High Detection Rates of Colorectal Neoplasia by Stool DNA Testing With a Novel Digital Melt Curve Assay

被引:88
作者
Zou, Hongzhi [1 ]
Taylor, William R. [1 ]
Harrington, Jonathan J. [1 ]
Hussain, Fareeda Taher Nazer [1 ]
Cao, Xiaoming [1 ]
Loprinzi, Charles L. [2 ]
Levine, Theodore R. [4 ]
Rex, Douglas K. [5 ]
Ahnen, Dennis [6 ,7 ]
Knigge, Kandice L. [8 ]
Lance, Peter [9 ]
Jiang, Xuan [10 ]
Smith, David I. [3 ]
Ahlquist, David A. [1 ]
机构
[1] Mayo Clin, Miles & Shirley Fiterman Div Gastroenterol & Hepa, Rochester, MN 55905 USA
[2] Mayo Clin, Div Med Oncol, Rochester, MN 55905 USA
[3] Mayo Clin, Div Expt Pathol, Rochester, MN 55905 USA
[4] Kaiser Permanente Med Care Program, Oakland, CA USA
[5] Indiana Univ, Sch Med, Div Gastroenterol, Indianapolis, IN USA
[6] Univ Colorado, Hlth Sci Ctr, Denver, CO USA
[7] Dept Vet Affairs Med Ctr, Denver, CO USA
[8] Oregon Hlth & Sci Univ, Div Gastroenterol, Portland, OR 97201 USA
[9] Univ Arizona, Arizona Canc Ctr, Tucson, AZ USA
[10] Peking Univ, Peoples Hosp, Div Gastroenterol & Hepatol, Beijing 100871, Peoples R China
关键词
FECAL-OCCULT-BLOOD; K-RAS MUTATIONS; CANCER PATIENTS; LUNG-CANCER; GEFITINIB; PLASMA; PCR; QUANTIFICATION; RESPONSIVENESS; SURVEILLANCE;
D O I
10.1053/j.gastro.2008.10.023
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Current stool DNA tests identify about half of individuals with colorectal cancers and miss most individuals with advanced adenomas. We developed a digital melt curve (DMC) assay to quantify low-abundance mutations in stool samples for detection of colorectal. neoplasms and compared this test with other approaches. Methods: We combined a melt curve assay with digital polymerase chain reaction and validated the quantitative range. We then evaluated its ability to detect neoplasms in 2 clinical studies. In study 1, stool samples from patients with colorectal tumors with known mutations (KRAS, APC, BRAF, TP53) were assayed. In study II, archived stool samples from patients with advanced adenomas containing known KRAS mutations were assayed, along with controls. Results were compared with those from the stool DNA test PreGenPlus (Exact Sciences, Marlborough, MA), Hemoccult, and HemoccultSensa (both Beckman-Coulter, Fullerton, CA). Results : The DMC assay detected samples in which only 0.1% of target genes were mutated. In study 1, the DMC assay detected known mutations in 28 (90%) of 31 tumor samples and 6 (75%) of 8 advanced adenoma samples. In study 11, the DMC assay detected 16 (59%) of 27 advanced adenoma samples that contained KRAS mutations, compared with 7% with the Hemoccult, 15% with the HemoccultSensa, and 26% with the PreGenPlus assays (P < .05 for each, compared with the DMC assay); specificities did not differ significantly. Conclusions: The DMC assay has a high level of sensitivity in detecting individuals with colon neoplasms and is better than current stool screening methods in detecting those with advanced adenomas. Further studies are indicated.
引用
收藏
页码:459 / 470
页数:12
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