Division of Hematology and Oncology, Department of Medicine, Massachusetts General Hospital Cancer Center and Harvard Medical School, Boston, Massachusetts.
University of California, San Francisco, Helen Diller Family Comprehensive Cancer Center (HDFCCC), San Francisco, California.
Clin Cancer Res. 2024 Jul 15;30(14):2964-2973. doi: 10.1158/1078-0432.CCR-23-3660.
Minimal residual disease (MRD) detection can identify the recurrence in patients with colorectal cancer (CRC) following definitive treatment. We evaluated a plasma-only MRD assay to predict recurrence and survival in patients with metastatic CRC who underwent curative intent procedures (surgery and/or radiotherapy), with or without (neo)adjuvant chemotherapy. The primary objective of this study was to assess the correlation of postprocedure tumor cell-free DNA detection status with radiographic disease recurrence.
Preprocedure and postprocedure longitudinal samples were collected from 53 patients and analyzed with a multiomic MRD assay detecting circulating tumor DNA (ctDNA) from genomic and epigenomic signals. Preprocedure and postprocedure ctDNA detection correlated with recurrence-free and overall survival (OS).
From 52 patients, 230/233 samples were successfully analyzed. At the time of data cutoff, 36 (69.2%) patients recurred with median follow-up of 31 months. Detectable ctDNA was observed in 19/42 patients (45.2%) with ctDNA analyzed 3 weeks postprocedure. ctDNA detection 3 weeks postprocedure was associated with shorter median recurrence-free survival (RFS; HR, 5.27; 95% CI, 2.31-12.0; P < 0.0001) and OS (HR, 12.83; 95% CI, 3.6-45.9; P < 0.0001). Preprocedure ctDNA detection status was not associated with RFS but was associated with improved OS (HR, 4.65; 95% CI, 1.4-15.2; P = 0.0111). Undetectable ctDNA preprocedure had notable long-term OS, >90% 3 years postprocedure.
In this cohort of oligometastatic CRC, detection of ctDNA preprocedure or postprocedure was associated with inferior outcomes even after accounting for known prognostic clinicopathologic variables. This suggests ctDNA may enhance current risk stratification methods helping the evaluation of novel treatments and surveillance strategies toward improving patient outcomes.
微小残留病灶 (MRD) 检测可在接受根治性治疗的结直肠癌 (CRC) 患者中确定复发。我们评估了一种仅检测血浆的 MRD 检测方法,以预测接受根治性治疗(手术和/或放疗)的转移性 CRC 患者的复发和生存情况,这些患者接受或未接受(新)辅助化疗。本研究的主要目的是评估术后肿瘤游离 DNA 检测状态与影像学疾病复发的相关性。
从 53 名患者中采集了术前和术后的纵向样本,并使用一种多组学 MRD 检测方法分析,该方法检测来自基因组和表观基因组信号的循环肿瘤 DNA (ctDNA)。术前和术后 ctDNA 检测与无复发生存 (RFS) 和总生存 (OS) 相关。
在 52 名患者中,成功分析了 230/233 份样本。在数据截止时,36 名 (69.2%) 患者出现复发,中位随访时间为 31 个月。在 42 名有 ctDNA 分析的患者中,有 19 名 (45.2%) 在术后 3 周时可检测到 ctDNA。术后 3 周时可检测到 ctDNA 与较短的中位 RFS (HR,5.27;95%CI,2.31-12.0;P<0.0001) 和 OS (HR,12.83;95%CI,3.6-45.9;P<0.0001) 相关。术前 ctDNA 检测状态与 RFS 无关,但与改善的 OS 相关 (HR,4.65;95%CI,1.4-15.2;P=0.0111)。术前不可检测到 ctDNA 的患者具有显著的长期 OS,术后 3 年的 OS 率>90%。
在这组寡转移性 CRC 患者中,即使考虑到已知的预后临床病理变量,术前或术后 ctDNA 的检测与不良结局相关。这表明 ctDNA 可能增强当前的风险分层方法,有助于评估新的治疗方法和监测策略,以改善患者的预后。