Preoperative rectal cancer staging with phased-array MR
Radiation Oncology volume 7, Article number: 29 (2012)
We retrospectively reviewed magnetic resonance (MR) images of 96 patients with diagnosis of rectal cancer to evaluate tumour stage (T stage), involvement of mesorectal fascia (MRF), and nodal metastasis (N stage).
Our gold standard was histopathology.
All studies were performed with 1.5-T MR system (Symphony; Siemens Medical System, Erlangen, Germany) by using a phased-array coil. Our population was subdivided into two groups: the first one, formed by patients at T1-T2-T3, N0, M0 stage, whose underwent MR before surgery; the second group included patients at Tx N1 M0 and T3-T4 Nx M0 stage, whose underwent preoperative MR before neoadjuvant chemoradiation therapy and again 4-6 wks after the end of the treatment for the re-staging of disease.
Our gold standard was histopathology.
MR showed 81% overall agreement with histological findings for T and N stage prediction; for T stage, this rate increased up to 95% for pts of group I (48/96), while for group II (48/96) it decreased to 75%.
Preoperative MR prediction of histologically involved MRF resulted very accurate (sensitivity 100%; specificity 100%) also after chemoradiation (sensitivity 100%; specificity 67%).
Phased-array MRI was able to clearly estimate the entire mesorectal fat and surrounding pelvic structures resulting the ideal technique for local preoperative rectal cancer staging.
Rectal cancer is one of the most common tumour in Europe and in the United States (40 cases in every 100,000 individuals)  with a poor prognosis caused by high risk of local recurrence and metastasis. The local recurrence is related to the extramural tumour spread into the mesorectum and to the tumour distance from circumferential resection margin (CRM). Imaging plays a crucial role in the preoperative management of rectal carcinoma because traditional techniques usually performed to make diagnosis (colonoscopy and digital rectal examination), do not adequately show important prognostic features such as depth of tumour spread T stage) or the extent of lymph node involvement (N stage) [2, 3].
At the present, the experts agreed that total mesorectal excision (TME) is the surgical approach of choice for rectal cancer, because it is able to reduce the local recurrence rate to less than 10% , improving the 5-year survival rate if compared with conventional surgery . Moreover, after surgery local recurrence risk increases if the CRM is involved from the tumour. In selected patients with involvement of MRF at the time of diagnosis, the use of preoperative radiation therapy is advocated and it has been shown to further reduce the local recurrence rate from 8.2% to 2.4% at 2 years [5, 6]. Using TME as surgical approach, MRF represents the CRM and consequently its involvement becomes the most important prognostic factor.
Due to this, preoperative staging techniques for rectal cancer should also distinguish patients with high risk of local recurrence and involvement of MRF, who might benefit from preoperative radiation therapy, from those patients at low risk, with the tumour located far from MRF, who might go directly to surgery. Then, it is always necessary to pay attention to the main risk factor for local recurrence that are: incomplete resection, nodal disease and distal tumour.
The aim of this report is to show that crucial role of phased-array MRI as technique of choice to preoperative locally stage rectal cancer, since it is the only technique able to accurately predict T and N stage and to depict the involvement of MRF.
Materials and methods
Between June 2005 - December 2008 we retrospectively reviewed 96 patients with histological diagnosis of rectal cancer, performed by endoscopical evaluation. This study population was subdivided into two groups: the first group was characterized by patients at T1-T2-T3 N0 M0 stage, whose underwent just a single MR examination before surgery. T3 stage patients, belonging to this group, despite the locally advanced disease, did not underwent neoadjuvant chemoradiation therapy, due to serious controindications to the treatment itself (such as chronic inflammatory disease, important diverticulitis, acute rheumatic disease, grave behaviour disease and the impossibility to maintain the treatment position). The second group included patients at Tx N1 M0 and T3-T4 Nx M0 stage of disease, whose underwent MR staging, then received neoadjuvant chemoradiation therapy and finally performed a second MR for the re-staging of disease.
The lesions were considered as T1 stage tumours when clearly limited to submucosa (Figure 1a-b) and as T2 stage tumours when limited to the rectal wall (Figure 2). It is important to underline the not always it is possible to distinguish tumour growth limited to the submucosa or the invasion to the muscolaris externa: anyway, in these cases it is not necessary to make the always difference because both tumours are treated with TME-surgery (only in a minority of cases a T1 tumour will be treated with local excision and in these cases, when MR cannot distinguish between T1 versus T2 stage, endorectal US may help to identify superficial tumours).
T3 stage tumours were considered those lesions with a growth through all wall layers and extended into the perirectal fat tissue (Figure 3a-c) while T4 stage lesions showed an invasion of surrounding structures like pelvic wall, vagina, prostate, seminal vescicle or bladder (Figure 4a-b).
All MR findings were compared with histological results.
MR imaging was performed with a 1.5- Siemens Medical System, Erlangen, Germany T MR imager (Symphony;) using a pelvic phased-array surface RF coil, necessary to reduce patient discomfort and to obtain higher spatial resolution images providing a full evaluation of rectal wall layers with the additional advantage of a large field of view.
All subjects were positioned in a supine, feet-first position with the lower edge of the coil placed at least 10 cm below the symphysis pubis in order to ensure adequate signal from the lower rectum and anorectal junction.
In our experience there was no need to use the endorectal coil because despite it may produce very high signal, its primary limitation is its small volume of sensitivity that is an insufficient anatomic detail from surrounding tissues to adequately stage rectal cancer. In fact, the area that can be imaged with endorectal coil amounts to a total distance of one coil diameter away from it that results in a very rapid drop in signal intensity beyond the immediate vicinity of the coil itself. Moreover, as with any other endoluminal technique, stenosis and stricturing, pain and discomfort, bowel wall motion, low lesions, lesions in the upper rectum and coil migration are all factors that hamper image acquisition.
No purgative bowel preparation or enemas, air-insufflation and contrast agents were administered. The use of intravenous antiperistaltic agents was not necessary to diminish movement in the small bowel since only the tumours of the lower two-thirds of the rectum were studied.
Multiplanar localizing images were obtained to select transverse, coronal and sagittal images with a T2- weighted fast spin-echo (FSE) sequence (repetition time msec/echo time msec, 4000-6000/100; 256 × 256 matrix, echo train length, 100-130; two signals acquired; sequence duration 3-5 minutes). These images were obtained with a 24-cm field of view and 4-mm-thick sections with no intersection gap. The sagittal images obtained were used to plan large field of view T2- weighted axial sections of the whole pelvis, from the iliac crest to the symphisis pubis (repetition time msec/echo time msec, 4000-6000/100; 256 × 256 matrix, echo train length, 100-130; two signals acquired; sequence duration 3-5 minutes). While the second series was being acquired, we again use the sagittal T2-weighted images obtained to plan to plan high-resolution T2-weighted thin-section axial images (repetition time msec/echo time msec, 4000-7000/100; 256 × 256 matrix, echo train length, 110-140; four signals acquired; sequence duration 5-7 minutes) through the rectal tumour and adjacent perirectal tissues. These images were performed perpendicularly to the long-axis of the tumour and rectal wall. The images were obtained by using a 16-cm field of view, a 3-mm section thickness and no intersection gap.
T1-weighted imaging (with/without contrast agent) was not performed, as it contributed any additional staging information to the analysis. No fat suppression was used to better delineate the tumour against the perirectal fat.
Some patients ( < 5%), either due to co-existing medical conditions or claustrophobia, found the scan impossible to tolerate. In these cases some of the sequences were omitted. Of all sequences the oblique high-resolution scans are the most important so the sagittal views is the only sequence which may be shortened by modifying the parameters and the large field of view. In these cases, axial T2-weighted images should be performed last and may be omitted if the patient is in considerable discomfort.
Pre-operative neo-adjuvant therapy has been shown to improve overall survival in patient with rectal carcinoma  especially when it is added to TME surgery in terms of local control. There is a need to improve overall survival and this may be achieved by delivering systemically active chemotherapy synchronously with pre-operative radiation. Moreover, to protract the therapy help to downstage rectal tumours, reducing the rate of patients with positive CRM (CRM+). Sometimes (20% of cases) chemoradiation therapy lead to complete destruction of tumour cells .
The challenge is to identify pre-operatively patients with high risk of local recurrence performing TME surgery alone and hence identify who may benefit from preoperative chemo-radiation.
In our study we used high-resolution phased-array coil MRI to allow better selection of patients who could have required pre-operative neo-adjuvant therapy from those who could have be safely treated with surgery alone. 48/96 patients underwent 5 weeks of pre-operative chemo-radiation therapy using standard dose radiation (45 Gy in 25 daily fractions) concurrently with systemically effective chemotherapy.
Pre-operative MRI restaging was planned to take place 4-6 weeks after completion of neo-adjuvant therapy. Surgery was performed within 2 weeks following this pre-operative MRI restaging (6-8 weeks after completion of neo-adjuvant therapy).
Specimen handlings and antomopathological technique
Good pathological reporting of rectal carcinoma is essential if we are to achieve the optimum possible results for patients with this tumour. There is nowadays good evidence that survival differs dramatically between surgeons and that the adoption of TME can improve local recurrence rates and survival [8–11].
After TME, each resected specimen was sent to the pathologist unopened and fresh (not in formalin). Not opening the specimen facilitates comparison with MRI which means an important quality control assessment for the radiologist. The specimen was photographed, prior and after inking, to allow audit of the quality of surgery. For a good resection the mesorectum should be smooth with no violation of the fat, good bulk to the mesorectum anteriorly and posteriorly and the distal margin should appear adequate with no coning near the tumour. No defect should be more than very superficial or 5 mm deep. Then the specimen was opened down to just above the tumour, but not through the tumour which was kept untouched to preserve assessment of the anterior aspect where CRM or peritoneal involvement may be seen. Anterior and posterior non-peritonealised surfaces were painted with ink.
After the resection surfaces were inked the specimen was fixed in formalin for a minimum of 3 days (72 hours). Good fixation allows thinner slices to be taken and thus a better assessment of tumour spread. The segment of the fixed specimen containing the tumour was then sectioned transversely at 5 mm intervals from 2 cm below to 2 cm above the tumour itself, producing slices that corresponded precisely to the MR sections.
Finally each slice was photographed and whole-mount histopathologic slices were cut and stained with hematoxylin-eosin. The extent of local tumor spread in each histopathologic slice was then assessed according to the TNM staging.
The local lymph nodes were identified and embedded, as should all the lymph nodes above and below the tumour.
The circumferential margin was considered involved if the tumour extended to within 1 mm of the circumferential excision margin.
The whole MR examination time was about 20 minutes, depending on the length of the tumour, and it was always well tolerated. Each MR image was interpreted by two experienced readers independently. The tumour, the layers of the rectal wall, the perirectal tissues and the mesorectal fascia were always well visualized in all patients (n = 96).
The zonal anatomy of the rectal wall was best appreciated on thin-section axial images where the three different layers may be easily recognized: the inner hypointense and hyperintense layers respectively represent mucosa and submucosa, while the hypointense inner and outer layers represent the muscolaris propria characterized by the inner circular muscle and the outer longitudinal muscle; the external hyperintense layer represents perirectal fat tissue (Figure 5).
Even very thin hypointense structures such as the mesorectal fascia was always identified independent of the body habitus of the patient, owing to the high contrast between the hypointense fascia and the hyperintense fat tissue in and outside the mesorectum.
Rectal carcinoma appeared as a higher signal intensity structure than rectal wall in all T2-weighted sequences so the infiltration was well appreciated thanks to the contrast between high-intermediate signal intensity of tumour and low signal intensity of surrounding muscle tissues. The fat tissue remained high in signal intensity and in this way, the tumour contrasted well also with the surrounding fat tissue (Figure 6).
Moreover, the major anatomic structures such as the levator ani muscle, the puborectal muscle, the internal and external anal sphincters, and the anal canal were easily evaluated (Figure 7a-b).
In the first group of pts MR demonstrated high accuracy in the prediction of correct T stage achieving an agreement rate with histology of 95%: in 2 cases, MRI overstaged attributing a T3 stage rather than a T2 (Table 1). Also for the identification of nodal disease (N stage) our diagnosis agreed accurately with histological data (94%) since MRI correctly assigned the N stage in 45/48 cases: in 2 patients MRI attributed a N1 stage while the histology did not confirm nodal disease; in 1 case MRI revealed no evidence of nodal involvement while histology reported N1 (Table 2) (Figure 8a-f).
Preoperative chemo-radiotherapy was administered to patients belonging to group II with locally advanced rectal cancer and then treated with TME. Locally advanced rectal cancer was defined as tumour extension through the bowel wall, based on clinical and MR evaluation, without associated distant metastases.
In this second group population of patients submitted to neoadjuvant therapy MRI correctly assigned tumour stage (T) in 36/48 cases with 75% of agreement with the histological results. In 12 cases MRI overstaged: 2 patients were staged as T2 rather than T1; 8 cases were staged as T3 rather than T2; 2 lesions were classified as T4 but resulted T3 at histology (Table 4).
MRI showed a sensibility of 100% and a specificity of 67% in prediction of a tumour-involved MRF (MRF+) as shown in table 5.
For nodal metastasis (N stage) MRI showed 92% accuracy with 2 cases of overstaging ( N1 stage rather than N0) and in 1 case MRI did not reveal any nodal involvement whereas histology reported N1 (Table 6).
Moreover, in this second group of patients phased-array MRI assessed also the treatment outcome. In fact, 22/48 cases resulted downstaged: 2 rectal cancer staged as T4 at preoperative MR became T3 lesions after chemoradiation; 14 cases staged as T3 have became T2 (Figure 10); 4 case staged as T3 downstaged to T1 and 2 cases staged as T2 resulted T1 at the end of the treatment.
Our study demonstrated the high accuracy of preoperative MRI in the prediction of correct T stage; the agreement with histopatholgy was about 95% and it correlated with the data reported in the most of the studies published in literature (65%-100%) [12–16].
For T staging, results of accuracy of phased-array coil have been demonstrated to be similar to those obtained with an endorectal coil, but with the advantage that also nodal staging and a detailed imaging of all anatomical structures above the pelvic floor is possible.
Moreover, there is no patient discomfort because no insertion of any rectal coil is needed: the patient have merely just to lie on the MR table and his/her comfort is further enhanced in our technique by using the feet-first supine position, resulting in fewer problems with claustrophobia.
MRI demonstrated high performance also to assign the correct tumour stage of small lesions confined to rectal wall: T1 (16/20) and T2 (18/28).
The most frequent diagnostic error caused by MRI consisted in correctly differentiated T2 from early T3 lesions: this overstaging was often caused by the presence of desmoplastic reaction within the peritumoral tissues that made difficult the MR differentiation between perirectal fat spiculation, caused by fibrosis alone from those containing viable tumour cells.
The major problems occurred when MRI was performed after neoadjuvant therapy because the agreement rate with histhological results comes down from 95 to 75% due to post-radiation oedema, inflammation, fibrosis and necrosis that made difficult a correct diagnosis.
As far as concern the prediction of MRF tumour invasion, MRI was extremely accurate achieving a sensibility and a specificity of 100% in the first group. Also for this aspect our results were in accordance with those published in literature, but decreased after neoadjuvant therapy (II group) (specificity, 67%).
A recent Dutch study introduced a profile very similar to our study as far as concerns the population of patients that performed neoadjuvant therapy (48/96); our data were indeed comparable with those (sensibility of 100%, specificity of 32-59%): in both cases the lowest values of specificity came from the overstaging. In the most of patients when disease was overstaged at MRI, a diffuse hypointense tissue infiltrating MRF, corresponded to sterilized areas of fibrosis at histological analysis. Indeed postchemoradiation MRI was not able to discriminate between the fibrotic spiculations in the perirectal fat and spiculations with contextually malignant cells at histological analysis .
The performances of MRI in the local staging of rectal cancer disease confirm the possibility of this technique to discriminate patients candidated to preoperative neoadjuvant therapy especially considering the high performances of MRI in defining MRF involvement. A recent trial reported that, in selected patients, with FMR+ at the moment of the diagnosis, the use of the preoperative radiation therapy is mandatory because reduces the recurrence rate from 8.2% to 2.4% to 2 years .
In our experience, radiologist can be sure that the MRF will be free, only when an intact rectal wall is detected.
In this respect, the present T-staging system have its shortcomings because it does not discriminate between cancers with a wide FMR and cancers with a close or involved FMR. Although most of those tumours are classified as stage T3, they have a different risk of local recurrence. In fact today it's unanimously agreed that the distance of the cancer from the CRM, represented by the MRF, is a more powerful predictor for the local recurrence rate, much more significant than the T stage. In particular, if the distance of the tumour from MRF is ≥ 5 mm, radiologist may consider the fascia uninvolved; if the distance is 2-5 mm the involvement is considered border-line; if it is ≤ 1 mm, MRF is involved.
As regard N stage, identification of nodal disease is still a diagnostic problem for the radiologist. Despite the identification of lymph nodes as small as 2-3 mm on high-spatial-resolution images, reliable detection of nodal metastasis presently is not possible. The radiologist assessment of nodal involvement generally relies on morphologic criteria such as the size and shape of the node. The problem with morphologic imaging, however, is that with enlarged nodes is difficult to distinguish between reactive and metastatic nodes, and with small nodes micrometastases are easily missed. An additional problem in rectal cancer is the high frequency of micrometastases in normal-sized nodes. In fact, there is currently no consensus about lymph node size vis-à-vis nodal involvement: some authors report any detectable lymph node, whereas others report only those lymph nodes that are larger than a given size (3 mm, 5 mm, or 10 mm) .
In our study nodal evaluation had been estimated with dimensional cut-off of 10 mm achieving an agreement rate with histology of 96% that was comparable with the values of literature but it is obvious that also our approach has been arbitrary.
However, results of early anatomic studies showed that over half of the metastatic nodes were within 3 cm of the primary tumour and were smaller than 5 mm in size [20–25]; these data evidently call in question the real validity of the dimensional criteria.
Our experience has confirmed that MR with phased-array coil is the technique of choice in the preoperative local staging of rectal cancer since it helps to estimate in a detailed and non-invasive way the entire mesorectal fat and all the surrounding pelvic structures, MRF included; moreover, it allows to identify the different risk group of patients helping to decide about the treatment and its outcome (downstaging with complete or incomplete response), and finally to optimize a complete excision allowing to those patients with an advantaced rectal cancer to benefit from a sphincter-preserving surgery.
Maier A, Fuchsjager M: Peroperative staging of rectal cancer. Eur J Radiol 2003, 47: 89-97. 10.1016/S0720-048X(03)00161-X
Tang R, Wang JY, Chen JS: Survival impact of lymph node metastasis in TNM stage III carcinoma of the colon and rectum. J Am Coll Surg 1995, 180: 705-712.
Willett CG, Badizadegan K, Ancukiewicz M, Shellito PC: Prognostic factors in stage T3N0 rectal cancer: do all patients require postoperative pelvic irradiation and chemotherapy? Dis Colon Rectum 1999, 42: 167-173. 10.1007/BF02237122
Kapiteijn E, Marijnen CA, Nagtegaal ID: Preoperative radiotherapy combined with total mesorectal excision for resectable rectal cancer. N Engl J Med 2001, 345: 638-646. 10.1056/NEJMoa010580
MacFarlane JK, Ryall RD, Heald RJ: Mesorectal excision for rectal cancer. Lancet 1993, 341: 457-460. 10.1016/0140-6736(93)90207-W
Beets-Tan RG, Beets GL: Rectal cancer: review with emphasis on MR imaging. Radiology 2004, 232: 773-783. 10.1148/radiol.2323031368
Bouzourene H, Bosman FT, Seelentag W: Importance of tumour regression assessment in predicting outcome in patients with locally advanced rectal carcinoma who are treated with pre-operative radiotherapy. Cancer 2002, 94: 1121-1130. 10.1002/cncr.10327
Heald RJ, Karanjia ND: Results of radical surgery for rectal cancer. World J Surg 1992,16(5):848-857. 10.1007/BF02066981
McArdle CS, Hole D: Imapct of variability among surgeons pn post-operative morbidity and mortality and ultimate survival. Br Med J 1991, 302: 1501-1505. 10.1136/bmj.302.6791.1501
MacFarlane JK, Ryall RD, Heald RJ: Mesorectal excision for rectal cancer. Lancet 1993,341(8843):457-460. 10.1016/0140-6736(93)90207-W
Hermanek P, Wiebelt H, Staimmer D, Riedl S: Prognostic factors of rectum carcinoma-experience of the german Multicentre Study SGCRC. German Study Group Colo-Rectal carcinoma. Tumori 1995,81(3 Suppl):60-64.
Blomqvist L, Machado M, Rubio C: Rectal tumor staging: MR imaging using pelvic phased-array and endorectal coils vs endoscopic ultrasonography. Eur Radiol 2000, 10: 653-660. 10.1007/s003300050979
Beets-Tan RG, Beets GL, Vliegen RF: Accuracy of magnetic resonance imaging in prediction of tumor-free resection margin in rectal cancer surgery. Lancet 2001, 357: 497-504. 10.1016/S0140-6736(00)04040-X
Blomqvist L, Holm T, Rubio C, Hindmarsh T: Rectal tumors: MR imaging with endorectal and/or phased-array coils, and histopathological staging on giant sections-a comparative study. Acta Radiol 1997, 38: 437-444.
Gagliardi G, Bayar S, Smith R, Salem RR: Preoperative staging of rectal cancer using magnetic resonance imaging with external phase-arrayed coils. Arch Surg 2002, 137: 447-451. 10.1001/archsurg.137.4.447
Brown G, Richards CJ, Newcombe RG: Rectal carcinoma: thin-section MR imaging for staging in 28 patients. Radiology 1999, 211: 215-222.
Vliegen RF, Beets GL, Beets-Tan RG: Mesorectal Fascia Invasion after Neoadjuvant Chemotherapy and Radiation Therapy for Locally Advanced Cancer: Accuracy of MR Imaging Prediction. Radiology 2008,246(2):454-462. 10.1148/radiol.2462070042
Goh V, Halligan S, Bartram CL: Local radiological staging of rectal cancer. Clin Radiol 2004, 59: 215-226. 10.1016/j.crad.2003.08.013
Kim JHC, Beets GL, Kim MJ, Kessels AG, Beets-Tan RG: High Resolution MR Imaging for nodal staging in rectal cancer: are there any criteria in addition to the size? Eur? Radiol 2004, 52: 78-83.
Iafrate F, Laghi A, Paolantonio P, Passariello R: Preoperative Staging of Rectal Cancer with MR IMaging: Correlation with Surgical and Histopathologic Findings. Radiographics 2006, 26: 701-714. 10.1148/rg.263055086
Brown G, Richards CJ, Bourne MW: Morphologic predictors of lymph node status in rectal cancer with use of high-spatial-resolution MR imaging with histopathologic comparison. Radiology 2003,227(2):371-377. 10.1148/radiol.2272011747
Monig SP, Baldus SE, Zirbes TK: Lymph node size and metastatic infiltration in colon cancer. Ann Surg Oncol 1999, 6: 579-581. 10.1007/s10434-999-0579-1
Bjelovic M, Kalezic V, Petrovic M: Correlation of macroscopic and histological characteristics in the regional lymph nodes of patients with rectal and sigmoidal adenocarcinoma. Hepatogastroenterology 1998, 45: 433-438.
Okizuka H, Sugimura K, Yshida T: Preoperative local staging of rectal carcinoma with MR imaging and a rectal balloon. J Magn Reson Imaging 1993, 3: 329-335. 10.1002/jmri.1880030207
Rafaelsen SR, Kronborg O, Fenger C: Digital rectal examination transrectal ultrasonography in staging of rectal cancer: a prospective, blind study. Acta Radiol 1994, 35: 300-304.
Supported in part by the SUIT-HEART Project: prot. n. 3317, 30/5/2011.
The authors declare that they have no competing interests.
SG: carried out the study and drafted the manuscript. PB: performed surgery. MC: performed anatomopathological evaluation. EF: participated in the design of the study. SF: participated in the anatomopathological evaluation. EC: participated in the anatomopathological evaluation. DC: coordinated the study. CB: coordinated the study and participate in its design. All authors read and approved the final manuscript
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Giusti, S., Buccianti, P., Castagna, M. et al. Preoperative rectal cancer staging with phased-array MR. Radiat Oncol 7, 29 (2012). https://doi.org/10.1186/1748-717X-7-29