Paskett Electra, Herndon James, Donohue Kathleen, Naughton Michelle, Grubbs Stephen, Pavy Michael, Hensley Martee, Stark Nancy, Kornblith Alice, Bittoni Marisa
College of Public Health and Comprehensive Cancer Center, The Ohio State University Comprehensive Cancer Center, 320 West 10th Avenue, Starling Loving Hall A356, Columbus, OH 43210-1240, USA.
Cancer. 2009 Mar 1;115(5):1109-20. doi: 10.1002/cncr.24140.
The Survivor's Health and Reaction (SHARE) study examined health-related quality of life (HRQL) in breast cancer patients who had participated in Cancer and Leukemia Group B Trial 8541 from 1985 to 1991.
In total, 245 survivors (78% of eligible patients) who were 9.4 to 16.5 years postdiagnosis (mean, 12.5 years postdiagnosis) completed HRQL surveys relating to 5 domains. Analyses examined HRQL domains according to 3 different chemotherapy dose levels that were administered in the original treatment trial: low-dose cyclophosphamide, doxorubicin, and fluorouracil (CAF) at 300 mg/m(2), 30 mg/m(2), and 300 x 2 mg/m(2), respectively, over 4 cycles; standard-dose CAF at 400 mg/m(2), 40 mg/m(2), and 400 x 2 mg/m(2), respectively, over 6 cycles; and high-dose CAF at 600 mg/m(2), 60 mg/m(2) and 600 x 2 mg/m(2), respectively, over 4 cycles.
In univariate analyses, a statistically significant difference was observed on the Medical Outcomes Study 36-item short form Physical Role Functioning subscale by treatment group, with lower mean scores in the standard treatment arm (mean, 65.05) compared with mean scores in the low-dose arm (mean, 74.66) and the high-dose arm (mean, 84.94; P.0001). However, multivariate analysis revealed that treatment arm no longer was statistically significant, whereas the following factors were associated with decreased physical role functioning: age >or=60 years (odds ratio [OR], 3.55; P = .006), increased comorbidity interference total score (OR, 1.64; P = .005), lower vitality (OR, 1.05; P = .0002), and increased menopausal symptoms (OR, 1.04 P = .02).
At 9.4-16.5 years after their original diagnosis, differences in physical role functioning among breast cancer survivors who had received 3 different dose levels of chemotherapy were explained by clinical and demographic variables, such as age, fatigue, menopausal symptoms, and comorbidities. Prospective studies are needed to further assess the role of these factors in explaining HRQL and physical role functioning among long-term survivors.
幸存者健康与反应(SHARE)研究调查了1985年至1991年参加癌症与白血病B组试验8541的乳腺癌患者的健康相关生活质量(HRQL)。
共有245名幸存者(占符合条件患者的78%)在确诊后9.4至16.5年(平均确诊后12.5年)完成了与5个领域相关的HRQL调查。分析根据原治疗试验中给予的3种不同化疗剂量水平检查HRQL领域:低剂量环磷酰胺、阿霉素和氟尿嘧啶(CAF),分别在4个周期内为300mg/m²、30mg/m²和300×2mg/m²;标准剂量CAF,分别在6个周期内为400mg/m²、40mg/m²和400×2mg/m²;高剂量CAF,分别在4个周期内为600mg/m²、60mg/m²和600×2mg/m²。
在单因素分析中,治疗组在医学结果研究36项简表身体角色功能子量表上观察到统计学上的显著差异,标准治疗组的平均得分(平均65.05)低于低剂量组(平均74.66)和高剂量组(平均84.94;P<0.0001)。然而,多因素分析显示治疗组不再具有统计学显著性,而以下因素与身体角色功能下降相关:年龄≥60岁(优势比[OR],3.55;P = 0.006)、合并症干扰总分增加(OR,1.64;P = 0.005)、活力较低(OR,1.05;P = 0.0002)和更年期症状增加(OR,1.04;P = 0.02)。
在最初诊断后的9.4至16.5年,接受3种不同剂量化疗的乳腺癌幸存者在身体角色功能方面的差异可由年龄、疲劳、更年期症状和合并症等临床和人口统计学变量来解释。需要进行前瞻性研究以进一步评估这些因素在解释长期幸存者的HRQL和身体角色功能方面的作用。