- Research article
- Open Access
- Open Peer Review
Across-province standardization and comparative analysis of time-to-care intervals for cancer
© Winget et al.; licensee BioMed Central Ltd. 2007
- Received: 27 February 2007
- Accepted: 04 October 2007
- Published: 04 October 2007
A set of consistent, standardized definitions of intervals and populations on which to report across provinces is needed to inform the Provincial/Territorial Deputy Ministries of Health on progress of the Ten-Year Plan to Strengthen Health Care. The objectives of this project were to: 1) identify a set of criteria and variables needed to create comparable measures of important time-to-cancer-care intervals that could be applied across provinces and 2) use the measures to compare time-to-care across participating provinces for lung and colorectal cancer patients diagnosed in 2004.
A broad-based group of stakeholders from each of the three participating cancer agencies was assembled to identify criteria for time-to-care intervals to standardize, evaluate possible intervals and their corresponding start and end time points, and finalize the selection of intervals to pursue. Inclusion/exclusion criteria were identified for the patient population and the selected time points to reduce potential selection bias. The provincial 2004 colorectal and lung cancer data were used to illustrate across-province comparisons for the selected time-to-care intervals.
Criteria identified as critical for time-to-care intervals and corresponding start and end points were: 1) relevant to patients, 2) relevant to clinical care, 3) unequivocally defined, and 4) currently captured consistently across cancer agencies. Time from diagnosis to first radiation or chemotherapy treatment and the smaller components, time from diagnosis to first consult with an oncologist and time from first consult to first radiation or chemotherapy treatment, were the only intervals that met all four criteria. Timeliness of care for the intervals evaluated was similar between the provinces for lung cancer patients but significant differences were found for colorectal cancer patients.
We identified criteria important for selecting time-to-care intervals and appropriate inclusion criteria that were robust across the agencies that did not result in an overly selective sample of patients to be compared. Comparisons of data across three provinces of the selected time-to-care intervals identified several important differences related to treatment and access that require further attention. Expanding this collaboration across Canada would facilitate improvement of and equitable access to quality cancer care at a national level.
- Lung Cancer Patient
- Cancer Care
- Colorectal Cancer Patient
- Cancer Agency
- Primary Interval
The Ten-Year Plan to Strengthen Health Care, established in September 2004  by the Provincial/Territorial Deputy Ministries of Health, united the Premiers of all Canadian provinces through a national plan for healthcare in the next decade. Improving access to and timeliness of care were identified as high priority areas for improving the Canadian health care system. As part of an exchange for federal funding to the provincial health care system, every province is expected to report "wait times" in five priority areas, including cancer.
Each province has tackled this responsibility differently, resulting in a set of inconsistently-defined intervals, patient subsets, and metrics used to report "wait times" that vary across provinces. In the case of cancer care, for example, Alberta is monitoring time from referral to first visit with an oncologist and time from the first visit to treatment (for chemotherapy and radiation therapy separately) , while Manitoba is monitoring time from "ready to treat" to radiation therapy . The health agencies of most provinces post "wait time" data online [2–7] in an attempt to be transparent and accountable to the public. Without a standardized reporting system, however, that unifies the definitions of care-step intervals to measure, patient populations to include, and metrics to report, it is not possible to properly evaluate progress across provinces for meeting the goals set forth in the Ten-Year Plan. Specifically, a set of consistent, standardized definitions of intervals and populations on which to report across provinces would allow provincial health-care agencies to discuss "wait times" in a unified manner, make across-province comparisons to identify policy-relevant strengths and deficiencies of each province in its care system, and learn from each other towards the achievement of the national Ten-Year Plan.
A large body of literature exists on issues associated with cancer care "wait times" nationally and internationally , however, the variability of methodologies used make comparison of results and use of information for decision-making difficult. In Canada, for example, there have been nine "wait-time" studies that measured time to care for colorectal and/or lung cancer patients [9–16]. All of them focused on measuring aspects of time to radiation therapy or time to surgery. Varying definitions of time points, study designs, patient populations and reporting metrics, however, make comparison of results impractical. Analyzing data on timeliness of care in a comparative fashion is a crucial research task for informing policy makers, health care providers, and other decision-makers towards improving the quality of patient care.
To address these concerns, researchers in the cancer agencies in three Canadian provinces (Alberta (AB), Saskatchewan (SK), and Manitoba (MB)) formed a collaborative team to develop and apply a unified methodology that is practical and useful in comparing and learning from each other, on time to cancer care in the three provinces. The cancer agencies in these provinces are responsible for non-surgical treatment of cancer in their jurisdictions. This manuscript describes the methodology developed from the collaboration and the overall analysis results as applied to invasive lung and colorectal cancer cases diagnosed in 2004 as the source population.
To initiate the project, we identified and assembled a group of stakeholders from each of the three cancer agencies to participate in a workshop to identify steps that our cancer agencies could take towards standardizing definitions and measures of relevant cancer care intervals. At the beginning of the workshop, presentations were made to inform one another on current, planned, and future activities for measuring and reporting "wait times" at each of the cancer agencies for both internal and external purposes. Criteria to define "relevance" were then discussed and identified. Various intervals and corresponding start and end time points were suggested and evaluated with respect to the criteria. Final intervals to pursue were then selected that met the criteria and for which analysis and evaluation could be completed within the one-year time frame of the project were selected. The general consensus-forming process was as follows. Ideas were generated via brainstorming followed by open discussion, including identification of pros and cons. Ideas were then synthesized, discussed further, as needed, and then final priorities and directions were voted on.
The expertise amongst stakeholders in the workshop was broadly based and included senior management, epidemiologists, surgeons, oncologists, nurses, a biostatistician, data analysts, quality assurance experts, system developers, and programmers. Final decisions were made by group consensus via informal voting after extensive discussion in workshops. In addition to workshops attended by the entire collaboration, a core group held additional meetings to clarify the data elements available, processes for data extraction, data completeness and quality, and ensure comparability of data across the three cancer agencies.
Consideration of time-to-care measurements as indicators for timely access to care served as the underpinning for discussions and decisions around the criteria for time points and intervals. The following characteristics were identified as requirements for standardizing such indicators for cancer: 1) relevant to patients (as opposed to relevant for internal organizational management), 2) clinically relevant, 3) time points are unequivocally definable, and 4) practical in a sense that data for relevant time points are routinely collected at the provincial cancer agencies in a consistent and high quality manner.
Based on the four criteria, we evaluated potential start and end time points for relevant time intervals. The time points and intervals considered included those that were being used in one of the three provinces and/or had been proposed in the literature. This process led us to the final time points and corresponding intervals to be used in the project.
In addition to the definition and selection of time intervals, we also identified inclusion criteria for the patient population. We selected lung and colorectal cancers diagnosed in 2004 as exemplary tumor sites to be analyzed for the purpose of evaluating and comparing measures for the selected intervals. The reasons for this choice were: disease incidence is high for both, they affect men and women, and treatment includes the main cancer treatment modalities (surgery, radiation, and chemotherapy) . The two cancers also contrast nicely in that prognosis is generally poor for lung cancer but good for colorectal cancer .
Sample selection criteria
Diagnosed 1,2 in 2004
Uncommon 3 histology
Multiple 4 cancers
Dead at diagnosis
In addition to identifying inclusion criteria for patients, it was also necessary to identify inclusion criteria for dates of the endpoints of the intervals (e.g., diagnosis to treatment). Initially data were evaluated that included dates within 18 months of diagnosis. We found that 95% of the patients received their first treatment in a cancer facility within 6 months. The remaining patients either had watchful waiting as their initial treatment plan or refused the recommended first treatment. Upon investigation of the data, we found that a very small proportion of patients were meeting with an oncologist or receiving treatment prior to diagnosis. This was a result of patients being referred prior to having a definitive diagnosis or errors in coding that have since been corrected. We, therefore, included dates of visits in the range between 30 days prior to diagnosis to 183 days (6 months) post-diagnosis.
The final dataset was reviewed by each province and quality assurance checks were run to ensure accuracy and completeness. Descriptive statistics and inverse Kaplan-Meier  graphs were generated for each interval of interest; the Log-Rank  test was used to test for differences between curves. Estimates for the 50th and 90th percentiles and their corresponding 95% confidence intervals were calculated non-parametrically. Chi-squared tests  were used to test differences between proportions. SAS® version 9.1 (Cary, NC, USA) was used to create the datasets and analyze them; graphs were made using Microsoft Excel®.
Description of provinces and corresponding cancer agencies
Province and cancer agency facts
661,185 sq. km
651,900 sq. km
649,950 sq. km
Annual cancer incidence1:
Cancer Agency: # of cancer facilities2 that provide:
Radiation and chemotherapy:
Time points and criteria for selecting standardized time-to-care intervals
Date of first:
Relevant to patients
Relevant to clinical care
Referral to cancer facility
Consensus not reached2
Consensus not reached2
Consult with oncologist
Ready to treat
Consensus not reached2
We considered three intervals with the four time points that satisfied the criteria; they were, time from: 1) diagnosis to first treatment in a cancer facility (that is, radiation or chemotherapy), 2) diagnosis to first consult with an oncologist, and 3) first consult with an oncologist to first treatment in a cancer facility. Interval (1), above, was selected as the primary interval of interest for comparison because, of the three intervals, it is the best summary measure of the total time-to-care experience of patients post-diagnosis. Times from diagnosis to first consult and from first consult to first radiation/chemotherapy were agreed to be important components of the primary interval. The provincial 2004 colorectal and lung cancer data are used to illustrate across-province comparisons.
Distribution (percent) of patient demographics of final population
Alberta (N = 1518)
SK (N = 642)
Manitoba (N = 749)
Alberta (N = 1585)
SK (N = 567)
Manitoba (N = 784)
Median and 90th percentile estimates for time-to-care for each care interval by cancer site and province
# days from diagnosis to 1stradiation or chemotherapy
# days from diagnosis to consult
# days from consult to 1stradiation or chemotherapy
Median (95% CI)
90% (95% CI)
Median (95% CI)
90% (95% CI)
Median (95% CI)
90% (95% CI)
69 (67, 74)
115 (110, 124)
50 (48, 53)
95 (89, 104)
21 (20, 21)
62 (56, 70)
77 (73, 85)
139 (132, 150)
63 (59, 69)
120 (113, 122)
14 (13, 18)
41 (36, 48)
74 (70, 77)
132 (122, 144)
57 (54, 60)
118 (107, 127)
14 (12, 19)
64 (51, 77)
31 (29, 34)
91 (84, 99)
25 (23, 26)
81 (72, 90)
8 (8, 9)
33 (30, 35)
41 (35, 45)
91 (80, 112)
30 (27, 33)
82 (71, 99)
10 (8, 14)
34 (30, 41)
36 (29, 41)
109 (95, 119)
25 (22, 28)
78 (70, 95)
8 (7, 12)
46 (41, 55)
The main goals of this project were to: 1) identify a set of criteria and variables needed to create comparable measures of important time-to-cancer-care intervals that could be applied across provinces and 2) to use the measures to compare time-to-care across participating provinces for lung and colorectal cancer patients diagnosed in 2004. Extensive communication and inclusion of a broad set of expertise ensured that the various perspectives of different types of stakeholders were included in the consensus-reaching process. This approach was needed to identify appropriate inclusion criteria that were robust across the agencies and did not result in an overly selective, or possibly biased, sample of patients to be compared. Application of the method to both lung and colorectal cancer patients provided examples for different types of cancer with different standard treatment practices.
Differences observed between provinces in the intervals depicted in Figures 2 and 3 for colorectal cancer patients suggest each cancer agency could learn from another to shorten the intermediary care intervals and subsequently shorten the overall diagnosis to first radiation/chemotherapy interval. Differences in time-to-care could be due to differences across provinces in the distribution of patient/disease charateristics, referral patterns, and/or treatment patterns, in addition to care-delivery differences. Patient characteristics were, however, comparable across the provinces (see Table 4). The distribution of stage at diagnosis for colorectal cancer patients across the provinces was also comparable (data not shown). Further investigations into referral patterns and treatment practices in the three provinces are underway to understand and explain the differences seen.
In Figures 1 and 2, the differences between lung and colorectal cancer patients are largely due to differences in treatment practice. Roughly 85% of the colorectal cancer patients had surgery prior to radiation or chemotherapy, whereas only about 13% of the lung cancer patients did. Surgery is more likely to be a colorectal cancer patient's first treatment while radiation or chemotherapy is more likely to be a lung cancer patient's first treatment. To a large extent then, these graphs represent time to first and second treatment for lung and colorectal cancer patients, respectively. Comparable differences would be expected to be seen between any tumor sites with similarly different order in their treatment modalities.
Ideally, one would like to compare time from diagnosis to first treatment and time from first treatment to second treatment. This, however, is not currently possible at a national level in Canada because a major treatment modality, surgery, is performed outside of the cancer agencies and many cancer agencies do not have routine access to cancer surgery data. Until dates for treatments received outside cancer agencies are routinely available, however, reporting time from diagnosis to first treatment oferred at the cancer agency is practical; at the very least it should be comparable for most Canadian cancer agencies. Based on an unpublished survey conducted by the Candian Association of Provincial Cancer Agencies (CAPCA) in 2006 at least seven provinces in Canada have the dates of diagnosis, consult with oncologist and first treatment in a cancer facility; the other three provinces may not have dates related to chemotherapy readily available (this information was not specifically captured in the survey) but have diagnosis date and dates related to radiation (consultations and treatment).
The Health Council of Canada recommends the definition of a waiting interval be time from initial referral to completion of the procedure . "Initial referral," in the context of cancer care, however, can have several meanings since patients may have multiple "initial" referrals as they are referred to surgeons and various types of oncologists. The clock of "waiting," however, begins at the time of diagnosis for the patient, thus diagnosis is a more appropriate start time. Furthermore, delays that occur between diagnosis and any of these "initial" referrals may be clinically relevant to quality of patient care. Regarding reporting, the Health Council suggests reporting the duration in 90th or 95th percentiles and adds that a wait-time reporting system should inform on the time for typical cases relative to existing benchmarks, duration of interval for outliers, and changes over time. Information on time-to-care alone is not enough, however, to properly inform policy on quality of care for cancer. Additional information such as the proportion of patients receiving certain care steps is also needed; short time-to-care intervals do not equal high quality if a large percentage of patients who should be receiving care are not.
An important limitation in the process used to identify criteria and select relevant time intervals was that we had one year of funding to perform the work; this prevented us from considering time points that were not currently being collected by our cancer agencies or pursuing external data sources. This restriction also prevented us from considering points of care that fall outside the care of the cancer agencies such as pre-diagnosis and post-treatment follow-up; equally important intervals of care for which information related to timeliness of care is needed. Due to the limited timeframe, our intent was to identify an initial step towards standardizing defintions and measures related to timeliness of care that would facilitate future decision-making and identify directions that would eventually include the cancer care continuum. In this intial step we did not include patients in our decision-making process which is also a limitation. A limitation in interpreting the analytic results is that although differences between tumor sites and provinces can be detected, additional data and information are needed to identify why differences exist.
In summary, production of standardized "wait-time" data across Canadian provinces will allow identification at the national level of problems which facilitate solutions and changes to current resource allocation and overall system improvements. Interpretation of the data in the context of practice guidelines, particularly as related to treatment modality and order, is essential to avoid incorrect interpretation of apparant relative delays. Production of standardized "wait-time" data requires close collaboration, at least initially, between the provinces to ensure comparability. This activity in and of itself may facilitate adoption of more efficient processes or models of care as differences and strengths between provinces are identified. Infrastructure must be developed to obtain dates of cancer surgery to enable comparisons of diagnosis to first and second treatment as well as facilitate evaluation of appropriate care.
Although there are many similarities between AB, SK, and MB with respect to the size of the provinces and organization of the cancer agencies, this collaboration has enabled us to identify several important differences related to treatment and access that require further attention. We expect that there are changes each organization could make that would decrease these differences resulting in improved access and quality of care for cancer patients. Expanding this collaboration across Canada would facilitate improvement of and equitable access to quality cancer care at a national level and reaching the goal of the Ten-Year Plan to Strengthen Health Care in Canada.
The authors thank the following workshop participants for their contribution to this study: Dr. H. Bryant, Ms J. Batemen, Ms P. Sayer, Mr T. Snodgrass and Ms E. Tamano (Calgary, Canada); Mr J. Koop, Dr M. Mohamed, Dr D. Popkin (Saskatoon, Canada); Mr J. Grossman, Mr B. Morton, Dr M. Jancewicz, (Regina, Canada); and Ms J Kostyra, Ms S. McFall, Mr A. Omsen, Ms K. Suderman, Dr M. Taylor, and Ms L. Venus (Winnipeg, Canada). The authors thank Ms. L. Harris, Librarian, for doing the literature searches and document delivery. CK was supported by a grant funded jointly by Canadian Institute for Health Research and the Provincial/Territorial Ministries of Health #76442. The funding organization had no role in the design or conduct of the study; the collection, analysis, or interpretation of the data; or the preparation, review, or approval of the manuscript.
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