| Literature DB >> 27384348 |
Jeanne Tie1, Yuxuan Wang2, Cristian Tomasetti3, Lu Li4, Simeon Springer2, Isaac Kinde5, Natalie Silliman2, Mark Tacey6, Hui-Li Wong7, Michael Christie8, Suzanne Kosmider9, Iain Skinner9, Rachel Wong10, Malcolm Steel11, Ben Tran12, Jayesh Desai7, Ian Jones13, Andrew Haydon14, Theresa Hayes15, Tim J Price16, Robert L Strausberg17, Luis A Diaz2, Nickolas Papadopoulos2, Kenneth W Kinzler2, Bert Vogelstein18, Peter Gibbs19.
Abstract
Detection of circulating tumor DNA (ctDNA) after resection of stage II colon cancer may identify patients at the highest risk of recurrence and help inform adjuvant treatment decisions. We used massively parallel sequencing-based assays to evaluate the ability of ctDNA to detect minimal residual disease in 1046 plasma samples from a prospective cohort of 230 patients with resected stage II colon cancer. In patients not treated with adjuvant chemotherapy, ctDNA was detected postoperatively in 14 of 178 (7.9%) patients, 11 (79%) of whom had recurred at a median follow-up of 27 months; recurrence occurred in only 16 (9.8 %) of 164 patients with negative ctDNA [hazard ratio (HR), 18; 95% confidence interval (CI), 7.9 to 40; P < 0.001]. In patients treated with chemotherapy, the presence of ctDNA after completion of chemotherapy was also associated with an inferior recurrence-free survival (HR, 11; 95% CI, 1.8 to 68; P = 0.001). ctDNA detection after stage II colon cancer resection provides direct evidence of residual disease and identifies patients at very high risk of recurrence.Entities:
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Year: 2016 PMID: 27384348 PMCID: PMC5346159 DOI: 10.1126/scitranslmed.aaf6219
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956