Graff Julie N, Mori Motomi, Li Hong, Garzotto Mark, Penson David, Potosky Arnold L, Beer Tomasz M
Division of Hematology and Medical Oncology, Oregon Health and Science University, Portland, Oregon 97239, USA.
J Urol. 2007 Apr;177(4):1307-12. doi: 10.1016/j.juro.2006.11.054.
Primary androgen suppression therapy for clinically localized prostate cancer is increasingly common in the United States despite a lack of supportive evidence for its use. We determined which demographic and clinical factors predict overall and cancer specific survival with this treatment strategy in patients enrolled in the Prostate Cancer Outcomes Study.
In 1994 to 1995 the Prostate Cancer Outcomes Study recruited 3,533 men diagnosed with prostate cancer. Clinical and treatment information was abstracted from medical records and demographic characteristics were obtained from patient surveys 6, 12, 24 and 60 months after diagnosis. Overall and cancer specific mortality was analyzed through December 2002 using the Kaplan-Meier method and Cox regression.
A total of 276 patients had organ confined (cT1-2) prostatic adenocarcinoma and received primary androgen suppression therapy within 1 year of diagnosis. Median followup for censored patients was 7.6 years (range 1.1 to 8.1). Five-year overall and cancer specific survival was 66% (95% CI 59-72) and 91% (95% CI 86-94), respectively. Independent predictors of shorter overall survival were patient age 75 years or older, prostate specific antigen 20 ng/ml or greater, Gleason score 7 or greater and abnormal digital rectal examination. Gleason score 7 or greater, prostate specific antigen 20 ng/ml or greater and a low comorbidity index were independent predictors of shorter cancer specific survival.
The use of primary androgen suppression therapy in the Prostate Cancer Outcomes Study data set resulted in 91% 5-year cancer specific survival. Advanced age, and factors that reflect tumor burden and biology were predictive of overall survival, while cancer specific survival was predicted by tumor factors and the burden of comorbid conditions. A nomogram for predicting overall survival at 5 years was constructed.
在美国,针对临床局限性前列腺癌的初始雄激素抑制治疗越来越普遍,尽管缺乏支持其使用的证据。我们在参与前列腺癌结局研究的患者中,确定了哪些人口统计学和临床因素可预测采用这种治疗策略时的总生存和癌症特异性生存情况。
1994年至1995年,前列腺癌结局研究招募了3533名被诊断为前列腺癌的男性。临床和治疗信息从病历中提取,人口统计学特征通过在诊断后6、12、24和60个月的患者调查获得。使用Kaplan-Meier法和Cox回归分析至2002年12月的总死亡率和癌症特异性死亡率。
共有276例患者患有器官局限性(cT1-2)前列腺腺癌,并在诊断后1年内接受了初始雄激素抑制治疗。截尾患者的中位随访时间为7.6年(范围1.1至8.1年)。5年总生存率和癌症特异性生存率分别为66%(95%CI 59-72)和91%(95%CI 86-94)。总生存时间较短的独立预测因素为年龄75岁或以上、前列腺特异性抗原20 ng/ml或更高、Gleason评分7或更高以及直肠指检异常。Gleason评分7或更高、前列腺特异性抗原20 ng/ml或更高以及低合并症指数是癌症特异性生存时间较短的独立预测因素。
在前列腺癌结局研究数据集中使用初始雄激素抑制治疗,5年癌症特异性生存率为91%。高龄以及反映肿瘤负荷和生物学特性的因素可预测总生存,而癌症特异性生存则由肿瘤因素和合并症负担预测。构建了一个预测5年总生存的列线图。