| Literature DB >> 29563323 |
Yuxuan Wang1, Lu Li2, Christopher Douville1, Joshua D Cohen1,3, Ting-Tai Yen4, Isaac Kinde5, Karin Sundfelt6, Susanne K Kjær7,8, Ralph H Hruban9, Ie-Ming Shih9, Tian-Li Wang9, Robert J Kurman9, Simeon Springer1, Janine Ptak1, Maria Popoli1, Joy Schaefer1, Natalie Silliman1, Lisa Dobbyn1, Edward J Tanner4, Ana Angarita4, Maria Lycke6, Kirsten Jochumsen10, Bahman Afsari2, Ludmila Danilova2, Douglas A Levine11, Kris Jardon12, Xing Zeng12, Jocelyne Arseneau12, Lili Fu12, Luis A Diaz1, Rachel Karchin13, Cristian Tomasetti14, Kenneth W Kinzler15, Bert Vogelstein15,16, Amanda N Fader17, Lucy Gilbert18, Nickolas Papadopoulos15.
Abstract
We report the detection of endometrial and ovarian cancers based on genetic analyses of DNA recovered from the fluids obtained during a routine Papanicolaou (Pap) test. The new test, called PapSEEK, incorporates assays for mutations in 18 genes as well as an assay for aneuploidy. In Pap brush samples from 382 endometrial cancer patients, 81% [95% confidence interval (CI), 77 to 85%] were positive, including 78% of patients with early-stage disease. The sensitivity in 245 ovarian cancer patients was 33% (95% CI, 27 to 39%), including 34% of patients with early-stage disease. In contrast, only 1.4% of 714 women without cancer had positive Pap brush samples (specificity, ~99%). Next, we showed that intrauterine sampling with a Tao brush increased the detection of malignancy over endocervical sampling with a Pap brush: 93% of 123 (95% CI, 87 to 97%) patients with endometrial cancer and 45% of 51 (95% CI, 31 to 60%) patients with ovarian cancer were positive, whereas none of the samples from 125 women without cancer were positive (specificity, 100%). Finally, in 83 ovarian cancer patients in whom plasma was available, circulating tumor DNA was found in 43% of patients (95% CI, 33 to 55%). When plasma and Pap brush samples were both tested, the sensitivity for ovarian cancer increased to 63% (95% CI, 51 to 73%). These results demonstrate the potential of mutation-based diagnostics to detect gynecologic cancers at a stage when they are more likely to be curable.Entities:
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Year: 2018 PMID: 29563323 PMCID: PMC6320220 DOI: 10.1126/scitranslmed.aap8793
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956