Colorectal cancer screening: The role of CT colonography

Abstract

Computed tomography colonography (CTC) in colorectal cancer (CRC) screening has two roles: one present and the other potential. The present role is, without any further discussion, the integration into established screening programs as a replacement for barium enema in the case of incomplete colonoscopy. The potential role is the use of CTC as a first-line screening method together with Fecal Occult Blood Test, sigmoidoscopy and colonoscopy. However, despite the fact that CTC has been officially endorsed for CRC screening of average-risk individuals by different scientific societies including the American Cancer Society, the American College of Radiology, and the US Multisociety Task Force on Colorectal Cancer, other entities, such as the US Preventive Services Task Force, have considered the evidence insufficient to justify its use as a mass screening method. Medicare has also recently denied reimbursement for CTC as a screening test. Nevertheless, multiple advantages exist for using CTC as a CRC screening test: high accuracy, full evaluation of the colon in virtually all patients, non-invasiveness, safety, patient comfort, detection of extracolonic findings and cost-effectiveness. The main potential drawback of a CTC screening is the exposure to ionizing radiation. However, this is not a major issue, since low-dose protocols are now routinely implemented, delivering a dose comparable or slightly superior to the annual radiation exposure of any individual. Indirect evidence exists that such a radiation exposure does not induce additional cancers.

Key Words: Computed tomography colonography; Colon neoplasms; Colon polyps; Colorectal cancer screening; Computed tomography colonography safety; Computed tomography colonography accuracy; Computed tomography colonography radiation exposure; Computed tomography colonography cost-effectiveness

INTRODUCTION

It is now 16 years since Vining et al[1] presented the first virtual images of the colon at the 1994 meeting of the Society of Gastrointestinal Radiologists. This marked the birth of “virtual colonoscopy” (VC), an intriguing name useful for marketing to patients, providers and the public, or “CT colonography” (CTC), the name most radiologists prefer.

When discussing the role of CTC in colorectal cancer (CRC) screening, it is necessary to separate the present and existent role from the potential one.

The present role is, without any further discussion, the integration into established screening programs as a replacement for barium enema (BE) in the case of incomplete colonoscopy (CC). In fact, since 2006 the American Gastroenterological Association (AGA) Clinical Practice and Economics Committee has endorsed CTC as the method of choice for colon investigation in cases of incomplete colonoscopy[2] and numerous evidence exists in the literature showing a clear superiority of CTC over BE in the detection of CRC and polyps[3-5]. It is also clear that performing CTC in patients with a positive Fecal Occult Blood Test (FOBT) would not be an efficient triage technique in terms of cost-effectiveness, due to the high prevalence of clinically relevant colonic lesions[6,7].

The potential role of CTC is to act as a first-line CRC screening modality. In this regard, it was in March 2008 that CTC obtained its major success: the American Cancer Society (ACS), the US Multi-Society Task Force on Colorectal Cancer and the American College of Radiology (ACR) released consensus guidelines on CRC screening for average-risk individuals. These guidelines distinguished diagnostic tests into two groups: those able to detect CRC, thus potentially reducing mortality (FOBT; Fecal Immunochemical stool Testing, FIT; and stool DNA testing), and those able to detect both polyps and cancer, thus potentially reducing both the incidence of and the mortality from CRC. This latter group of tests includes CC, sigmoidoscopy, BE and - for the first time - also CTC, with the recommendation that it be performed every 5 years starting at 50 years of age[8]. Unfortunately, this position did not remain unequivocal: in fact, the US Preventive Services Task Force (USPSTF) considered the evidence insufficient because of the unknown impact of both extra-colonic findings and radiation exposure, the poor data on cost and cost-effectiveness, and the still unsolved problem of ideal bowel preparation[9]. Other associations, such as the Asia Pacific Working Group on Colorectal Cancer[10] and the American College of Gastroenterology[11], consider CTC a second-line screening test for those unwilling or unable to undergo CC and for those in whom CC was incomplete. Furthermore, in 2008 in the USA, the Centers for Medicare and Medicaid Services denied the reimbursement of screening exams done with CTC[12].

These facts mean on one hand that CTC is considered useful by clinicians, but, on the other hand, that radiologists have much to do until this imaging method is implemented for screening, as testified by a survey conducted among US primary care physicians (PCP)[13]. When asked which diagnostic tests they perceive as being very effective in reducing CRC mortality, 22% answered CTC vs 95% CC; and when asked which test they would recommend for CRC screening, most respondents indicated CC (95%) and FOBT (80%), but only about 5% answered CTC.

Keeping in mind these facts, the potential role of CTC in CRC screening will be discussed in the next paragraphs, taking into consideration that an ideal screening test is not yet available and that any screening test is a compromise among four major variables: efficacy, compliance, safety and cost.

EFFICACY

The issue of diagnostic accuracy of CTC for CRC and polyps has been debated for a long time, because of the conflicting results in some of the papers published in the literature[14-16]. This has been recently confirmed by a meta-analysis showing that “CTC is highly specific for the detection of colorectal polyps and tumors” and that “some studies reported high sensitivities, but the results of the studies were highly heterogeneous, while the studied variables explained only part of this discrepancy”[17].

These results led researchers to design three important studies: two large, multicenter trials testing the performance of CTC in comparison with CC in respectively asymptomatic subjects at average risk, i.e. a typical screening population [the American College of Radiology Imaging Network (ACRIN) trial performed in the USA][18] and in a mixed population of asymptomatic subjects at risk higher-than-average and in patients referred for a positive FOBT [Italian Multicenter Polyps Accuracy CTC study (IMPACT) trial][19]; and one multicenter trial [Special Interest Group in Gastrointestinal and Abdominal Radiology (SIGGAR) trial run in the UK] conducted on symptomatic patients with the aim to detect CRC[20]. In particular, the ACRIN trial tried to minimize the variables possibly affecting CTC performance. For this reason only ≥ 16-row MDCT scanners were used, patients were administered oral contrast agent for stool tagging together with cathartic agent and training of the radiologists observing the images was an important component of the study. In particular, CTC readers were obligated to have read at least 500 cases, or to have attended a 1.5-d training course, and all had to pass a certified exam in which they detected at least 90% of adenomas 1 cm or larger in 50 cases. More than half of the readers had to undergo additional training in order to pass the certified exam initially and, with additional training, all the readers eventually passed.

Results from ACRIN and IMPACT have been recently published[18,19], whereas those from SIGGAR[20] are still under data analysis. Both the ACRIN and IMPACT trials reported per-patient sensitivity of 90% for polyps > 10 mm and 78%-84% for polyps larger than 6 mm; per-patient specificity was extremely high as well, over 85% independently of lesion size (Table 1). The major drawback of ACRIN was represented by the poor positive predictive value (PPV) (23% for polyps ≤ 10 mm), which might negatively affect a screening program, leading to useless CC, with patient discomfort, embarrassment of radiologists, potential risk of complications and increased costs. Unfortunately there is no explanation for these data, unless one would claim a psychological attitude to overcall in order to reach the threshold of 90% for clinically significant polyps despite a loss in specificity. A definitely better PPV was documented in the IMPACT trial (62% for lesions larger than 6 mm) as well as in studies obtained in high-experience centers, the University of Wisconsin (PPV, 91.5%) and a group of Korean hospitals (PPV, 69% for lesions > 6 mm and 92% for those > 10 mm)[21,22].

Table 1 Results from major trials on a per-patient basis: sensitivity, specificity, positive and negative predictive values.

Multicenter trials	All polyp size	Polyps (≥5 mm)	Polyps (≥6 mm)	Polyps (≥7 mm)	Polyps (≥8 mm)	Polyps (≥9 mm)	Polyps (≥10 mm)
Per patient sensitivity
ACRIN	N/A	65%	78%	84%	87%	90%	90%
IMPACT	N/A	N/A	85%	86%	88%	91%	91%
Munich	84%	91%	N/A	N/A	N/A	N/A	92%
Per patient specificity
ACRIN	N/A	89%	88%	87%	87%	86%	86%
IMPACT	N/A	N/A	88%	87%	86%	85%	85%
Munich	47%	93%	N/A	N/A	N/A	N/A	98%
Per patient PPV
ACRIN	N/A	45%	40%	35%	31%	25%	23%
IMPACT	N/A	N/A	62%	N/A	N/A	N/A	N/A
Munich	48%	N/A	70%	N/A	N/A	N/A	79%
Per patient NPV
ACRIN	N/A	95%	98%	99%	99%	99%	99%
IMPACT	N/A	N/A	96%	N/A	N/A	N/A	N/A
Munich	84%	N/A	98%	N/A	N/A	N/A	99%

Results are categorized according to polyp size. PPV: Positive predictive value; NPV: Negative predictive value; N/A: Not assessable.

However, the negative predictive values in both the ACRIN and the IMPACT trials was rather high, approaching 100%; this is extremely important in order to reassure negative patients about the significance of the examination.

Excellent results were also obtained in the Munich Colorectal Cancer Prevention Trial[23], a single-center study where around 300 asymptomatic subjects underwent low-dose CTC in comparison with other screening tests (CC, sigmoidoscopy and FOBT).

It is noteworthy to mention that in a screening project offered by the University of Wisconsin[24], after 2 years of recruitment over 3000 subjects of two different, non-randomized groups underwent CTC and CC. The detection rate for advanced adenomas was 3.2% for CTC and 3.4% for CC (difference not statistically significant), with the advantage of a large reduction in the number of polypectomies in the CTC group without any complication as opposed to seven perforations which occurred in the CC group.

Despite the good results there are still some open issues under debate within the radiological as well as the gastroenterological communities. These are the significance of diminutive (< 6 mm) polyps, the management of intermediate (6-9 mm) lesions, the detection rate for non-polypoid, flat lesions and the impact of the extra-colonic findings.

According to a very recent systematic review[25] of published studies reporting the distribution of advanced adenomas in asymptomatic screening cohorts, diminutive polyps have a minimal clinical impact. In fact, the frequency of advanced lesions among patients whose largest polyp was ≤ 5 mm, 6-9 mm, < 10 mm, and > 10 mm in size was 0.9%, 4.9%, 1.7%, and 73.5%, respectively (Figure 1). As a consequence, a 6-mm polyp size threshold for polypectomy referral would identify over 95% of subjects with advanced adenomas, whereas a 10-mm threshold would identify 88% of cases. From a cost-effectiveness point of view, detection and removal of all polyps including those smaller than 5 mm, would be very inefficient, with a cost per year of life gained > $460 000[26], absolutely unacceptable in terms of cost-effectiveness. It is also true that this approach, not removing diminutive polyps, necessitates an extensive education of patients and PCP. In fact, according to a recently published survey[27], the majority of patients, PCP and gastroenterologists would not choose to follow up small polyps identified by CTC with CC because of the fear of missing precancerous lesions.

Figure 1 Sessile polyp: adenoma with low-grade dysplasia. A: Coronal reformatted image showing a polypoid lesion (arrow), partly surrounded by tagged fluid (asterisks); B: The same lesion as shown on 3D endoluminal view (arrow); C: Conventional colonoscopy.

The management of intermediate (6 to 9 mm) lesions is also under debate, despite the fact that today any polyp 6 mm or larger should be preferably referred for CC and polypectomy, also according to ACS CRC screening guidelines[2]. However, evidence does exist from cost-effectiveness[28] as well as follow-up[29] studies indicating that, for the future, polyp follow-up might be an alternative to referral for CC and polypectomy. These data have been recently reinforced by studies conducted with CC and subsequent polypectomy, where the rate of advanced adenoma in 6-9 mm polyps was demonstrated to be 6.6%[30].

A potential disadvantage of CTC would be the possible impaired ability to detect non-polypoid, flat lesions (Figure 2). This issue deserves some consideration. First of all, flat lesions represent a subset of sessile polyps, and according to a recent publication[31] the overall prevalence in a screening population is around 5.8% (if flat lesions are defined as those with a height not exceeding 0.5 of the diameter[32]). However, within this definition, slightly elevated lesions are also included, which, in some cases, may be classified as sessile. For this reason, an elevation not higher than 3 mm is often used, especially for small lesions not larger than 2-3 cm. The other important remarks are that “completely flat lesions are exceedingly rare” and that depressed lesions are less than 1% of all colorectal lesions and only a quarter of those are observed in a screening population. This means that the majority of non-polypoid lesions are at least slightly elevated and this works in favor of the possible detection with CTC. Unfortunately, at the moment only few and conflicting data about the sensitivity of CTC for flat lesions are available. At the beginning disappointing results were published[33,34], because of technical limitations as well as readers’ experience. More recently, better results were reported, with sensitivity in the range of 80%-90% for flat adenocarcinomas[32,35]. These results seem to be confirmed by a recent retrospective analysis of the data from the ACRIN trial showing a sensitivity of 89% for flat adenomas ≤ 6 mm (at the prospective analysis, sensitivity was 68%) (Fidler J, presented at ACRIN meeting, October 1, 2009).

Figure 2 Non-polypoid (flat) lesion: advanced adenoma. A: On 2D axial computed tomography image an irregularly thickened fold (arrow) is detected; B: On 3D endoluminal image the lesion is better appreciated (black arrow), in particular if compared with the normal adjacent colonic folds (white arrows); C: The same lesion at colonoscopy before removal.

The impact of extra-colonic findings will be discussed in the paragraph concerning costs.

COMPLIANCE (ADHESION TO A SCREENING PROGRAM)

Compliance means adhesion of healthy individuals to a screening program. This is a very complex issue, long debated in the literature and presently without a solution, since virtually in any Western country a high proportion of adults 50 years of age or older have not undergone any CRC screening test[36]. Colonoscopy, considered to be the most effective screening method, suffers from a very low participation rate. Very recent data from Italy[37] underline the difficulties and barriers in implementing a CC population screening, at least through primary care. Reported participation in a CC screening arm was extremely low in Southern Italy (2.8%), and higher, but still disappointing, in North-Central Italy (12.4%).

To increase screening uptake is extremely important, since the adhesion rate of the invited population directly affect the efficiency of the program. For example, if we consider that the efficacy of CC in reducing the incidence of CRC is around 76%[38], the efficiency with regard to CRC prevention rate, considering an adhesion rate of 20%, drops to 15% (76% × 20% = 15%).

The question is whether CTC would be able to increase screening uptake. The three most common deterrents that patients expressed about receiving CC were bowel preparation, embarrassment and fear of discomfort[39,40]. The advantage of CTC is the use of a gentler preparation or unprepped (laxative-free) examination[41]. Furthermore, the pain related to colon distension by air may be minimized by the use of carbon dioxide delivered by an electronic pump. The use of carbon dioxide is also associated with a faster absorption, making the patient more comfortable immediately after the examination[42].

Unfortunately, only few data are available regarding adhesion rate and CTC. In a study conducted in Western Australia[43], 2000 people were invited and 28.4% accepted to undergo CTC for screening, with 62% of them preferring CTC over optical colonoscopy. The fact remains that we need data resulting from real screening experiences.

SAFETY

CTC is a safe test, definitely safer than colonoscopy. The results of different surveys show a perforation rate associated with CTC ranging between 0.06% and 0.08%[44,45], even lower in screening[46], compared with 0.1%-0.2% for diagnostic colonoscopy[47]. It should also be noted that the comparison between CTC and CC is very difficult, with the risk of overestimating the clinically significant perforations at CTC, because of the much higher sensitivity of CT in the detection of even tiny air bubbles. In fact, most of the perforations reported in a UK survey[44] were treated conservatively, without surgical intervention. CTC complications in most of the cases are due to technical factors, such as the use of a rigid catheter for bowel distension (now replaced by thin rubber devices), manual distension with air (now minimized by the use of an electronic pump delivering carbon dioxide and able to control pressure and volume), inexpert personnel and incorrect patient selection.

Other complications occasionally reported have been vasovagal reactions due to colonic overdistention[48].

The main potential drawback of screening with CTC is the exposure to ionizing radiation[49] and the consequent theoretical risk of inducing cancer. The risk is theoretical because there are still many uncertainties with regard to the true effects of ionizing radiation at low doses, such as those used in diagnostic radiology[50,51]. According to the Health Physics Society[52], “below 5-10 rem (50-100 mSv) (which includes occupational and environmental exposures), risks of health effects are either too small to be observed or are nonexistent”; and the French Academy report[53] stated that the linear no-threshold (LNT) hypothesis for assessing the risk associated with low doses is not based on scientific evidence. However, in contrast, the International Commission on Radiological Protection (ICRP)[54] and the Biological Effects of Ionizing Radiation (BEIR) VII report[55] considered LNT as the best method to assess low dose exposures, in order to be more conservative and more protective towards patients because of the multiple uncertainties. Unfortunately even if this hypothesis may be true it cannot be proved since we have little direct evidence of harm below 100 mSv.

Even if the LNT hypothesis is considered the most accurate, the problem of radiation exposure of patients undergoing CTC seems to be minimal. In fact, the mean exposure in the case of a screening examination has been calculated in a recent survey[56] to be around 5-6 mSv, which is twice the normal background radiation exposure in the US (2.5-3.0 mSv per year)[57]. In addition we have to consider, in a screening scenario, that CTC should be repeated every 5 years, not earlier. For a radiation dose of around 5-8 mSv at age 50 years, the lifetime risk of death from cancer varies between 0.02% and 0.03%[58]. If we think about cost/benefit of the examination, this minor risk should be compared with the theoretical risk of CRC in average risk individuals, which is around 5%[59].

A more precise idea about the amount of radiation exposure comes from a comparison with other categories of workers continuously exposed to low dose radiation, such as, for example, airline crews and nuclear workers. As an example, the value of 5-6 mSv, to be received in a screening scenario every 5 years, should be compared with radiation exposure of airline crews, who are submitted to an average of 5 mSv per year every single year of their activity, with a long life exposure close to 80 mSv. A recent survey of airline pilots from eight different European countries has shown no increase in mortality from radiation-induced cancers over a 30-year period of time[60]. Similar data were observed in nuclear workers in two recently published experiences[61,62].

COSTS

Cost analysis is a very difficult task, especially in the absence of real data and based only on mathematical models. Among the studies published in the literature[63-69] 5 out of 7 are in favor of CC and only two were able to demonstrate a better cost-effectiveness of CTC. A recent review of the literature[70] has pointed out the profound differences among the models as well as the weakness of such an approach, where a minimal variation of a single input may completely alter the final results. As an example, if the cost ratio between CTC and CC is ≤ 0.7, the model is usually in favor of CTC, but if the cost of CTC is higher than 80% of the cost of CC, it will be CC which is the most cost effective method. Another very important issue, adhesion rate, is never taken into account in the models, where it is considered to be equal among the different screening tests, although this is probably not the case. In addition, differences in healthcare systems, reimbursement, cost of the equipment and personnel are other important variables affecting the final outcome.

When considering cost, the issue of extra-colonic findings should be taken into account. The detection of extra-colonic findings can be considered a potential advantage of CTC, since previously unknown life-threatening diseases, which are not insignificant[71], can be diagnosed and treated, with a clear impact on patients’ life expectancy. However, the major problem is the extra time necessary for reporting these findings and the cost induced by unnecessary investigation of common benign abnormalities, especially because of their high prevalence[72,73]. In a recent publication[74], the mean cost per patient was $31.02 for nonsurgical and $67.54 for surgical work-up procedures. Although extra-colonic findings have been traditionally regarded as an additional cost, they have been recently considered as a potential benefit (i.e. detection of unsuspected abdominal aortic aneurysm or renal cancer), able to improve CTC cost-effectiveness[75].

CONCLUSION

In conclusion, CTC has a present role in CRC screening programs, i.e. the replacement of BE in the case of incomplete colonoscopy. The potential role is the proposal of CTC as a first-line CRC screening modality. In this setting, CTC has clear advantages, such as accuracy, safety and subject acceptance. Further research should be warranted to clarify, in particular, two aspects: the uptake rate of the general population and the real cost and benefits derived from a CTC screening program.