Kumar Ambuj, Soares Heloisa P, Balducci Lodovico, Djulbegovic Benjamin
H. Lee Moffitt Cancer Center and Research Institute at the University of South Florida, Tampa, FL 33612, USA.
J Clin Oncol. 2007 Apr 1;25(10):1272-6. doi: 10.1200/JCO.2006.09.2759.
Elderly patients share the majority of the disease burden in cancer. Although 61% of new cancer cases occur among elderly, they comprise only 25% of the patients enrolled onto randomized clinical trials (RCTs). A systematic review to assess the accurate participation of elderly patients in RCTs has not been performed.
We reviewed all consecutively completed phase III RCTs conducted by five National Cancer Institute-sponsored cooperative groups. Published papers and study protocols were used for data extraction. We used a cutoff age of 65 years to define elderly patients. For trials that did not exclusively enroll elderly, data were extracted on number of participants 65 years of age. Outcome between the innovative and the standard treatment was compared.
Of 345 studies, only one trial exclusively enrolled elderly patients (0.28%); 57% of the trials (n = 197) had no stratification by age, and 12% of the studies had a stratification age 65 years (n = 42). Overall survival in the trial exclusively enrolling elderly favored the newer treatments (hazard ratio [HR], 0.69; 95% CI, 0.47 to 1.02; P = .06). Additionally, in trials enrolling more than 40% of elderly, survival and event-free survival favored the innovative treatments (HR for survival, 0.91; 95% CI, 0.84 to 0.99; P = .03; HR for event-free survival, 0.85; 95% CI, 0.72 to 1.01; P = .07). Treatment-related mortality was similar in both the innovative and standard treatment groups (HR, 0.91; 95% CI, 0.47 to 1.78; P = .8).
Our data indicate that enrollment of elderly in experimental RCTs is not associated with increased harm to this patient population. Increased participation of elderly may help in finding new treatments that are clinically applicable specifically to this cohort of patients.
老年患者承担着癌症疾病负担的大部分。尽管61%的新发癌症病例发生在老年人中,但他们仅占参与随机临床试验(RCT)患者的25%。尚未进行系统评价来评估老年患者在RCT中的准确参与情况。
我们回顾了由五个美国国立癌症研究所赞助的合作组连续完成的所有III期RCT。已发表的论文和研究方案用于数据提取。我们使用65岁的年龄界限来定义老年患者。对于并非专门纳入老年患者的试验,提取65岁参与者的数量数据。比较创新治疗与标准治疗的结果。
在345项研究中,仅有一项试验专门纳入老年患者(0.28%);57%的试验(n = 197)未按年龄分层,12%的研究分层年龄为65岁(n = 42)。专门纳入老年患者的试验中的总生存期有利于新治疗(风险比[HR],0.69;95%可信区间[CI],0.47至1.02;P = 0.06)。此外,在纳入超过40%老年患者的试验中,生存期和无事件生存期有利于创新治疗(生存期HR,0.91;95%CI,0.84至0.99;P = 0.03;无事件生存期HR,0.85;95%CI,0.72至1.01;P = 0.07)。创新治疗组和标准治疗组的治疗相关死亡率相似(HR,0.91;95%CI,0.47至1.78;P = 0.8)。
我们的数据表明,老年患者参与实验性RCT与对该患者群体的伤害增加无关。增加老年患者的参与可能有助于找到专门适用于该患者群体的临床适用新治疗方法。