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

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 comp...

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Veröffentlicht in:Gastroenterology (New York, N.Y. 1943) N.Y. 1943), 2009-02, Vol.136 (2), p.459-470
Hauptverfasser: Zou, Hongzhi, Taylor, William R, Harrington, Jonathan J, Hussain, Fareeda Taher Nazer, Cao, Xiaoming, Loprinzi, Charles L, Levine, Theodore R, Rex, Douglas K, Ahnen, Dennis, Knigge, Kandice L, Lance, Peter, Jiang, Xuan, Smith, David I, Ahlquist, David A
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container_issue 2
container_start_page 459
container_title Gastroenterology (New York, N.Y. 1943)
container_volume 136
creator Zou, Hongzhi
Taylor, William R
Harrington, Jonathan J
Hussain, Fareeda Taher Nazer
Cao, Xiaoming
Loprinzi, Charles L
Levine, Theodore R
Rex, Douglas K
Ahnen, Dennis
Knigge, Kandice L
Lance, Peter
Jiang, Xuan
Smith, David I
Ahlquist, David A
description 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 I, 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 I, the DMC assay detected known mutations in 28 (90%) of 31 tumor samples and 6 (75%) of 8 advanced adenoma samples. In study II, 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.
doi_str_mv 10.1053/j.gastro.2008.10.023
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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 I, 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 I, the DMC assay detected known mutations in 28 (90%) of 31 tumor samples and 6 (75%) of 8 advanced adenoma samples. In study II, 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 &lt; .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.</description><identifier>ISSN: 0016-5085</identifier><identifier>EISSN: 1528-0012</identifier><identifier>DOI: 10.1053/j.gastro.2008.10.023</identifier><identifier>PMID: 19026650</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adenoma - diagnosis ; Adenoma - genetics ; Aged ; Case-Control Studies ; Colorectal Neoplasms - diagnosis ; Colorectal Neoplasms - genetics ; Diagnostic Tests, Routine - methods ; DNA, Neoplasm - genetics ; Feces ; Female ; Gastroenterology and Hepatology ; Humans ; Male ; Mass Screening - methods ; Middle Aged ; Mutation ; Occult Blood ; Polymerase Chain Reaction - methods ; Proto-Oncogene Proteins - genetics ; Proto-Oncogene Proteins B-raf - genetics ; Proto-Oncogene Proteins p21(ras) ; ras Proteins - genetics ; Sensitivity and Specificity ; Tumor Suppressor Protein p53 - genetics</subject><ispartof>Gastroenterology (New York, N.Y. 1943), 2009-02, Vol.136 (2), p.459-470</ispartof><rights>AGA Institute</rights><rights>2009 AGA Institute</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c461t-a8987b56962872869f7802ba653dfef7688c4737c481d3f64a4324576278dc813</citedby><cites>FETCH-LOGICAL-c461t-a8987b56962872869f7802ba653dfef7688c4737c481d3f64a4324576278dc813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1053/j.gastro.2008.10.023$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19026650$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zou, Hongzhi</creatorcontrib><creatorcontrib>Taylor, William R</creatorcontrib><creatorcontrib>Harrington, Jonathan J</creatorcontrib><creatorcontrib>Hussain, Fareeda Taher Nazer</creatorcontrib><creatorcontrib>Cao, Xiaoming</creatorcontrib><creatorcontrib>Loprinzi, Charles L</creatorcontrib><creatorcontrib>Levine, Theodore R</creatorcontrib><creatorcontrib>Rex, Douglas K</creatorcontrib><creatorcontrib>Ahnen, Dennis</creatorcontrib><creatorcontrib>Knigge, Kandice L</creatorcontrib><creatorcontrib>Lance, Peter</creatorcontrib><creatorcontrib>Jiang, Xuan</creatorcontrib><creatorcontrib>Smith, David I</creatorcontrib><creatorcontrib>Ahlquist, David A</creatorcontrib><title>High Detection Rates of Colorectal Neoplasia by Stool DNA Testing With a Novel Digital Melt Curve Assay</title><title>Gastroenterology (New York, N.Y. 1943)</title><addtitle>Gastroenterology</addtitle><description>Background &amp; 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 I, 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 I, the DMC assay detected known mutations in 28 (90%) of 31 tumor samples and 6 (75%) of 8 advanced adenoma samples. In study II, 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 &lt; .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. 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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 I, 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 I, the DMC assay detected known mutations in 28 (90%) of 31 tumor samples and 6 (75%) of 8 advanced adenoma samples. In study II, 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 &lt; .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.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>19026650</pmid><doi>10.1053/j.gastro.2008.10.023</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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subjects Adenoma - diagnosis
Adenoma - genetics
Aged
Case-Control Studies
Colorectal Neoplasms - diagnosis
Colorectal Neoplasms - genetics
Diagnostic Tests, Routine - methods
DNA, Neoplasm - genetics
Feces
Female
Gastroenterology and Hepatology
Humans
Male
Mass Screening - methods
Middle Aged
Mutation
Occult Blood
Polymerase Chain Reaction - methods
Proto-Oncogene Proteins - genetics
Proto-Oncogene Proteins B-raf - genetics
Proto-Oncogene Proteins p21(ras)
ras Proteins - genetics
Sensitivity and Specificity
Tumor Suppressor Protein p53 - genetics
title High Detection Rates of Colorectal Neoplasia by Stool DNA Testing With a Novel Digital Melt Curve Assay
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