National Surgical Adjuvant Breast and Bowel Project, Pittsburgh, PA, USA.
Ann Surg Oncol. 2010 Apr;17(4):959-66. doi: 10.1245/s10434-009-0881-y.
The objective of this study is to conduct a pooled analysis of National Surgical Adjuvant Breast and Bowel Project (NSABP) colon trials involving surgery and surgery plus 5-fluorouracil and leucovorin (5-FU/LV) to compare survival and establish a baseline from which to evaluate future studies.
All patients enrolled in NSABP adjuvant trials C-01 through C-05 with stage II and III disease who were treated with surgery or with surgery plus 5-FU/LV were examined for overall survival (OS), disease-free survival (DFS), and recurrence-free interval (RFI). Time-to-event by treatment group was examined using adjusted Kaplan-Meier estimates and multivariable Cox regression analysis.
There were 2,966 eligible patients: 693 (23%) surgery and 2,273 (77%) surgery plus 5-FU/LV; 1,255 (42%) stage II and 1,711 (58%) stage III. Age > or =60 years [hazard ratio (HR) = 1.36, P < 0.0001], male gender (HR = 1.20, P = 0.0012), and more nodes positive or fewer nodes examined (P < 0.0001) were associated with worse survival. At 5 years, the adjusted OS was 0.62 [confidence interval (CI) = 0.60-0.63] in the surgery group and 0.76 (CI = 0.74-0.78) in the surgery plus 5-FU/LV group. Treatment with 5-FU/LV was associated with improved outcome compared with surgery: OS (HR = 0.62, P < 0.0001), DFS (HR = 0.66, P < 0.0001) and RFI (HR = 0.64, P < 0.0001). Improved OS with adjuvant treatment was seen in both stage II (HR = 0.58, 95% CI = 0.48-0.71) and stage III disease (HR = 0.65, 95% CI = 0.55-0.75).
This analysis demonstrates that treatment of colon cancer patients with 5-FU/LV following surgery provides benefit over surgery alone and can provide anticipated survival outcomes with which to compare modern adjuvant trials.
本研究旨在对美国国家癌症研究所外科辅助乳腺和肠道项目(NSABP)的结肠试验进行汇总分析,这些试验涉及手术以及手术加氟尿嘧啶和亚叶酸(5-FU/LV)治疗,旨在比较生存情况并建立一个基准,以便评估未来的研究。
所有入组 NSABP 辅助试验 C-01 至 C-05、患有 II 期和 III 期疾病且接受手术或手术加 5-FU/LV 治疗的患者,均对总生存(OS)、无病生存(DFS)和无复发生存(RFI)进行了检查。采用调整后的 Kaplan-Meier 估计值和多变量 Cox 回归分析,对治疗组的时间至事件进行了检查。
共有 2966 例符合条件的患者:693 例(23%)接受手术治疗,2273 例(77%)接受手术加 5-FU/LV 治疗;1255 例(42%)为 II 期,1711 例(58%)为 III 期。年龄≥60 岁[风险比(HR)=1.36,P<0.0001]、男性(HR=1.20,P=0.0012)和更多淋巴结阳性或更少淋巴结检查(P<0.0001)与生存情况较差相关。5 年时,手术组调整后的 OS 为 0.62(置信区间[CI]为 0.60-0.63),手术加 5-FU/LV 组为 0.76(CI=0.74-0.78)。与手术相比,5-FU/LV 治疗与改善结局相关:OS(HR=0.62,P<0.0001)、DFS(HR=0.66,P<0.0001)和 RFI(HR=0.64,P<0.0001)。辅助治疗可改善 II 期(HR=0.58,95%CI=0.48-0.71)和 III 期疾病(HR=0.65,95%CI=0.55-0.75)患者的 OS。
本分析表明,结直肠癌患者手术后接受 5-FU/LV 治疗优于单独手术,并且可以提供预期的生存结果,以便与现代辅助试验进行比较。