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放射学分期对识别适合新辅助化疗的高危结肠癌患者的准确性:一项多中心经验。

Accuracy of radiological staging in identifying high-risk colon cancer patients suitable for neoadjuvant chemotherapy: a multicentre experience.

机构信息

Department of Surgery, Mayday University Hospital, Croydon, Surrey, UK.

出版信息

Colorectal Dis. 2012 Apr;14(4):438-44. doi: 10.1111/j.1463-1318.2011.02638.x.

DOI:10.1111/j.1463-1318.2011.02638.x
PMID:21689323
Abstract

AIM

A pilot study was undertaken to determine the accuracy of computed tomography (CT) staging in identifying patients with high-risk colon cancers who would be considered as candidates for a neoadjuvant therapy trial (FOxTROT) and those at low risk (T1/T2) who would be excluded.

METHOD

Participating radiologists from 19 centres attended workshops for standardization of image interpretation according to previously defined prognostic criteria: good prognosis tumours, including, T1/T2; intermediate prognosis, T3 < 5 mm tumour invasion beyond the muscularis propria (MP); and poor prognosis tumours, including T3 with tumour extension ≥ 5 mm beyond the MP or T4. The CT findings were compared with histopathology as the reference standard.

RESULTS

Of 94 patients with radiological and pathological data, 71% were categorized by CT as having a poor prognosis. The sensitivity and specificity of CT in identifying these tumours were 87% (95% CI, 74-94) and 49% (95% CI, 33-65). Sensitivity and specificity for tumour infiltration beyond the MP (T3/T4 vs T1/T2) were 95% (95% CI, 87-98) and 50% (95% CI, 22-77), respectively. Including all CT-staged T3 and T4 patients in the trial would have increased the proportion eligible for entry to 89% (n = 84) without affecting the false-positive rate of 7%. Some 20% of T3/T4 patients would have been ineligible for FOxTROT because of synchronous metastases.

CONCLUSION

In a multicentre setting, CT scanning identified high-risk (T3/4) colon cancers with minimal overstaging of T1/T2 tumours, thus establishing the feasibility of radiologically guided neoadjuvant chemotherapy.

摘要

目的

本研究旨在通过前瞻性临床试验(FOxTROT)评估计算机断层扫描(CT)分期对高危结肠癌患者的准确性,以便确定哪些患者有必要接受新辅助治疗,哪些患者为低危(T1/T2)而无需接受新辅助治疗。

方法

19 个中心的放射科医生参加了标准化图像解释的研讨会,这些研讨会是根据先前定义的预后标准进行的:包括 T1/T2 的预后良好肿瘤;T3 肿瘤侵犯固有肌层(MP)<5mm 且预后中等的肿瘤;包括 T3 肿瘤侵犯 MP 超过 5mm 或 T4 肿瘤的预后不良肿瘤。将 CT 结果与组织病理学作为参考标准进行比较。

结果

94 例有影像学和病理学数据的患者中,71%的患者 CT 分期为预后不良。CT 识别这些肿瘤的敏感性和特异性分别为 87%(95%CI,74-94)和 49%(95%CI,33-65)。肿瘤侵犯固有肌层(T3/T4 与 T1/T2)的敏感性和特异性分别为 95%(95%CI,87-98)和 50%(95%CI,22-77)。如果将所有 CT 分期为 T3 和 T4 的患者纳入试验中,那么符合条件的患者比例将增加到 89%(n=84),而不会影响 7%的假阳性率。大约 20%的 T3/T4 患者由于同步转移而不符合 FOxTROT 条件。

结论

在多中心环境中,CT 扫描可识别高危(T3/4)结肠癌,对 T1/T2 肿瘤的过度分期较少,从而为放射引导新辅助化疗的可行性提供了依据。

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