Abstract
Background:
The benefits from expedited diagnosis of symptomatic cancer are uncertain. We aimed to analyse the relationship between stage of colorectal cancer (CRC) and the primary and specialist care components of the diagnostic interval.
Methods:
We identified seven independent data sets from population-based studies in Scotland, England, Canada, Denmark and Spain during 1997–2010 with a total of 11 720 newly diagnosed CRC patients, who had initially presented with symptoms to a primary care physician. Data were extracted from patient records, registries, audits and questionnaires, respectively. Data sets were required to hold information on dates in the diagnostic interval (defined as the time from the first presentation of symptoms in primary care until the date of diagnosis), symptoms at first presentation in primary care, route of referral, gender, age and histologically confirmed stage. We carried out reanalysis of all individual data sets and, using the same method, analysed a pooled individual patient data set.
Results:
The association between intervals and stage was similar in the individual and combined data set. There was a statistically significant convex (∩-shaped) association between primary care interval and diagnosis of advanced (i.e., distant or regional) rather than localised CRC (P=0.004), with odds beginning to increase from the first day on and peaking at 90 days. For specialist care, we saw an opposite and statistically significant concave (∪-shaped) association, with a trough at 60 days, between the interval and diagnosis of advanced CRC (P<0.001).
Conclusions:
This study provides evidence that longer diagnostic intervals are associated with more advanced CRC. Furthermore, the study cannot define a specific ‘safe’ waiting time as the length of the primary care interval appears to have negative impact from day one.
Keywords: delayed diagnosis, waiting lists, tumour staging, colorectal cancer, primary health-care, bias
The diagnostic interval for cancer is defined as the time from first presentation of symptoms in primary care to diagnosis (Weller et al, 2012). There is a general public perception – largely shared by health professionals – that prolonged diagnostic intervals lead to poorer cancer outcome (Richards, 2009). Existing epidemiological evidence on the relationship between diagnostic interval and outcomes in colorectal cancer (CRC) is contradictory, most of it suggesting no statistically significant association (Ramos et al, 2007, 2008; Neal et al, 2015). Many of these studies are undermined by negative bias due to confounding by indication and lead-time, but the lack of clear evidence has nonetheless led some to question the current use of healthcare and research resources to reduce cancer delays (Rupassara et al, 2006; Murchie et al, 2014).
Most CRC patients present initially to a primary care physician (PCP) and are subsequently referred to specialist cancer centres for assessment and investigation (Hamilton and Sharp, 2004; Hamilton, 2010; Hansen et al, 2011; Banks et al, 2014). National guidelines such as the English NICE Guidance, the Scottish SIGN Guidelines and the Danish Cancer Patient Pathways, recommend urgent referral of patients with alarm signs and symptoms, including unexplained weight loss, change in bowel habit and/or rectal bleeding (NICE, 2005; SIGN, 2003; Probst et al, 2012). However, over half of people subsequently diagnosed with colorectal cancer have no alarm signs or symptoms at initial presentation to a PCP (Hamilton et al, 2005). These patients may experience longer diagnostic intervals, perhaps as a result of not being referred until alarm symptoms develop, or because they are ineligible for an urgent appointment (Neal et al, 2014; Jensen et al, 2014a).
We propose a temporal and relational way of understanding the association between time to diagnosis and CRC outcomes. In short, the temporal idea is that cancers become gradually easier to detect with time due to the exponential growth of tumours. The relational idea is that doctors exert their ability to identify cancer by virtue of the role they perform within the relational network to which they belong. It is our hypothesis that symptomatic cancer patients are being sorted and diagnosed at different pace based on their gradually changing clinical indications, and on the respective diagnostic tools available in primary and specialist care. This must be taken into account when analysing the prognostic influence of delays.
We identified seven CRC cohort studies to create a data set sufficiently large to investigate the association between time to diagnosis and CRC outcomes. To call attention to the inevitable problem of confounding by indication and explain continued lack of evidence, we analysed stage of CRC as a flexible function of the length of time under PCP care and specialist care, respectively.
Materials and methods
We identified seven studies with data sets from Scotland, England, Canada, Denmark and Spain from population-based studies of incident CRC patients diagnosed between 1997 and 2010. Data sets were required to hold information on dates in the diagnostic interval (Weller et al, 2012), symptoms at first presentation in primary care, route of referral, gender, age and stage. All but one (ALBERTA) have published their results (Robertson et al, 2004; Hamilton et al, 2005; Stapley et al, 2006; Korsgaard et al, 2006a, 2006b; Esteva et al, 2007, 2013; Rubin et al, 2011; Lyratzopoulos et al, 2013; Murchie et al, 2014; Jensen et al, 2014b). The individual studies are summarised in Table 1 and more extensively described in the Supplementary Material I.
Table 1. Study characteristics of seven colorectal cancer cohort data sets.
| Cohort name | CRUX | CAPER | CRCDK | ALBERTA | CAP | DECCIRE | NACDPC |
|---|---|---|---|---|---|---|---|
| Project | Comparing rural and urban cancer care | Cancer prediction in Exeter | Colorectal cancer in Denmark | Not named | Cancer in primary care | Delay cancer colon i recto | National audit of cancer diagnosis in primary care |
| Reference | Robertson et al, 2004; Murchie et al, 2014 | Hamilton et al, 2005; Stapley et al, 2006 | Korsgaard et al, 2006a, 2006b; Iversen et al, 2009 | Unpublished | Jensen et al, 2014a, 2014b | Esteva et al, 2007, 2013 | Rubin et al, 2011; Lyratzopoulos et al, 2013 |
| Population | Scotland | England | Denmark | Canada | Denmark | Spain | England |
| Region/county | Highland and Grampian regions | Devon county | Aarhus, Ringkoebing and Ribe counties | Province of Alberta | Aarhus County (CAP1) Central and Southern DK (CAP2) All of Denmark (CAP3) | Baleares, Galicia, Valencia, Catalunya and Aragón regions | 1170 volunteering practices from 20 Cancer Networks representing 14% of all practices in England |
| Study period | Jan 1997–Dec 1998 | Jan 1998–Dec 2002 | Jan 2001–July 2002 | Jan 2004–Dec 2008 | Sept 2004–Aug 2005 (CAP1) Oct 2007–Sept 2008 (CAP2) May 2010–Aug 2010 (CAP3) | Sept 2006–Sept 2008 | April 2009–April 2010 |
| Study design | Registry-based | Registry-based | Patient-based | Registry-based | PCP-based | Patient-based | PCP-based |
| Identification | Scottish Cancer Registry | Exeter Cancer Registry | Hospital departments | Provincial Cancer Registry | Hospital Discharge Registry | Hospital departments | English Cancer Networks |
| Disease classification | ICD-10 C18, C19 and C20 | ICD-O-3 8140, 8480, 8490, 8020 | ICD-10 C18, C19 and C20 | ICD-10 C18, C19 and C20 | ICD-10 C18, C19 and C20 | ICD-9 153–154 | ICD-10 C18, C19 and C20 |
| Validation | Histological confirmation | Histological confirmation | Histological confirmation (Pathology reports) | Histological confirmation | Histological confirmation (Danish Cancer Registry) | Histological confirmation (pathology reports) | Practice records including hospital correspondence |
| Data sources | Primary care records and governmental hospital admissions data | Electronic primary care record | Interviewer-administered patient questionnaires | Physician billings and hospital records | PCP-questionnaires requesting dates from electronic patient files and hospital discharge letters | Patient interviews combined with review of primary care and hospital records | PCP-audit tool requesting dates from practice records and hospital correspondence |
| Definitions | Algorithm | Case-Control review | Interview | Algorithm | Questionnaire | Interview and review | Audit |
| Date of presentation | Earliest recorded colorectal cancer symptom in the year before diagnosis | Earliest recorded colorectal cancer symptom in the year before date of diagnosis | ‘When did you first present the above stated symptoms to a doctor?’ | The earlier of: first recorded CRC symptom or PCP visit prior to first CRC procedure in the year before diagnosis | ‘When did the patient first present to your practice with symptoms which you think are related to the current cancer diagnosis?’ | Researchers browsed primary care records | First notification to any health-care professional working within the Primary Health-Care Team about a probable symptom or sign of cancer |
| Date of referral | Date of first PCP referral or date of emergency admission to hospital | Not collected | ‘When were you referred to hospital for further investigation?’ | Date of first PCP visit prior to colonoscopy or other CRC-related procedure | ‘At which date did you/your practice decide to refer the patient for further investigation?’ | Researchers browsed primary care records, but not in the Aragón region (n=214) | Referral to secondary care for further investigation or management of probable symptom or sign of cancer |
| Date of diagnosis | Scottish Cancer Registry incidence date | Date of positive histology or date given by the specialist | ‘What decisive examination led to your current hospitalisation?’ | Date in cancer registry which is almost always the date of first positive histology | Danish Cancer Registry incidence date | Date of positive histology (date of the first pathology report) | Not collected |
| Tumour stage | Dukes | Dukes | Dukes and TNM | TNM | TNM | TNM | SEER 2–4 |
| Symptom data | 17 CRC symptoms (ICPC) | 11 CRC symptoms (ICPC) | 17 CRC symptoms (patients’ first symptom experience) | 12 CRC symptoms | 11–22 cancer symptoms presented in primary care | 9 CRC symptoms (patients’ first symptom experience) | 11 CRC symptoms (ICPC) |
| Emergency admission | Type of first hospital visit=A&E and emergency admission according to hospital admission data | Surgical admission for suspected bowel obstruction or perforation with CRC diagnosed during admission | ‘How were you admitted to the surgical department’ response: acute or sub-acute admission | Emergency admission with CRC-related issue within 7 days prior to diagnosis | Acute or sub-acute admission according to National Patient Registry NB: Not collected for the second and third subcohort (n=1569) | Route to diagnosis=emergency department according to hospital record | Type of referral=emergency according to primary care record (audit tool) |
Abbreviations: CRC=colorectal cancer; ICD-10=International Classification of Diseases 10th revision; ICD-9 International Classification of Diseases 9th revision; ICD-O-3=WHO International Classification of Disease for Oncology; ICPC=International Classification of Primary Care; PCP=primary care physician; SEER=Surveillance, Epidemiology and End Results (cancer reporting standard of the National Cancer Institute); TNM=Tumour, node, metastasis.
Study characteristics of seven colorectal cancer cohort data set.
Study population
All cohorts described in this study were from jurisdictions with publicly funded, universal health-care systems, in which PCPs act as gatekeepers from primary to specialist care. Newly diagnosed CRC patients were identified in discharge registries, hospital or primary care records. From each data set, we included all patients aged 20 years and over who had attended primary care before the cancer diagnosis. Screen-detected cases were excluded, as were those diagnosed as a result of emergency presentation with no prior contact with primary care. To render the data sets uniform, we only included patients with recorded CRC symptoms or CRC-related visits in the year before diagnosis (Stapley et al, 2006).
Defining exposures, outcome and covariates
We defined and calculated three exposure variables as illustrated on Figure 1: (1) The primary care interval (time from first presentation to referral to a cancer specialist centre); (2) the secondary care interval (time from referral to diagnosis); and (3) the total diagnostic interval (time from first presentation to diagnosis) based on information on date of first presentation of symptoms in primary care and date of referral to a cancer specialist centre, and date of diagnosis, as defined in the Aarhus Statement (Weller et al, 2012). All data sets, except the NACDPC, recorded the date of diagnosis, defined as date of first histological confirmation of the malignancy in accordance with the hierarchy produced by the European Network of Cancer Registries (Supplementary Material I).
Figure 1.
Definition of exposure variables. We calculated three exposure variables based on information on date of first presentation of symptoms in primary care (B); date of referral to a cancer specialist centre (C); and date of diagnosis (D). ‘The primary care interval’ is defined as (B, C)=time from first presentation to referral to a cancer specialist centre. ‘The secondary care interval’ is defined as (C, D)=time from referral to diagnosis). ‘The total diagnostic interval’ is defined as (B, D)=time from first presentation to diagnosis. Information on date of first symptom (A) was not available.
The primary outcome of the study was stage of CRC as defined by the local registry or provincial cancer registry in the case of the ALBERTA cohort (Table 1). All data sets included histologically confirmed stage, except the NACDPC data set, which used a simplified staging equating to SEER stages 0–3 that was determined by the PCP using information contained in cancer specialist letters. We used T, N and M and not Dukes’ stage where both were available. Stage data were re-categorised to localised, regional, distant, or unknown; and then further simplified to a binary variable of advanced (i.e., distant or regional) vs localised CRC (Supplementary Table 1 shows the algorithm for colorectal cancer staging according to classification system).
All data sets included data on gender, age at diagnosis and presenting symptoms. ‘Alarm symptoms at first presentation’ (yes/no), were defined based on whether patients’ reported symptom(s) merited urgent referral according to the UK’s NICE guidelines (NICE, 2005; Neal et al, 2014) (Supplementary Table 2 shows the pre-specified lists of colorectal cancer symptoms recorded in each data set).
Statistical analyses
Each data set was analysed separately, then combined for pooled individual patient data analysis. Time intervals are presented as medians with interquartile intervals (IQI). To test for confounding factors related to clinical triage, we estimated the difference in median care intervals between patients with and without ‘alarm symptoms’ and ‘emergency admission’ or not using quantile regression analysis (Supplementary Table 3; Supplementary Figures 4 and 5).
To avoid assuming a linear or piecewise constant association between care intervals and stage, we treated primary and secondary care intervals as continuous variables, using restricted cubic splines with three knots and 30 days as the reference point (Durrleman and Simon, 1989). We estimated the odds ratio of being diagnosed with advanced vs localised CRC as a function of the length of each care interval using logistic regression. We adjusted for age (20–64/65–74/⩾75 years), gender and alarm symptoms. With the combined data, we allowed for between-data set variability by adjusting for cohort. We combined interval data with no attention to distributions or weights. Eight sensitivity analyses tested the robustness of the model (Supplementary Table 5).
We tested each model against a model with no care interval term using the Wald test. A two-sided P-value of 0.05 or less was defined as significant. Analyses were done using Stata v. 14 (StataCorp LP, College Station, TX, USA).
Results
In total, the seven data sets included 15 023 incident CRC patients. Of these, 1584 (11%) did not consult a PCP before their diagnosis of CRC, and 1719 had incomplete data; these were excluded. Of the remaining 11 720 patients, 11 187 (95%) had information on primary care interval; 9163 (78%) on secondary care interval and 9696 (83%) on the total diagnostic interval. Stage information was available for 92% (Table 1 and Figure 2).
Figure 2.
Patient flow for each colorectal cancer cohort data set and all data combined. CAP=Cancer in Primary Care; CAPER=Cancer Prediction in Exeter; CRC=colorectal cancer; CRCDK=Colorectal Cancer in Denmark; CRUX=Comparing Rural and Urban Cancer Care; DECCIRE=Delay Cancer Colon i Recto; NACDPD=National Audit of Cancer Diagnosis in Primary Care.
The median age for all patients combined was 70 years; 56% were males, 59% presented with alarm symptoms, 20% were emergency hospital admissions, 61% had colon and 39% rectal cancer; 44% had localised CRC. Clinical features were remarkably similar for each of the seven cohorts, except for the proportion of patients presenting with alarm symptoms, which varied from 49% (DECIRRE) to 78% (CAPER); and the proportion of emergency admissions, which varied from 10% (CRCDK) to 43% (DECCIRE) (Table 2).
Table 2. Clinical features for patients attending general practice before diagnosis displayed for each colorectal cancer cohort data set and all data combined.
| CRUX | CAPER | CRCDK | ALBERTA | CAP | DECCIRE | NACDPC | COMBINED | |
|---|---|---|---|---|---|---|---|---|
| n (%) | n (%) | n (%) | n (%) | n (%) | n (%) | n (%) | n (%) | |
| Study subjects | 802 (7) | 319 (3) | 613 (5) | 5657 (48) | 1841 (16) | 464 (4) | 2024 (17) | 11 720 (100) |
| Time intervals, median (IQI) days | ||||||||
| Primary care interval | 12 (2–64) | NA | 6 (0–45) | 3 (0–48) | 1 (0–21) | 14 (0–50)a | 6 (0–32) | 5 (0–39) |
| Secondary care interval | 21 (3–47) | NA | 14 (7–29) | 18 (6–46) | 23 (9–45) | 38 (17–82)a | NA | 20 (7–46) |
| Diagnostic interval | 55 (21–148) | 97 (44–218) | 31 (13–84) | 47 (18–109) | 35 (16–73) | 67 (28–132) | NA | 46 (18–105) |
| Alarm symptoms of cancer | ||||||||
| No | 306 (38) | 70 (22) | 236 (38) | 2708 (48) | 617 (34) | 237 (51) | 631 (31) | 4805 (41) |
| Yes | 496 (62) | 249 (78) | 377 (62) | 2949 (52) | 1224 (66) | 227 (49) | 1393 (69) | 6915 (59) |
| Emergency admission | ||||||||
| No | 592 (74) | 264 (83) | 551 (90) | 4486 (79) | 204 (75)b | 263 (57) | 1739 (86) | 8099 (80) |
| Yes | 210 (26) | 55 (17) | 62 (10) | 1171 (21) | 68 (25)b | 201 (43) | 285 (14) | 2052 (20) |
| Tumour site | ||||||||
| Colon | 498 (62) | 196 (61) | 368 (60) | NA | 1147 (62) | 264 (57) | NA | 2473 (61) |
| Rectum | 304 (38) | 123 (39) | 245 (40) | NA | 694 (38) | 200 (43) | NA | 1566 (39) |
| Sex | ||||||||
| Females | 350 (44) | 154 (48) | 280 (46) | 2378 (42) | 883 (48) | 177 (38) | 940 (46) | 5162 (44) |
| Males | 452 (56) | 165 (52) | 333 (54) | 3279 (58) | 958 (52) | 287 (62) | 1084 (54) | 6558 (56) |
| Age at diagnosis | ||||||||
| 20–64 years | 206 (26) | 80 (25) | 217 (35) | 2184 (39) | 599 (33) | 142 (31) | 614 (30) | 4042 (34) |
| 65–74 years | 276 (34) | 96 (30) | 200 (33) | 1567 (28) | 583 (32) | 145 (31) | 582 (29) | 3449 (29) |
| ⩾75 years | 320 (40) | 143 (45) | 196 (32) | 1906 (34) | 659 (36) | 177 (38) | 828 (41) | 4229 (36) |
| Median age (IQI) | 72 (64–79) | 73 (65–80) | 70 (62–77) | 69 (59–77) | 71 (62–79) | 72 (62–78) | NA | 70 (60–78) |
| Stage | ||||||||
| Localised | 341 (43) | 167 (52) | 299 (49) | 2709 (48) | 586 (32) | 213 (46) | 823 (41) | 5138 (44) |
| Regional | 251 (31) | 91 (29) | 186 (30) | 1536 (27) | 488 (27) | 128 (28) | 647 (32) | 3327 (28) |
| Distant | 99 (12) | 37 (12) | 114 (19) | 1140 (20) | 438 (24) | 84 (18) | 448 (22) | 2360 (20) |
| Unknown | 111 (14) | 24 (8) | 14 (2) | 272 (5) | 329 (18) | 39 (8) | 106 (5) | 895 (8) |
Abbreviation: NA=not available.
In the DECCIRE data set, the primary and secondary care intervals were only recorded in the Baleares, Galicia, Valencia and Catalunya regions (n=250).
Emergency admission was only recorded in the 1st subcohort of the CAP data set (n=272).
Clinical features for patients attending general practice before diagnosis displayed for each colorectal cancer cohort data set and all data combined.
Total diagnostic interval and its primary care and secondary care components
The overall median primary care interval was 5 days (interquartile interval (IQI): 0–39), ranging from 2 days (IQI: 0–21) in CAP to 14 days (IQI: 0–64) in CRUX. Thirty nine per cent of patients were referred immediately after presentation (i.e., primary care interval of zero days) varying from 14% in CRUX to 46% in the CAP and ALBERTA cohorts (Supplementary Figure 1). The overall median secondary care interval was 20 days (IQI: 7–46) and varied from 14 days (IQI: 7–29) in CRCDK to 38 days (IQI: 17–82) in DECCIRE (Table 2; Supplementary Figure 2). The overall median diagnostic interval was 46 days (IQI: 18–105) ranging from 35 days in CAP to 97 days in CAPER (Table 2; Supplementary Figure 3).
The adjusted care intervals were significantly shorter for patients with alarm symptoms and for patients with emergency admissions. Overall, patients waited an additional 6 (95% confidence interval (CI): 4–7) days from presentation to referral and an additional 9 (95% CI: 7–10) days from referral to diagnosis at the 50th percentile if they had no alarm symptoms. An emergency admission shortened the secondary care interval by 18 (95% CI: 17–19) days at the 50th percentile. Alarm symptoms consistently shortened the length of the primary care interval in each cohort, whereas emergency admissions more convincingly affected the length of the secondary care interval (Supplementary Table 3; Supplementary Figures 4 and 5).
Primary and secondary care diagnostic intervals and stage of CRC
For the combined cohort, we observed a significant trend for a concave, ∩-shaped association with increasing and subsequently decreasing odds of advanced CRC with longer primary care intervals (P=0.004). The point-wise estimates showed that the adjusted odds of being diagnosed with an advanced stage tumour increased from the first day, and were around 8% (95% CI: 2–12%) higher for patients who waited 90 days compared to 30 days from first presentation to referral (Figure 3, blue curve). For the secondary care interval, we saw the reverse effect: a significant ∪-shaped association with decreasing and subsequently increasing odds of advanced CRC with longer secondary care intervals (P<0.001) (Figure 3, red curve). Crude estimates were similar to the adjusted curves on Figure 3 (not shown).
Figure 3.
The risk of being diagnosed with advanced colorectal cancer as a function of time to diagnosis. Estimated odds ratios of being diagnosed with advanced (distant or regional) vs localised colorectal cancer as a function of the length of the primary care interval (blue) and the secondary care interval (red) analysed for all cohorts combined (patients with unknown tumour stage excluded). We adjusted for age, gender, alarm symptoms and cohort. The area around the fitted curves indicates 95% confidence limits. The spikes below the curves show the distribution of the primary care interval (blue) and secondary care interval (red) on a squared scale. The grey horizontal lines indicate the chosen reference point of 30 days (see logistic regression details in Supplementary Table'4, Supplementary Material IV). Crude estimates are not shown.
The cohort-specific associations were consistent with the overall trend (Figures 4 and 5), but the primary care interval model was only significant for CRUX (P=0.03); and the secondary care interval model was only significant for ALBERTA (P<0.001) and CAP (P<0.001) data. For the total diagnostic interval, we found decreasing odds of advanced CRC with longer intervals (P<0.001), but not achieving significance in individual cohorts (Supplementary Figure 6).
Figure 4.
The risk of being diagnosed with advanced colorectal cancer as a function of time from presentation to referral. Estimated odds ratios of being diagnosed with advanced (distant or regional) vs localised colorectal cancer as a function of the length of the primary care interval (time from first presentation of symptoms to referral); analysed for six cohorts (in total 10 333 patients). We excluded patients with unknown tumour stage excluded and adjusted for age, gender and alarm symptoms at first presentation. The grey dashed curves with 95% confidence limits are fitted on the combined data sets with grey spikes showing the distribution of the care intervals on a squared scale. The grey horizontal lines indicate the chosen reference point of 30 days. Crude estimates are not shown.
Figure 5.
The risk of being diagnosed with advanced colorectal cancer as a function of time from referral to diagnosis. Estimated odds ratios of being diagnosed with advanced (distant or regional) vs localised colorectal cancer as a function of the length of the secondary care interval (time from referral to diagnosis) analysed for five cohorts (in total 8415 patients). We excluded patients with unknown tumour stage and adjusted for age, gender and alarm symptoms at first presentation. The grey dashed curves with 95% confidence limits are fitted on the combined data sets with grey spikes showing the distribution of the care intervals on a squared scale. The grey horizontal lines indicate the chosen reference point of 30 days. Crude estimates are not shown.
The findings were similar after including patients with unknown tumour stage (915 patients) or restricting the analysis to patients with/without alarm symptoms or with/without emergency admission. Excluding the 41% of patients with zero days of primary care interval (zero-inflation) decreased the primary care interval trend. These sensitivity analyses are shown in Supplementary Table 5.
Discussion
In this unique pooled individual patient data analysis of seven cohorts with 11 720 incident CRC patients attending primary care with symptoms before diagnosis, the odds of advanced CRC increased with longer primary care intervals up to ∼90 days, after which the odds decreased. Conversely, the odds of advanced CRC decreased with longer secondary care intervals up to ∼60 days, after which the odds slowly increased. Both of these associations were statistically significant and the trends were consistent across data sets. No clear trend was noted across individual cohorts for the total diagnostic intervals.
Strengths and limitations
The key strength of this study lies in the large number of cases, from seven data sets in five countries with comparable systems of universal health-care. By excluding screen-detected patients and those without PCP involvement, the results are relevant to all health-care systems featuring primary care gate-keeping. However, the proportions of patients presenting as an emergency are not routinely recorded outside the UK, so we cannot know whether varying sizes of this proportion have affected our results. The data were sufficiently detailed to enable care intervals to be analysed as a continuous variable, enabling us to utilise recent methodological advances in a larger sample (Tørring et al, 2011, 2012). A fundamental strength of the study is that lead-time bias cannot explain results, as we used stage as our outcome measure, rather than survival time.
A number of limitations exist due to the cross-sectional study design, which does not permit direct inference of causality. Dates for interval calculations may have been recorded systematically differently across different data sets. Although the ascertainment of dates accorded with best practice in all cases (Weller et al, 2012), no gold standard data source exists for interval measures. Studies show good agreement between patient and PCP recorded dates of diagnosis (Adelstein et al, 2008); but dates of first presentation are usually more accurately recorded for alarm symptoms than for non-specific symptoms (Lynch et al, 2008). Furthermore, registry-based interval measures may be affected by the data collection methods, with some symptoms unrecorded, whereas others are potentially unrelated to the cancer (Stapley et al, 2006; Tate et al, 2009). Registry-based studies are highly dependent on underlying algorithms and cut-points; they benefit from high inclusion rates, but potentially have non-differential misclassification of date of first presentation. To ensure that registry-based recorded symptoms were likely to be related to the cancer, we only included recorded CRC symptoms or CRC-related visits in the year before diagnosis. Even so, registry-based measures were longer than PCP-reported time points (Table 2; Supplementary Figures 1–3).
Missing information bedevils all studies on staging, and may have biased results if the quality of staging was associated with diagnostic timeliness. Although we used benchmarked registries and approaches to produce comparable stage information (Tucker et al, 1999; Ostenfeld et al, 2012; Walters et al, 2013; Benitez-Majano et al, 2016), it is conceivable that there was some bias to exclusion of more advanced cases in some data sets, reflecting those dying during admission or treatment. The main effect of such information bias would be increased variation and fewer cases with short intervals and advanced stages, and thus towards no association between time and stage. Hence, our estimates are perhaps underestimates of the real association.
Despite differences in data sources and construction, the clinical features of patients were remarkably similar for each of the seven individual data sets, and they produced strikingly similar results suggesting that selection and information biases were not major methodological limitations.
Unmeasured confounding by factors such as socioeconomic status, co-morbidity, or tumour grade/aggressiveness, which were not universally available, may have influenced the results. We partly mitigated this by adjusting for alarm symptoms and emergency admissions, reducing confounding by indication.
Given the observed trends, it is difficult to predict the direction of bias. However, most of the potential biases from selection, information, confounding, and confounding by indication inherited from the different study designs are likely to have caused negative bias towards and even beyond the null-hypothesis (i.e., odds ratio=1).
When interpreting the results from the combined data sets, the weight of information contributed by each study is relevant. In a sensitivity analysis excluding ALBERTA (50–61% of subjects) we found almost identical results (Supplementary Table 5).
Comparison with findings from other studies
The study builds on a recent systematic review of the association between time to diagnosis and cancer outcome for all types of cancers, which called for higher quality and larger studies that addressed basic issues of bias (Neal et al, 2015). Few studies have considered the possibility that the associations may vary for different components of the diagnostic pathway (Afzelius et al, 1994; Crawford et al, 2002). They support our interpretation that the basis for assignment of delay (the sorting of patients) change during the diagnostic pathway and that interval-specific models are necessary to achieve valid comparisons of delay and mortality. Our findings also confirm a non-monotonic relationship between delay and stage, and thus consolidate important points made by Maguire and others, but in a much larger cohort enabling more valid models (Maguire et al, 1994; Tørring et al, 2011, 2012; Murchie et al, 2014).
Underlying mechanisms
It is a widely held assumption that the waiting time paradox can be explained by the effect of high-risk precursors such as phenotype, biological virulence or tumour aggressiveness, which are thought to act as unmeasured confounders that mask the effect of the exposure (Afzelius et al, 1994; Crawford et al, 2002; Symonds, 2002; Neal et al, 2015). However, some studies have shown that a significant proportion of cancers present with symptoms that are vague or non-specific, with the underlying problem more difficult to detect and act upon in time (Korsgaard et al, 2006b; Jensen et al, 2014a). It is reasonable to assume that symptomatic cancer patients are sorted and diagnosed at different pace based on their gradually changing clinical indications, and on the respective diagnostic tools available in primary and specialist care.
We believe the finding of a two-sided ‘waiting time paradox’ (lower odds of advanced CRC for very long primary care intervals and higher odds of advanced CRC for very short secondary care intervals) reflects confounding by indication, a bias stemming from the inherent difference in the prognosis of patients given different medical priority in primary care vs specialist care.
In primary care, PCPs will expedite patients using a fast-track cancer patient pathway or emergency admission if the patient’s ill-health is obvious. At the same time, PCPs may be more reluctant to refer those with low-risk symptoms, leading to use of normal waiting list referral or watchful-waiting. As many patients in primary care do not fall squarely into either of these categories, delays should be less contingent upon prognosis and thus more randomly distributed in the large group of intermediate patients. We, therefore, propose that the observed increasing odds of advanced CRC with longer primary care intervals up to ∼90 days reflects the actual effect of primary care delays.
In contrast, when a patient is first seen in specialist care, primary care triage has already taken place—making the probability of CRC higher. Furthermore, the specialist’s greater clinical experience of patients with CRC and ready access to hospital-based investigations ensures that patients with advanced disease attending specialist care are diagnosed and treated very quickly; those with less advanced disease are managed less urgently. Hence, negative bias (where the observed effect is lower than the true value) probably explains the decreasing odds of advanced CRC with time and may explain why many CRC studies to date have failed to reject the null-hypothesis of no association between delays and outcome (Ramos et al, 2007, 2008; Neal et al, 2015). As with previous studies, we found no clear association between the total diagnostic interval and stage, presumably due to the conflicting selection-effects of primary care and secondary care intervals. As a final, tentative point, we propose that the observation of increasing odds of advanced CRC with secondary care intervals longer than ∼60 days could reflect the effect of false negative tests or unnecessary delays in investigation and/or treatment.
Clinical implications
We cannot define a specific ‘safe’ waiting time as the length of the primary care interval appears to have a negative impact from day one. It follows that patients with CRC, without alarm symptoms at presentation, are most at risk of a prolonged diagnostic interval.
Cancer diagnostic delays cannot be completely eradicated, so resources must be used proportionately to the objective of finding cancer sooner. Reducing the primary care interval by lowering the threshold for urgent referral and enabling easier direct access to investigations by PCPs, may provide the greatest benefit, as other recent studies indicate (Maclean et al, 2015; Moller et al, 2015).
The study displays the immense complexity and difficulty of diagnosing cancer. Further research on similar combined data sets from longitudinal studies, using the same novel analytical approach, should now be conducted to confirm the relative impact of primary and secondary care diagnostic intervals on outcomes in patients with other cancers.
Conclusion
This study provides evidence that longer primary care and secondary care intervals are associated with more advanced CRC. The finding of similar trends when using different sources of information, for different time periods and in different health-care systems (of Scotland, England, Canada, Denmark and Spain) strengthens the belief that the results can be generalised to other health-care systems around the world.
Acknowledgments
The authors are all members of the Cancer in Primary Care Research International (CaPRI) Network. We are thankful to the CRUX, CAPER, ALBERTA, CRCDK, DECCIRE, CAP and NACDPC research teams for contributing data as well as detailed knowledge about the way it was collected. We are equally thankful to the participating general practices, hospitals, service agencies, and patients for their time and involvement. In addition, we would like to express our gratitude to associate professor Morten Frydenberg from the Department of Biostatistics at Aarhus University for statistical support and making programmes available for generating cubic splines with specific reference values (centercsplines.ado) and estimates with standard errors for linear combinations (calcest.ado) in Stata (applied in Figures 3, 4, 5 and in Supplementary Figure 6). To bioinformatics Martin Krzywinski at the Genome Science Centre in Vancouver for his advice on improving the data visualisation of Figure 3. To Jochim Terhaar sive Droste from the Department of Gastroenterology and Hepatology, VU University Medical Centre, Amsterdam for his initial collaboration and willingness to share data from the Northern Holland cohort. The workgroup sincerely thanks Dr Fiona Walter and the Early Diagnosis Group at Cambridge’s Primary Care Unit for providing a perfect space for thinking, working and writing together in the autumn of 2014.
Disclaimer
The guarantor, MLT, affirms that this manuscript is an honest, accurate, and transparent account of the study being reported; that no important aspects of the study have been omitted; and that all discrepancies from the study as planned have been explained.
Ethical approval
MLT was granted permission to analyse data according to the laws in each country. The CRUX study was approved by the Privacy Advisory Committee of ISD Scotland. According to the North of Scotland Research Ethics Committee formal ethical approval was not required. Research and Development approval was granted from NHS Grampian. In the CAPER study ethical approval was obtained from North and East Devon local research ethics committee. All patients in the CRCDK study signed an informed consent form and the study was approved by the Danish Data Protection Agency and the Ethical Committees of Aarhus, Ringkoebing and Ribe counties. The principle investigator of the ALBERTA data set obtained necessary regulatory approvals to send data to MLT. The CAP study was approved by the Danish Data Protection Agency. The Danish Health and Medicines Authority gave permission to obtain information from the PCPs’ medical records. Health research ethics was not required. The DECCIRE study was approved by the Primary Health-Care Committee of each health district and by the Ethical and Clinical Research Committee of each participating region in Spain. The NACDPC audit was approved as an audit by the Research and Audit committees of the Primary Care Trusts of participating practices. Permission to use anonymised data for research purposes was granted by the NACDPC oversight group.
Funding
The CaPri Colorectal Cancer Collaboration project received no formally targeted donations, but, the primary author MLT co-ordinated the work as part of her postdoctoral studies at the Research Centre for Cancer Diagnosis in Primary Care (CaP), funded by the Novo Nordisk Foundation and the Danish Cancer Society. The CRUX study was funded by NHS Grampian Research Endowment Award 11/26, and a grant from The Colorectal Study Fund (a NHS Grampian Endowment fund). The CAPER study was funded by the Department of Health, UK. The CRCDK study was supported by grants from Western Danish Research Forum, Danish Medical Research Council, Dagmar Marshall’s Fund and the Danish Cancer Society. The ALBERTA was funded by the National Cancer Institute of Canada, Alberta Cancer Foundation, and the Canadian Institute of Health Research. The CAP study was supported by the Novo Nordisk Foundation, the Danish Cancer Society, the Health Foundation, the Tryg Foundation, and the Central Denmark Region’s ‘Praksisforskningsfond’. The DECCIRE study was financed with grants from the Ministry of Health, Carlos III Institute, and also received support from the Health Promotion and Preventive Activities-Primary Health-Care Network, sustained by the Ministry of Health in Spain. The NACDPC study was financed by the Department of Health, England. The sponsors were not involved in any part of the studies.
Author contributions
GR and MLT initiated the CaPRI Colorectal Cancer Collaboration Workgroup and came up with the idea for the study. MLT, PM and GR evolved the study design in subsequent meetings and discussions. All authors collaborated on drafting an analysis plan and prepared their individual data sets in accordance with the agreed protocol. The author and data custodian of the CRCDK data, M Lautrup is identical with M Korsgaard as cited in the reference list. MLT co-ordinated communication with and data acquisition from involved research groups, performed the statistical analyses, and wrote the paper together with PM. She (MLT) is the guarantor. GR, PV and WH provided critical revision of the intellectual content of the manuscript. All authors had full access to their own data set and take full responsibility for the accuracy of the data description and analysis. All authors contributed to the writing of and approved the final manuscript.
Footnotes
Supplementary Information accompanies this paper on British Journal of Cancer website (http://www.nature.com/bjc)
This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License.
The authors declare no conflict of interest.
Supplementary Material
References
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