Tagore Kuldeep S, Lawson Michael J, Yucaitis Joy A, Gage Rhonda, Orr Tashia, Shuber Anthony P, Ross Michael E
University of California Davis Medical Center, Sacramento, USA.
Clin Colorectal Cancer. 2003 May;3(1):47-53. doi: 10.3816/CCC.2003.n.011.
Colorectal cancer is the second-leading cause of cancer death. New noninvasive options for screening capable of diagnosing cancer at an early stage are needed to improve compliance and reduce mortality. This study was designed to provide an estimate of the sensitivity and specificity of a multitarget assay panel (MTAP) of stool DNA changes. Eighty patients with advanced colorectal neoplasia and 212 control subjects provided stool samples before colonoscopy. Patients with hereditary colorectal cancer syndromes were excluded. The MTAP included 21 specific mutations in the adenomatous polyposis coli (APC), p53, and K-ras genes, a microsatellite instability marker (BAT-26), and a marker of abnormal apoptosis (DNA Integrity Assay). All samples were analyzed in the clinical laboratory at EXACT Sciences. Multitarget assay panel detected 33 of 52 patients (63.5%, 95% confidence interval [CI], 49.0%-76.4%) with invasive colorectal cancer, including 26 of 36 (72.2%) with node-negative disease (American Joint Committee on Cancer [AJCC] stage I/II) and 7 of 16 (43.7%) with advanced disease (AJCC stage III/IV). Sixteen of 28 patients (57.1%; 95% CI, 37.2%-75.5%) with advanced adenomas (lesions containing high-grade dysplasia, villous adenomas, or tubular adenomas > 1 cm in size) were detected, including 6 of 7 (85.7%) with high-grade dysplasia and 10 of 21 (47.6%) with other advanced adenomas. Specificity was 96.2% (95% CI, 92.7%-98.4%) in patients with either no colorectal lesions or diminutive polyps. Multitarget assay panel has better sensitivity than that reported with use of Hemoccult(R) II in fecal occult blood testing, with similar specificity. Sensitivity appeared to be equally high for patients with node-negative and advanced disease, as well as for advanced adenomas. This study contained a disproportionately high number of distal cancers and, as such, may not be representative of results in proximal lesions. Although a prospective study in an average-risk population is needed to validate these findings, MTAP may offer an important noninvasive option for population-based screening.
结直肠癌是癌症死亡的第二大原因。需要新的能够在早期诊断癌症的非侵入性筛查方法,以提高筛查的依从性并降低死亡率。本研究旨在评估一种粪便DNA变化多靶点检测面板(MTAP)的敏感性和特异性。80例晚期结直肠肿瘤患者和212例对照者在结肠镜检查前提供了粪便样本。排除患有遗传性结直肠癌综合征的患者。MTAP包括腺瘤性息肉病(APC)、p53和K-ras基因中的21个特定突变、一个微卫星不稳定性标志物(BAT-26)以及一个异常凋亡标志物(DNA完整性检测)。所有样本均在EXACT Sciences的临床实验室进行分析。多靶点检测面板在52例浸润性结直肠癌患者中检测出33例(63.5%,95%置信区间[CI],49.0%-76.4%),其中36例(72.2%)无淋巴结转移疾病(美国癌症联合委员会[AJCC] I/II期)患者中检测出26例,16例(43.7%)晚期疾病(AJCC III/IV期)患者中检测出7例。28例晚期腺瘤(包含高级别上皮内瘤变、绒毛状腺瘤或直径>1 cm的管状腺瘤的病变)患者中检测出16例(57.1%;95% CI,37.2%-75.5%),其中7例高级别上皮内瘤变患者中检测出6例(85.7%),21例其他晚期腺瘤患者中检测出10例(47.6%)。在无结直肠病变或微小息肉的患者中,特异性为96.2%(95% CI,92.7%-98.4%)。多靶点检测面板的敏感性高于粪便潜血检测中使用的Hemoccult(R) II报告的敏感性,特异性相似。对于无淋巴结转移和晚期疾病患者以及晚期腺瘤患者,敏感性似乎同样高。本研究中远端癌症的比例过高,因此可能不代表近端病变的结果。尽管需要在平均风险人群中进行前瞻性研究来验证这些发现,但MTAP可能为基于人群的筛查提供一种重要的非侵入性选择。