Circulating tumor DNA analysis detects minimal residual disease and predicts recurrence in patients with stage II colon cancer

Jeanne Tie(The University of Melbourne), Yuxuan Wang(Howard Hughes Medical Institute), Cristian Tomasetti(Johns Hopkins University), Lu Li(Johns Hopkins University), Simeon Springer(Howard Hughes Medical Institute), Isaac Kinde(PapGene (United States)), Natalie Silliman(Howard Hughes Medical Institute), Mark Tacey(The University of Melbourne), Hui‐Li Wong(The University of Melbourne), Michael Christie(The Royal Melbourne Hospital), Suzanne Kosmider(Western Health), Iain Skinner(Western Health), Rachel Wong(Walter and Eliza Hall Institute of Medical Research), Malcolm Steel(Eastern Health), Ben Tran(The University of Melbourne), Jayesh Desai(The University of Melbourne), Ian T. Jones(The Royal Melbourne Hospital), Andrew Haydon(The Alfred Hospital), Theresa Hayes(St John of God Hospital), Timothy Price(Queen Elizabeth Hospital), Robert L. Strausberg(Ludwig Cancer Research), Luis A. Díaz(Howard Hughes Medical Institute), Nickolas Papadopoulos(Howard Hughes Medical Institute), Kenneth W. Kinzler(Howard Hughes Medical Institute), Bert Vogelstein(Howard Hughes Medical Institute), Peter Gibbs(The University of Melbourne)
Science Translational Medicine
July 6, 2016
Cited by 1,461Open Access
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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.


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