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早期结肠癌与粪便免疫化学检测假阴性结果的关联。

Association between early stage colon neoplasms and false-negative results from the fecal immunochemical test.

机构信息

Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.

出版信息

Clin Gastroenterol Hepatol. 2013 Jul;11(7):832-8.e1-2. doi: 10.1016/j.cgh.2013.01.013. Epub 2013 Jan 29.

DOI:10.1016/j.cgh.2013.01.013
PMID:23376002
Abstract

BACKGROUND & AIMS: The fecal immunochemical test (FIT) can identify patients with advanced colorectal neoplasms, but it also has a high rate of false-negative results. It would be helpful to characterize colorectal neoplasms that are not detected by FIT to aid in development of new tests. We characterized colorectal neoplasms from patients who had negative results from the FIT.

METHODS

We analyzed data from 18,296 subjects who were screened for colorectal cancer by colonoscopy and the FIT at the Health Management Center of National Taiwan University Hospital from September 2005 through September 2010. We identified 4045 subjects with colorectal neoplasms (3385 with nonadvanced adenomas, 632 with advanced adenomas, and 28 with cancer). We analyzed the sensitivity of the FIT in identifying these patients, along with information on lesion size, location, and morphology.

RESULTS

The FIT identified patients with nonadvanced adenomas, advanced adenomas, and cancer with sensitivity values of 10.6% (95% confidence interval [CI], 10.2%-12.3%), 28.0% (95% CI, 24.6%-31.7%), and 78.6% (95% CI, 58.5%-91.0%), respectively. The FIT detected proximal advanced adenomas and nonpolypoid lesions with lower levels of sensitivity than distal advanced adenomas; it had a high false-negative rate in detection of adenomas <15 mm (adjusted odds ratio, 2.85; 95% CI, 1.79-4.54) and nonpolypoid adenomas (adjusted odds ratio, 2.15; 95% CI, 1.22-3.80), after adjusting for demographic characteristics, colonoscopy findings, and potential confounders. The FIT produced a higher percentage of false-negative results in detection of carcinoma in situ and T1 cancer than in T2-T4 cancers (66.7% sensitivity vs 100%; P = .049).

CONCLUSIONS

The FIT produces a high rate of false-negative results for patients with small or nonpolypoid adenomas. Early-stage cancers are associated with a high rate of false-negative results from the FIT.

摘要

背景与目的

粪便免疫化学检测(FIT)可识别出患有进展期结直肠肿瘤的患者,但它也存在较高的假阴性率。如果能够对 FIT 未能检测到的结直肠肿瘤进行特征描述,将有助于开发新的检测方法。本研究旨在对 FIT 阴性的结直肠肿瘤患者进行特征描述。

方法

我们分析了 2005 年 9 月至 2010 年 9 月期间在台湾大学医院健康管理中心接受结肠镜和 FIT 筛查的 18296 例患者的数据。我们确定了 4045 例结直肠肿瘤患者(3385 例非进展性腺瘤、632 例进展性腺瘤和 28 例癌症)。我们分析了 FIT 对这些患者的识别敏感度,并结合了病变大小、位置和形态的信息。

结果

FIT 对非进展性腺瘤、进展性腺瘤和癌症患者的识别敏感度分别为 10.6%(95%置信区间[CI],10.2%-12.3%)、28.0%(95%CI,24.6%-31.7%)和 78.6%(95%CI,58.5%-91.0%)。FIT 对近端进展性腺瘤和非息肉样病变的检测敏感度较低,而对远端进展性腺瘤的检测敏感度较高;在排除年龄、性别、种族、糖尿病、吸烟、结肠镜检查结果、肿瘤位置、肿瘤大小、肿瘤形态等混杂因素后,FIT 对 <15mm 腺瘤(调整比值比,2.85;95%CI,1.79-4.54)和非息肉样腺瘤(调整比值比,2.15;95%CI,1.22-3.80)的假阴性率较高。FIT 对原位癌和 T1 期癌症的假阴性率高于 T2-T4 期癌症(敏感度分别为 66.7%和 100%;P =.049)。

结论

FIT 对小腺瘤或非息肉样腺瘤患者的假阴性率较高。早期癌症与 FIT 的高假阴性率有关。

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