4.6 Article

Early dynamics of circulating tumor DNA predict chemotherapy responses for patients with esophageal cancer

Journal

CARCINOGENESIS
Volume 42, Issue 10, Pages 1239-1249

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/carcin/bgab088

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Funding

  1. Keiryokai Collaborative Research Grant [131, 136]
  2. KAKENHI [16H01578, 16K19951, 16K19952, 16H06279, 17K10605, 19K09224, 20K09064]
  3. Grants-in-Aid for Scientific Research [16K19951, 16H01578, 17K10605, 19K09224, 20K09064, 16K19952] Funding Source: KAKEN

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Early changes in circulating tumor DNA (ctDNA) following the first cycle of chemotherapy accurately predict later treatment responses in esophageal squamous cell cancer (ESCC) patients. The study shows that the dynamics of ctDNA can better predict total volume reductions and overall survival rates in ESCC patients.
We investigated whether early circulating tumor DNA (ctDNA) changes, measured using digital PCR (dPCR), can predict later chemotherapy responses in esophageal squamous cell cancer (ESCC). We compared the dynamics of ctDNA and tumor volumes during chemotherapy in 42 ESCC. The accuracy of predictions of later chemotherapy responses was evaluated by the ratio of the variant allele frequency of ctDNA (post-/pre-ctDNA) and the total tumor volume (post-/pre-volume) before and after an initial chemotherapy cycle using a receiver-operating characteristic curve analysis. Total positive and negative objective responses (ORs) were defined as either >50 or <= 50% reductions, respectively, in the total tumor volume at the end of first-line chemotherapy. Mutation screening of 43 tumors from 42 patients revealed 96 mutations. The pretreatment dPCR-ctDNA data were informative in 38 patients, using 70 selected mutations (1-3 per patient). The areas under the curve (AUCs) for the post-/pre-volume and post-/pre-ctDNA levels used in predicting the total OR were 0.85 and 0.88, respectively. The optimal cutoff value of post-/pre-ctDNA was 0.13. In 20 patients with post-/pre-volume >= 50%, the total OR could be predicted by the post-/pre-ctDNA with high accuracy; the AUC by post-/pre-ctDNA was higher than that by post-/pre-volume (0.85 versus 0.76, respectively). Patients with low post-/pre-ctDNA (n = 18) had a significantly better overall survival rate than those with high post-/pre-ctDNA (n = 20; P = 0.03). Early ctDNA changes after an initial cycle of chemotherapy predict later responses to treatment with high accuracy in ESCC patients. .

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