Division of Hematology and Oncology, Department of Medicine, University of Virginia, Charlottesville, VA, USA.
J Natl Cancer Inst. 2012 Feb 8;104(3):211-27. doi: 10.1093/jnci/djr524. Epub 2012 Jan 20.
The addition of oxaliplatin to adjuvant 5-fluorouracil (5-FU) improves survival of patients with stage III colon cancer in randomized clinical trials (RCTs). However, RCT participants are younger, healthier, and less racially diverse than the general cancer population. Thus, the benefit of oxaliplatin outside RCTs is uncertain.
Patients younger than 75 years with stage III colon cancer who received chemotherapy within 120 days of surgical resection were identified from five observational data sources-the Surveillance, Epidemiology, and End Results registry linked to Medicare claims (SEER-Medicare), the New York State Cancer Registry (NYSCR) linked to Medicaid and Medicare claims, the National Comprehensive Cancer Network (NCCN) Outcomes Database, and the Cancer Care Outcomes Research & Surveillance Consortium (CanCORS). Overall survival (OS) was compared among patients treated with oxaliplatin vs non-oxaliplatin-containing adjuvant chemotherapy. Overall survival for 4060 patients diagnosed during 2004-2009 was compared with pooled data from five RCTs (the Adjuvant Colon Cancer ENdpoinTs [ACCENT] group, n = 8292). Datasets were juxtaposed but not combined using Kaplan-Meier curves. Covariate and propensity score adjusted proportional hazards models were used to calculate adjusted survival hazard ratios (HR). Stratified analyses examined effect modifiers. All statistical tests were two-sided.
The survival advantage associated with the addition of oxaliplatin to adjuvant 5-FU was evident across diverse practice settings (3-year OS: RCTs, 86% [n = 1273]; SEER-Medicare, 80% [n = 1152]; CanCORS, 88% [n = 129]; NYSCR-Medicaid, 82% [n = 54]; NYSCR-Medicare, 79% [n = 180]; and NCCN, 86% [n = 438]). A statistically significant improvement in 3-year overall survival was seen in the largest cohort, SEER-Medicare, and in the NYSCR-Medicare cohort (non-oxaliplatin-containing vs oxaliplatin-containing adjuvant therapy, adjusted HR of death: pooled RCTs: HR = 0.80, 95% CI = 0.70 to 0.92, P = .002; SEER-Medicare: HR = 0.70, 95% CI = 0.60 to 0.82, P < .001; NYSCR-Medicare patients aged ≥65 years: HR = 0.58, 95% CI = 0.38 to 0.90, P = .02). The association between oxaliplatin treatment and better survival was maintained in older and minority group patients, as well as those with higher comorbidity.
The addition of oxaliplatin to 5-FU appears to be associated with better survival among patients receiving adjuvant colon cancer treatment in the community.
在随机临床试验(RCT)中,奥沙利铂联合辅助 5-氟尿嘧啶(5-FU)可改善 III 期结肠癌患者的生存。然而,RCT 参与者比一般癌症人群更年轻、更健康、种族多样性更小。因此,奥沙利铂在 RCT 之外的获益尚不确定。
从五个观察性数据来源中确定了年龄小于 75 岁且在手术切除后 120 天内接受化疗的 III 期结肠癌患者:监测、流行病学和最终结果(SEER)注册数据库与医疗保险索赔相关联(SEER-医疗保险)、纽约州癌症登记处(NYSCR)与医疗补助和医疗保险索赔相关联、国家综合癌症网络(NCCN)结果数据库和癌症护理结果研究和监测联盟(CanCORS)。比较接受奥沙利铂治疗与不含奥沙利铂的辅助化疗的患者的总生存期(OS)。比较了 2004-2009 年诊断的 4060 例患者的总生存期与来自五个 RCT 的汇总数据(辅助结肠癌终点[ACCENT]组,n=8292)。使用 Kaplan-Meier 曲线对数据集进行并列但不合并。使用协变量和倾向评分调整的比例风险模型计算调整后的生存风险比(HR)。分层分析检查了效应修饰剂。所有统计检验均为双侧。
在不同的实践环境中,添加奥沙利铂到辅助 5-FU 中与生存优势相关(3 年 OS:RCT,86%[n=1273];SEER-医疗保险,80%[n=1152];CanCORS,88%[n=129];NYSCR-医疗补助,82%[n=54];NYSCR-医疗保险,79%[n=180];NCCN,86%[n=438])。在最大的队列 SEER-医疗保险和 NYSCR-医疗保险队列中,观察到 3 年总生存的显著改善(非奥沙利铂组与奥沙利铂组的辅助治疗,调整死亡风险的 HR:汇总 RCT:HR=0.80,95%CI=0.70 至 0.92,P=0.002;SEER-医疗保险:HR=0.70,95%CI=0.60 至 0.82,P<.001;年龄≥65 岁的 NYSCR-医疗保险患者:HR=0.58,95%CI=0.38 至 0.90,P=0.02)。在年龄较大和少数民族患者以及合并症较高的患者中,奥沙利铂治疗与更好的生存之间的关联仍然存在。
在社区接受辅助结肠癌治疗的患者中,添加奥沙利铂到 5-FU 似乎与更好的生存相关。