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. 2020 Sep 10;13:1499–1512. doi: 10.2147/RMHP.S262171

Cost-Effectiveness Analysis of Colorectal Cancer Screening: A Systematic Review

Farhad Khalili 1, Behzad Najafi 2, Fariborz Mansour-Ghanaei 3, Mahmood Yousefi 4,, Hadi Abdollahzad 5, Ali Motlagh 6
PMCID: PMC7490076  PMID: 32982508

Abstract

Introduction

Colorectal cancer (CRC) is a significant health problem with an increasing incidence worldwide. Screening is one of the ways, in which cases and deaths of CRC can be prevented. The objective of this systematic review was to evaluate the cost-effectiveness of the different CRC screening techniques and to specify the efficient technique from a cost-effectiveness perspective.

Methods

The economic studies of CRC screening in general populations (average risk), aged 50 years and above were reviewed. Two reviewers independently reviewed the titles, abstracts, and full-texts of the studies in five databases: Cochrane, Embase, Scopus, Web of Science and PubMed. The disagreements between reviewers were resolved through the authors’ consensus. The main outcome measures in this systematic review were the incremental cost-effectiveness ratio (ICER) of screening versus no-screening and then in comparison with other screening techniques. The ICER is defined by the difference in cost between two possible interventions, divided by the difference in their effect.

Results

Eight studies were identified and retained for the final analysis. In this study, when screening techniques were compared to no-screening, all CRC screening techniques showed to be cost-effective. The lowest ICER calculated was $PPP −16265/quality-adjusted life-year (QALY) (the negative ICERs were between purchasing power parity in US dollar ($PPP) −16265/QALY to $PPP −1988/QALY, whereas the positive ICERs were between $PPP 1257/QALY to $PPP 55987/QALY). For studies comparing various screening techniques, there was great heterogeneity in terms of the structures of the analyses, leading to diverse conclusions about their incremental cost-effectiveness.

Conclusion

All CRC screening techniques were cost-effective, compared with the no-screening methods. The cost-effectiveness of the various screening techniques mainly was dependent on the context-specific parameters and highly affected by the framework of the cost-effectiveness analysis. In order to make the studies comparable, it is important to adopt a reference-based methodology for economic evaluation studies.

Keywords: incremental cost-effectiveness ratio, screening techniques, economic evaluation, colorectal cancer

Introduction

Among the world mostly diagnosed cancers, colorectal cancer (CRC) takes the third place in males and the second in females, worldwide.1

In 2018, there were an estimated 1.8 million new CRC cases and 861,663 deaths in both sexes at all ages (0–85+ years). This is already becoming a major public health problem across the world.1,2 The attributable cases and deaths of CRC can be avoided through early diagnosis. Screening for finding cases at the early stages of the disease is a well-known strategy of controlling disease, in fact, early detection of cancer helps to remove precancerous lesions and prevent cancer from reaching advanced stages. While the European Union recommends screening by a fecal occult blood test (FOBT), in the US the guidelines recommend people older than 50 years, to choose among several recommended strategies.3,4

Screening programs often target people with apparently healthy conditions, and active screening tends to be delivered collectively. Thus, the number of people using screening services is usually higher than the true number of patients. This in turn has implications for high costs per diagnosed patient. In an optimal situation, the return of benefits to society due to the implementation of screening should outweigh the associated costs. In essence, understanding this situation depends on some basic factors like the prevalence of the disease, accuracy of screening methods, target population, and cost of each strategy.5 Economic evaluation is a systematic and formal way of assessing the costs and benefits of screening interventions. There are several techniques for screening of CRC; colonoscopy, which is one of the most popular interventions, has been associated with relatively high but better accuracy performance;6 in contrast, the FOBT has advantages over colonoscopy in terms of being less costly and easy to perform. The fecal immunochemical test (FIT), which is also called either immunochemical FOBT or IFOBT, is usually favored because it does not need any dietary restriction, and it has higher specificity when it is compared to guaiac-based FOBT (G-FOBT).7,8 Furthermore, the non-invasive hybrid screening techniques, which is a stool DNA test (S-DNA test), have recently been approved by the US Food and Drug Administration (FDA).9,10 The characteristics of different types of screening techniques are presented in Appendix 1.

We performed a systematic review to retrieve the evidence on the cost-effectiveness of the various CRC screening methods. The study was designed to focus on the most recent studies, which have been conducted worldwide, since 2012.

This review aimed to explore the cost-effectiveness of the different screening strategies, either in comparison with no-screening or other techniques, in the average-risk population.

Methods

Search Strategy

We conducted this systematic review based on the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines,11 and following the Cochrane Handbooks for systematic reviews.12 The search strategy used in this review was registered in Prospero13 (registration number: CRD42018081676). The approach for identifying studies and extracting the data has been described in earlier studies, and performed in the economic evaluation of CRC screening techniques.14,15 Five databases were searched for identifying relevant studies, including Cochrane, Embase, Scopus, Web of Science, PubMed. We used a specific search strategy for each database and the following key terms were used: “colorectal cancer”, “cost-effectiveness” and “screening”. Our search was restricted to studies written in English and published between January 2012 and December 2018, and then updated until June 2020. In order to find the studies not covered by our database searches and studies in gray literature, we manually looked at the reference lists of the studies and contacted the authors of the concerned studies. The studies were chosen, according to the similar inclusion and exclusion criteria, as in the US Preventive Services Task Force (USPSTF) review.16

The inclusion criteria were: 1) Studies that focused on CRC screening, 2) Studies that aimed at average risk17 populations, aged 50 years and above, 3) Studies that reported the Incremental Cost-Effectiveness Ratio (ICER) or provided data for ICER calculation, 4) Studies that outlined cost per quality-adjusted life-year (QALY) gained or cost per life-year gained, 5) Studies that had full economic evaluations, and 6) Studies published in English.

The exclusion criteria were as follows: 1) Articles that reported only cost per cancer detected, cost per patient screened and cost per death prevented, 2) Non-original studies, 3) Opportunistic screening, and 4) Short-term decision trees.

Data Extraction and Quality Assessment

Firstly, two reviewers independently assessed the titles and abstracts of the retrieved studies and then excluded the irrelevant studies based on the developed criteria. When the articles could not be located based on the title and abstract, the full-text was evaluated. The disagreements between reviewers about inclusion and exclusion of studies were resolved through the authors’ consensus or by the third reviewer. For data collection, we designed a data extraction form containing 1) Details of bibliography, 2) Study design, including aim and cases of studies, time horizon, interventions and alternatives, costs included in the study, sources of screening cost, outcome measures for effectiveness, data sources that are relevant to the outcome, study’s perspective, modeling sensitivity analysis and discount rate for both costs and outcomes, and 3) Main results and conclusions. Data extracted from each article were included in the table for each of the techniques under consideration such as FIT, Flexible Sigmoidoscopy (FS), FOBT, Multi-target Stool DNA (MT- S-DNA), colonoscopy, double-contrast barium enema (based on the age of the subjects and the time intervals of 2, 5 and10 years). To compare different alternatives, costs were updated to purchasing power parity (PPP) in 2017, using the Consumer Price Index (CPI) for medical care and PPP conversion factor. The ICER was the primary outcome measure in this systematic review, for comparing the screening and no-screening methods, and then in comparison with other screening techniques. The ICERs calculated as either cost per life-year gained or cost per QALY.

graphic file with name M1.gif

In this systematic review, the threshold is defined as a standard threshold in the country of origin where the paper was published, while for the countries that did not report any threshold, the World Health Organization (WHO) recommended guideline was used.1820 The criterion for assessing the cost-effectiveness was based on the recommended WHO threshold for cost-effectiveness analysis. According to this criterion, if the value of an ICER for a given intervention falls below the specified value of three-time the Gross Domestic Product (GDP) per capita, then it is considered as a cost-effective strategy.

We used the Drummond 10-point checklist, which is a standard procedure for the quality assessment of economic evaluation studies, for qualitative assessment of studies, in order to confirm their methodological quality.21 All questions had three options for the answer, including “yes”, “cannot tell” and “no”, and the corresponding value for each item was 1, 0.5 and 0, respectively. The reason for choosing a 0.5 value for the “cannot tell” response was that the information about that item was not complete. For items that were not relevant, we considered score 1.

Results

Study Selection

A flow diagram, based on the PRISMA, for choosing the relevant studies has been shown in Figure 1. In primary search, we identified 1701 relevant studies, which were published after January 2012. Removing the duplicates (841 papers) resulted in 830 articles for further analysis. After examining the title and abstracts of these studies, 92 articles were identified for full-text review and additional analysis. Finally, we found eight studies from 92 fully reviewed articles, which met our criteria. In Table 1, we have introduced the characteristics of these studies. Table 1 represents the details of methods and results, such as the lists of the models, study population, time horizon, screening techniques, the perspective of the study and outcome measure for each study, sources of cost information, type of costs, currency (type and year), discount rate, side effects, approach for expressing uncertainty and important variables in the sensitivity analysis. The results show that one study reported costs per life years saved (LYS) from CRC screening,22 six reported costs per QALYs only,2328 and two reported both costs per LYS and costs per QALY.29 All studies examined one or more of the available screening techniques, as well as a no-screening alternative. The perspectives of the analyses were societal or third-party payers.

Figure 1.

Figure 1

The methods to identify studies based on the inclusion criteria.

Note: Adapted from Moher D, Liberati A, Tetzlaff J, Altman DG, The PRISMA Group (2009). Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement. PLoS Med 6(7): e1000097.30

Table 1.

The Characteristics of the Included Studies

Characteristics Wong22 Dinh23 Ladabaum24 Sharaf25 Sharp26 Dan27 James28 Wong29
Model type Markov Archimedes Markov Markov Markov process Markov Markov Markov
Study Population GP (50 year over) GP 50–75 GP 50, 65 and older GP(65–71) GP(55–74) GP(50–75) GP(50–100) GP(50–70)
Time horizon 25 years Lifetime 30 years Lifetime Lifetime Lifetime 30 years 20 years
Screening technique No-screening
G-FOBT yearly and 2-year
I-FOBT(FIT) yearly and 2-year
Colonoscopy 10-year
No-screening
FIT/sigmoidoscopy
FIT yearly/COLOx1
FIT yearly
Sigmoidoscopy 5-year
colonoscopy 10-year
No-screening
FIT every 2 years
FIT yearly
MT-s DNA every 3 years
Colonoscopy 10-year
No-screening
FS once
FOBT yearly
FS every 5 years
FIT yearly
Colonoscopy every 10 years
FS 5-year+ FIT yearly
No-screening
biennial G FOBT at ages (55–74)
biennial FIT at ages (55–74)
FSIG once at age 60
No-screening, FIT early, barium enema 5-year,
sigmoidoscopy 5-year, sigmoidoscopy 5-year+ FIT early, stool DNA every 5 years, single colonoscopy
colonoscopy 10-year, colonography10-year, FIT early+ colonoscopy 10-year
No-screening
FIT yearly
colonoscopy 10-year
stool DNA3-year
sigmoidoscopy5-year
No-screening
FS5-year at ages 50–70 for male and female
Colonoscopy 10-year at ages 50–60–70 for male and female
FS5-year at ages 50–55 (female)
FS5-year at ages 50–65 (female)
FS5-year at ages 50–70 (female)+colonoscopy10-year
Perspective Third-party payer (healthcare service provider) Societal Third-party payer Third-party payer Third-party payer Societal Societal Third-party payer
(healthcare service provider)
Out-come Data sources LYs or QALYs/experimental studies QALYs/Systematic review QALYs/Observational and experimental studies QALYs/Systematic review QALYs/Systematic review QALYs/Systematic review QALYs/review of literature LYs/experimental studies
Type of cost included Direct Direct Direct Direct Direct Indirect- Direct Indirect- Direct Direct
Source of screening cost Hong Kong Government Printers
(Government Gazette)
Medicare Medicare payment Medicare DRG-2 article Governments
restructured hospitals in Singapore
Medicare and private insurance Hong Kong Government Printers
(Government Gazette)
FOBT $PPP NR NR NR 25.25 10 NR NR NR
FIT $PPP NR 2.6 19 25.25 15 33 22 NR
Barium enema NR NR NR NR NR 115.3 NR NR
Colonoscopy $PPP 1351 570.3 1416 708.07 842 708.1 1075 1351
Sigmoidoscopy $PPP NR 184.4 NR 185.52 194 219.6 185.8 368
Sigmoidoscopy
+FIT $PPP
NR NR NR NR NR NR NR NR
Stool DNA NR NR 661 NR NR 329.3 NR NR
Virtual Colonography $PPP NR NR NR NR 550 866.15 NR 713
FIT+ Colonoscopy $PPP NR NR NR NR NR NR NR NR
Polypectomy, $PPP 267 172 NR 1112.05 NR NR NR 267
Treatment of perforation, $PPP 15002 NR 23058 15652.14 13215 26346.7 NR 15002
Indirect costs, $ Wong22 Dinh23 Ladabaum24 Sharaf25 Sharp26 Dan27 James28 Wong29
Screen program cost * $PPP NR NR NR NR NR 4.17 NR NR
Transport and wage loss $PPP NR NR NR NR NR 1207.6 NR NR
Localized, $PPP NR NR 3599 2482.1 47129 14106.7 2831 23014
Regional, $PPP NR NR 4795 3307.6 62229 25084.3 3080 37986
Distant, $PPP NR NR 99381 78866.7 46380 46930.1 12317 99761
Side effects Bleeding or perforation NR Perforation- major hemorrhage Perforation- hemorrhage Major bleeding- bowel
perforation- deaths due to
perforation
Major bleeding- Bowel
Perforation- Deaths due to
perforation
NR Bleeding or perforation
Currency (type and year) U.S dollar-2009 U.S dollar- 2010 U.S dollars 2015 U.S dollar- 2010 € 2008 U.S dollar- 2009 U.S dollar 2014 U.S dollar-NR
Discount rate 3.5% 3% 3% 3% 4% 3% 3% 3%
Approach to expressing uncertainty Deterministic and PSA One-way sensitivity One-way and multiway sensitivity One-way sensitivity analyses PSA and One-way sensitivity analyses One-way and multi-way sensitivity One-way and two-way sensitivity analyses,
PSA
1-way sensitivity
Important variables in sensitivity analysis Model parameters
And outputs (compliance rates of screening, utilities, discount rate)
Compliance rates, interval between FIT screenings, performance
characteristics of FIT and colonoscopy, costs of FIT, colonoscopy,
and CRC treatments, and discount rate
All model inputs: costs- utility, sensitivity, specificity, side effect, interval screening Costs of the tests, the costs of CRC care, the
risk of CRC
Discount rate, costs of screening tests, costs of managing colorectal
cancer
Incidence of colorectal cancer, secondary and tertiary adherence, and cost of colonoscopy, specificity and sensitivity of tests All inputs model (specificity and sensitivity of tests, costs of the tests Compliance rates of screening, specificity and sensitivity of tests, costs of the tests

Note: *The cost of screening program includes: screening center manpower staffing/training/case-tracking/registry/public education audit/quality control.

Abbreviations: GP, general population; FIT, fecal immunochemical test; MT-s DNA, multi-target stool DNA; FS once, flexible sigmoidoscopy once; FOBT, fecal occult blood test; QALYs, quality-adjusted life-year; LYS, life years saved; NR, not reported; PSA, probabilistic sensitivity analysis; CRC, colorectal cancer; NR, not reported.

Cost-Effectiveness of Common Alternative Techniques of Screening vs No-Screening

The results of the present study showed that the screening for CRC led to a decrease in the deaths from CRC in adults above 50 years of age, who were at average risk for CRC. The results demonstrated that screening by any technique was cost-effective. For one study, the cost of screening techniques ($PPP 2028 per person to $PPP 2428 per person) was less than the cost of no-screening ($PPP 3580 per person).23 In the remaining of the studies, the costs of no-screening were between $PPP 240 per person and $PPP 8422 per person, and for the alternative screening techniques, the costs were exceeding these ranges. In this systematic review, all the studies revealed that any type of screening strategies is more effective than the no-screening technique. The minimum ICER calculated in $PPP was −16265/QALY (the negative ICERs were between $PPP −16265/QALY to $PPP –1988/QALY, whereas the positive ICERs were between $PPP 1257/QALY to $PPP 55987/QALY).23 Table 2 shows the details of extracted data for alternative techniques, in comparison to the no-screening strategy.

Table 2.

The Incremental Cost-Effectiveness Ratios of Different Techniques for CRC, in Contrast to the No-Screening Method

Screening Test Study/Reference
Wong22 Dinh23 Ladabaum24 Sharaf25 Sharp26 Dan27 Kingsley28 Wong29
FIT 2-year 4328 - −11391 - 1306 - - -
FIT yearly 4587 −16169 −7970 −7243 - 34580 −6005 -
FIT+COLOx1a - −12695 - - - - - -
FIT+sigmoidoscopy - −12243 - −1988 - 47205 - -
Sigmoidoscopy once - - - −11,712 1257 25981 - -
Sigmoidoscopy 5-year - - −3330 - 45448 −3109 40237
Colonoscopy 10-year 5265 −10400 15283 2959 - 38745 3316 22391
Single Colonoscopy - - - - - 43911 - -
Stool DNA - 30014 - - - 48205 16046 -
Virtual colonography 5-y - - - - - 49830 - -

Notes: The negative ICER indicates that the new technique is less costly and more effective. The positive ICERs refer to those techniques that are more costly and more effective; both numerators and denominators are positive.

Abbreviation: aCOLOx1, colonoscopy once.

Overall, from the studies that examining only one method of screening, in four studies, the FIT was more effective and less costly than the no-screening strategy. The FIT every 2-year and FIT yearly screening techniques were more effective and less costly than the no-screening, among all techniques.

Studies also assessed the mixed method screening and found that annual FIT/COLOx1 (colonoscopy once) and FIT/sigmoidoscopy were more effective and less costly than the no-screening method (FIT/COLOx1 and FIT/sigmoidoscopy, gained 0.11 and 0.112 QALYs per person, and saved $PPP 1396 and 1371 per person, respectively).23

In two studies, sigmoidoscopy was dominant, compared to the no-screening technique.2325 In fact, sigmoidoscopy once and sigmoidoscopy every 5 years were less costly and more effective than the no-screening method. Single sigmoidoscopy had an ICER below $28,000/QALY, indicating the dominance of this technique to no-screening technique, in the given context-specific threshold.27

Colonoscopy every 10-year, beginning at either 50 or 70 years of age, for both sexes also dominated the no-screening.29 Only one out of seven studies showed that performing colonoscopy every 10-year was more effective and less costly than no-screening.23 Actually, this technique had an ICER lower than other techniques. In addition, only one out of seven studies reported a single colonoscopy technique. We found that the single colonoscopy was cost-effective, in comparison to the no-screening strategy, according to the given threshold.27 The studies that reported the cost-effectiveness analysis for the newer technologies of stool DNA and virtual colonography every 5-year, revealed that both techniques were cost-effective, in comparison to the no-screening strategy.24,27,28

Comparison of Different Screening Techniques

We identified eight studies, examined multiple screening methods (FOBT, FIT, colonoscopy, sigmoidoscopy and the combination of S-DNA test, FIT and sigmoidoscopy) and reached diverse conclusions about their ICER. In three studies, annual/biennial FIT was compared to annual/biennial FOBT, showing that the ICER for annual/biennial FIT in all studies was below the accepted threshold, and thus suggesting a cost-effective strategy. Also in two out of three studies, the annual FIT was more effective and less costly than annual FOBT. The analysis performed by Ladabaum et al24 showed that yearly FIT was cost-effective when it was compared to FIT performed every 2 years (see Table 3). The comparisons made between annual FIT and sigmoidoscopy every 5-year showed that annual FIT was dominant in four out of five studies. In two of those studies, annual FIT showed less cost and more effectiveness, in comparison with sigmoidoscopy every 5-year.22,25 Only in the analysis conducted by Dan and colleagues,27 the annual FIT dominated by both single sigmoidoscopy and sigmoidoscopy every 5-year or had an ICER higher than $50,000/per QALY (see Table 4). When FOBT was compared to sigmoidoscopy of every 5-year and sigmoidoscopy once, it was observed that all the studies had an ICER below $50000/per QALY. In the study of Sharaf et al25 the annual FOBT was more effective and less costly than sigmoidoscopy once (see Table 5). When sigmoidoscopy every 10-year or sigmoidoscopy every 5-year plus annual FIT was compared to FIT yearly, it was revealed that in four out of five studies the sigmoidoscopy every 10-year or sigmoidoscopy every 5-year plus annual FIT had an ICER of above $50000/per QALY and was dominated (see Table 6).25,27 Colonoscopy every 10-year in one out of five studies was cost-effective, in comparison with the FIT yearly and annual FOBT. A study by Wong et al represented that colonoscopy every 10-year was more effective and less costly than annual FOBT (see Table 7).22 Also in one out of two comparisons, colonoscopy every 10-year was dominant, compared to the sigmoidoscopy every 5-year plus annual FIT.27 However, in another study that sigmoidoscopy every 5-year plus annual FIT considered as a base technique, and was compared to colonoscopy every 10-year, we observed less cost and more effectiveness, in comparison to the colonoscopy every 10-year (see Table 8).25

Table 3.

The Calculated Incremental Cost-Effectiveness Ratios When Using FIT Yearly vs FIT Every 2-Year, and FOBT Yearly

Author/Technique C Q ICER Threshold Optimal Strategy
Sharaf25
 FIT yearly 2090 18.7456 −9327 $US 50000 FIT yearly was dominant
 FOBT yearly 2187 18.7352
Sharp26
 FIT 2-yearly 1443 10.984 563 WHO Recommendation FIT 2-yearly was cost-effective a
 FOBT 2-yearly 1434 10.968
Wong22
 FIT yearly 7371 15.5491 −1504 $US 50000 FIT yearly was dominant
 FOBT yearly 7845 15.2339
Wong22
 FIT 2-yearly 6606 15.4203 1328 $US 50000 FIT 2-yearly was cost-effective
 FOBT 2-yearly 6136 15.0687
Ladabaum24
 FIT yearly 2450 18.747 33167 $US 50000 FIT yearly was cost-effective
 FIT 2-year 2251 18.741

Notes: In this table, for each study, the first row shows the new technique that is compared with the old technique, presented in the second row. The negative ICER indicates that the new technique is less costly and more effective. The positive ICERs refer to those techniques that are more costly and more effective; both numerators and denominators are positive. aBased on the context threshold.

Abbreviations: C, costs per person ($PPP); Q, QALYs (quality-adjusted life-year); ICER, incremental cost-effectiveness ratio; FOBT, fecal occult blood testing; FIT, fecal immunochemical testing.

Table 4.

The Calculated Incremental Cost-Effectiveness Ratios When Using FIT Alone vs Flexible Sigmoidoscopy (FS)

Author/Technique C Q ICER Threshold Optimal Strategy
Dinh23
 FIT yearly 2028.2 15.771 −15896 $US 50000 FIT yearly was dominant
 FS 5-year 2425.6 15.746
Sharaf25
 FIT yearly 2090 18.7456 −39167 $US 50000 FIT yearly was dominant
 FS 5-year 2419 18.7372
Dan27
 FIT yearly 378.73 16.393 60370 $US 50000 FIT yearly was dominated
 Single FS 318.36 16.392
Kingsley28
 FIT yearly 1607 19.506 −11370 $US 50000 FIT yearly was dominant
 FS 5-year 1914 19.479
Sharaf25
 FIT yearly 2090 18.7372 −5920 $US 50000 FIT yearly was dominant
 FS once 2341 18.6948
Dan27
 FIT yearly 378.73 16.393 88920 $US 50000 FIT yearly was dominated
 FS 5-year 467.65 16.394

Notes: In this table, for each study the first row shows the new technique that is compared with the old technique, written in the second row. The negative ICER indicates that the new technique is less costly and more effective.

Abbreviations: C, costs per person ($PPP); Q, QALYs (quality-adjusted life-year); ICER, incremental cost-effectiveness ratio; FOBT, fecal occult blood testing; FIT, fecal immunochemical testing; FS 5-year, flexible sigmoidoscopy every 5 years; FS once flexible sigmoidoscopy once in lifetime.

Table 5.

The Calculated Incremental Cost-Effectiveness Ratios When Using FOBT Alone vs Flexible Sigmoidoscopy (FS)

Author/Technique C Q ICER Threshold Optimal Strategy
Sharaf25
 FOBT yearly 2178 18.7352 120500 $US 50000 FOBT yearly was dominated
 Sigmoidoscopy 5-year 2419 18.7372
Sharp26
 FOBT 2-year 1434 10.968 19500 WHO Recommendation FOBT 2-year was cost-effective a
 Sigmoidoscopy once 1395 10.966
Sharaf25
 FOBT yearly 2178 18.7352 $US 50000 FOBT yearly was dominant
 (FS Once)Sigmoidoscopy once 2341 18.6948 −4035

Notes: In this table, for each study, the first row shows the new technique that is compared with the old technique, written in the second row. The negative ICER indicates that the new technique is less costly and more effective. The positive ICERs refer to those techniques that are more costly and more effective; both numerators and denominators are positive. aBased on the context threshold.

Abbreviations: C, costs per person ($PPP); Q, QALYs (quality-adjusted life-year); ICER, incremental cost-effectiveness ratio; FOBT, fecal occult blood testing yearly; FIT, fecal immunochemical testing yearly; FS once, flexible sigmoidoscopy once in lifetime.

Table 6.

The Calculated Incremental Cost-Effectiveness Ratios When Using FIT+ Sigmoidoscopy vs FIT

Author/Technique C Q ICER Threshold Optimal Strategy
Dinh23
 FIT early+ sigmoidoscopy 5-year 2209.1 15.787 11306 $US 50000 FIT early+ FS 5-year was cost-effective a
 FIT yearly 2028.2 15.771
Sharaf25
 FS 5-year + FIT yearly 2492 18.7469 309231 $US 50000 FS 5-year + FIT yearly was dominated
 FIT yearly 2090 18.7456
Dan27
 FS 5-year + IFOBT yearly 570.85 16.396 64040 $US 50000 FS 5-year + IFOBT yearly was dominated
 IFOBT yearly 378.73 16.393

Notes: In this table, for each study, the first row shows the new technique that is compared with the old technique, written in the second row. The negative ICER indicates that the new technique is less costly and more effective. The positive ICERs refer to those techniques that are more costly and more effective; both numerators and denominators are positive. aBased on the context threshold.

Abbreviations: C, costs per person ($PPP); Q, QALYs (quality-adjusted life-year); ICER, incremental cost-effectiveness ratio; FOBT, fecal occult blood testing; FIT, fecal immunochemical testing.

Table 7.

The Calculated Incremental Cost-Effectiveness Ratios When Using Colonoscopy vs FIT and FOBT

Author/Technique C Q ICER Threshold Optimal Strategy
Dinh23
 Colonoscopy 10-year 2384.3 15.79 17805 $US 50000 Colonoscopy 10-year was cost-effective a
 FIT yearly 2028.2 15.77
Ladabaum24
 Colonoscopy 10-year 4248 18.746 443778 $US 50000 Colonoscopy 10-year was dominated
 FIT 2-year 2251 18.741
Sharaf25
 Colonoscopy 10-year 2871 18.7443 75165 $US 50000 Colonoscopy 10-year was dominated
 FOBT yearly 2187 18.7352
Wong22
 Colonoscopy 10-year 6911 15.3586 −7490 $US 50000 Colonoscopy 10-year was dominant
 G-FOBT yearly 7845 15.2339
Kingsley28
 Colonoscopy 10-year 2474 19.517 78818 $US 50000 Colonoscopy 10-year was dominated
 FIT yearly 1607 19.506

Notes: In this table, for each study, the first row shows the new technique that is compared with the old technique, written in the second row. The negative ICER indicates that the new technique is less costly and more effective. The positive ICERs refer to those techniques that are more costly and more effective; both numerators and denominators are positive. aBased on the context threshold.

Abbreviations: C, costs per person ($PPP); Q, QALYs (quality-adjusted life-year); ICER, incremental cost-effectiveness ratio; G-FOBT, guaiac fecal occult blood testing; FIT, fecal immunochemical testing.

Table 8.

The Calculated Incremental Cost-Effectiveness Ratios When Using Colonoscopy vs FIT + Sigmoidoscopy

Author/Technique C Q ICER Threshold Optimal Strategy
Dinh23
 Colonoscopy 10 year 2384.3 15.79 58400 $US 50000 Colonoscopy 10-year was dominated
 FIT yearly+ sigmoidoscopy 5-year 2209.1 15.787
Dan27
 Colonoscopy 10-year 899.08 16.406 32823 $US 50000 Colonoscopy 10-year was cost-effective a
 Sigmoidoscopy 5-year + IFOBT yearly 570.85 16.396

Notes: In this table, for each study, the first row shows the new technique that is compared with the old technique, written in the second row. The positive ICERs refer to those techniques that are more costly and more effective; both numerators and denominators are positive. aBased on the context threshold.

Abbreviations: C, costs per person ($PPP); Q, QALYs (quality-adjusted life-year); ICER, incremental cost-effectiveness ratio; IFOBT, fecal occult blood testing; FIT, fecal immunochemical testing.

When colonoscopy every 10-year was compared with S-DNA test (3-year and 5-year), colonoscopy test had an ICER below $50000/per QALY and was dominant with 100% of the certainty. Only one study showed that the virtual colonography every 5-year was less cost-effective when compared to the established technique (see Table 9).27

Table 9.

The Calculated Incremental Cost-Effectiveness Ratios When Using Colonoscopy vs Stool DNA

Author/Technique C Q ICER Threshold Optimal Strategy
Ladabaum24
 Colonoscopy 10-year 4248 18.7455 −323438 $US 50000 Colonoscopy 10-year was dominant
 MT-s DNA 3-year 5283 18.7423
Dan27
 Colonoscopy 10-year 899.08 16.406 28432 $US 50000 Colonoscopy 10-year was cost-effective a
 Stool DNA 5-year 614.76 16.396
Kingsley28
 Colonoscopy 10-year 2474 19.517 −111600 $US 50000 Colonoscopy 10-year was dominant
 Stool DNA 3-year 3590 19.507

Notes: In this table, for each study, the first row shows the new technique that is compared with the old technique, written in the second row. The negative ICER indicates that the new technique is less costly and more effective. The positive ICERs refer to those techniques that are more costly and more effective; both numerators and denominators are positive. aBased on the context threshold.

Abbreviations: C, costs per person ($PPP); Q, QALYs (quality-adjusted life-year); ICER, incremental cost-effectiveness ratio; MT-S DNA 3-year, multi-target stool DNA every 3-year.

Discussion

There are multiple methods, policies, and interventions for screening for CRC. These methods are used in combination or alone. These mean that we have numerous strategies for the screening of CRC, and evaluating of those strategies in terms of costs and effectiveness is, to some extent, a complex task.

As the results of this systematic review demonstrated, the CRC screening by any technique is cost-effective, in comparison with the no-screening method.

Three studies reported the cost-effectiveness analysis for the S-DNA test. The results showed that the S-DNA test was cost-effective, in comparison to the no-screening. However, this technique was less cost-effective when compared with other screening techniques (namely, colonoscopy every 10-year, barium enema 5-year, sigmoidoscopy, FIT and virtual colonography every 5-year). In our systematic review, only one study reported that the virtual colonography every 5-year was cost-effective, in comparison to the no-screening method. However, the virtual colonography every 5-year was not cost-effective when it was compared to other techniques.27 Virtual colonography every 5-year is a non-invasive procedure that potentially can be ideal for subjects who avoid invasive procedures, such as colonoscopy and FS. Although this technique has advantages, such as a reduction in complications of colonoscopy (bowel perforation, major bleeding, and deaths due to perforation), more resources need to be allocated to get the same effectiveness, in comparison with the colonoscopy.

Based on our results, there was no consensus about starting and endpoint screening ages, but it seems that the age of 50 years was the most appropriate for initiation. Kingsley et al28 examined the starting and stopping ages of screening in their analysis from the age 50 until age 100 or death, but in conclusion, they did not recommend any type of screening for people above the age of 80. The prevalence and incidence rates of CRC at different ages determine which screening technique is the most cost-effective.

In this study, two out of eight studies had reported the prevalence rate of CRC at age 50, and the decrease of CRC incidence in different screening techniques had been discussed. However, there has been no examination of the prevalence rate of CRC at different ages and the choice of age-appropriate screening techniques, which have an impact on the cost-effectiveness of screening techniques.

Overall, changes in the sensitivity and specificity of screening tests will have a different effect on the cost-effectiveness of CRC screening techniques. In the current review, four out of eight studies have demonstrated that the changes in sensitivity and specificity of the screening tests have a moderate impact on ICER, and for the other studies, this impact is minimal. For instance, in the study of Dan et al27 it is shown that when the specificity and sensitivity of CRC screening tests varied from 50% to 99%, moderate impacts were observed on the cost-effectiveness of CRC screening techniques. Thereby, screening techniques may be dominated or may no longer be cost-effective.

Although most of the models used in the studies are the same (Markov model), due to the differences in cost and effectiveness of screening strategies such as time horizon, variety of techniques in different studies, differences in sensitivity and specificity rate, it is not feasible in practice to determine which strategy is the optimal technique. Dinh et al and Kingsley et al analyzed the colonoscopy but the cost of complications was not included in the model.23,28 These factors may be one of the main reasons, leading to inconsistency in the results of the different studies.

In addition, our findings showed that all studies conducted the sensitivity analysis with alternative assumptions to examine the uncertainty with parameters. Five studies used the Monte Carlo simulation to investigate the uncertainty of the model. Uncertainty among various parameters was assessed in each study by one-way, multi-way, and probabilistic sensitivity analysis (PSA). In 37.5% of cases with sensitivity analysis, there was no change in the results or the effect of change in parameters was not significant. For instance, in the study by Dinh et al23 changes in the variables had not had a significant effect on the ICER, when the FIT/COLOx1 was compared to FIT and COLO.

In 62.5% of the studies, it was found that changing the parameters had a significant effect on the results. A study conducted by Dan and colleagues showed that the risk of CRC and the cost of colonoscopy accompanied by uncertainty.27 When the cost of colonoscopy was less than $300 regardless of the risk of CRC, colonoscopy was the dominant technique. When the cost of colonoscopy was above the $300, the IFOBT was considered the dominant technique in lower incidence levels of CRC, whereas, for the higher incidence level, the sigmoidoscopy revealed to be more cost-effective than the other techniques.

Limitation

One limitation when evaluating the cost-effectiveness and costing is that studies take place in different countries with different contexts, prices, and costs and at different times. Therefore, these need to be considered when decision-makers interested to use the overall results or some components of the cost-effectiveness analyses for different settings and times. It is recommended that in order to compare and value the cost differences over time, it should be adjusted by the inflation rate, and across countries should be adjusted by PPP. These adjustments are apart from the adjustment required for the differences in conducting processes. The magnitude of indirect costs in cancers is outstanding, and theoretically, the sum of the direct and indirect costs is almost a reflection of the cost of opportunity lost due to cancer.

Even though indirect costs constitute a significant part of the cancer costs and it is about a societal perspective, but only few studies included these types of costs in their analyses. This leads to an underestimation of the cancer costs and heterogeneity arises when there is an intention for comparing the results. In this review, we found that there are also other heterogeneous parameters such as time horizons, perspectives, and types of the models and included states that make it difficult to compare various outcomes one by one in different contexts.

One of the less paid subjects in a cost-effectiveness analysis is the threshold level for different countries. There is a general agreement that the threshold level for each country should be context-specific, but there is a discrepancy among the methods used for the implementation of the thresholds for different health systems. Furthermore, even for the same health systems, the threshold is kept constant for quite a long time. In some countries, it might be necessary to adjust the threshold in relation to the inflation rate.

Since the feasibility and acceptability of using screening tests according to the context of the study, is one of the important factors, but it was discussed in just one out of eight studies. For example, colonoscopy is an invasive method for screening and many people do not prefer to use it in the first step. Therefore, future studies should examine the feasibility of using screening tests and consider patient preference in the selection of alternative tests.

Conclusion

Our review showed that all CRC screening techniques are cost-effective when compared with no-screening, but there is no agreement between the results of the various studies to determine the optimal technique. The newer technologies of virtual colonography and S-DNA were not cost-effective, compared with conventional techniques (FIT, sigmoidoscopy, and conventional colonoscopy). Although both techniques were less cost-effective than other techniques, S-DNA and virtual colonography are non-invasive procedures, making them a potentially ideal choice for subjects who like to avoid any invasive procedures. Finally, additional analyses are necessary to determine the optimal technique.

To compare and utilize the results of the different studies, there should be some observations like inflation, PPP, threshold levels and the subject preference for accepting the interventions.

Acknowledgments

We extend our sincere thanks to all authors who responded to our communications and shared with us their original data and documents. This paper was extracted from the master’s thesis of FK, supervised by MY and supported by Tabriz University of Medical Sciences (Approval ID: IR.TBZMED.REC.1396.936)

Disclosure

The authors report no conflicts of interest in this work.

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