Abstract

BackgroundClinical management of rectal cancer patients relies on pre-operative staging. Studies however continue to report moderate degrees of over/understaging as well as inter-observer variability. The aim of this study was to determine the sensitivity, specificity and accuracy of tumor size for predicting T and N stages in pre-operatively untreated rectal cancers.MethodsWe examined a test cohort of 418 well-documented patients with pre-operatively untreated rectal cancer admitted to the University Hospital of Basel between 1987 and 1996. Classification and regression tree (CART) and logistic regression analysis were carried out to determine the ability of tumor size to discriminate between early (pT1-2) and late (pT3-4) T stages and between node-negative (pN0) and node-positive (pN1-2) patients. Results were validated by an external patient cohort (n = 28).ResultsA tumor diameter threshold of 34 mm was identified from the test cohort resulting in a sensitivity and specificity for late T stage of 76.3%, and 67.4%, respectively and an odds ratio (OR) of 6.67 (95%CI:3.4-12.9). At a threshold value of 29 mm, sensitivity and specificity for node-positive disease were 94% and 15.5%, respectively with an OR of 3.02 (95%CI:1.5-6.1). Applying these threshold values to the validation cohort, sensitivity and specificity for T stage were 73.7% and 77.8% and for N stage 50% and 75%, respectively.ConclusionsTumor size at a threshold value of 34 mm is a reproducible predictive factor for late T stage in rectal cancers. Tumor size may help to complement clinical staging and further optimize the pre-operative management of patients with rectal cancer.

Highlights

  • Clinical management of rectal cancer patients relies on pre-operative staging

  • Clinical management of patients with rectal cancer depends significantly on pre-operative staging. Parameters such as cT and cN stage obtained by magnetic resonance imaging (MRI), computed tomography (CT) or endorectal ultrasonography (EUS) are crucial in selecting patients for pre-operative neoadjuvant therapy [1,2]

  • Whereas EUS or CT seem to be more accurate for the detection of early T1/T2 cancer, understaging with CT has been described for T3 tumors in comparison to MRI [10,11,12,13]

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Summary

Introduction

Clinical management of rectal cancer patients relies on pre-operative staging. The aim of this study was to determine the sensitivity, specificity and accuracy of tumor size for predicting T and N stages in pre-operatively untreated rectal cancers. Clinical management of patients with rectal cancer depends significantly on pre-operative staging. Recent studies report variability in the accuracy of pre-operative staging of rectal cancer. All three methods (CT, MRI and EUS) can lead to moderate rates of over- or understaging of T and N stages compared to histology in pre-operatively untreated patients [5,6,7,8,9,10]. Detection of novel prognostic factors capable of complementing clinical staging is warranted to identify patients in the pre-operative setting with locally advanced disease

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