Davidoff Cancer Center, Rabin Medical Center, Petah Tikva; Faculty of Medicine, Tel Aviv University, Tel Aviv.
Oncology Department, Lin Medical Center, Haifa; Rappaport Faculty of Medicine, Technion Israeli Institute of Technology, Haifa.
ESMO Open. 2024 Aug;9(8):103648. doi: 10.1016/j.esmoop.2024.103648. Epub 2024 Aug 12.
The 12-gene Oncotype DX Colon Recurrence Score® result quantifies the recurrence risk in stage II/III colon cancer (CC). This real-world study investigated stage II CC patients whose treatment decisions incorporated the Recurrence Score® (RS) result.
This retrospective analysis of a prospectively designed cohort included all stage II, mismatch repair-proficient CC patients who underwent 12-gene testing through Clalit between January 2011 and December 2016 and had available data with a minimum 3-year follow-up.
The analysis included 938 patients {median age 68 [interquartile range (IQR) 60-76] years; 96% T3 tumors}. The median RS was 26 (IQR 19-33) and the three RS categories (0-29, 30-40, 41-100) included 65%, 24%, and 11% of patients, respectively. Chemotherapy (CT) use differed significantly between the three RS categories (14%, 36%, and 60%, respectively; P < 0.001). The CT and observation-only groups were imbalanced with worse clinicopathologic characteristics in the former. Among observation-only patients, Kaplan-Meier (KM) estimates for recurrence-free interval (RFI) and CC-specific survival (CCSS) differed significantly between the three RS categories (P < 0.001). Clinical outcomes by treatment (CT versus observation) within each RS category revealed no differences in RFI and CCSS in the RS 0-29 and 30-40 categories. In contrast, in the RS 41-100 category, the difference in RFI trended toward significance (P = 0.066), and for CCSS, a statistically significant difference was observed, with better outcomes among CT-treated patients (P = 0.035).
RS results are prognostic in stage II CC. Among RS 41-100 patients, outcomes were better in CT-treated versus observation-only patients despite worse clinicopathologic characteristics, suggesting that CT confers clinical benefit in high-risk patients.
12 基因 Oncotype DX 结肠癌复发评分®结果定量评估 II 期/III 期结肠癌(CC)的复发风险。本真实世界研究调查了纳入复发评分®(RS)结果的 II 期 CC 患者的治疗决策。
这是一项前瞻性设计队列的回顾性分析,纳入了 2011 年 1 月至 2016 年 12 月期间通过 Clalit 进行 12 基因检测且至少有 3 年随访数据的所有 II 期、错配修复功能正常的 CC 患者。
分析纳入了 938 例患者(中位年龄 68 [四分位距(IQR)60-76] 岁;96% T3 肿瘤)。中位 RS 为 26(IQR 19-33),三个 RS 类别(0-29、30-40、41-100)分别包含 65%、24%和 11%的患者。三个 RS 类别之间的化疗(CT)使用率差异显著(分别为 14%、36%和 60%;P < 0.001)。CT 组和观察组之间的临床病理特征不平衡,前者更差。在观察组中,三个 RS 类别之间的无复发生存率(RFI)和结肠癌特异性生存率(CCSS)的 Kaplan-Meier(KM)估计值差异显著(P < 0.001)。在每个 RS 类别内按治疗(CT 与观察组)进行的临床结果显示,RS 0-29 和 30-40 类别之间的 RFI 和 CCSS 无差异。相比之下,在 RS 41-100 类别中,RFI 的差异有统计学意义(P = 0.066),CCSS 也存在统计学差异,CT 治疗患者的结果更好(P = 0.035)。
RS 结果在 II 期 CC 中具有预后意义。在 RS 41-100 患者中,尽管临床病理特征较差,但 CT 治疗与观察组相比,RFI 结果更好,提示 CT 为高危患者带来临床获益。