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ctDNA-based molecular residual disease and survival in resectable colorectal cancer

  • Yoshiaki Nakamura,
  • Jun Watanabe,
  • Naoya Akazawa,
  • Keiji Hirata,
  • Kozo Kataoka,
  • Mitsuru Yokota,
  • Kentaro Kato,
  • Masahito Kotaka,
  • Yoshinori Kagawa,
  • Kun-Huei Yeh,
  • Saori Mishima,
  • Hiroki Yukami,
  • Koji Ando,
  • Masaaki Miyo,
  • Toshihiro Misumi,
  • Kentaro Yamazaki,
  • Hiromichi Ebi,
  • Kenji Okita,
  • Atsushi Hamabe,
  • Hiroki Sokuoka,
  • Satoshi Kobayashi,
  • George Laliotis,
  • Vasily N. Aushev,
  • Shruti Sharma,
  • Adham Jurdi,
  • Minetta C. Liu,
  • Alexey Aleshin,
  • Matthew Rabinowitz,
  • Hideaki Bando,
  • Hiroya Taniguchi,
  • Ichiro Takemasa,
  • Takeshi Kato,
  • Daisuke Kotani,
  • Masaki Mori,
  • Takayuki Yoshino,
  • Eiji Oki

摘要

The interim analysis of the CIRCULATE-Japan GALAXY observational study demonstrated the association of circulating tumor DNA (ctDNA)-based molecular residual disease (MRD) detection with recurrence risk and benefit from adjuvant chemotherapy (ACT) in resectable colorectal cancer (CRC). This updated analysis with a 23-month median follow-up, including 2,240 patients with stage II–III colon cancer or stage IV CRC, reinforces the prognostic value of ctDNA positivity during the MRD window with significantly inferior disease-free survival (DFS; hazard ratio (HR): 11.99, P < 0.0001) and overall survival (OS; HR: 9.68, P < 0.0001). In patients who experienced recurrence, ctDNA positivity correlated with shorter OS (HR: 2.71, P < 0.0001). The significantly shorter DFS in MRD-positive patients was consistent across actionable biomarker subsets. Sustained ctDNA clearance in response to ACT was an indicator of favorable DFS and OS compared to transient clearance (24-month DFS: 89.0% versus 3.3%; 24-month OS: 100.0% versus 82.3%). True spontaneous clearance rate with no clinical recurrence was 1.9% (2/105). Overall, our findings provide evidence for the utility of ctDNA monitoring for post-resection recurrence and mortality risk stratification that could be used for guiding adjuvant therapy.