TY - JOUR
T1 - Circulating Tumor DNA Analysis Guiding Adjuvant Therapy in Stage II Colon Cancer
AU - for the DYNAMIC Investigators
AU - Tie, Jeanne
AU - Cohen, Joshua D.
AU - Lahouel, Kamel
AU - Lo, Serigne N.
AU - Wang, Yuxuan
AU - Kosmider, Suzanne
AU - Wong, Rachel
AU - Shapiro, Jeremy
AU - Lee, Margaret
AU - Harris, Sam
AU - Khattak, Adnan
AU - Burge, Matthew
AU - Harris, Marion
AU - Lynam, James
AU - Nott, Louise
AU - Day, Fiona
AU - Hayes, Theresa
AU - McLachlan, Sue Anne
AU - Lee, Belinda
AU - Ptak, Janine
AU - Silliman, Natalie
AU - Dobbyn, Lisa
AU - Popoli, Maria
AU - Hruban, Ralph
AU - Lennon, Anne Marie
AU - Papadopoulos, Nicholas
AU - Kinzler, Kenneth W.
AU - Vogelstein, Bert
AU - Tomasetti, Cristian
AU - Gibbs, Peter
N1 - Publisher Copyright:
Copyright © 2022 Massachusetts Medical Society.
PY - 2022/6/16
Y1 - 2022/6/16
N2 - BACKGROUND The role of adjuvant chemotherapy in stage II colon cancer continues to be debated. The presence of circulating tumor DNA (ctDNA) after surgery predicts very poor recurrence-free survival, whereas its absence predicts a low risk of recurrence. The benefit of adjuvant chemotherapy for ctDNA-positive patients is not well understood. METHODS We conducted a trial to assess whether a ctDNA-guided approach could reduce the use of adjuvant chemotherapy without compromising recurrence risk. Patients with stage II colon cancer were randomly assigned in a 2:1 ratio to have treatment decisions guided by either ctDNA results or standard clinicopathological features. For ctDNA-guided management, a ctDNA-positive result at 4 or 7 weeks after surgery prompted oxaliplatin-based or fluoropyrimidine chemotherapy. Patients who were ctDNA-negative were not treated. The primary efficacy end point was recurrence-free survival at 2 years. A key secondary end point was adjuvant chemotherapy use. RESULTS Of the 455 patients who underwent randomization, 302 were assigned to ctDNA-guided management and 153 to standard management. The median follow-up was 37 months. A lower percentage of patients in the ctDNA-guided group than in the standard-management group received adjuvant chemotherapy (15% vs. 28%; relative risk, 1.82; 95% confidence interval [CI], 1.25 to 2.65). In the evaluation of 2-year recurrence-free survival, ctDNA-guided management was noninferior to standard management (93.5% and 92.4%, respectively; absolute difference, 1.1 percentage points; 95% CI, −4.1 to 6.2 [noninferiority margin, −8.5 percentage points]). Three-year recurrence-free survival was 86.4% among ctDNA-positive patients who received adjuvant chemotherapy and 92.5% among ctDNA-negative patients who did not. CONCLUSIONS A ctDNA-guided approach to the treatment of stage II colon cancer reduced adjuvant chemotherapy use without compromising recurrence-free survival.
AB - BACKGROUND The role of adjuvant chemotherapy in stage II colon cancer continues to be debated. The presence of circulating tumor DNA (ctDNA) after surgery predicts very poor recurrence-free survival, whereas its absence predicts a low risk of recurrence. The benefit of adjuvant chemotherapy for ctDNA-positive patients is not well understood. METHODS We conducted a trial to assess whether a ctDNA-guided approach could reduce the use of adjuvant chemotherapy without compromising recurrence risk. Patients with stage II colon cancer were randomly assigned in a 2:1 ratio to have treatment decisions guided by either ctDNA results or standard clinicopathological features. For ctDNA-guided management, a ctDNA-positive result at 4 or 7 weeks after surgery prompted oxaliplatin-based or fluoropyrimidine chemotherapy. Patients who were ctDNA-negative were not treated. The primary efficacy end point was recurrence-free survival at 2 years. A key secondary end point was adjuvant chemotherapy use. RESULTS Of the 455 patients who underwent randomization, 302 were assigned to ctDNA-guided management and 153 to standard management. The median follow-up was 37 months. A lower percentage of patients in the ctDNA-guided group than in the standard-management group received adjuvant chemotherapy (15% vs. 28%; relative risk, 1.82; 95% confidence interval [CI], 1.25 to 2.65). In the evaluation of 2-year recurrence-free survival, ctDNA-guided management was noninferior to standard management (93.5% and 92.4%, respectively; absolute difference, 1.1 percentage points; 95% CI, −4.1 to 6.2 [noninferiority margin, −8.5 percentage points]). Three-year recurrence-free survival was 86.4% among ctDNA-positive patients who received adjuvant chemotherapy and 92.5% among ctDNA-negative patients who did not. CONCLUSIONS A ctDNA-guided approach to the treatment of stage II colon cancer reduced adjuvant chemotherapy use without compromising recurrence-free survival.
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U2 - 10.1056/NEJMoa2200075
DO - 10.1056/NEJMoa2200075
M3 - Article
C2 - 35657320
AN - SCOPUS:85132197310
SN - 0028-4793
VL - 386
SP - 2261
EP - 2272
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 24
ER -