Department of Medical Oncology, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Saint-Antoine, Paris, France.
Sorbonne Université, Paris, France.
J Clin Oncol. 2020 May 20;38(15):1702-1710. doi: 10.1200/JCO.19.01960. Epub 2020 Mar 13.
A post hoc analysis of all pathologic reports from patients with stage III CC included in the IDEA France phase III study (ClinicalTrials.gov identifier: NCT00958737) investigating the duration of adjuvant fluorouracil, leucovorin, and oxaliplatin or capecitabine and oxaliplatin therapy (3 6 months) was performed. The primary objective was to determine the prognostic impact of TD on disease-free survival (DFS). The effect of the addition of TD to LNM count on pN restaging was also evaluated. A multivariable analysis was performed to establish the association between TD and DFS.
Of 1,942 patients, 184 (9.5%) had TDs. The pN1a/b and pN1c populations showed similar DFS. TD-positive patients had worse prognosis compared with TD-negative patients, with 3-year DFS rates of 65.6% (95% CI, 58.0% to 72.1%) and 74.7% (95% CI, 72.6% to 76.7%; = .0079), respectively. On multivariable analysis, TDs were associated with a higher risk of recurrence or death (hazard ratio [HR], 1.36; = .0201). Other adverse factors included pT4 and/or pN2 disease (HR, 2.21; < .001), the 3 months of adjuvant treatment (HR, 1.29; = .0029), tumor obstruction (HR, 1.28; = .0233), and male sex (HR, 1.24; = .0151). Patients restaged as having pN2 disease (n = 35, 2.3%) had similar DFS as patients initially classified as pN2.
The presence of TDs is an independent prognostic factor for DFS in patients with stage III CC. The addition of TD to LNM may help to better define the duration of adjuvant therapy.
对 IDEA France 期 3 研究中包含的所有 III 期结肠癌患者的病理报告进行了事后分析(ClinicalTrials.gov 标识符:NCT00958737),该研究调查了氟尿嘧啶、亚叶酸钙和奥沙利铂或卡培他滨和奥沙利铂辅助治疗(3 6 个月)的持续时间。主要目的是确定 TD 对无病生存(DFS)的预后影响。还评估了 TD 对 LNM 计数的附加作用对 pN 分期的影响。进行了多变量分析以确定 TD 与 DFS 之间的关联。
在 1942 名患者中,有 184 名(9.5%)患者有 TDs。pN1a/b 和 pN1c 人群的 DFS 相似。TD 阳性患者的预后比 TD 阴性患者差,3 年 DFS 率分别为 65.6%(95%CI,58.0%至 72.1%)和 74.7%(95%CI,72.6%至 76.7%; =.0079)。多变量分析显示,TDs 与复发或死亡的风险增加相关(风险比[HR],1.36; =.0201)。其他不利因素包括 pT4 和/或 pN2 疾病(HR,2.21; <.001)、辅助治疗 3 个月(HR,1.29; =.0029)、肿瘤阻塞(HR,1.28; =.0233)和男性(HR,1.24; =.0151)。重新分期为 pN2 疾病的患者(n = 35,2.3%)与最初分类为 pN2 的患者的 DFS 相似。
TDs 的存在是 III 期结肠癌患者 DFS 的独立预后因素。TD 对 LNM 的附加作用可能有助于更好地定义辅助治疗的持续时间。