Sweat Susan D, Bergstralh Erik J, Slezak Jeffrey, Blute Michael L, Zincke Horst
Department of Urology and Section of Biostatistics, Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA.
J Urol. 2002 Aug;168(2):525-9.
Factors important for determining appropriate therapy for localized prostate cancer are biopsy tumor grade, patient age and co-morbidity. We estimated the probability of dying from prostate cancer or other competing causes stratified by age at diagnosis and clinical histological grade in men diagnosed with clinically nonmetastatic prostate cancer who were treated with radical prostatectomy.
A total of 751 men comprised a retrospective cohort with clinically nonmetastatic prostate cancer diagnosed and treated with bilateral pelvic lymphadenectomy and radical prostatectomy at our institution between 1971 and 1984. All patients were between 55 and 74 years old (median age 65) at diagnosis and they were followed a median of 14.7 years. The cumulative incidence of prostate cancer death or death from any cause was estimated using methods of competing risk survival analysis.
Overall 435 men died with 32% of the deaths attributable to prostate cancer. In 62%, 27% and 11% of patients the Charlson co-morbidity score was 0, 1 and 2+, respectively. The only significant predictor of death from prostate cancer was clinical Gleason score (p <0.001), while only age and Charlson co-morbidity score were significant independent predictors of death from other causes (p <0.001). The estimated cumulative incidence of prostate cancer death after considering competing risks increased with Gleason score regardless of patient age. In men with Gleason scores 2 to 4, 5, 6, 7 and 8 to 10 disease the cumulative incidence of prostate cancer death within 20 years was 6% to 7%, 10% to 13%, 15% to 19%, 29% to 35% and 36% to 43%, respectively, depending on age at diagnosis. Clinical stages T2 and T3 outcomes were indistinguishable.
This study shows that for any given Gleason score the prostate cancer death rate is similar in older and younger patients with few to no co-morbidities. Men with a score of 7 to 10 were at 29% to 43% risk of death from prostate cancer even when cancer was diagnosed as late as age 74 years and treated surgically.
对于确定局限性前列腺癌的合适治疗方法而言,重要因素包括活检肿瘤分级、患者年龄及合并症。我们评估了在接受根治性前列腺切除术治疗的临床非转移性前列腺癌男性患者中,按诊断时年龄和临床组织学分级分层的死于前列腺癌或其他竞争原因的概率。
共有751名男性构成一个回顾性队列,他们于1971年至1984年在我们机构被诊断为临床非转移性前列腺癌,并接受了双侧盆腔淋巴结清扫术和根治性前列腺切除术。所有患者诊断时年龄在55至74岁之间(中位年龄65岁),中位随访时间为14.7年。使用竞争风险生存分析方法估计前列腺癌死亡或任何原因死亡的累积发生率。
总体上435名男性死亡,其中32%的死亡归因于前列腺癌。Charlson合并症评分在62%、27%和11%的患者中分别为0、1和2+。前列腺癌死亡的唯一显著预测因素是临床Gleason评分(p<0.001),而仅年龄和Charlson合并症评分是其他原因死亡的显著独立预测因素(p<0.001)。考虑竞争风险后,前列腺癌死亡的估计累积发生率随Gleason评分增加,与患者年龄无关。在Gleason评分2至4、5、6、7以及8至10的疾病患者中,20年内前列腺癌死亡的累积发生率分别为6%至7%、10%至13%、15%至19%、29%至35%以及36%至43%,具体取决于诊断时的年龄。临床分期T2和T3的结果无差异。
本研究表明,对于任何给定的Gleason评分,合并症少或无合并症的老年和年轻患者的前列腺癌死亡率相似。Gleason评分为7至10的男性,即使在74岁时才诊断出癌症并接受手术治疗,死于前列腺癌的风险仍为29%至43%。