Skip to main content
Cancers logoLink to Cancers
. 2024 Jan 15;16(2):366. doi: 10.3390/cancers16020366

Non-Curative Treatment Choices in Colorectal Cancer: Predictors and Between-Hospital Variations in Denmark: A Population-Based Register Study

Søren Rattenborg 1,2,3,*, Torben Frøstrup Hansen 2,3,4, Sören Möller 5,6, Erik Frostberg 1,3, Hans Bjarke Rahr 1,2,3
Editor: Eero Pukkala
PMCID: PMC10814909  PMID: 38254854

Abstract

Simple Summary

Despite universal free healthcare and national treatment guidelines, between-hospital variation in treatment choices for colorectal cancer has been reported in several countries. It is unknown whether this variation may be ascribed to simple variations in clinical case mix or to differences in socioeconomic status or even attitudes and traditions among patients and healthcare professionals. This study examined factors associated with non-curative treatment choices and with refraining from recommended chemotherapy in colorectal cancer in Denmark in 2009–2018. We found that non-curative surgical treatment was associated with being old and frail and having widespread cancer and low weight. Not having chemotherapy was also associated with previous treatment complications and living alone. Marked variations in non-curative treatment between hospitals were found, even after taking a wide range of plausible explanations into account. The reason for these variations is unknown and requires further examination.

Abstract

Background: Variations in treatment choices have been reported in colorectal cancer (CRC). In the context of national recommendations, we aimed to elucidate predictors and between-hospital variations in refraining from curatively intended surgery and adjuvant chemotherapy in potentially curable colorectal cancer. Methods: A total of 34,116 patients diagnosed with CRC from 2009 to 2018 were included for analyses on non-curative treatment in this register-based study. Subsequently 8006 patients were included in analyses on adjuvant treatment. Possible predictors included patient-, disease-, socioeconomic- and perioperative-related factors. Logistic regressions were utilized to examine the predictors of a non-curative aim of treatment and no adjuvant chemotherapy. Results: The predictors of non-curative treatment were high age, poor performance, distant metastases and being underweight. Predictors for no adjuvant treatment were high age, poor performance, kidney disease, postoperative complications and living alone. For both outcomes we found between-hospital variations to be present. Conclusions: Non-curative overall treatment and refraining from adjuvant chemotherapy were associated with well-known risk factors, but the former was also associated with being underweight and the latter was also associated with living alone. Marked between-hospital variations were found and should be examined further.

Keywords: colorectal cancer, oncology, predictors, surgery

1. Introduction

The cornerstone in the curative treatment of colorectal cancer (CRC) is surgery. Of the almost 4000 patients diagnosed with CRC in Denmark in 2022, 68% were treated surgically with curative intent [1]. Treatment choices rest on national and European guidelines which have been in place for at least two decades [2,3,4,5], but the final decisions are made together with the individual patient, taking a multitude of patient- and disease-related factors, as well as patient preferences, into account.

The most common reason for refraining from curatively intended surgery is disseminated disease, although palliative surgery may be needed to manage acute problems such as bowel obstruction. Sometimes patients themselves decline curative treatment, and in other cases the surgeon will recommend against major surgery based on an assessment of performance status, age and comorbidity. In these cases, the choice may be compromised oncologic resection or no resection at all [6].

Although the aforementioned characteristics are the major predictors for the non-curative treatment of CRC, factors such as socioeconomic status and psychiatric disease could be important as well, as they are related to adverse outcomes [7,8,9]. Finally, clinical experience, traditions and attitudes may vary between individual surgeons, hospitals, and even countries. Majano et al. examined differences between four Northern European countries in CRC survival and were able to relate them to marked differences in resection rates [10].

The use of adjuvant therapy may also vary. Commonly accepted guidelines recommend adjuvant chemotherapy after curatively intended surgery for Union for International Cancer Control (UICC) stage III cancer [2,3,4]. The evidence of benefit from adjuvant therapy in UICC stage II CRC is more conflicting, but the European Society for Medical Oncology (ESMO) together with the Danish guidelines suggest adjuvant therapy if specific high risk features (e.g., pT4 tumor, fewer than 12 lymph nodes examined in the specimen) are present together with proficient mismatch repair (pMMR) status and favorable performance status [2,3,4]. Present guidelines suggest adjuvant treatment, after relevant risk assessment [2,3,4], consisting of fluoropyrimidines alone or in combination with oxaliplatin. In stage II colon cancer with high risk features, the Danish guidelines suggest fluoropyrimidine monotherapy, while the addition of oxaliplatin is recommended in stage III in patients below the age of 70 [2,3]. For rectal cancer, adjuvant chemotherapy is only recommended in those without neoadjuvant radiochemotherapy [2,4]. Those with upper rectal cancer have the same indications as colon cancer, while for mid and lower rectal cancer fluoropyrimidines as a monotherapy are recommended [2,4]. In certain cases, local radiotherapy can be applied [4].

However, in spite of national guidelines for both the surgical and oncological treatment of CRC, recent annual reports by the Danish Colorectal Cancer Group have found marked between-hospital variations in, e.g., the proportion of patients having surgery for rectal cancer (45–88%) [1] and adjuvant chemotherapy for stage III colon cancer (67–92% and 55–93%) [1,11]. The reason for these variations is unknown, but it may be speculated to reflect the differences in case mix between hospitals that we have shown previously [9].

The aim of this study was to elucidate predictors and between-hospital variations in refraining from curatively intended surgery and adjuvant chemotherapy in potentially curable colorectal cancer.

2. Materials & Methods

2.1. Study Design and Population

This study is a register-based Danish national cohort study. The data were extracted from the Danish Colorectal Cancer Group (DCCG) database [12], the National Patient Registry (NPR) under the Danish National Health Authority [13] and Statistics Denmark (SD) [13].

The cohort consists of 44,471 adults with a first-time diagnosis of CRC in the years 2009–2018. The cohort and covariates are thoroughly described in Rattenborg et al. [9].

2.2. Specific Primary Exclusion Criteria for This Study

In this study we focused on patients with potentially curable disease. Therefore, we added the following exclusion criteria (Figure 1):

  • Incompatibility between the tumor location and resection procedure registered in the DCCG (e.g., primary tumor in the right colon and rectal resection), or synchronous cancer;

  • Patients in whom curative surgery was not an option (e.g., patients who died before surgery or patients not offered surgery because of disseminated disease);

  • Non-elective surgery;

  • Rare and poorly characterized aims of treatment or an unspecified aim of treatment;

  • The presence of distant metastasis (UICC stage IV) was not an exclusion criterion, provided that the surgeon had not registered disseminated disease as the reason for no surgery.

Figure 1.

Figure 1

Flowchart of inclusion and exclusion in analyses. Abbreviations: CRC, colorectal cancer; DCCG, Danish Colorectal Cancer Group.

2.3. The Stratification of the Cohort by Overall Treatment Goal

Patients were stratified into four different groups based on their intended treatment registered in the DCCG database: operative treatment with curative intent (OT-CUR); operative treatment with compromised or palliative intent (OT-NCUR); non-operative treatment because the patient declined (NOT-NO); and non-operative treatment due to comorbidity (NOT-CO). ‘Compromised surgery’ was defined as a suboptimal oncological resection chosen to minimize the surgical trauma in a frail patient. The ‘palliative surgery’ category had rather few elective patients registered and therefore it was fused with the ‘compromised surgery’ category for our purpose. Data were collected from the DCCG.

2.4. Specific Secondary Exclusion Criteria for Adjuvant Oncological Treatment

Patients in the OT-CUR group and with UICC stage II or III disease and with at least one high-risk feature for benefit (inclusion criteria) of adjuvant therapy, according to national recommendations [2,5], were eligible for analysis, if no exclusion criteria were present. Or, in other words, patients in whom adjuvant chemotherapy was indicated according to national guidelines were eligible for analysis. These changed over the decade studied, and for each patient, we applied the criteria in force at the time of that patient’s operation (Supplementary Table S1). Patients > 80 years old were excluded, since it was (by the authors) considered a general rule of thumb for no benefit of adjuvant therapy during the whole period. Patients only having local or unspecified resections were excluded from this analysis, as well as (in some years) patients with deficient mismatch repair (dMMR) status, age > 75 years and World Health Organization (WHO) performance status (PS) > 2 (Figure 1 and Supplementary Table S1). Recommended adjuvant chemotherapy regimes were, through the whole period, fluoropyrimidine, and possibly leucovorin, and oxaliplatin, depending on the aforementioned risk assessment [2,5]. We grouped included patients as having any or no adjuvant chemotherapy treatment. Data on adjuvant chemotherapy were collected via the DCCG from the NPR.

2.5. Predictors and Covariates

2.5.1. Demographics, Lifestyle and Performance Score

Sex, age groups (<50, 50–64, 65–74, 75–84 or ≥85), body mass index (BMI) according to WHO classification (underweight, normal, overweight, obese) [14], alcohol consumption in units per week (0–14, >14 units) and smoking status (never, ex-smoker, current smoker), American Association of Anesthesiologists (ASA) score (I–V, unknown) and WHO performance status (PS) (0–4, unknown) were included as covariates. Data were collected from the DCCG.

2.5.2. Comorbidity

Comorbidity was reported on an overall level as an aggregated Charlson comorbidity index [15] score (0, 1, 2, 3+) in descriptive tables with updated weights [16]. International Classification of Disease 10th edition (ICD-10) codes for CRC were excluded. Only dichotomous comorbidity variables were included in the regression analyses, based on ICD-10 and Anatomical Therapeutic Chemical Classification System (ATC) codes, as reported recently [9]. In brief, the included somatic domains were cardiovascular disease, chronic pulmonary disease, diabetes, dementia, liver disease, kidney disease, chronic nerve disease, other cancer or tumors and connective tissue disease, and the included psychiatric domains were affective disorders, schizophrenia spectrum disorders, disorder of adult personality and behavior and disorders due to psychoactive substance abuse. ICD-10 codes were collected from the NPR and ATC codes from the prescription database at SD.

2.5.3. Socioeconomic Factors

Educational level (short, medium, long, unknown or unclassified) [17], annual household income in Danish kroner (DKK) (1st–4th quartile or unknown) and cohabitation status (cohabitating, alone, unknown) were included. Data were collected from SD.

2.5.4. Disease-Related Factors

The primary tumor was defined as located in either the colon or the rectum. Clinical presentation with distant metastases at the time of diagnosis was included (yes, no, unknown), as well as information on pretreatment discussion at a multidisciplinary team (MDT) conference (yes, no, unknown). The hospital responsible for the definitive treatment was included in the analyses. These hospitals were identified by letters A to Q, ordered by total patient volume (low to high). Data were collected from the DCCG.

2.5.5. Covariates Included Only in Regression Models for Adjuvant Chemotherapy

In addition to the aforementioned variables, the following variables were of interest in the adjuvant chemotherapy analysis: mismatch repair (MMR) status was categorized as proficient MMR (pMMR), deficient MMR (dMMR) or unknown and collected from the DCCG. In the study period, the most common neoadjuvant radio-chemotherapy regime for rectal cancer was 50.4 Gray in 28 fractions and fluoropyrimidine, applied mainly for T4 and T3 (depending on suspected involvement of margins) [2,5]. Neoadjuvant therapy was categorized as no, yes or unknown for those with rectal cancer only and was collected from the DCCG and via the DCCG from the NPR. Data on postoperative medical and surgical complications within 30 days after surgery were included (no, yes or unknown) and collected from the DCCG.

2.6. Statistical Methods

Descriptive statistics were applied to examine between-hospital variations in outcome variables. For group comparisons (e.g., between two different proportions) we estimated 95% confidence intervals (CI).

In order to examine predictors for non-curative treatment aims, a multivariable multinomial logistic regression model was utilized. The outcome variable was the aim of treatment with the OT-CUR group as the comparison level. The relevant covariates were included. We applied the Hosmer-Lemeshow test with twenty groups to investigate the goodness of model fit. Results are presented as relative risk ratios (RR) with corresponding 95% CI.

In order to examine predictors for refraining from adjuvant chemotherapy, a multivariable logistic regression model was built for colon and rectal cancer, respectively. The possible outcomes were any kind of adjuvant chemotherapy, with no adjuvant chemotherapy as the comparison level. As mentioned briefly above, exclusion criteria in force at the time of the operation of each particular patient were used to define the population with the indication for adjuvant chemotherapy. Since some of these exclusion criteria may have predicted non-treatment with adjuvant chemotherapy before they were included in national recommendations, we included these criteria in our analysis. To balance the analysis we recoded age, MMR and neoadjuvant therapy to non-applicable (n-a) in the periods when they were exclusion criteria. The exact distribution (without n-a) is reported. Results from this model are presented as odds ratios (OR) with corresponding 95% CI. Sensitivity analyses with a reduction of hospitals to tertiles (low, medium, high) of the total volume of patients were done in order to examine if hospital volume was a predictor.

Missing data were included for all analyses and treated as an unknown level for each variable. We did not perform imputation. Data were stored and managed on the secure servers of Statistics Denmark, using Stata IC/17 (StataCorp LCC, 4905 Lakeway Drive, College Station, TX, USA) for analysis. Data were only extracted after anonymization.

2.7. Ethics and Permisson

This study was approved by the DCCG and Danish Clinical Quality Program (DCCG-2018-03-08a) and the Danish Data Protection Agency (jr. no 18/15252). No other approvals were required under Danish law [18].

3. Results

For the overall analyses, 34,116 patients were included in this study (Figure 1).

3.1. The Characteristics of Overall Treatment Aims

Table 1 shows an overview of the included cohort, stratified by the aim of treatment. The majority (90%) had OT-CUR, with five percent having OT-NCUR. Three percent had NOT-NO and three percent had NOT-CO. During the study period, the proportion of patients receiving curative treatment was consistent. The proportion of patients who had OT-NCUR decreased from eight to three percent over the study period, while proportions of NOT-NO and NOT-CO were relatively constant during the study period.

Table 1.

Characteristics of 34,116 patients with colorectal cancer diagnosed in the years 2009–2018 in Denmark by overall treatment aim.

OT-CUR
(N = 30,548)
OT-NCUR
(N = 1678)
NOT-NO
(N = 1007)
NOT-CO
(N = 883)
Total
(N = 34,116)
N % N % N % N % N %
Sex
  Male 16,777 55 897 53 498 49 497 56 18,669 55
  Female 13,771 45 781 47 509 51 386 44 15,447 45
Age group
  <50 1261 4 70 4 15 1 0 0 1346 4
  50–64 7612 25 304 18 70 7 32 4 8018 24
  65–74 11,683 38 496 30 146 14 151 17 12,476 37
  75–84 8074 26 520 31 313 31 345 39 9252 27
  85+ 1918 6 288 17 463 46 355 40 3024 9
ASA score
  I 7162 23 180 11 <45 4 <5 0 7387 22
  II 16,793 55 781 47 <235 23 <75 8 17,882 52
  III 5835 19 557 33 289 29 387 44 7068 21
  IV + V 264 1 101 6 43 4 133 15 541 2
  Unknown 494 2 59 4 399 40 286 32 1238 4
WHO performance status
  0 11,421 37 230 14 75 7 10 1 11,736 34
  1 3782 12 246 15 122 12 74 8 4224 12
  2 1054 3 160 10 134 13 159 18 1507 4
  3 + 4 248 1 78 5 105 10 246 28 677 2
  Unknown 14,043 46 964 57 571 57 394 45 15,972 47
Location of cancer
  Colon 20,058 66 1097 65 560 56 514 58 22,229 65
  Rectum 10,490 34 581 35 447 44 369 42 11,887 35
cM category
  cM0 27,514 90 488 29 650 65 629 71 29,281 86
  cM1 2686 9 1142 68 223 22 168 19 4219 12
  Unknown 348 1 48 3 134 13 86 10 616 2
MDT conference
  Yes 19,678 64 1068 64 435 43 485 55 21,666 64
  No 8496 28 383 23 182 18 160 18 9221 27
  Unknown 2374 8 227 14 390 39 238 27 3229 9
Charlson score
  0 23,180 76 1087 65 609 60 342 39 25,218 74
  1 2569 8 154 9 104 10 124 14 2951 9
  2 3247 11 202 12 177 18 211 24 3837 11
  3+ 1552 5 235 14 117 12 206 23 2110 6
Smoking status
  Never a smoker 10,969 36 520 31 179 18 142 16 11,810 35
  Ex-smoker 11,377 37 555 33 178 18 223 25 12,333 36
  Active smoker 5132 17 296 18 89 9 97 11 5614 16
  Unknown 3070 10 307 18 561 56 421 48 4359 13
Alcohol consumed per week (units 1)
  0–14 24,024 79 1249 74 415 41 412 47 26,100 77
  >14 3745 12 147 9 46 5 53 6 3991 12
  Unknown 2779 9 282 17 546 54 418 47 4025 12
WHO body mass index class
  Underweight 741 2 111 7 38 4 57 6 947 3
  Normal 12,014 39 738 44 279 28 258 29 13,289 39
  Overweight 10,878 36 428 26 164 16 143 16 11,613 34
  Obese 5231 17 206 12 61 6 54 6 5552 16
  Unknown 1684 6 195 12 465 46 371 42 2715 8
Highest educational level 2
  Short 10,684 35 728 43 461 46 429 49 12,302 36
  Medium 13,635 45 620 37 302 30 299 34 14,856 44
  Long 5363 18 227 14 96 10 86 10 5772 17
  Unknown or unclassified 866 3 103 6 148 15 69 8 1186 3
Annual household income
  1st quartile 6909 23 557 33 404 40 311 35 8181 24
  2nd quartile 7257 24 451 27 332 33 332 38 8372 25
  3rd quartile 7857 26 385 23 172 17 154 17 8568 25
  4th quartile 8419 28 276 16 94 9 86 10 8875 26
  Unknown 106 0 9 0 5 0 0 0 120 0
Cohabitation status
  Cohabiting 19,096 63 873 52 311 31 303 34 20,583 60
  Alone <11,415 37 <805 48 <700 69 580 66 13,492 40
  Unknown <40 0 <5 0 <5 0 0 0 41 0

In order to avoid showing identifiable data some numbers have been changed to <N. 1 One unit = 12 g of pure ethanol. 2 International Standard Classification of Education (ISCED) 2011. Abbreviations: ASA, American Society of Anesthesiologists; WHO, World Health Organization; MDT, treatment decisive multidisciplinary team conference; OT-CUR, operative treatment with curative intent; OT-NCUR, operative treatment with compromised/palliative intent; NOT-NO, non-operative treatment due to patient decline; NOT-CO, non-operative treatment due to patient comorbidity.

3.2. The Characteristics of Patients with a Curative Treatment Aim

The patients in the OT-CUR group were generally younger, had a lower ASA score and PS, lower Charlson scores, higher educational level, higher annual household income and were more often cohabiting (Table 1). The majority of OT-CUR patients had a segmental resection, while 6% had a local resection (e.g., endoscopic mucosal resection). Also, a few patients (<1%) in this group did not actually receive any curative operative treatment although the intention of the treatment before surgery was curative.

3.3. The Characteristics of Patients with a Non-Curative Treatment Aim

The non-curatively treated patients were characterized by higher age, ASA, PS and Charlson score, short educational level and lower annual household income, and were more frequently living alone (Table 1).

OT-CUR and OT-NCUR were more common among patients with colon cancer rather than rectum cancer, while NOT-NO and NOT-CO were less often found in colon cancer patients (Table 1). The most predominant types of surgery in OT-NCUR were resection (47%), relief of obstruction (42%), local resections (7%) or only exploration (4%) (not shown in tables).

Looking at the data descriptively, non-curative treatment varied from 8 to 13% between hospitals as seen in Figure 2. OT-NCUR treatment varied from 2 to 7%. NOT-NO and NOT-CO varied only a few percentages between hospitals, 2 to 4%, and 1 to 4%, respectively.

Figure 2.

Figure 2

Proportions of non-curative aim of treatment by hospital (A–Q). Abbreviations: OT, operative treatment; NOT, non-operative treatment.

3.3.1. The Predictors of Non-Curative Treatment in a Multinomial Model

The highest RR values among the predictors of OT-NCUR were distant metastases and advanced age, ASA or PS (Table 2). To a lesser degree BMI, dementia, other cancer disease at diagnosis and rectal location were predictors of OT-NCUR. Between-hospital variations in RR varied significantly, with RR as low as 0.3.

Table 2.

Multivariable multinomial logistic regression of a non-curative aim of treatment with curative surgical treatment as the comparison level for 34,116 colorectal cancer patients.

OT-NCUR NOT-NO NOT-CO
RR 95% CI p RR 95% CI p RR 95% CI p
Sex (ref. female)
  Male 1.1 [0.99–1.27] 0.072 1.2 [1.03–1.45] 0.022 1.4 [1.20–1.75] 0.000
Age group (ref. 50–64)
  <50 1.1 [0.81–1.51] 0.520 1.2 [0.66–2.35] 0.495 - - -
  65–74 1.0 [0.84–1.19] 0.985 1.2 [0.89–1.70] 0.210 2.4 [1.55–3.73] 0.000
  75–84 1.3 [1.09–1.58] 0.004 2.5 [1.85–3.49] 0.000 4.6 [2.99–7.15] 0.000
  85+ 3.4 [2.73–4.34] 0.000 10.8 [7.74–15.13] 0.000 16.6 [10.51–26.09] 0.000
ASA score (ref. I)
  II 1.5 [1.23–1.82] 0.000 1.0 [0.70–1.45] 0.983 2.7 [0.85–8.86] 0.090
  III 2.1 [1.69–2.67] 0.000 1.3 [0.90–1.98] 0.156 10.0 [3.11–32.00] 0.000
  IV + V 7.4 [5.13–10.63] 0.000 2.9 [1.72–4.98] 0.000 41.9 [12.70–138.17] 0.000
  Unknown 2.5 [1.71–3.62] 0.000 15.3 [10.02–23.37] 0.000 100.1 [30.82–324.87] 0.000
WHO performance status (ref. 0)
  1 2.2 [1.74–2.67] 0.000 2.9 [2.10–3.99] 0.000 7.6 [3.85–15.20] 0.000
  2 4.4 [3.39–5.75] 0.000 8.3 [5.88–11.68] 0.000 33.8 [17.12–66.55] 0.000
  3 + 4 7.1 [4.97–10.19] 0.000 21.4 [14.34–31.83] 0.000 146.2 [73.10–292.60] 0.000
  Unknown 1.5 [1.13–1.88] 0.003 1.7 [1.16–2.43] 0.006 6.4 [3.17–12.95] 0.000
Location of cancer (ref. colon)
  Rectum 1.2 [1.06–1.39] 0.004 3.4 [2.86–4.05] 0.000 3.2 [2.67–3.92] 0.000
cM category (ref. cM0)
  cM1 28.9 [25.47–32.81] 0.000 4.6 [3.76–5.61] 0.000 4.1 [3.23–5.11] 0.000
  Unknown 5.1 [3.65–7.20] 0.000 4.3 [3.05–6.01] 0.000 3.2 [2.22–4.69] 0.000
MDT conference (ref. yes)
  No 0.9 [0.77–1.06] 0.231 1.1 [0.85–1.36] 0.558 0.7 [0.57–0.96] 0.021
  Unknown 0.9 [0.71–1.15] 0.424 4.0 [2.88–5.51] 0.000 2.2 [1.52–3.16] 0.000
Comorbidity
  Cardiovascular disease 0.9 [0.78–1.02] 0.091 1.1 [0.88–1.32] 0.454 1.4 [1.06–1.75] 0.015
  Chronic pulmonary disease 1.0 [0.85–1.11] 0.674 0.9 [0.78–1.11] 0.412 1.2 [0.99–1.43] 0.061
  Diabetes 0.9 [0.79–1.12] 0.508 1.0 [0.80–1.24] 0.965 1.1 [0.90–1.39] 0.299
  Dementia 2.2 [1.55–3.10] 0.000 1.2 [0.78–1.71] 0.471 1.8 [1.27–2.58] 0.001
  Liver disease 1.3 [0.75–2.31] 0.342 1.1 [0.51–2.35] 0.812 4.3 [2.52–7.19] 0.000
  Kidney disease 1.1 [0.75–1.50] 0.744 1.2 [0.83–1.72] 0.342 1.4 [1.02–1.94] 0.040
  Nerve disease 1.2 [0.72–1.90] 0.522 0.7 [0.39–1.34] 0.303 0.9 [0.54–1.57] 0.776
  Other cancer 1.4 [1.18–1.61] 0.000 1.1 [0.86–1.37] 0.473 1.4 [1.10–1.75] 0.006
  Connective tissue disease 1.0 [0.78–1.18] 0.689 0.9 [0.70–1.18] 0.455 1.1 [0.86–1.42] 0.453
  Affective disorder 0.9 [0.78–1.04] 0.163 1.1 [0.92–1.33] 0.274 1.3 [1.07–1.56] 0.008
  Schizophrenia spectrum disorder 0.8 [0.36–1.65] 0.503 2.3 [1.06–4.90] 0.035 2.3 [1.01–5.31] 0.048
  Personality and behavior disorder 0.6 [0.20–1.95] 0.413 1.9 [0.55–6.34] 0.317 1.2 [0.27–5.63] 0.787
  Psychoactive drug abuse disorder 0.9 [0.70–1.26] 0.681 0.9 [0.64–1.40] 0.782 1.2 [0.80–1.66] 0.445
Smoking status (ref. non-smoker)
  Ex-smoker 1.0 [0.86–1.14] 0.865 0.9 [0.68–1.08] 0.195 1.0 [0.80–1.33] 0.823
  Active smoker 1.0 [0.86–1.22] 0.788 1.2 [0.87–1.55] 0.323 1.1 [0.83–1.59] 0.413
  Unknown 1.2 [0.95–1.61] 0.115 2.0 [1.38–2.78] 0.000 1.4 [0.97–2.12] 0.074
Alcohol consumed per week (units 1) (ref. 0–14)
  >14 0.8 [0.65–0.99] 0.037 1.1 [0.77–1.51] 0.665 1.1 [0.75–1.52] 0.734
  Unknown 1.1 [0.85–1.43] 0.475 1.8 [1.31–2.56] 0.000 1.8 [1.26–2.60] 0.001
WHO Body mass index class (ref. normal weight)
  Underweight 1.9 [1.47–2.48] 0.000 1.6 [1.11–2.44] 0.013 2.3 [1.58–3.39] 0.000
  Overweight 0.7 [0.65–0.86] 0.000 0.9 [0.69–1.05] 0.139 0.8 [0.61–1.00] 0.046
  Obese 0.8 [0.67–0.97] 0.022 0.7 [0.53–0.98] 0.037 0.6 [0.39–0.78] 0.001
  Unknown 0.9 [0.73–1.21] 0.620 1.7 [1.25–2.21] 0.001 2.5 [1.88–3.42] 0.000
Highest educational level 2 (ref. long)
  Short 1.1 [0.90–1.32] 0.383 0.9 [0.68–1.20] 0.467 0.9 [0.69–1.31] 0.747
  Medium 1.0 [0.81–1.17] 0.753 0.8 [0.60–1.06] 0.120 0.9 [0.63–1.18] 0.356
  Unknown or unclassified 1.3 [0.97–1.81] 0.073 1.4 [0.93–1.98] 0.109 0.9 [0.58–1.42] 0.681
Annual household income (ref. 4th quartile)
  1st quartile 1.2 [0.97–1.45] 0.102 1.5 [1.10–2.03] 0.011 1.4 [0.96–1.92] 0.086
  2nd quartile 1.2 [0.97–1.44] 0.089 1.6 [1.20–2.16] 0.002 1.4 [1.03–2.00] 0.031
  3rd quartile 1.1 [0.95–1.37] 0.166 1.2 [0.92–1.68] 0.148 1.0 [0.71–1.41] 0.994
  Unknown 1.8 [0.67–4.58] 0.250 3.0 [0.72–12.78] 0.130 - - -
Cohabitation status (ref. cohabiting)
  Alone 1.2 [1.03–1.32] 0.017 1.7 [1.39–1.97] 0.000 1.4 [1.14–1.66] 0.001
  Unknown 0.8 [0.13–4.90] 0.803 0.3 [0.01–4.52] 0.349 - - -
Hospital (ref. Q)
  A 1.2 [0.85–1.80] 0.272 1.8 [1.04–3.26] 0.037 1.2 [0.63–2.15] 0.635
  B 1.1 [0.76–1.62] 0.581 0.6 [0.33–0.99] 0.044 0.2 [0.12–0.49] 0.000
  C 0.6 [0.42–0.90] 0.012 0.6 [0.31–1.03] 0.064 0.4 [0.20–0.73] 0.004
  D 0.7 [0.50–1.05] 0.092 1.8 [1.16–2.77] 0.009 1.0 [0.57–1.58] 0.857
  E 0.3 [0.23–0.48] 0.000 0.9 [0.57–1.48] 0.716 0.4 [0.22–0.73] 0.003
  F 1.2 [0.90–1.62] 0.216 2.6 [1.74–3.92] 0.000 1.8 [1.13–2.74] 0.012
  G 0.9 [0.70–1.28] 0.709 0.7 [0.43–1.14] 0.151 0.5 [0.29–0.81] 0.006
  H 1.0 [0.73–1.30] 0.870 2.8 [1.93–4.17] 0.000 1.5 [0.95–2.27] 0.085
  I 0.3 [0.24–0.49] 0.000 1.1 [0.73–1.77] 0.583 1.7 [1.07–2.56] 0.023
  J 0.8 [0.57–1.01] 0.060 1.8 [1.17–2.65] 0.007 1.5 [0.94–2.37] 0.087
  K 1.1 [0.83–1.37] 0.613 0.8 [0.52–1.22] 0.300 1.2 [0.79–1.81] 0.399
  L 0.6 [0.44–0.78] 0.000 1.3 [0.85–1.87] 0.254 0.7 [0.44–1.09] 0.115
  M 0.7 [0.50–0.89] 0.005 1.0 [0.68–1.52] 0.923 1.4 [0.92–2.02] 0.128
  N 0.8 [0.58–1.02] 0.068 2.0 [1.40–2.87] 0.000 1.5 [1.04–2.28] 0.030
  O 0.8 [0.58–0.99] 0.040 0.8 [0.57–1.25] 0.401 0.6 [0.38–0.89] 0.013
  P 1.3 [0.96–1.64] 0.100 2.6 [1.75–3.74] 0.000 2.1 [1.41–3.20] 0.000
Year of diagnosis 0.9 [0.88–0.96] 0.000 1.2 [1.14–1.27] 0.000 1.2 [1.12–1.25] 0.000
Intercept 0.0 [0.01–0.01] 0.000 0.0 [0.00–0.00] 0.000 0.0 [0.00–0.00] 0.000

1 One unit = 12 g of pure ethanol. 2 International Standard Classification of Education (ISCED) 2011. p-values < 0.05 in bold. Abbreviations: RR, relative risk ratio; CI, confidence interval; ASA, American Society of Anesthesiologists; WHO, World Health Organization; MDT, treatment decisive multidisciplinary team; OT-CUR, operative treatment with curative intent; OT-NCUR, operative treatment with compromised/palliative intent; NOT-NO, non-operative treatment due to patient decline; NOT-CO, non-operative treatment due to patient comorbidity. Goodness of fit test: p-value= 0.000.

The highest RR among the predictors of both NOT-NO and NOT-CO were high age, ASA and PS (Table 2). Also, rectal cancer, year of diagnosis, distant metastases, BMI and living alone were predictors of both non-operative aims. A range of comorbidities were, not surprisingly, predictors of NOT-CO, while low income was a predictor of NOT-NO. Between-hospital variations in RR shared patterns for NOT-NO and NOT-CO, with RR up to 2.8 for NOT-NO and between 0.3 and 2.1 for NOT-CO. In a sensitivity analysis, where hospitals were contracted to tertiles (1st, 2nd and 3rd) of the total volume of patients, the only outcome which was markedly different with volume was NOT-CO, with a RR for the low volume tertile of 0.61 (95% CI 0.49–0.77) using the high volume tertile as the comparison level (not shown in table).

3.3.2. Adjuvant Chemotherapy

For analyses on adjuvant chemotherapy, 8006 patients with an indication for adjuvant chemotherapy were included (Figure 1). An overview is seen in Table 3. The majority of patients received adjuvant therapy (72%), with the largest proportion in patients with colon cancers. The majority (81%) of UICC stage III received adjuvant treatment, while only 42% of stage II had treatment. Those who did not receive adjuvant chemotherapy were generally of higher age, had a higher ASA and/or Charlson score, had a shorter education, had a lower annual household income, were living alone and had more often had complications within 30 days after surgery. The unadjusted between-hospital variations are seen from Figure 3.

Table 3.

Overview of 8006 colorectal cancer patients with an indication for adjuvant chemotherapy in the years 2009–2018.

Colon Rectum
Treatment with Adjuvant Therapy Treatment with Adjuvant Therapy
No treatment Treatment Total No treatment Treatment Total
N % N % N % N % N % N %
Sex
  Male 818 55 2151 53 2969 53 456 62 1055 61 1511 62
  Female 682 45 1909 47 2591 47 274 38 661 39 935 38
Age group
  <50 15 1 251 6 266 5 24 3 143 8 167 7
  50–64 289 19 1348 33 1637 29 184 25 702 41 886 36
  65–74 679 45 1881 46 2560 46 336 46 691 40 1027 42
  75–79 517 34 580 14 1097 20 186 25 180 10 366 15
ASA score
  I 205 14 1243 31 1448 26 133 18 636 37 769 31
  II 758 51 2323 57 3081 55 423 58 912 53 1335 55
  III 475 32 443 11 918 17 167 23 147 9 314 13
  IV + V 36 2 7 0 43 1 <10 1 <5 0 8 0
  Unknown 26 2 44 1 70 1 <5 0 <20 1 20 1
WHO performance status
  0 374 25 1601 39 1975 36 175 24 751 44 926 38
  1 216 14 380 9 596 11 72 10 99 6 171 7
  2 80 5 63 2 143 3 <25 3 <15 1 34 1
  3 + 4 26 2 8 0 34 1 <5 0 <5 0 5 0
  Unknown 804 54 2008 49 2812 51 457 63 853 50 1310 54
UICC stage
  II 695 46 557 14 1252 23 329 45 174 10 503 21
  III 805 54 3503 86 4308 77 401 55 1542 90 1943 79
Neoadjuvant therapy
  No 502 69 1468 86 1970 81
  Yes 228 31 248 14 476 19
Mismatch repair status
  pMMR 971 65 2918 72 3889 70 517 71 1381 80 1898 78
  dMMR 251 17 422 10 673 12 15 2 22 1 37 2
  Missing MMR 278 19 720 18 998 18 198 27 313 18 511 21
Postoperative medical complication < 30 days
  No 1136 76 3559 88 4695 84 531 73 1565 91 2096 86
  Yes 237 16 167 4 404 7 128 18 83 5 211 9
  Unknown 127 8 334 8 461 8 71 10 68 4 139 6
Postoperative surgical complication < 30 days
  No 1018 68 3271 81 4289 77 375 51 1253 73 1628 67
  Yes 360 24 468 12 828 15 290 40 396 23 686 28
  Unknown 122 8 321 8 443 8 65 9 67 4 132 5
Charlson score
  0 1008 67 3341 82 4349 78 543 74 1476 86 2019 83
  1 160 11 287 7 447 8 64 9 87 5 151 6
  2 223 15 317 8 540 10 89 12 121 7 210 9
  3+ 109 7 115 3 224 4 34 5 32 2 66 3
Smoking status
  Never a smoker 457 30 1587 39 2044 37 205 28 690 40 895 37
  Ex-smoker 572 38 1493 37 2065 37 286 39 612 36 898 37
  Active smoker 313 21 661 16 974 18 170 23 297 17 467 19
  Unknown 158 11 319 8 477 9 69 9 117 7 186 8
Alcohol consumed per week (units 1)
  0–14 1181 79 3269 81 4450 80 559 77 1394 81 1953 80
  >14 185 12 511 13 696 13 100 14 221 13 321 13
  Unknown 134 9 280 7 414 7 71 10 101 6 172 7
WHO Body mass index class
  Underweight 47 3 73 2 120 2 35 5 17 1 52 2
  Normal 582 39 1513 37 2095 38 284 39 659 38 943 39
  Overweight 502 33 1471 36 1973 35 254 35 671 39 925 38
  Obese 269 18 821 20 1090 20 124 17 316 18 440 18
  Unknown 100 7 182 4 282 5 33 5 53 3 86 4
Highest educational level 2
  Short 600 40 1216 30 1816 33 306 42 476 28 782 32
  Medium 655 44 1923 47 2578 46 301 41 835 49 1136 46
  Long 203 14 836 21 1039 19 104 14 373 22 477 20
  Unknown or unclassified 42 3 85 2 127 2 19 3 32 2 51 2
Annual household income
  1st quartile 425 28 704 17 1129 20 211 29 266 16 477 20
  2nd quartile 411 27 848 21 1259 23 160 22 320 19 480 20
  3rd quartile 375 25 1127 28 1502 27 194 27 475 28 669 27
  4th quartile 283 19 1374 34 1657 30 160 22 650 38 810 33
  Unknown 6 0 7 0 13 0 5 1 5 0 10 0
Cohabitation status
  Cohabiting 873 58 2879 71 3752 67 444 61 1256 73 1700 70
  Alone <630 42 <1185 29 <1810 32 <285 39 <460 27 <745 30
  Unknown <5 0 <5 0 <5 0 <5 0 <5 0 <5 0

In order to avoid showing identifiable data some numbers are changed to <n. 1 One unit = 12 g of pure ethanol. 2 International Standard Classification of Education (ISCED) 2011. Abbreviations: ASA, American Society of Anesthesiologists; WHO, World Health Organization; MDT, treatment decisive multidisciplinary team; pMMR, proficient mismatch repair; dMMR, deficient mismatch repair.

Figure 3.

Figure 3

Proportion of patients receiving adjuvant chemotherapy by hospital (A–Q). Hospital A and B only treat colon cancer.

3.3.3. The Predictors of Adjuvant Chemotherapy in a Logistic Regression Model

The multivariable logistic regression tables for having any adjuvant treatment for colon and rectal cancer respectively are shown in Table 4. The most significant predictors associated with not receiving adjuvant therapy (and thereby having a low OR for receiving adjuvant therapy) for both colon and rectum were as follows: high age, ASA III and PS 1 or 2–4, respectively, together with kidney disease, postoperative complications, living alone and earlier years of surgery. For colon specifically, dementia, liver disease, other cancer and dMMR were also predictors, while obesity was found to be a predictor of receiving treatment. For rectum, nerve disease, neoadjuvant treatment and being underweight were predictors of no treatment. The adjusted OR for hospitals varies from 0.6 to 4.5 and 1.8 to 5.4 for colon and rectum, respectively. In sensitivity analyses, a low volume tertile was a predictor in colon (OR 0.77, 95% CI 0.65–0.92), but not in rectum. It should be noted that for rectum, the two hospitals with the lowest numbers had only 11 and 44 cases in the whole period, but even without these, the resulting OR of a low volume tertile was still insignificant. Some other variables were significantly associated with the outcome, but had a 95% CI very close to 1.

Table 4.

Multivariable logistic regression of receiving adjuvant chemotherapy for 8006 stage II or III colorectal cancer patients with an indication for adjuvant chemotherapy treatment.

Colon Rectum
OR 95% CI p OR 95%CI p
Sex (ref. female)
  Male 0.90 [0.77–1.04] 0.161 1.18 [0.93–1.48] 0.170
Age group (ref. 50–64)
  <50 3.68 [2.09–6.51] 0.000 1.44 [0.84–2.47] 0.180
  65–74 0.79 [0.65–0.94] 0.010 0.62 [0.47–0.80] 0.000
  75–79 0.34 [0.27–0.42] 0.000 0.28 [0.20–0.38] 0.000
  N-a 0.93 [0.54–1.60] 0.790 0.23 [0.09–0.54] 0.001
ASA score (ref. I)
  II 0.78 [0.63–0.95] 0.016 0.77 [0.58–1.02] 0.066
  III 0.35 [0.27–0.46] 0.000 0.48 [0.32–0.72] 0.000
  IV + V 0.09 [0.04–0.22] 0.000 0.58 [0.09–3.70] 0.565
  Unknown 0.45 [0.24–0.84] 0.011 3.79 [0.75–19.32] 0.108
WHO performance status (ref. 0)
  1 0.81 [0.64–1.04] 0.096 0.63 [0.41–0.95] 0.029
  2 0.63 [0.41–0.97] 0.037 0.43 [0.18–1.04] 0.062
  3 + 4 0.29 [0.11–0.72] 0.008 0.22 [0.02–2.51] 0.224
  N-a 1
  Unknown 1.32 [0.99–1.76] 0.055 1.28 [0.82–2.02] 0.280
Comorbidity
  Cardiovascular disease 0.93 [0.79–1.10] 0.407 0.90 [0.71–1.15] 0.402
  Chronic pulmonary disease 0.96 [0.81–1.13] 0.607 0.99 [0.76–1.30] 0.947
  Diabetes 0.80 [0.65–0.97] 0.027 0.82 [0.60–1.13] 0.234
  Dementia 0.28 [0.12–0.66] 0.004 0.37 [0.12–1.15] 0.085
  Liver disease 0.48 [0.25–0.91] 0.024 0.59 [0.14–2.49] 0.476
  Kidney disease 0.41 [0.25–0.66] 0.000 0.29 [0.12–0.74] 0.009
  Nerve disease 0.62 [0.32–1.22] 0.166 0.25 [0.08–0.81] 0.020
  Other cancer 0.74 [0.59–0.93] 0.010 0.77 [0.53–1.12] 0.175
  Connective tissue disease 0.77 [0.59–1.01] 0.055 0.88 [0.57–1.34] 0.539
  Affective disorder 0.87 [0.73–1.04] 0.124 1.04 [0.78–1.39] 0.805
  Schizophrenia spectrum disorder 0.36 [0.13–1.01] 0.052 0.36 [0.07–1.88] 0.227
  Disorder of adult personality and behaviour 1.02 [0.29–3.59] 0.981 0.25 [0.06–1.04] 0.056
  Psychoactive drug abuse disorder 0.98 [0.71–1.36] 0.906 1.00 [0.59–1.70] 0.993
Microsatellite status of tumor (ref. pMMR)
  dMMR 0.41 [0.33–0.51] 0.000 0.62 [0.22–1.73] 0.357
  N-a 0.29 [0.25–0.35] 0.000 1.22 [0.78–1.93] 0.384
  Missing MMR 0.77 [0.58–1.00] 0.051 1.01 [0.63–1.61] 0.968
Postoperative medical complication < 30 days (ref. no)
  Yes 0.41 [0.32–0.52] 0.000 0.28 [0.20–0.40] 0.000
  Unknown 1.14 [0.67–1.93] 0.624 0.59 [0.25–1.42] 0.237
Postoperative surgical complication < 30 days (ref. no)
  Yes 0.46 [0.38–0.56] 0.000 0.41 [0.33–0.52] 0.000
  Unknown 0.89 [0.53–1.51] 0.669 1.21 [0.49–2.96] 0.680
Smoking status (ref. non-smoker)
  Ex-smoker 0.96 [0.82–1.14] 0.675 0.76 [0.59–0.97] 0.031
  Active smoker 0.84 [0.68–1.04] 0.112 0.74 [0.54–1.00] 0.048
  Unknown 1.01 [0.69–1.47] 0.964 1.19 [0.69–2.05] 0.536
Alcohol consumed per week (units 2) (ref. 0–14)
  >14 1.05 [0.84–1.31] 0.682 0.93 [0.68–1.27] 0.638
  Unknown 1.11 [0.74–1.65] 0.616 0.52 [0.31–0.90] 0.019
WHO body mass index class (ref. normal weight)
  Underweight 0.78 [0.49–1.23] 0.289 0.30 [0.15–0.62] 0.001
  Overweight 1.12 [0.95–1.32] 0.191 1.29 [1.01–1.65] 0.038
  Obese 1.46 [1.19–1.80] 0.000 1.35 [0.99–1.84] 0.056
  Unknown 0.90 [0.61–1.32] 0.591 1.34 [0.68–2.64] 0.403
Highest educational level 3 (ref. long)
  Short 0.77 [0.62–0.97] 0.026 0.79 [0.57–1.10] 0.167
  Medium 0.84 [0.68–1.04] 0.106 0.97 [0.72–1.32] 0.867
  Unknown or unclassified 0.67 [0.42–1.06] 0.088 0.98 [0.45–2.14] 0.951
Annual household income (ref. 4th quartile)
  1st quartile 0.78 [0.62–0.99] 0.042 0.86 [0.61–1.22] 0.406
  2nd quartile 0.87 [0.69–1.08] 0.199 1.02 [0.73–1.42] 0.927
  3rd quartile 0.88 [0.72–1.08] 0.207 0.95 [0.71–1.27] 0.721
  Unknown 0.20 [0.04–0.92] 0.039 0.11 [0.02–0.72] 0.021
Cohabitation status (ref. cohabiting)
  Alone 0.70 [0.60–0.82] 0.000 0.70 [0.56–0.89] 0.003
  Unknown 0.29 [0.01–12.22] 0.517 1.83 [0.10–32.09] 0.680
Year of surgery 1.13 [1.07–1.20] 0.000 1.17 [1.02–1.33] 0.021
Hospital (ref. Q)
  A 3.57 [2.29–5.57] 0.000 - - -
  B 1.24 [0.83–1.83] 0.295 - - -
  C 2.56 [1.69–3.89] 0.000 0.77 [0.18–3.29] 0.722
  D 0.64 [0.43–0.96] 0.030 0.55 [0.29–1.06] 0.073
  E 1.59 [1.06–2.40] 0.026 1.38 [0.73–2.61] 0.317
  F 2.50 [1.74–3.58] 0.000 5.53 [1.98–15.41] 0.001
  G 3.36 [2.25–5.01] 0.000 2.45 [1.45–4.14] 0.001
  H 1.82 [1.26–2.62] 0.001 1.82 [1.04–3.20] 0.036
  I 2.97 [2.01–4.38] 0.000 2.77 [1.61–4.77] 0.000
  J 2.21 [1.55–3.16] 0.000 1.91 [1.16–3.15] 0.011
  K 1.96 [1.28–3.02] 0.002 2.20 [1.42–3.40] 0.000
  L 2.76 [1.93–3.97] 0.000 2.21 [1.37–3.58] 0.001
  M 2.35 [1.65–3.35] 0.000 2.49 [1.43–4.33] 0.001
  N 4.42 [3.08–6.37] 0.000 4.02 [2.42–6.68] 0.000
  O 1.37 [0.97–1.93] 0.072 1.12 [0.73–1.72] 0.607
  P 2.19 [1.58–3.02] 0.000 2.50 [1.51–4.14] 0.000
Neoadjuvant therapy (ref. no)
  Yes - - - 0.32 [0.24–0.43] 0.000
  N-a - - - 0.62 [0.38–1.00] 0.051
Intercept 4.60 [2.59–8.16] 0.000 3.02 [1.28–7.11] 0.011

1 omitted from analysis due to collinearity with age group n-a. 2 One unit = 12 g of pure ethanol. 3 International Standard Classification of Education (ISCED) 2011. p-values < 0.05 in bold. Abbreviations: OR, odds ratio; CI, confidence interval; ASA, American Society of Anesthesiologists; WHO, World Health Organization; MDT, treatment decisive multidisciplinary team; pMMR, proficient mismatch repair; dMMR, deficient mismatch repair. Goodness of fit test: p-value 0.55 (Colon) and 0.67 (Rectum).

4. Discussion

4.1. A Review of Aim and Results

We aimed to elucidate predictors and between-hospital variations in refraining from curatively intended surgery in potentially curable colorectal cancer. We analysed this in a cohort study of patients diagnosed with CRC during the years 2009–2018, using the Danish national registers. Similarly, we aimed to examine predictors and between-hospital variations in refraining from adjuvant chemotherapy recommended in national CRC treatment guidelines. We wish to emphasize that we are confident that the actual treatment choices in each case were made for good reasons, and we did not intend to judge hospitals whose treatment patterns seemed to deviate from those of others. We only wanted to identify overall predictors for the treatment choices and to investigate whether these predictors could explain between-hospital variation in adjusted analyses.

Generally speaking, the most clinically significant results were those whose coefficients (RR or OR) deviated markedly from 1 (e.g., 0.75 or 1.25), but also had 95% confidence intervals which deviated markedly from 1 (e.g., not including 0.90 or 1.10). In light of this, we found, for the multivariable analysis of overall treatment aim, that advanced age, ASA and PS, as well as distant metastases at diagnosis and being underweight, were predictors of all non-curative treatment aims. Apart from BMI, all of these are well-established predictors for adverse outcomes. For OT-NCUR, dementia and other cancer were also predictors, compared with an aim of curatively intended surgery. Specifically for non-operative treatment, having a rectal tumor, being in the lower two quartiles of household income and living alone were predictors compared with OT-CUR. For NOT-CO, dementia, liver disease and other cancer were found to be predictors, which is not surprising. The between-hospital variations in the overall aim of treatment were found to vary significantly even after multivariable adjustments for all three non-curative aims of treatment. It may be noted that the treatment choices did not seem complementary, i.e., hospitals with a significantly positive coefficient for NOT-NO generally also had a positive coefficient for NOT-CO.

We found that refraining from adjuvant treatment was predicted by high age and ASA, kidney disease, postoperative complications and living alone, both for colon and rectum cancer. Age and ASA are markers for patient frailty, and kidney disease is important for tolerance of adjuvant chemotherapy [3]. Postoperative complications can lead to a prolonged hospital stay and deranged performance and thereby affect the presumed effect and tolerability of chemotherapy [19]. For colon cancer specifically, PS, dementia and dMMR were also predictors. For rectum cancer specifically, nerve disease, neoadjuvant treatment and being underweight were also predictors. The between-hospital variations in use of adjuvant chemotherapy were significant even after multivariable adjustments in both colon and rectum cancer.

4.2. A Discussion of Related Studies

As shown in Table 1, we found a distribution between treatment strategies of 90% (OT-CUR), 5% (OT-NCUR), 3% (NOT-NO) and 3% (NOT-CO). We have no knowledge of other studies that are directly comparable. Giesen et al. had a mean of 95% resected patients for non-metastatic CRC in the Netherlands [20]. We found being underweight to be a predictor of non-curative treatment. In an earlier study, we found obesity to be protective of 90-day mortality [9], which seems in line with our findings in the present study. Axt et al. found that weight loss was associated with postoperative complications [21], unfortunately we have no information on pretreatment weight loss. We also found that living alone was associated with non-operative treatment aims. It is well established that lower socioeconomic status is associated with an adverse outcome of CRC in population-based studies [7,22,23] and this correlates with our findings of low income being associated with NOT-NO. In our study, not all socioeconomic factors were predictors. As shown by others, the effect of each socioeconomic factor does not necessarily point in the same direction due to different causal mechanisms and associations with specific covariates and outcomes [24,25]. We found variations between hospitals in all three non-curative treatment aims, however with rather low numbers, especially for OT-NCUR. Giesen et al. found that resection rates vary between hospitals in the Netherlands, but that they did not translate into differences in mortality [20]. In a Swedish study, Ljunggren et al. found variations in metastatic surgery for CRC between university hospitals and non-university hospitals, but no difference in the hospital volume of patients [26], while an English study by Downing et al. found that hospitals participating in interventional studies had better survival than those who did not [27]. We did not include data on university hospitals nor participation in interventional studies. Regarding adjuvant chemotherapy treatment, Babaei et al. found between-hospital variations in stage II with risk factors (17–38%) and stage III (55–68%) in a register-based study conducted in the Netherlands, Sweden and Belgium [28]. If you ask the oncologists about adherence to national guidelines on adjuvant therapy in the Netherlands, 66% and 84% agreement was found for stage II and III, respectively [29]. Shared decision-making is on the rise, also in Denmark, but is not implemented in guidelines yet [30]. Probably this had little effect on between-hospital variations in our study of patients from the years 2009 to 2018. The goodness of fit (GOF) test of the overall analysis returned a very low p-value (Table 2) and the interpretation of this is important. A significant GOF test is not surprising in a large cohort and just implies to the reader that on a population level (or hospital-specific level), these relative risk ratios are plausible, but should not be used on an individual level.

We also found that 28% of the patients with an indication for adjuvant chemotherapy did not have any adjuvant treatment, with differences between stage II (58%) and III (19%). DCCG has set a desired target level for commencing adjuvant therapy of 80–90% for stage III CRC [1], which is in line with our findings, as seen from Table 3. In the latest annual report from the United Kingdom, 61% of stage III colon cancer received a major resection followed by adjuvant chemotherapy in 2019 (latest pre-COVID-19 pandemic numbers) [31]. We found that refraining from adjuvant treatment was predicted by living alone, which is in line with the socioeconomic indicators found in a recent systematic review and meta-analysis [32]. Our findings of variations between hospitals are in line with annual reports from the United Kingdom and Denmark, although the latter is with rather low numbers per hospital [1,31].

4.3. Strength and Limitations

This study has some limitations. First, the period these patients are collected from is rather old (2009–2018) and this can affect the generalizability of our results. Secondly, we have missing data on some variables such as reason for no referral for adjuvant therapy evaluation, WHO performance status (which is missing in the majority of patients as seen in Table 1) and clinical TN category at diagnosis (although metastases at diagnosis is included). Third, it is worth mentioning that we pooled ypT and pT categories in the analyses on adjuvant therapy. Those with a good response on neoadjuvant therapy probably have less of an effect from adjuvant therapy and vice versa [2], and this could affect the adjuvant treatment decision. We have insufficient data on this and we suspect this to have little impact on our overall conclusions. Fourth, we did not include genetic markers, such as KRAS. ESMO guidelines do not recommend the inclusion of these, due to a lack of utility in the adjuvant treatment decision-making process [3]. The strengths of this study are mainly its size, including a large cohort with almost 100% coverage of the national population [33], but also the prospective collection of data (although retrospectively extracted) from the national registries.

4.4. Perspectives

Refraining from curative treatment is more widespread in some hospitals than in others, even when adjusting for various predictors. No desirable proportions per hospital are applicable, since these discussions are complex with patients at a very vulnerable point in their lives and the decisions are a subject of personal preferences. Further elaboration into this research area requires further data on the impact of treatment choices on survival, morbidity and quality of life. Also, research into tools aiding shared decision-making could probably promote further equity for these patients in making well-informed decisions.

5. Conclusions

An intended non-curative aim of treatment in colorectal cancer was associated with age, performance status and distant metastases. Refraining from indicated adjuvant chemotherapy was also associated with age and performance status, but also with living alone, kidney disease and postoperative complications. Between-hospital variations in treatment choices were found, even in adjusted analyses, and should be examined further.

Acknowledgments

The authors are grateful for the data provided by the DCCG and the Danish Clinical Quality Program.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/cancers16020366/s1, Table S1: Overview of inclusion and exclusion criteria and changes over the study period regarding national recommendation of treatment with adjuvant oncological treatment after curative re-section of stage II and III colorectal cancer.

Author Contributions

Conceptualization, S.R., S.M., E.F. and H.B.R.; Data curation, S.R., S.M. and E.F.; Formal analysis, S.R., S.M. and E.F.; Funding acquisition, S.R., S.M., E.F. and H.B.R.; Investigation, S.R.; Methodology, S.R., T.F.H., S.M., E.F. and H.B.R.; Project administration, S.R., E.F. and H.B.R.; Visualization, S.R., E.F. and H.B.R.; Writing—original draft, S.R.; Writing—review & editing, S.R., T.F.H., S.M., E.F. and H.B.R. All authors have read and agreed to the published version of the manuscript.

Institutional Review Board Statement

According to Danish law, a register-based study does not require approval from an ethics review board.

Informed Consent Statement

Since this is a register-based study, no consent from patients was required under Danish law [17].

Data Availability Statement

Data were obtained under a license granted specifically for this study and cannot be made available according to Danish legislation. Researchers can apply for data at www.dst.dk, www.sundhedsdatastyrelsen.dk and www.rkkp.dk (accessed on 8 January 2024).

Conflicts of Interest

The authors declare no conflict of interest.

Funding Statement

This study was funded by the Region of Southern Denmark (jr. no. 20/45132) and University Hospital Lillebaelt.

Footnotes

Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

References

  • 1.DCCG Landsdækkende Database for Kræft i Tyk- Og Endetarm (DCCG.dk). National Årsrapport. [Danish Colorectal Cancer Group (DCCG) Annual Report] 2022. [(accessed on 12 December 2023)]. Available online: https://dccg.dk/arsrapporter/
  • 2.DCCG Oversigt over DCCG’s Aktuelle Retningslinjer. [Overview of Current National Guidelines of Danish Colorectal Cancer Group (DCCG)] [(accessed on 28 September 2023)]. Available online: https://dccg.dk/retningslinjer/
  • 3.Argilés G., Tabernero J., Labianca R., Hochhauser D., Salazar R., Iveson T., Laurent-Puig P., Quirke P., Yoshino T., Taieb J., et al. Localised colon cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 2020;31:1291–1305. doi: 10.1016/j.annonc.2020.06.022. [DOI] [PubMed] [Google Scholar]
  • 4.Glynne-Jones R., Wyrwicz L., Tiret E., Brown G., Rödel C., Cervantes A., Arnold D., ESMO Guidelines Committee Rectal cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 2017;28((Suppl. 4)):iv22–iv40. doi: 10.1093/annonc/mdx224. [DOI] [PubMed] [Google Scholar]
  • 5.DCCG Oversigt over DCCG’s Tidligere Retningslinjer. [Overview of Former National Guidelines of Danish Colorectal Cancer Group (DCCG)] [(accessed on 29 September 2023)]. Available online: https://dccg.dk/tidligere-retningslinjer/
  • 6.Maeda H., Takahashi M., Seo S., Hanazaki K. Frailty and Colorectal Surgery: Review and Concept of Cancer Frailty. J. Clin. Med. 2023;12:5041. doi: 10.3390/jcm12155041. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Sundhedsstyrelsen Social Ulighed i Sundhed Og Sygdom. Udviklingen i Danmark i Perioden 2010–2017 [Social Inequality in Health and Disease. Development in Denmark from 2010–2017] [(accessed on 28 September 2023)]. Available online: https://www.sst.dk/da/udgivelser/2020/social-ulighed-i-sundhed-og-sygdom.
  • 8.Protani M.M., Alotiby M.K.N., Seth R., Lawrence D., Jordan S.J., Logan H., Kendall B.J., Siskind D., Sara G., Kisely S. Colorectal cancer treatment in people with severe mental illness: A systematic review and meta-analysis. Epidemiol. Psychiatr. Sci. 2022;31:e82. doi: 10.1017/S2045796022000634. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Rattenborg S., Möller S., Frostberg E., Rahr H.B. Uneven Between-Hospital Distribution of Patient-Related Risk Factors for Adverse Outcomes of Colorectal Cancer Treatment: A Population-Based Register Study. Clin. Epidemiol. 2023;15:867–880. doi: 10.2147/CLEP.S411392. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Benitez Majano S., Di Girolamo C., Rachet B., Maringe C., Guren M.G., Glimelius B., Iversen L.H., Schnell E.A., Lundqvist K., Christensen J., et al. Surgical treatment and survival from colorectal cancer in Denmark, England, Norway, and Sweden: A population-based study. Lancet Oncol. 2019;20:74–87. doi: 10.1016/S1470-2045(18)30646-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.DCCG Landsdækkende Database for Kræft i Tyk- Og Endetarm. Årsrapport. [Danish Colorectal Cancer Group Database (DCCG) Annual Report] 2021. [(accessed on 12 December 2023)]. Available online: https://dccg.dk/arsrapporter/
  • 12.Ingeholm P., Gögenur I., Iversen L.H. Danish Colorectal Cancer Group Database. Clin. Epidemiol. 2016;8:465–468. doi: 10.2147/CLEP.S99481. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Schmidt M., Schmidt S.A.J., Adelborg K., Sundbøll J., Laugesen K., Ehrenstein V., Sørensen H.T. The Danish health care system and epidemiological research: From health care contacts to database records. Clin. Epidemiol. 2019;11:563–591. doi: 10.2147/CLEP.S179083. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.World Health Organization (WHO) Obesity and Overweight. [(accessed on 31 October 2023)]. Available online: https://www.who.int/en/news-room/fact-sheets/detail/obesity-and-overweight.
  • 15.Charlson M.E., Pompei P., Ales K.L., MacKenzie C.R. A new method of classifying prognostic comorbidity in longitudinal studies: Development and validation. J. Chronic Dis. 1987;40:373–383. doi: 10.1016/0021-9681(87)90171-8. [DOI] [PubMed] [Google Scholar]
  • 16.Quan H., Li B., Couris C.M., Fushimi K., Graham P., Hider P., Januel J.M., Sundararajan V. Updating and validating the Charlson comorbidity index and score for risk adjustment in hospital discharge abstracts using data from 6 countries. Am. J. Epidemiol. 2011;173:676–682. doi: 10.1093/aje/kwq433. [DOI] [PubMed] [Google Scholar]
  • 17.UNESCO International Standard Classification of Education, ISCED 2011. 2012, 86. [(accessed on 7 December 2023)]. Available online: https://uis.unesco.org/en/topic/international-standard-classification-education-isced.
  • 18.Thygesen L.C., Daasnes C., Thaulow I., Brønnum-Hansen H. Introduction to Danish (nationwide) registers on health and social issues: Structure, access, legislation, and archiving. Scand. J. Public Health. 2011;39((Suppl. 7)):12–16. doi: 10.1177/1403494811399956. [DOI] [PubMed] [Google Scholar]
  • 19.Turner M.C., Farrow N.E., Rhodin K.E., Sun Z., Adam M.A., Mantyh C.R., Migaly J. Delay in Adjuvant Chemotherapy and Survival Advantage in Stage III Colon Cancer. J. Am. Coll. Surg. 2018;226:670–678. doi: 10.1016/j.jamcollsurg.2017.12.048. [DOI] [PubMed] [Google Scholar]
  • 20.Giesen L.J.X., van Erning F.N., Vissers P.A.J., Maas H., Rutten H.J.T., Lemmens V., Dekker J.W.T. Inter-hospital variation in resection rates of colon cancer in the Netherlands: A nationwide study. Eur. J. Surg. Oncol. 2019;45:1882–1886. doi: 10.1016/j.ejso.2019.06.012. [DOI] [PubMed] [Google Scholar]
  • 21.Axt S., Wilhelm P., Spahlinger R., Rolinger J., Johannink J., Axt L., Kirschniak A., Falch C. Impact of preoperative body mass index and weight loss on morbidity and mortality following colorectal cancer-a retrospective cohort study. Int. J. Color. Dis. 2022;37:1983–1995. doi: 10.1007/s00384-022-04228-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Frederiksen B.L., Osler M., Harling H., Ladelund S., Jørgensen T. Do patient characteristics, disease, or treatment explain social inequality in survival from colorectal cancer? Soc. Sci. Med. 2009;69:1107–1115. doi: 10.1016/j.socscimed.2009.07.040. [DOI] [PubMed] [Google Scholar]
  • 23.Van den Berg I., Buettner S., van den Braak R., Ultee K.H.J., Lingsma H.F., van Vugt J.L.A., Ijzermans J.N.M. Low Socioeconomic Status Is Associated with Worse Outcomes After Curative Surgery for Colorectal Cancer: Results from a Large, Multicenter Study. J. Gastrointest. Surg. 2020;24:2628–2636. doi: 10.1007/s11605-019-04435-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Darin-Mattsson A., Fors S., Kåreholt I. Different indicators of socioeconomic status and their relative importance as determinants of health in old age. Int. J. Equity Health. 2017;16:173. doi: 10.1186/s12939-017-0670-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Geyer S., Hemstrom O., Peter R., Vagero D. Education, income, and occupational class cannot be used interchangeably in social epidemiology. Empirical evidence against a common practice. J. Epidemiol. Community Health. 2006;60:804–810. doi: 10.1136/jech.2005.041319. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Ljunggren M., Weibull C.E., Rosander E., Palmer G., Glimelius B., Martling A., Nordenvall C. Hospital factors and metastatic surgery in colorectal cancer patients, a population-based cohort study. BMC Cancer. 2022;22:907. doi: 10.1186/s12885-022-10005-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Downing A., Morris E.J., Corrigan N., Sebag-Montefiore D., Finan P.J., Thomas J.D., Chapman M., Hamilton R., Campbell H., Cameron D., et al. High hospital research participation and improved colorectal cancer survival outcomes: A population-based study. Gut. 2017;66:89–96. doi: 10.1136/gutjnl-2015-311308. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Babaei M., Balavarca Y., Jansen L., Lemmens V., van Erning F.N., van Eycken L., Vaes E., Sjövall A., Glimelius B., Ulrich C.M., et al. Administration of adjuvant chemotherapy for stage II-III colon cancer patients: An European population-based study. Int. J. Cancer. 2018;142:1480–1489. doi: 10.1002/ijc.31168. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Keikes L., van Oijen M.G.H., Lemmens V.E.P.P., Koopman M., Punt C.J.A. Evaluation of Guideline Adherence in Colorectal Cancer Treatment in The Netherlands: A Survey Among Medical Oncologists by the Dutch Colorectal Cancer Group. Clin. Color. Cancer. 2018;17:58–64. doi: 10.1016/j.clcc.2017.10.007. [DOI] [PubMed] [Google Scholar]
  • 30.Maes-Carballo M., Gómez-Fandiño Y., García-García M., Martín-Díaz M., De-Dios-de-Santiago D., Khan K.S., Bueno-Cavanillas A. Colorectal cancer treatment guidelines and shared decision making quality and reporting assessment: Systematic review. Patient Educ. Couns. 2023;115:107856. doi: 10.1016/j.pec.2023.107856. [DOI] [PubMed] [Google Scholar]
  • 31.NBOCA National Bowel Cancer Audit. Annual Report 2022. 2022. [(accessed on 7 December 2023)]. Available online: https://www.nboca.org.uk/reports/?filter_date=2022.
  • 32.Konradsen A.A., Lund C.M., Vistisen K.K., Albieri V., Dalton S.O., Nielsen D.L. The influence of socioeconomic position on adjuvant treatment of stage III colon cancer: A systematic review and meta-analysis. Acta Oncol. 2020;59:1291–1299. doi: 10.1080/0284186X.2020.1772501. [DOI] [PubMed] [Google Scholar]
  • 33.Klein M.F., Gögenur I., Ingeholm P., Njor S.H., Iversen L.H., Emmertsen K.J. Validation of the Danish Colorectal Cancer Group (DCCG.dk) database-on behalf of the Danish Colorectal Cancer Group. Color. Dis. 2020;22:2057–2067. doi: 10.1111/codi.15352. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Data Availability Statement

Data were obtained under a license granted specifically for this study and cannot be made available according to Danish legislation. Researchers can apply for data at www.dst.dk, www.sundhedsdatastyrelsen.dk and www.rkkp.dk (accessed on 8 January 2024).


Articles from Cancers are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)

RESOURCES