Non-Invasive Detection Of Urothelial Cancer Through The Analysis Of Driver Gene Mutations And Aneuploidy
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Tarih
2018Yazar
Springer, Simeon U.
Chen, Chung-Hsin
Pena, Maria Del Carmen Rodriguez
Li, Lu
Douville, Christopher
Wang, Yuxuan
Cohen, Joshua David
Taheri, Diana
Silliman, Natalie
Schaefer, Joy
Ptak, Janine
Dobbyn, Lisa
Papoli, Maria
Kinde, Isaac
Afsari, Bahman
Tregnago, Aline C.
Bezerra, Stephania M.
VandenBussche, Christopher
Fujita, Kazutoshi
Ertoy, Dilek
Cunha, Isabela W.
Yu, Lijia
Bivalacqua, Trinity J.
Grollman, Arthur P.
Diaz, Luis A.
Karchin, Rachel
Danilova, Ludmila
Huang, Chao-Yuan
Shun, Chia-Tung
Turesky, Robert J.
Yun, Byeong Hwa
Rosenquist, Thomas A.
Pu, Yeong-Shiau
Hruban, Ralph H.
Tomasetti, Cristian
Papadopoulos, Nickolas
Kinzler, Ken W.
Vogelstein, Bert
Dickman, Kathleen G.
Netto, George J.
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Current non-invasive approaches for detection of urothelial cancers are suboptimal. We developed a test to detect urothelial neoplasms using DNA recovered from cells shed into urine. UroSEEK incorporates massive parallel sequencing assays for mutations in 11 genes and copy number changes on 39 chromosome arms. In 570 patients at risk for bladder cancer ( BC), UroSEEK was positive in 83% of those who developed BC. Combined with cytology, UroSEEK detected 95% of patients who developed BC. Of 56 patients with upper tract urothelial cancer, 75% tested positive by UroSEEK, including 79% of those with non-invasive tumors. UroSEEK detected genetic abnormalities in 68% of urines obtained from BC patients under surveillance who demonstrated clinical evidence of recurrence. The advantages of UroSEEK over cytology were evident in low-grade BCs; UroSEEK detected 67% of cases whereas cytology detected none. These results establish the foundation for a new non-invasive approach for detection of urothelial cancer.