Frontiers in Oncology (Nov 2022)

Postoperative circulating tumor DNA detection is associated with the risk of recurrence in patients resected for a stage II colorectal cancer

  • Adrien Grancher,
  • Ludivine Beaussire,
  • Ludivine Beaussire,
  • Sylvain Manfredi,
  • Karine Le Malicot,
  • Marie Dutherage,
  • Vincent Verdier,
  • Claire Mulot,
  • Olivier Bouché,
  • Jean-Marc Phelip,
  • Charles-Briac Levaché,
  • Philippe Deguiral,
  • Sophie Coutant,
  • David Sefrioui,
  • Jean-François Emile,
  • Pierre Laurent-Puig,
  • Frédéric Bibeau,
  • Pierre Michel,
  • Nasrin Sarafan-Vasseur,
  • Côme Lepage,
  • Frederic Di Fiore,
  • Frederic Di Fiore

DOI
https://doi.org/10.3389/fonc.2022.973167
Journal volume & issue
Vol. 12

Abstract

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Circulating tumor DNA (ctDNA) is reported to be promising in localized colorectal cancer (CRC). The present study aimed to retrospectively evaluate the impact of ctDNA in patients with a resected stage II CRC from the PROGIGE 13 trial with available paired tumor and blood samples. A group of recurrent patients were matched one-to-one with nonrecurrent patients according to sex, tumor location, treatment sequence, and blood collection timing. CtDNA was analyzed by digital PCR according to NGS of tumors. Disease-free survival (DFS) and overall survival (OS) were analyzed based on ctDNA, and the risks of recurrence and death were determined. A total of 134 patients were included, with 67 patients in each group. At least one alteration was identified in 115/134 tumors. Postoperative ctDNA was detected in 10/111 (9.0%) informative samples and was detected more frequently in the recurrent group (16.7% versus 1.8%; p = 0.02). The median DFS of ctDNA+ versus ctDNA- patients was 16.8 versus 54 months (p = 0.002), respectively, and the median OS was 51.3 versus 69.5 months (p = 0.03), respectively. CtDNA was associated with recurrence (ORa = 11.13, p = 0.03) and death (HRa = 3.15, p = 0.01). In conclusion, the presence of postoperative ctDNA is associated with both recurrence and survival in stage II CRC.

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