Journal of Surgery

Computed Tomography as a Single Modality for Preoperative Tumor Staging for Locally Advanced Rectal Cancer. A Descriptive Tomographic Scoring System

by Benjamen Person1,3, Dorit Eizenberg2, Abeer Masarwi1, Arie Bitterman1,3Wissam Khoury1,3*

1Department of General Surgery , Carmel Medical center, Haifa, Israel

2Depatment of Radiology, Carmel Medical Center, Haifa, Israel

3Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel

*Corresponding Author: Wissam Khoury, Department of General Surgery, Carmel Medical center, Haifa, Israel

Received Date: 06 May 2026

Accepted Date: 12 May 2026

Published Date: 14 May 2026

Citation: Person B, Eizenberg D, Masarwi A, Bitterman A, Khoury W (2026) Computed Tomography as a Single Modality for Preoperative Tumor Staging for Locally Advanced Rectal Cancer. A Descriptive Tomographic Scoring System. J Surg 11: 11623 DOI: https://doi.org/10.29011/2575-9760.011623

Abstract

Background: Accurate preoperative staging of rectal cancer includes a rectal Magnetic Resonance Imaging(MRI) or Endorectal Ultrasound(ERUS) as a standard of care. Often, a locally advanced rectal tumor is demonstrated on a staging Computerized Tomography(CT) scan that is usually performed prior to the MRI. In certain cases the MRI may not add clinical information that would influence the treatment plan. The purpose of this study was to evaluate in which cases MRI could potentially be deferred at the time of decision making.

Methods: A retrospective study that included all the patients with rectal cancer who were treated in the department of surgery at Carmel medical center from 2017 to 2020 was undertaken. All the patients were routinely staged by CT and MRI or ERUS. The CT descriptive findings regarding the rectum were divided into 4 common findings, each receiving a score of 1 or 0: rectal wall thickening, peri-rectal fat haziness, enlarged peri-rectal lymph nodes and penetration into adjacent structures or organs. The summation of the scores of these findings results in a total score between 0 and 4. The patients were divided into 2 groups: Group A with low CT scores of 0 or 1, and group B with scores of 2-4. The decision on preoperative Chemoradiotherapy (CRT) was made according to the disease stage on MRI/ERUS regardless of the CT scores.

Results: Eighty patients were included in the study. Complete data were available for 74 patients.  Group A included 42 patients and

Group B – 32 patients. Based on the results of the staging by CT and MRI/ERUS, in group A 40/42 patients required preoperative Chemoradiotherapy(CRT) and in group B all the patients (32/32) required preoperative CRT (p-0.21). In most cases in group A the patients required preoperative CRT based on the results of the MRI/ERUS in spite of low CT scores; however, in group B the patients had high CT scores which correlated to high disease stages on MRI/ERUS as well, and all of them required preoperative CRT.

Conclusions: CT tends to understage rectal cancer compared to MRI or ERUS. High CT scores may correlate to the clinical tumor stage. As such, immediate staging MRI/ERUS may be unnecessary; however, in patients with low CT scores, a staging MRI is mandatory.

Keywords: Computerized Tomography; Locally Advanced Rectal Cancer; Preoperative Chemoradiotherapy; Scoring System

Introduction

The current standard of preoperative staging of rectal cancer includes a rectal Magnetic Resonance Imaging (MRI) or Endorectal Ultrasound (ERUS) for evaluation of the stage of local disease, and a Computerized Tomography (CT) for assessing the stage of systemic disease [1,2]. Accurate preoperative staging determines the appropriate treatment sequence, where low stage tumors can undergo upfront surgery, and higher stage, locally advanced tumors usually require preoperative Chemoradiotherapy (CRT) [3,4]. The diagnostic accuracy of CT, MRI and ERUS for preoperative staging of rectal tumors was assessed in several studies in which the modalities had relatively comparable results [5-13]. While high-resolution MRI is generally considered superior for rectal cancer staging – particularly in assessing tumor depth, mesorectal fascia involvement and Circumferential Resection Margin (CRM) status – there are specific areas where CT shows comparable performance, notably, in early-stage tumors and nodal status [513]. MRI is superior to CT for identifying tumor penetration into the rectal wall primarily because of its superior soft tissue contrast and spatial resolution, which allow for precise differentiation of the rectal wall layers and surrounding structures. In particular, the high-resolution T2-weighted MRI sequences, provides excellent contrast between the different rectal wall layers. CT, in contrast, cannot reliably distinguish rectal wall layers due to limited softtissue contrast resolution.  CT cannot show these distinctions clearly; it often detects gross wall thickening or irregular outer margins, but not precise wall layer involvement.The role of CT for Locally Advanced Rectal Cancer (LARC) staging has been previously discussed in terms of mesorectum and mesorectal fascia invasion [7-10]. Deep invasion of mesorectum can be easily identified by CT, MRI and ERUS, while for superficial invasion it may be challenging and MRI is usually required. In such circumstances, decision making based on CT findings is not well established yet. However, due to a better availability of CT scanners and in order to rule out metastatic disease, in most cases the staging CT is performed prior to MRI and ERUS. We hypothesized that in cases in which the reported CT results described a locally advanced rectal tumor, the added value of the MRI and ERUS that might influence the treatment plan would be minimal, thus the decision to proceed with preoperative CRT could be made based on the results of the CT alone. In these cases, the MRI exam could be deferred in order to not delay treatment. Additionally, given the limited CT soft tissue contrast resolution, the radiologists usually use descriptive parameters rather than actual TNM terminology when reporting the local extent of the rectal tumor. Using standard terms in the CT report may provide better tools to determine the appropriate treatment. In an attempt to achieve this goal, we propose a simple scoring system that translates standard descriptive CT findings into numeric parameters. These descriptive findings are often discussed in the standard CT reports.

Methods

After obtaining an IRB approval following the Helsenki declaration, we performed a retrospective analysis that included all the patients with mid and low rectal cancer, defined as ≤ 10 cm from anal verge, who were treated in the department of surgery at Carmel Medical Center in Haifa, Israel from 2017 to 2020. Patients and tumor characteristics were collected. With regard to oncologic work-up, all the patients underwent colonoscopy and were routinely evaluated by CT and MRI or ERUS. Based on the radiologic findings a decision was made on preoperative CRT or upfront surgery. CT and MRI scans were performed at multiple institutions and image interpretations were reported by different senior radiologists and were reevaluated by an experienced body radiologist at our institute. ERUS was performed by a single experienced colorectal surgeon. Findings with regard to local tumor extent were retrieved from the MRI and ERUS reports. After reviewing all the CT reports, we found 4 descriptive findings that were most commonly reported by radiologists in the CT reports regarding the extent of rectal tumors: rectal wall thickening or space occupying lesion, peri-rectal fat haziness, enlarged/ prominent peri-rectal lymph nodes and penetration into adjacent organs or structures. The absence or presence of each of these findings in the CT report received a score of 0 or 1 respectively, comprising a total potential CT score between 0 (none of the findings was reported), and 4 (all of the findings were reported). Since each parameter may reflect a degree of locally advanced disease, we classified patients into two subgroups; low and high probability for advanced disease. Group A – patients with low CT scores of 0 or 1 (low probability), and Group B – patients with high CT scores of 2-4 (high probability). In all the patients, the decision on preoperative CRT was made per the standard of care according to the disease stage on MRI/ ERUS regardless of the CT scores. Patients in whom the stage on MRI or ERUS was at least T3 and/or N+ were referred for preoperative CRT.

Statistical Analysis

Continuous variables are presented by mean, and Standard Deviation (SD) or median & (interquartile range) IQR. The categorical variables are presented in percentages. Differences between the groups of high and low CT score were evaluated using Chi Square with Yates correction or Fisher exact test for the categorical variables and Independent t-test for the continuous variables. P<0.05 was considered statistically significant.

Results

Between 2017 and 2020, 80 patients were assessed and treated for mid and low rectal cancer, of whom complete data were available in 74 patients (F=49). The patients were classified into two groups according to low and high CT scores. There were 42 patients in group A (low score) and 32 patients in group B (high score). Patients’ and tumor characteristics are listed in Table 1.  Median tumor distance from anal verge was 7cm (1-10) in group A and 6cm (1-10) in group B (p-0.41). Sixty-six patients underwent low anterior resection, 5 patients - abdominoperineal resection and three patients did not undergo surgery. Postoperative tumor stage was comparable between groups (p- 0.9) (Table 1). Advanced preoperative local tumor stage did not correlate with postoperative pathology findings. Most patients were stage I or stage II tumor. In the entire cohort 13.5% experienced complete pathological response, 7 patients in the low CT score group and 3 patients in the high CT score group. In group A, out of 42 patients who had low CT scores, the tumor stage on MRI and/or ERUS was actually at least T3/N+ in 40 patients, and they were referred for CRT per the standard of care. Only in 2 patients in this group the tumor stage on MRI/ERUS correlated to the low CT score, and they were referred for upfront surgery. In group B, all 32 patients had a high CT score and locally advanced tumors on MRI/ERUS, and all of them were referred for CRT. We compared the CT results to MRI/ERUS, with the latter studies being the gold standard for decision making for preoperative CRT.

                                                      Low CT score (n=42)

High CT score (n=32)

P

M/F

26/16

23-Sep

0.37

Age

67 (51-93)

65 (33-84)

0.41

ASA score

2.15+/-0.6

2.07+/-0.6

0.71

Tumor AV distance (cm)

7 (1-10)

6 (1-10)

0.42

Histopathology

No residual tumor

Stage I

Stage II

7

15

8

3

8

10

0.9

Stage III

8

8

Stage IV

3

1

No surgery

1

2

Type of operation

Low anterior resection

39

27

0.89

Abdominoperineal resection

2

3

No surgery

1

2

CT- Computerized Tomography, ASA – American Society of Anesthesiology, AV- Anal Verge

Table 1: Patients’ and tumor characteristics.

Discussion

The routine preoperative staging process of rectal cancer includes abdominal and chest CT and pelvic MRI. Their results often allow for a decision making on the appropriate treatment sequence. In the majority of cases, the staging CT is performed prior to the MRI/ ERUS, and in most cases the degree of local spread of the rectal tumor can be assessed based on that CT scan. Herein we showed that in selected cases, when a locally advanced rectal tumor is clearly visualized on CT, it may be reasonable to proceed with neoadjuvant chemoradiation without MRI. Examples for cases when CT is sufficient: Bulky tumor with clear extramural spread where CRM is obviously threatened; CT shows invasion into adjacent structures (unequivocal T4); patient is not a candidate for surgery and CRT is either palliative or aimed at downsizing for further decisions or when there is high clinical urgency and MRI is unavailable or contraindicated. Our hypothesis was that in such cases in which the CT shows an obvious locally advanced rectal cancer, the tomographic findings will usually suggest a high CT score, and the additional information achieved by a subsequent MRI/ERUS does not influence the immediate treatment plan of whether to refer the patient to preoperative CRT or not (Table 2). As such, the MRI/ERUS could be deferred in the immediate workup time, thus expediting the preoperative treatment. There is a definitive advantage of MRI over CT in terms of rectal cancer staging. In order to improve CT performance and accessibility in rectal cancer staging, we created a new scoring system based on routine CT findings. Since the radiological report of the CT scan uses descriptive terms rather than standard staging terminology, we designed a simple scoring system to convert descriptive wording to numeric parameters, hence a “CT score”, regarding the degree of local spread of rectal cancer – as described above. The score is based on 4 common reported findings on CT scan reports, assuming that the higher the score – the more advanced is the rectal cancer. We divided the patients into 2 groups of low and high CT scores and reviewed their treatment course that was determined by appropriate local staging by MRI/ERUS.

Interestingly, the vast majority of our patients, in both score groups (72/74), were diagnosed with locally advanced rectal cancer and had preoperative CRT. Only 2 patients, with low CT score, skiped preoperative CRT and underwent upfront surgery based on MRI/ ERUS findings. These data suggest that MRI/ERUS are probably more accurate than CT for determining the degree of local spread of rectal cancer in patients with low CT scores, in whom the CT tends to underestimate the degree of local disease, as opposed to patients with high CT scores (locally advanced tumors), where the results of the MRI/ERUS concur with the results of the CT, thus creating some form for redundancy. As such, we believe that MRI/ERUS are mandatory in patients with low CT score, i.e. no remarkable local tomographic findings, prior to treatment planning. These patients may be misdiagnosed with T2 or early T3 tumors.

                                                                        Low CT score (n=42)

High CT score  (n-32)

Staging modality

MRI

32

23

ERUS

9

7

Both MRI and ERUS

1

2

CT score

0

19

1

23

2

17

3

14

4

1

CT- Computerized Tomography, MRI- Magnetic Resonance Imaging, ERUS-Endorectal Ultrasound

Table 2: Staging modalities and CT scores.

The superiority of MRI over CT is well established in T2- early T3 tumors. MRI offers high accuracy, clear visualization of tissue planes, and precise measurements needed for treatment planning. It accurately visualizes muscularis propria (low T2 signal) and perirectal fat (high T2 signal) because of its superior soft tissue contrast and spatial resolution [14], which allow for precise differentiation of the rectal wall layers and surrounding structures. Therefore, in patients with low score group where discrimination between T2 or early T3 tumors may be limited, MRI is highly recommended since it may obviate CRT. While CT has limited capability to discriminate between bowel layers, it can suggest invasion when there is gross thickening or spiculated/nodular margins beyond the rectal wall [15]. Such a scenario probably represents a high CT score, where more than one tomographic parameters are usually noticed, i.e. bowel thickening, fat haziness or enlarged lymph nodes. Patients may be considered for preoperative CRT. All patients with high CT score in the present study have locally advanced disease per MRI and required preoperative CRT. Indeed, CT cannot reliably measure the depth of tumor extension into perirectal fat, but treatment planning can be initiated and MRI can be performed down the road.  Moreover, based on CT findings, patients may also be considered for total neoadjuvant CRT (TNT) when enlarged lymph nodes are identified, since CT has high sensitivity and specificity in diagnosing lymphadenopathy [16]. Compared to CT, MRI can obviously notice tumor signal extending into perirectal fat, often with nodular or bulging appearance and can provide depth measurement of penetration (T3a-d:<1 mm to >15 mm) [14]. However, when CT score is high, MRI did not change treatment plan. This is of further importance, since CT is much more available than MRI. For example, in Israel we have 4.73 MRI scanners per 1 million population compared to 15.4 scanners per million population in the OECD countries. The average waiting time for MRI is 20-40 business days. On the other hand, the availability of CT scanners is 8.3 per million compared to 24.8 in the OECD, the 30th out of 33 countries. Still, the waiting time for CT exam is significantly shorter than the waiting time for MRI [17,18].  Therefore, by using the new scoring system, in selected cases, treatment can be expedited. Furthermore, CT may be useful if MRI is contraindicated such as in patients with metallic implants. In such cases, the decision making on preoperative CRT can be made based on the CT findings, in particular, in patients with large, bulky tumors [19]. ERUS availability and accuracy are also to be considered.

This is an invasive tool, operator dependent, inaccurate in terms of tumor penetration into the bowel layers and beyond, with a long waiting list in areas with no availability of MRI.  Consequently, one can argue about the efficacy of ERUS as a substitute for MRI to expedite preoperative treatment. In this study we did not discuss the correlation of the histopathological results of the resected specimens to the radiological stages. We showed that the preoperative radiologic local staging did not correlate with the postoperative histopathology findings, since CRT causes a downstaging in a significant percentage of patients [20-22].  In our view such a comparison would be inaccurate. This study has several limitations. The first is its retrospective nature. The second is that CT reports are not intended for reporting on the local stage of rectal cancer, thus radiologists may not elaborate on all the findings related to local disease progression. In this study we had a group of 19 patients in whom the CT score was 0. This does not necessarily mean that there were no findings related to the rectal tumor, rather it is more likely that they were not described by the interpreting radiologist. However, it is expected that when these findings are missing in the report, it is probably because the findings were not outstanding and therefore were ignored by the radiologist. The third caveat is that our study may not be appropriate for patients in whom restaging after CRT completion is crucial for further treatment planning or amendment. MRI is indicated in these cases. Nevertheless, we believe that the previously described situations on imaging modalities availability exist in numerous countries and areas worldwide, and in order to not delay CRT and surgical treatment for rectal cancer, patients with locally advanced, bulky tumors can be treated based on the results of the CT alone, and the CT score presented here can aid in achieving this goal by producing standardized CT reports. In particular, this premise is appropriate for patients who are candidates for preoperative treatment, i.e. bulky circumferential tumors who will surely require CRT. Thus, preoperative CRT can be expedited based on the CT results alone. While MRI remains the preferred modality for most preoperative assessments, CT may still play a supportive or alternative role in selected cases.

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