Division of Abdominal Imaging and Interventional Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Clin Radiol. 2013 Oct;68(10):e524-31. doi: 10.1016/j.crad.2013.05.094. Epub 2013 Jul 2.
To evaluate the role of pretreatment apparent diffusion coefficient (ADC) as a predictor of treatment response and local recurrence in patients with locally advanced rectal cancer who underwent neoadjuvant therapy.
Forty-nine patients who underwent preoperative diffusion-weighted magnetic resonance imaging (MRI) followed by neoadjuvant chemoradiation and surgery were enrolled in the study. The mean tumour ADC was measured independently from multiple, non-overlapping regions of interest (ROIs) to cover the entire tumour area on a single section by two radiologists and patients were followed postoperatively for a median of 16.4 months. Diagnostic accuracy of ADC for predicting treatment response and recurrence was evaluated using the area under the receiver-operating characteristic (ROC) curve, sensitivity, specificity, and predictive values. Univariate and multivariate analyses including clinical tumour (cT) staging, carcinoembryonic antigen (CEA) level, lymph-node involvement, tumour grade, surgical margin, vascular involvement, and ADC were performed with respect to recurrence. Interobserver agreement of ADC values was assessed.
Twenty patients showed response to neoadjuvant therapy and recurrence was noted in 17 patients. Low pretreatment ADC, MRI findings of cT4 staging, and node involvement were significantly related to poor treatment response. Sensitivity and specificity of ADC = 0.833 × 10(-3) mm(2)/s for prediction of treatment response was 75 and 48% for reader 1 and 65 and 52% for reader 2, respectively. Univariate and multivariate analyses identified pretreatment tumour ADC as the only predictive factor for recurrence. Sensitivity and specificity of ADC = 0.833 × 10(-3) mm(2)/s for prediction of recurrence was 86 and 77% for reader 1 and 80 and 69% for reader 2, respectively. Interobserver agreement for measuring ADC was good with a kappa value of 0.70.
Pretreatment rectal tumour ADC values may be an early biomarker for predicting treatment response and local recurrence in patients who underwent neoadjuvant chemoradiation.
评估治疗前表观扩散系数(ADC)作为预测接受新辅助治疗的局部晚期直肠癌患者治疗反应和局部复发的指标的作用。
本研究纳入了 49 例接受术前磁共振弥散加权成像(MRI)检查,然后接受新辅助放化疗和手术的患者。两名放射科医生独立地从多个、非重叠的感兴趣区域(ROI)测量肿瘤的平均 ADC 值,以覆盖单一切面的整个肿瘤区域,患者在术后中位数随访 16.4 个月。通过接受者操作特征(ROC)曲线下面积、敏感性、特异性和预测值来评估 ADC 预测治疗反应和复发的诊断准确性。对 ADC 值与复发相关的临床肿瘤(cT)分期、癌胚抗原(CEA)水平、淋巴结受累、肿瘤分级、手术切缘、血管受累以及 ADC 值进行单因素和多因素分析。评估了 ADC 值的观察者间一致性。
20 例患者对新辅助治疗有反应,17 例患者出现复发。低治疗前 ADC 值、MRI 的 cT4 分期和淋巴结受累与治疗反应不良显著相关。读者 1 预测治疗反应的 ADC 值为 0.833×10(-3)mm(2)/s 的敏感性和特异性分别为 75%和 48%,读者 2 分别为 65%和 52%。单因素和多因素分析确定治疗前肿瘤 ADC 是复发的唯一预测因素。读者 1 预测复发的 ADC 值为 0.833×10(-3)mm(2)/s 的敏感性和特异性分别为 86%和 77%,读者 2 分别为 80%和 69%。ADC 值测量的观察者间一致性良好,kappa 值为 0.70。
治疗前直肠肿瘤 ADC 值可能是预测接受新辅助放化疗的患者治疗反应和局部复发的早期生物标志物。