TY - JOUR
T1 - Detection of endometrial precancer by a targeted gynecologic cancer liquid biopsy
AU - Martignetti, John A.
AU - Pandya, Deep
AU - Nagarsheth, Nimesh
AU - Chen, Ying
AU - Camacho, Olga
AU - Tomita, Shannon
AU - Brodman, Michael
AU - Ascher-Walsh, Charles
AU - Kolev, Valentin
AU - Cohen, Samantha
AU - Harkins, Timothy T.
AU - Schadt, Eric E.
AU - Reva, Boris
AU - Sebra, Robert
AU - Dottino, Peter
N1 - Funding Information:
This study was supported in part by funding from the Gordon family, the Ruttenberg family, the Goldstone family, and the Varadi Ovarian Initiative in Cancer Education (VOICE). The funders had no role in study design, data collection, or its analysis.
Publisher Copyright:
© 2018 Martignetti et al.
PY - 2018/12
Y1 - 2018/12
N2 - Endometrial cancer is the most common gynecologic malignancy in industrialized countries, and both its incidence and its associated mortality are increasing. The “liquid biopsy” is becoming an important transformative precision oncology tool, but barriers intrinsic to blood sampling have limited its use in early cancer detection. We hypothesized that using a more targeted sample for analysis-namely, a uterine lavage-should provide a more sensitive and specific diagnostic test for endometrial cancer. Using a custom 12-gene endometrial cancer panel, molecular analysis of uterine lavage fluid from an asymptomatic 67-yr-old female without histopathologic evidence of premalignant lesions or cancer in her uterine tissue revealed two oncogenic PTEN mutations. Ten months later, the patient returned with postmenopausal bleeding and a single microscopic focus of endometrial cancer. DNA isolated and sequenced from laser-capture microdissected tumor tissue revealed the same two PTEN mutations. These mutations were unlikely to occur by chance alone (P < 3 × 10 −7 ). This illustrative case provides the first demonstration that future, tumor-specific mutations can be identified in an asymptomatic individual without clinical or pathologic evidence of cancer by using already established sequencing technologies but targeted sampling methods. This finding provides the basis for new opportunities in early cancer screening, detection, and prevention.
AB - Endometrial cancer is the most common gynecologic malignancy in industrialized countries, and both its incidence and its associated mortality are increasing. The “liquid biopsy” is becoming an important transformative precision oncology tool, but barriers intrinsic to blood sampling have limited its use in early cancer detection. We hypothesized that using a more targeted sample for analysis-namely, a uterine lavage-should provide a more sensitive and specific diagnostic test for endometrial cancer. Using a custom 12-gene endometrial cancer panel, molecular analysis of uterine lavage fluid from an asymptomatic 67-yr-old female without histopathologic evidence of premalignant lesions or cancer in her uterine tissue revealed two oncogenic PTEN mutations. Ten months later, the patient returned with postmenopausal bleeding and a single microscopic focus of endometrial cancer. DNA isolated and sequenced from laser-capture microdissected tumor tissue revealed the same two PTEN mutations. These mutations were unlikely to occur by chance alone (P < 3 × 10 −7 ). This illustrative case provides the first demonstration that future, tumor-specific mutations can be identified in an asymptomatic individual without clinical or pathologic evidence of cancer by using already established sequencing technologies but targeted sampling methods. This finding provides the basis for new opportunities in early cancer screening, detection, and prevention.
UR - http://www.scopus.com/inward/record.url?scp=85058741331&partnerID=8YFLogxK
U2 - 10.1101/mcs.a003269
DO - 10.1101/mcs.a003269
M3 - Article
C2 - 30301868
AN - SCOPUS:85058741331
SN - 2373-2873
VL - 4
JO - Cold Spring Harbor molecular case studies
JF - Cold Spring Harbor molecular case studies
IS - 6
M1 - a003269
ER -