia (1, 2). Around 80 Australians die each week from CRC; however, if detected early it can be treated successfully (3). The Australian National Health and Medical Research Council and Cancer Australia have developed evidence-based guidelines for optimal care in the clinical management of CRC (4, 5). These guidelines recommend that patients should receive site- and stage-specific care including preoperative assessment, surgery, and adjuvant therapy where appropriate. Specifically, primary surgical resection is recommended for stage I to III CRC, except for low-grade stage I where local excision is appropriate; adjuvant chemotherapy for all node-positive colon cancers; adjuvant preoperative or postoperative radiotherapy for high risk rectal cancers; and chemotherapy for metastatic CRC. The guidelines also recommend less than 30 days between diagnosis and surgery, and receipt of treatment in specialist cancer centers or from specialist surgeons (5). To date, it is unclear whether these guidelines are adhered to uniformly across Australia.
In Australia, survival from CRC differs according to geographical location, with mortality rates higher in regional and remote areas compared to major cities (1, 6–8). Geographical variations in access to recommended treatments may contribute to the noted disparities in survival and other outcomes. Only 78 sites across Australia deliver radiotherapy treatment (42% private providers), with the majority of these located in capital cities or major regional centers (9). An analysis of available radiotherapy services in Australia in 2009 found that only 38% of cancer patients for whom radiotherapy was the appropriate treatment could be treated within the current service capacity, with lower percentages expected in regional and rural Australia (10). Geographical differences in surgery and chemotherapy also exist as there are reported gaps in the percentage of non-metropolitan hospitals with medical oncologists or specialist surgeons, and reports of administration of chemotherapy by staff without oncology training (11, 12).
Residents in metropolitan areas have increased access to services, and access to hospitals and surgeons with higher caseloads; factors known to be associated with better clinical outcomes (13, 14). However, few population-level datasets in Australia include comprehensive treatment data or clinical management information (15), and to date, there has been no aggregation and synthesis of available data. This evidence gap hampers our understanding of disparities in clinical care and how these might influence cancer outcomes. A preliminary survey of the literature regarding geographic disparities in outcomes for patients diagnosed with CRC highlighted a lack of clear, consistent findings and identified a need for a more in-depth examination of differences in clinical management (8). Thus, the primary aim of this systematic review was to understand the nature of geographical variations in the clinical management of CRC (including surgery, chemotherapy, and radiotherapy) in Australia, incorporating clinical reports as well as peer-reviewed literature.
Methods
The review methodology was planned and carried out following the PRISMA statement for the conduct and reporting of systematic reviews (16). The review protocol was registered with PROSPERO; registration number CRD42016042666 (https://www.crd.york.ac.uk/PROSPERO/display_record.asp?ID=CRD42016042666).
Eligibility Criteria
Studies were included if the data were from cohorts of Australian individuals with CRC; reflected outcomes pertaining to clinical management; and compared non-metropolitan vs metropolitan patients. Qualitative studies, review articles, editorials, books, commentaries, and conference abstracts were excluded.
Search Strategy
PubMed, CINAHL, Embase, ProQuest, and Informit databases were searched for articles published in English from 1990 to 26th February 2018. Search strings included terms relating to “colorectal cancer” or “bowel cancer,” “clinical management,” “treatment,” “chemotherapy,” “radiotherapy,” or “surgery.” Terms relating to geographical disparities included “metropolitan,” “urban,” “rural,” “remote” or “regional,” and “Australia.”
Gray literature searches were conducted through targeted Internet searches of state and federal government health websites, non-government cancer association (e.g., state Cancer Council groups) websites, web search engines (Google), and manual hand searching of reference lists of included articles.
Screening and Data Extraction
After removing duplicates, titles and abstracts were independently screened by two reviewers for relevance according to the selection criteria. Full text versions of potentially eligible articles were then assessed for inclusion by two independent reviewers. Reviewer discrepancies were discussed and resolved within the project team where necessary.
Criteria for data extraction were determined prior to review. Summary data for each study included design, data sources, participants, geographic classification system, dates of data collection, clinical management details, and key trends. Extracted data were synthesized descriptively.
Quality Assessment
The methodological quality of each paper meeting the inclusion criteria was assessed using a tool previously developed for research in breast cancer, based on the Newcastle–Ottawa Scale for assessing quality in non-randomized studies (17, 18). Studies were scored according to the extent that they met each of nine criteria ranging from high risk of bias (score of 0), intermediate risk of bias (score of 1), and low risk of bias (score of 2). Criteria scores were then summed and categorized as “high” (14–18), “moderate” (9–13), or “low” (<9) quality. Study quality appraisal was carried out by two authors, and a third author resolved disagreements between the initial two reviewing authors.
Results
The search strategy yielded 690 records in total. After removal of duplicates, 681 records were screened by title and abstract. Of those, 153 full-text articles were potentially relevant and assessed for eligibility. Following assessment, 17 studies were included in the final review, comprising 12 peer-reviewed articles and 5 gray literature reports (Figure 1). Because of the diverse nature of the study designs, a quantitative synthesis was not possible and a narrative review of individual studies is provided.
Figure 1. PRISMA flow diagram of included studies.
Table 1 presents the key characteristics of all 17 included studies. Eight studies (47%) were of moderate quality, including all five gray literature reports. All other included studies (53%) were high quality indicating they have samples that were representative of the population, variables were collected through secure records, important confounders were controlled for, and statistical methods were appropriate and well presented.
Table 1. Characteristics of included studies.
Main Findings
Surgery
Eight studies reported on surgical management. Three studies reported no significant variation in rates of surgical treatment according to place of residence, for all stage cancers (15) or metastatic disease (27, 32). Five studies reported geographical variations in aspects of surgical management, although methodologies varied greatly. A retrospective data linkage study found that patients residing in remote areas of Western Australia were more likely to receive surgery compared to patients residing in any other area (25). However, when location of hospital was considered, patients were more likely to receive surgery when their first admission was to a metropolitan facility rather than a rural hospital (25, 28). A Queensland audit report suggested that it was more likely for patients residing in metropolitan areas to have surgery less than 30 days after diagnosis, compared to patients in outer regional and remote areas (31). A retrospective cohort analysis from New South Wales reported that among rectal cancer patients there was a longer delay until surgery for individuals living in rural areas, but this was not the case for colon cancer patients (24). A clinicians report from NSW examined preoperative investigations, and reported that patients residing in highly accessible areas were significantly more likely to have had recommended tests such as colonoscopy, sigmoidoscopy, and scans for distant metastases compared to those living in less accessible areas (13).
Chemotherapy
Eight studies examined chemotherapy management. Three studies indicated that chemotherapy for stage III colon cancer was less likely to be received by patients residing in rural and remote areas than metropolitan areas (15, 19, 33). One study found equivalent rates of chemotherapy management between patients residing in metropolitan and rural areas across each line of treatment, although higher proportions of metropolitan patients received combination chemotherapy in the first-line, and rural patients had increased use of the oral prodrug capecitabine as first-line treatment compared to metropolitan patients (27). In contrast, two Queensland studies reported a similar number of chemotherapy cycles, regimen types, and dose-intensities used in both rural and urban areas (22, 30). Two retrospective cohort studies reported no geographical variation in receipt of chemotherapy (28, 29).
Radiotherapy
Five studies examined radiotherapy management in rectal cancer patients, with four reporting geographical disparities in radiotherapy use. Specifically, one retrospective cohort study reported lower utilization of radiotherapy in patients residing in rural Victoria that was not explained by age; a pattern that was more prominent in men than women (26). One cohort study conducted in New South Wales reported variability in receipt of radiotherapy as being attributable to location of hospital rather than place of residence, with radiotherapy less likely to occur in rural hospitals (28). In contrast, a New South Wales study of clinician reports suggested that patients residing in highly accessible areas had lower use of radiotherapy than non-metropolitan areas; however, this study had small numbers of rectal cancer patients in moderately accessible and remote areas (20). One national cross-sectional study reported that patients residing in rural areas were less likely to receive preoperative radiotherapy for high-risk rectal cancer although it is unclear whether these patterns are indicative of patient characteristics, physician recommendations, or health service accessibility (23). Only one retrospective data-linkage study found no differences in radiotherapy for stage II and stage III rectal cancer according to location of residence in South Australia (15).
Discussion
The current review found inconsistent evidence relating to geographical disparities in clinical management of CRC in Australia. While some studies showed no differences in treatment by location of residence, other studies reported that patients with CRC in non-metropolitan areas of Australia are less likely to receive optimal care. This was particularly true for studies where the outcome was radiotherapy utilization. The evidence gathered in this review highlights key issues with consistency in current data collection and reporting regarding CRC treatments and clinical management. In particular, the review highlights the importance of recording location of treatment as well as location of residence; gaps in data collection at a population-level; and large variability in the methodologies used to investigate and report on geographical disparity. There is significant capacity for future research to focus on these critical issues, as well as aspects missing from the current literature such as treatment completion rates and reasons for non-receipt of adjuvant therapies.
Population level data collected in cancer registries internationally provides information on all cancers occurring in a certain population (34). The type of data that cancer registries can provide is varied, and while most provide information on incidence and mortality, currently many registries, including those in Australia, do not routinely collect data on stage at diagnosis or treatment details (35). Hospital registries and other sources of clinical data may have this information available, but it is generally limited to a single institution or health service area. In clinical practice, factors such as position of the tumor, lymph node invasion, involved margins, as well as individual factors such as age, and comorbidities influence CRC treatment decisions (4, 36), yet, detailed clinical information is not available at the population level. This significantly hampers research efforts attempting to understand disparities in CRC management. The findings of the current review emphasize a need for more comprehensive data collection, particularly, in this era of electronic data. This might involve the use of standardized reporting database software such as electronic health records, whereby variables such as patients’ residence, hospital location, treatment type, tumor stage, and comorbidities are recorded and able to be linked to cancer registry data. As the use of electronic health records and capacity for data-linkage expands in Australia, and worldwide, these provide a useful avenue for the collection of clinical management data for CRC patients, with the ability to share information across networks. The digital collection of cancer management data at the population level could result in complex databases to be used for a multitude of previously unanswered research questions (37).
Several studies reported that clinical management for CRC was less optimal in non-metropolitan areas of Australia. For instance, some studies reported that when non-metropolitan patients underwent surgery for CRC, it was more likely to be delayed and less likely to be preceded by preoperative investigations, radiotherapy for rectal cancer patients was underutilized in non-metropolitan areas, and non-metropolitan patients with stage III colon cancer were less likely to receive recommended chemotherapy treatment. Despite potential differences in the provision of chemotherapy across geographic locations, chemotherapy regimens were generally found to be similar across metropolitan and non-metropolitan areas (22, 30). However, one study indicated that oral chemotherapy was more likely to be used for rural patients with metastatic disease (27). The advantages of oral regimens over chemotherapy by infusion include convenience, flexibility in location of administration, and reduced toxicity-related hospitalization, which may be of benefit to patients in non-metropolitan areas (38–40). For these reasons, the use of innovative chemotherapy regimens is a promising solution for overcoming the barrier of distance for optimal CRC treatment.
Previous studies in Canada, the United States, and the United Kingdom have also reported less optimal treatment provided to non-metropolitan CRC patients (41–43), although again evidence is mixed (41). A number of international studies have reported that geographic variability in the treatment of CRC may be reflective of the different population compositions in regional areas, as well as hospital volume and service availability. For instance, older patients, black patients, and patients of lower socioeconomic status (SES) were less likely to receive recommended treatments and more likely to have poorer outcomes (43–47). As rural Australia is also characterized by populations with lower education, lower SES, more advanced age, and higher rates of Indigenous populations (12, 48), these sociodemographic factors may explain many of the treatment differences reported in the current review. If SES, ethnicity, and demographic characteristics are explanations for geographical disparity in cancer treatment resulting in poorer cancer outcomes, there is an issue of inequality that needs to be urgently addressed.
Studies that reported data comparing regional and metropolitan facilities, rather than basing geographic location on patient’s home address, generally reported less optimal clinical management in non-metropolitan areas. This may suggest that there are important differences in the quality of treatment for patients receiving treatment in regional areas. If disparities in clinical management of CRC are explained to some extent by accessibility to appropriate services, then changes to health service delivery may be an appropriate solution (11, 49). To date, increased use of telehealth, the development of approved oral chemotherapy regimens, and the requirement for overseas trained health workers to work in rural and regional areas are strategies implemented to help overcome the challenge of distance (38, 50–52). The results of this review suggest that planning for health service delivery must continue to adapt and focus on overcoming barriers due to distance. In particular, high priority areas are the recruitment and retention of specialist staff in non-metropolitan areas, reduction of wait times, and tailoring services to individuals of low SES, increased age, multiple comorbidities, and indigenous populations.
Based on evidence presented above, it appears that clinical management of CRC in non-metropolitan Australia may be less than optimal; however, this may be due to a range of patient and provider factors that correspond to geographic location. As evidence in this area is limited, one major contribution of the current review is to motivate future research. Future studies will need to collect more detailed data on clinical indicators, health professionals decision-making, and patient preferences to shed light on potential variations in CRC treatment. To provide optimal treatment equitably to patients with CRC, a better understanding of the underlying causes of geographical variations in treatment is required. Digital data collection tools provide an opportunity to address this. Further investigation into the relative contribution of patient, provider, and health system factors to geographical disparities in clinical management is essential. Subsequently, interventions designed to improve the quality of care can then be directed at those patients most likely to benefit from them, such as the provision of extra care from nurse navigators by assessing and monitoring “at risk” patients. Additionally, health services can use this information to adapt appropriately to suit the needs of regional populations, for instance, through the extended use of tele-oncology models of care, oral chemotherapy regimens, or the development of outreach radiotherapy facilities to improve quality of care for those living outside city centers. Not only is this of relevance in Australia but also to countries with similar geographic distributions and population characteristics such as the US, Canada, and the UK.
Limitations
This review is limited by the small number of studies and the use of inconsistent methodology across studies. The variation in population samples, and use of different geographical classifications made direct comparisons between studies difficult. Above all, research identifying geographical disparities in cancer outcomes is hindered by the lack of accurate patient and treatment data at a population level. The use of digital systems to collect and record clinical management information would enhance understanding of variations in cancer outcomes and inform policy and clinical guidelines. The reviewed studies emphasize the need for better data collection and reporting, and highlight the need for the use of data linkage to gather comprehensive clinical management data.
Conclusion
The present review provides specific information on clinical management differences across geographic regions in Australia. This synthesis of existing literature highlights significant issues both for data collection and reporting at the population level, an issue of relevance worldwide. Improvements in cancer outcomes in regional areas will require enhanced capacity to accurately track, and respond to, geographical disparities. Through the use of electronic health records, data linkage and future research, it is important to investigate differences in clinical management of CRC across geographical locations, and in particular, the patient, professional, or health service factors, which contribute to these disparities. Causes for disparities in treatment are found not only in the individual patients and their social environments but also in the location and quality of the health-care system. It is recommended that population-level data regarding clinical management of CRC is routinely collected to improve health outcomes and inform future guidelines and policy.
Author Contributions
All authors have made substantial contributions to acquisition, analysis, and interpretation of data, and drafting the manuscript. JD, SC, SM, and JA provided substantial contribution to conception of the work, and revised the work for important intellectual content. FC-W, AR, and MI carried out searches, screening, and extraction. Study quality appraisal was carried out by AR and FC-W and moderated by MI. BG and MH contributed to conception of work, edited, and critically revised the manuscript. Each author has participated sufficiently in the work and takes responsibility for appropriate portions of the content. All authors have read and have given final approval of the version to be published.
Conflict of Interest Statement
The authors declare that the preparation of this article was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The reviewers DG and RK and the handling Editor declared their shared affiliation.
References
2. Ferlay J, Soerjomataram I, Ervik M, Dikshit R, Eser S, Mathers C, et al. GLOBOCAN 2012: Cancer Incidence and Mortality Worldwide. Lyon, France: International Agency for Research on Cancer (2014) [cited 2015 Jan 16]. Available from: http://globocan.iarc.fr
3. ACIM. Australian Cancer Incidence and Mortality (ACIM) Books: Colorectal Cancer. Canberra: AIHW (2016).
4. National Health and Medical Research Council. Guidelines for the Prevention, Early Detection and Management of Colorectal Cancer. Sydney: The Cancer Council Australia and Australian Cancer Network (2005).
5. Department of Health and Human Services. Optimal Care Pathway for People with Colorectal Cancer. Melbourne, Australia: Victorian Government (2015).
6. Valery PC, Coory M, Stirling J, Green AC. Cancer diagnosis, treatment, and survival in Indigenous and non-Indigenous Australians: a matched cohort study. Lancet (2006) 367(9525):1842–8. doi:10.1016/S0140-6736(06)68806-5
7. Cunningham J, Rumbold AR, Zhang X, Condon JR. Incidence, aetiology, and outcomes of cancer in Indigenous peoples in Australia. Lancet Oncol (2008) 9(6):585–95. doi:10.1016/S1470-2045(08)70150-5
8. Ireland M, March S, Crawford-Williams F, Cassimatis M, Aitken JF, Hyde MK, et al. A systematic review of geographical differences in management and outcomes for colorectal cancer in Australia. BMC Cancer (2017) 17:95. doi:10.1186/s12885-017-3067-1
9. Australian Institute of Health and Welfare. Radiotherapy in Australia 2015-16. Canberra: AIHW (2017).
10. Morgan GW, Barton M, Atkinson C, Millar J, Kumar Gogna N, Yeoh E. ‘GAP’ in radiotherapy services in Australia and New Zealand in 2009. J Med Imaging Radiat Oncol (2010) 54(3):287–97. doi:10.1111/j.1754-9485.2010.02172.x
11. Underhill C, Bartel R, Goldstein D, Snodgrass H, Begbie S, Yates P, et al. Mapping oncology services in regional and rural Australia. Aust J Rural Health (2009) 17(6):321–9. doi:10.1111/j.1440-1584.2009.01106.x
13. Armstrong K, O’Connell D, Leong D, Spigelman A, Armstrong BK. The New South Wales Colorectal Cancer Care Survey 2000 – Part 1 Surgical Management. Kings Cross, NSW: The Cancer Council NSW (2004).
14. Wilson A, Marlow NE, Maddern GJ, Barraclough B, Collier NA, Dickinson IC, et al. Radical prostatectomy: a systematic review of the impact of hospital and surgeon volume on patient outcome. ANZ J Surg (2010) 80(1–2):24–9. doi:10.1111/j.1445-2197.2009.05172.x
15. Beckmann KR, Bennett A, Young GP, Roder DM. Treatment patterns among colorectal cancer patients in South Australia: a demonstration of the utility of population-based data linkage. J Eval Clin Pract (2014) 20(4):467–77. doi:10.1111/jep.12183
16. Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gøtzsche PC, Ioannidis JPA, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration. BMJ (2009) 339:b2700. doi:10.1136/bmj.b2700
17. Youl PH, Dasgupta P, Youlden D, Aitken JF, Garvey G, Zorbas H, et al. A systematic review of inequalities in psychosocial outcomes for women with breast cancer according to residential location and Indigenous status in Australia. Psychooncology (2016) 25(10):1157–67. doi:10.1002/pon.4124
18. Wells G, Shea B, O’connell D, Peterson J, Welch V, Losos M, et al. The Newcastle-Ottawa Scale (NOS) for Assessing the Quality of Nonrandomised Studies in Meta-Analyses. Ottawa: Ottawa Health Research Institute (1999) [cited 2016 May 11]. Available from: http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp
19. Armstrong K, O’Connell D, Leong D, Spigelman A, Armstrong BK. The New South Wales Colorectal Cancer Care Survey 2000 – Part 2 Chemotherapy Management. Kings Cross, NSW: The Cancer Council NSW (2005).
20. Armstrong K, O’Connell D, Leong D, Spigelman A, Armstrong BK. The New South Wales Colorectal Cancer Care Survey 2000 – Part 3 Radiotherapy Management. Kings Cross, NSW: The Cancer Council NSW (2007).
21. Beckmann KR, Bennett A, Young GP, Cole SR, Joshi R, Adams J, et al. Sociodemographic disparities in survival from colorectal cancer in South Australia: a population-wide data linkage study. BMC Health Serv Res (2016) 16:24. doi:10.1186/s12913-016-1263-3
22. Chan BA, Larkins SL, Evans R, Watt K, Sabesan S. Do teleoncology models of care enable safe delivery of chemotherapy in rural towns? Med J Aust (2015) 203(10):406–6.e6. doi:10.5694/mja15.00190
23. Clinical Governance Unit. The National Colorectal Cancer Care Survey: Australian Clinical Practice in 2000. Melbourne, Australia: National Cancer Control Initiative (2002).
24. Goldsbury D, Harris MF, Pascoe S, Olver I, Barton M, Spigelman A, et al. Socio-demographic and other patient characteristics associated with time between colonoscopy and surgery, and choice of treatment centre for colorectal cancer: a retrospective cohort study. BMJ Open (2012) 2(3):e001070. doi:10.1136/bmjopen-2012-001070
25. Hall SE, Holman CD, Platell C, Sheiner H, Threlfall T, Semmens J. Colorectal cancer surgical care and survival: do private health insurance, socioeconomic and locational status make a difference? ANZ J Surg (2005) 75(11):929–35. doi:10.1111/j.1445-2197.2005.03583.x
26. Henry MJ, Jones P, Morrissy K, Matheson LM, Pitson G, Healy P, et al. Radiotherapy in the Barwon South Western Region: a rural perspective. J Med Imaging Radiat Oncol (2014) 58(5):612–7. doi:10.1111/1754-9485.12208
27. Hocking C, Broadbridge VT, Karapetis C, Beeke C, Padbury R, Maddern GJ, et al. Equivalence of outcomes for rural and metropolitan patients with metastatic colorectal cancer in South Australia. Med J Aust (2014) 201(8):462–6. doi:10.5694/mja14.00046
28. Jorgensen ML, Young JM, Dobbins TA, Solomon MJ. Does patient age still affect receipt of adjuvant therapy for colorectal cancer in New South Wales, Australia? J Geriatr Oncol (2014) 5(3):323–30. doi:10.1016/j.jgo.2014.02.007
29. Morris M, Platell C, Fritschi L, Iacopetta B. Failure to complete adjuvant chemotherapy is associated with adverse survival in stage III colon cancer patients. Br J Cancer (2007) 96:701–7. doi:10.1038/sj.bjc.6603627
30. Pathmanathan S, Burgher B, Sabesan S. Is intensive chemotherapy safe for rural cancer patients? Int Med J (2013) 43(6):643–9. doi:10.1111/imj.12083
31. Queensland Government. Queensland Colorectal Cancer Audit 2016. Brisbane: Queensland Cancer Control Analysis Team (2016).
32. Singla A, Broadbridge V, Mittinty M, Beeke C, Maddern GJ. Rural populations have equal surgical and survival outcomes in metastatic colorectal cancer. Aust J Rural Health (2014) 22(5):249–56. doi:10.1111/ajr.12133
33. Young JM, Leong DC, Armstrong K, O’Connell D, Armstrong BK, Spigelman AD, et al. Concordance with national guidelines for colorectal cancer care in New South Wales: a population-based patterns of care study. Med J Aust (2007) 186:292–5.
34. Silva I. Reality TV. In: Creber G, editor. The Television Genre Book. London: British Film Institute (1999). p. 134–7.
35. Forsea A-M. Cancer registries in Europe – going forward is the only option. Ecancermedicalscience (2016) 10:641. doi:10.3332/ecancer.2016.641
36. Labianca R, Nordlinger B, Beretta GD, Mosconi S, Mandalà M, Cervantes A, et al. Early colon cancer: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol (2013) 24(Suppl_6):vi64–72. doi:10.1093/annonc/mdt354
37. Fleming M, Kirby B, Penny KI. Record linkage in Scotland and its applications to health research. J Clin Nurs (2012) 21(19–20):2711–21. doi:10.1111/j.1365-2702.2011.04021.x
38. Sabesan S, Larkins S, Evans R, Varma S, Andrews A, Beuttner P, et al. Telemedicine for rural cancer care in North Queensland: bringing cancer care home. Aust J Rural Health (2012) 20(5):259–64. doi:10.1111/j.1440-1584.2012.01299.x
39. Malet-Martino M, Martino R. Clinical studies of three oral prodrugs of 5-fluorouracil (capecitabine, UFT, S-1): a review. Oncologist (2002) 7(4):288–323. doi:10.1634/theoncologist.7-4-288
40. Bhattacharyya GS. Oral systemic therapy: not all “win-win”. Indian J Med Paediatric Oncol (2010) 31(1):1–3. doi:10.4103/0971-5851.68844
41. Campbell NC, Elliott AM, Sharp L, Ritchie LD, Cassidy J, Little J. Impact of deprivation and rural residence on treatment of colorectal and lung cancer. Br J Cancer (2002) 87(6):585–90. doi:10.1038/sj.bjc.6600515
42. Eldin NS, Yasui Y, Scarfe A, Winget M. Adherence to treatment guidelines in stage II/III rectal cancer in Alberta, Canada. Clin Oncol (2012) 24(1):e9–17. doi:10.1016/j.clon.2011.07.005
43. Sankaranarayanan J, Watanabe-Galloway S, Sun J, Qiu F, Boilesen EC, Thorson AG. Age and rural residence effects on accessing colorectal cancer treatments: a registry study. Am J Manag Care (2010) 16(4):265–73.
44. Ayanian JZ, Zaslavsky AM, Fuchs CS, Guadagnoli E, Creech CM, Cress RD, et al. Use of adjuvant chemotherapy and radiation therapy for colorectal cancer in a population-based cohort. J Clin Oncol (2003) 21(7):1293–300. doi:10.1200/jco.2003.06.178
45. Hines RB, Markossian TW. Differences in late-stage diagnosis, treatment, and colorectal cancer-related death between rural and urban African Americans and whites in Georgia. J Rural Health (2012) 28(3):296–305. doi:10.1111/j.1748-0361.2011.00390.x
46. Le H, Ziogas A, Lipkin SM, Zell JA. Effects of socioeconomic status and treatment disparities in colorectal cancer survival. Cancer Epidemiol Prev Biomarkers (2008) 17(8):1950–62. doi:10.1158/1055-9965.EPI-07-2774
47. Aarts MJ, Lemmens VE, Louwman MW, Kunst AE, Coebergh JW. Socioeconomic status and changing inequalities in colorectal cancer? A review of the associations with risk, treatment and outcome. Eur J Cancer (2010) 46(15):2681–95. doi:10.1016/j.ejca.2010.04.026
48. Baxter J, Gray M, Hayes A. Families in Regional, Rural, and Remote. Australia, Melbourne: AIFS (2011).
49. Amgen Australia Pty Ltd. Access to Cancer Treatment in Non-Metropolitan Areas of Australia. Barton, ACT: Deloitte Access Economics (2011) [cited 2016 Aug 4]. Available from: https://www2.deloitte.com/au/en/pages/economics/articles/access-cancer-treatment-non-metropolitan-australia.html
50. Department of Health. Review of Australian Government Health Workforce Programs. International Recruitment, Support and Regulation. Canberra, Australia: Department of Health (2013) [updated 2013 May 24; cited 2017 Jan 20]. Available from: http://www.health.gov.au/internet/publications/publishing.nsf/Content/work-review-australian-government-health-workforce-programs-toc~chapter-6-managing-supply-health-workers-meet-community-needs~chapter-6-international-recruitment-support-regulation
51. Chapman A, Shakespeare T, Turner M. Improving access to radiotherapy for regional cancer patients – the National Radiotherapy Single Machine Unit Trial. Cancer Forum (2007) 31(2):74–7.
52. Hoff PM, Ansari R, Batist G, Cox J, Kocha W, Kuperminc M, et al. Comparison of oral capecitabine versus intravenous fluorouracil plus leucovorin as first-line treatment in 605 patients with metastatic colorectal cancer: results of a randomized phase III study. J Clin Oncol (2001) 19(8):2282–92. doi:10.1200/JCO.2001.19.8.2282
Keywords: colorectal cancer, rural health, health disparity, cancer treatment, systematic review
Citation: Crawford-Williams F, March S, Ireland MJ, Rowe A, Goodwin B, Hyde MK, Chambers SK, Aitken JF and Dunn J (2018) Geographical Variations in the Clinical Management of Colorectal Cancer in Australia: A Systematic Review. Front. Oncol. 8:116. doi: 10.3389/fonc.2018.00116
Received: 12 September 2017; Accepted: 29 March 2018;
Published: 16 May 2018
Edited by:
Kieran Sheahan, St. Vincent’s University Hospital, IrelandReviewed by:
David Gibbons, St. Vincent’s University Hospital, IrelandRory Patrick Kennelly, University College Dublin, Ireland
Cornelis F. M. Sier, Leiden University, Netherlands
Jacintha Noelle O’Sullivan, Trinity College, Dublin, Ireland
Copyright: © 2018 Crawford-Williams, March, Ireland, Rowe, Goodwin, Hyde, Chambers, Aitken and Dunn. 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 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: Fiona Crawford-Williams, fiona.crawford-williams@usq.edu.au