基于 ctDNA 的分子残留疾病与可切除结直肠癌的生存。

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

机构信息

Department of Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Translational Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan.

出版信息

Nat Med. 2024 Nov;30(11):3272-3283. doi: 10.1038/s41591-024-03254-6. Epub 2024 Sep 16.

Abstract

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.

摘要

CIRCULATE-Japan GALAXY 观察性研究的中期分析表明,循环肿瘤 DNA(ctDNA)基于分子残留疾病(MRD)检测与可切除结直肠癌(CRC)的复发风险和辅助化疗(ACT)获益相关。这项更新的分析中位随访时间为 23 个月,包括 2240 例 II-III 期结肠癌或 IV 期 CRC 患者,该分析强化了 ctDNA 阳性在 MRD 窗口期的预后价值,无病生存期(DFS;风险比(HR):11.99,P<0.0001)和总生存期(OS;HR:9.68,P<0.0001)显著降低。在发生复发的患者中,ctDNA 阳性与较短的 OS 相关(HR:2.71,P<0.0001)。MRD 阳性患者的 DFS 明显缩短在具有可操作生物标志物亚组中一致。与短暂清除相比,ACT 后持续的 ctDNA 清除是 DFS 和 OS 良好的指标(24 个月 DFS:89.0%比 3.3%;24 个月 OS:100.0%比 82.3%)。无临床复发的真正自发性清除率为 1.9%(2/105)。总之,我们的研究结果为 ctDNA 监测在术后复发和死亡率分层中的效用提供了证据,这可能用于指导辅助治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57ee/11564113/d6648c649be0/41591_2024_3254_Fig1_HTML.jpg

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