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[ subject:"Oncology." ]
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Circulating tumor DNA as a candidate...
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Anand, Sanya.
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Circulating tumor DNA as a candidate biomarker for ovarian cancer surveillance and prognosis.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Circulating tumor DNA as a candidate biomarker for ovarian cancer surveillance and prognosis./
作者:
Anand, Sanya.
面頁冊數:
60 p.
附註:
Source: Masters Abstracts International, Volume: 55-03.
Contained By:
Masters Abstracts International55-03(E).
標題:
Genetics. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=1605980
ISBN:
9781339354415
Circulating tumor DNA as a candidate biomarker for ovarian cancer surveillance and prognosis.
Anand, Sanya.
Circulating tumor DNA as a candidate biomarker for ovarian cancer surveillance and prognosis.
- 60 p.
Source: Masters Abstracts International, Volume: 55-03.
Thesis (M.S.)--Icahn School of Medicine at Mount Sinai, 2016.
While CA-125 is an FDA-approved biomarker used for monitoring ovarian cancer, levels can rise non-specifically in patients with non-cancerous conditions and stay within a normal range in the presence of persistent disease, making CA-125 inadequate for screening and surveillance. We have developed an efficient pipeline that identifies cancer-specific mutations in each patient's tumor and monitors circulating tumor DNA (ctDNA) levels using droplet digital PCR. Using this platform, we tested and detected ctDNA in 11/12 patients with ovarian cancer. Undetectable levels of ctDNA post-treatment were associated with improved overall survival (p = 0.0179). In six patients, ctDNA levels were detectable prior to CA-125 levels rising above the threshold level of 35 U/ml, indicating that ctDNA has the potential to be a more sensitive and broadly applicable tumor marker for ovarian cancer than CA-125.
ISBN: 9781339354415Subjects--Topical Terms:
530508
Genetics.
Circulating tumor DNA as a candidate biomarker for ovarian cancer surveillance and prognosis.
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While CA-125 is an FDA-approved biomarker used for monitoring ovarian cancer, levels can rise non-specifically in patients with non-cancerous conditions and stay within a normal range in the presence of persistent disease, making CA-125 inadequate for screening and surveillance. We have developed an efficient pipeline that identifies cancer-specific mutations in each patient's tumor and monitors circulating tumor DNA (ctDNA) levels using droplet digital PCR. Using this platform, we tested and detected ctDNA in 11/12 patients with ovarian cancer. Undetectable levels of ctDNA post-treatment were associated with improved overall survival (p = 0.0179). In six patients, ctDNA levels were detectable prior to CA-125 levels rising above the threshold level of 35 U/ml, indicating that ctDNA has the potential to be a more sensitive and broadly applicable tumor marker for ovarian cancer than CA-125.
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