Non-invasive detection of urothelial cancer through the analysis of driver gene mutations and aneuploidy - PubMed (original) (raw)
doi: 10.7554/eLife.32143.
Chung-Hsin Chen # 3, Maria Del Carmen Rodriguez Pena # 4 5, Lu Li 6, Christopher Douville 7, Yuxuan Wang 1 2, Joshua David Cohen 1 2, Diana Taheri 4 8, Natalie Silliman 1 2, Joy Schaefer 1 2, Janine Ptak 1 2, Lisa Dobbyn 1 2, Maria Papoli 1 2, Isaac Kinde 1 2, Bahman Afsari 9 10, Aline C Tregnago 4, Stephania M Bezerra 11, Christopher VandenBussche 4, Kazutoshi Fujita 12, Dilek Ertoy 13, Isabela W Cunha 11, Lijia Yu 5, Trinity J Bivalacqua 14, Arthur P Grollman 15 16, Luis A Diaz 17, Rachel Karchin 7 9, Ludmila Danilova 10 13, Chao-Yuan Huang 3, Chia-Tung Shun 18, Robert J Turesky 19 20, Byeong Hwa Yun 19 20, Thomas A Rosenquist 15, Yeong-Shiau Pu 3, Ralph H Hruban 4, Cristian Tomasetti 6 10, Nickolas Papadopoulos 1 2, Ken W Kinzler 1 2, Bert Vogelstein 1 2, Kathleen G Dickman 15 16, George J Netto 4 5
Affiliations
- PMID: 29557778
- PMCID: PMC5860864
- DOI: 10.7554/eLife.32143
Non-invasive detection of urothelial cancer through the analysis of driver gene mutations and aneuploidy
Simeon U Springer et al. Elife. 2018.
Erratum in
- Correction: Non-invasive detection of urothelial cancer through the analysis of driver gene mutations and aneuploidy.
Springer SU, Chen CH, Rodriguez Pena MDC, Li L, Douville C, Wang Y, Cohen JD, Taheri D, Silliman N, Schaefer J, Ptak J, Dobbyn L, Papoli M, Kinde I, Afsari B, Tregnago AC, Bezerra SM, VandenBussche C, Fujita K, Ertoy D, Cunha IW, Yu L, Bivalacqua TJ, Grollman AP, Diaz LA, Karchin R, Danilova L, Huang CY, Shun CT, Turesky RJ, Yun BH, Rosenquist TA, Pu YS, Hruban RH, Tomasetti C, Papadopoulos N, Kinzler KW, Vogelstein B, Dickman KG, Netto GJ. Springer SU, et al. Elife. 2018 Nov 12;7:e43237. doi: 10.7554/eLife.43237. Elife. 2018. PMID: 30418154 Free PMC article.
Abstract
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.
Keywords: bladder; cancer; cancer biology; chromosomes; genes; human; liquid biopsy; renal pelvis; ureter; urine.
© 2018, Springer et al.
Conflict of interest statement
SS, CC, MR, LL, CD, YW, JC, DT, NS, JS, JP, LD, MP, IK, BA, AT, SB, CV, KF, DE, IC, LY, TB, AG, LD, RK, LD, CH, CS, RT, BY, TR, YP, RH, CT, KD, GN No competing interests declared, NP Founder of Personal Genome Diagnostics and PapGene and advises Sysmex-Inostics. These companies and others have licensed technologies from Johns Hopkins, of which BV, KK, and NP are inventors on a patent (U.S. 20140227705 A1) and receive royalties. The terms of these arrangements are managed by the university in accordance with its conflict of interest policies. Luis A Diaz: Member of the board of directors of Personal Genome Diagnostics (PGDx) and Jounce Therapeutics. LAD holds equity in PapGene, Personal Genome Diagnostics (PGDx) and Phoremost. He is a paid consultant for Merck, PGDx and Phoremost. LAD is an inventor of licensed intellectual property related to technology for ctDNA analyses and mismatch repair deficiency for diagnosis and therapy from Johns Hopkins University. These licenses and relationships are associated with equity or royalty payments to LAD. The terms of all these arrangements are being managed by Johns Hopkins and Memorial Sloan Kettering in accordance with their conflict of interest policies. In addition, in the past 5 years, LAD has participated as a paid consultant for one-time engagements with Caris, Lyndra, Genocea Biosciences, Illumina and Cell Design Labs. KK Ken W Kinzler: Founder of Personal Genome Diagnostics and PapGene and advises Sysmex-Inostics. These companies and others have licensed technologies from Johns Hopkins, of which BV, KK, and NP are inventors on a patent (U.S. 20140227705 A1) and receive royalties. The terms of these arrangements are managed by the university in accordance with its conflict of interest policies. BV Bert Vogelstein: Founder of Personal Genome Diagnostics and PapGene and advises Sysmex-Inostics. These companies and others have licensed technologies from Johns Hopkins, of which BV, KK, and NP are inventors on a patent (U.S. 20140227705 A1) and receive royalties. The terms of these arrangements are managed by the university in accordance with its conflict of interest policies.
Figures
Figure 1.. Schematic of the approach used to evaluate urinary cells in this study.
UroSEEK assay is designed to detect urothelial neoplasms that are in direct contact with urine (A) of variable pathologic stages originating in upper urinary tract (B) or bladder (C).
Figure 2.. Flow diagram indicating the number of patients in the three cohorts evaluated in this study and summarizing the salient findings.
Cytology was performed on only a subset of the patients (see main text).
Figure 3.. Fraction of mutations found in the ten-gene panel in 231 urinary cell samples assessed in the BC early detection cohort, 56 urinary cell samples assessed in the UTUC cohort, and 132 urinary cell samples assessed in the BC surveillance cohort.
Figure 4.. Venn diagram showing the distribution of positive results for each of the three UroSEEK assays for the (A) BC early detection (B) UTUC and (C) BC surveillance cohorts.
URO = Ten gene panel, TERT = TERT promoter region, ANEU = Aneuploidy test.
Figure 5.. Bar graphs of the lead time between a positive UroSEEK test and the detection of disease at the clinical level in the (A) BC early detection and (B) BC surveillance cohorts.
Figure 6.. Bar graphs representing the performance of Cytology vs. UroSEEK in diagnosis of low- and high-grade urothelial neoplasms in the early detection and surveillance BC cohorts and the UTUC cohort.
References
- Allory Y, Beukers W, Sagrera A, Flández M, Marqués M, Márquez M, van der Keur KA, Dyrskjot L, Lurkin I, Vermeij M, Carrato A, Lloreta J, Lorente JA, Carrillo-de Santa Pau E, Masius RG, Kogevinas M, Steyerberg EW, van Tilborg AA, Abas C, Orntoft TF, Zuiverloon TC, Malats N, Zwarthoff EC, Real FX. Telomerase reverse transcriptase promoter mutations in bladder cancer: high frequency across stages, detection in urine, and lack of association with outcome. European Urology. 2014;65:360–366. doi: 10.1016/j.eururo.2013.08.052. - DOI - PubMed
- Bettegowda C, Sausen M, Leary RJ, Kinde I, Wang Y, Agrawal N, Bartlett BR, Wang H, Luber B, Alani RM, Antonarakis ES, Azad NS, Bardelli A, Brem H, Cameron JL, Lee CC, Fecher LA, Gallia GL, Gibbs P, Le D, Giuntoli RL, Goggins M, Hogarty MD, Holdhoff M, Hong SM, Jiao Y, Juhl HH, Kim JJ, Siravegna G, Laheru DA, Lauricella C, Lim M, Lipson EJ, Marie SK, Netto GJ, Oliner KS, Olivi A, Olsson L, Riggins GJ, Sartore-Bianchi A, Schmidt K, Shih lM, Oba-Shinjo SM, Siena S, Theodorescu D, Tie J, Harkins TT, Veronese S, Wang TL, Weingart JD, Wolfgang CL, Wood LD, Xing D, Hruban RH, Wu J, Allen PJ, Schmidt CM, Choti MA, Velculescu VE, Kinzler KW, Vogelstein B, Papadopoulos N, Diaz LA. Detection of circulating tumor DNA in early- and late-stage human malignancies. Science Translational Medicine. 2014;6:224ra24. doi: 10.1126/scitranslmed.3007094. - DOI - PMC - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- T32 GM007309/GM/NIGMS NIH HHS/United States
- P30 CA077598/CA/NCI NIH HHS/United States
- P30 CA006973/CA/NCI NIH HHS/United States
- P30 CA008748/CA/NCI NIH HHS/United States
- R01 ES019564/ES/NIEHS NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical