Tong L, Ahn C, Symanski E, Lai D, Du X L
Division of Epidemiology, Human Genetics, and Environmental Sciences, University of Texas School of Public Health, Houston Department of Clinical Sciences.
Department of Clinical Sciences Harold C. Simmons Cancer Center, UT Southwestern Medical Center, Dallas.
Ann Oncol. 2014 Jun;25(6):1234-42. doi: 10.1093/annonc/mdu131. Epub 2014 Mar 27.
Abundant evidences have shown that newly developed chemotherapy regimens improved 5-year survival rate of colorectal cancer (CRC) patients over the past two decades. However, their impact on risk of death from leading causes among elderly patients is still poorly understood.
A retrospective cohort study of 69 718 elderly CRC patients with their first primary tumors in 1992-2009, identified from the 12 areas of Surveillance, Epidemiology, and End Results-Medicare linked database with their Medicare claims up to 2010. Multivariate Cox regression models were used to assess the effect of newly developed chemotherapy regimens, comorbidities, and chemotherapy related toxicities on cause-specific death and their temporal patterns among elderly CRC patients.
The leading causes of death among CRC patients were CRC, circulation disorders, and secondary cancers, which accounted for 51.4%, 25%, and 4.6% of all-cause death, respectively. Patients diagnosed in more recent diagnostic time periods were significantly less likely to die of CRC [period 2: 5-year hazard ratio = 0.94, 95% confidence interval (CI) 0.90-0.97; period 3: 0.86, 0.83-0.90], circulation disorders (period 2: 0.94, 0.88-1.00; period 3: 0.80, 0.75-0.87), and more likely to die of secondary cancer (period 3: 1.42, 1.20-1.68) compared with those diagnosed in period 1. Charlson comorbidities index and the selected pre-existing comorbidities were significantly associated with increased 5-year risk of death from all three leading causes. Both hematological and gastric toxicity were associated with reduced risk of death from CRC and circulation disorders. The association between diagnostic time period and risk reduction in death from CRC depended on chemotherapy treatment (P < 0.0001). Subgroup analyses showed that the chemotherapy-dependent significant risk reduction was seen in patients with stage II-III CRC, patients without comorbidities, and patients without toxicities (P < 0.0001 for all).
The newly developed chemotherapy regimens were associated with the decreased risk of mortality from CRC.
大量证据表明,在过去二十年中,新研发的化疗方案提高了结直肠癌(CRC)患者的5年生存率。然而,它们对老年患者主要死因死亡风险的影响仍知之甚少。
一项回顾性队列研究,纳入了1992 - 2009年首次诊断为原发性肿瘤的69718例老年CRC患者,这些患者来自监测、流行病学和最终结果 - 医疗保险关联数据库的12个地区,并拥有截至2010年的医疗保险理赔记录。采用多变量Cox回归模型评估新研发的化疗方案、合并症以及化疗相关毒性对老年CRC患者特定病因死亡及其时间模式的影响。
CRC患者的主要死因是CRC、循环系统疾病和继发性癌症,分别占全因死亡的51.4%、25%和4.6%。与第1阶段诊断的患者相比,在更近诊断时间段诊断的患者死于CRC的可能性显著降低[第2阶段:5年风险比 = 0.94,95%置信区间(CI)0.90 - 0.97;第3阶段:0.86,0.83 - 0.90],死于循环系统疾病的可能性也降低(第2阶段:0.94,0.88 - 1.00;第3阶段:0.80,0.75 - 0.87),而死于继发性癌症的可能性增加(第3阶段:1.42,1.20 - 1.68)。Charlson合并症指数和选定的既往合并症与所有三种主要死因的5年死亡风险增加显著相关。血液学毒性和胃部毒性均与CRC和循环系统疾病死亡风险降低相关。诊断时间段与CRC死亡风险降低之间的关联取决于化疗治疗(P < 0.0001)。亚组分析表明,在II - III期CRC患者、无合并症患者和无毒副作用患者中观察到了化疗依赖性的显著风险降低(所有P < 0.0001)。
新研发的化疗方案与CRC死亡率降低相关。