首页> 外文期刊>The Journal of Urology >Comparing prostate specific antigen triggers for intervention in men with stable prostate cancer on active surveillance.
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Comparing prostate specific antigen triggers for intervention in men with stable prostate cancer on active surveillance.

机译:比较前列腺特异抗原引发剂对积极监测稳定前列腺癌的男性进行干预。

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PURPOSE: We determined the proportion of men with nonprogressive prostate cancer on active surveillance who had a trigger for treatment using various measures of prostate specific antigen kinetics. MATERIALS AND METHODS: A prospective phase II study of patients with favorable clinical parameters (stage T1b-T2b N0M0, Gleason sum 7 or less, prostate specific antigen 15 ng/ml or less) on active surveillance was initiated in 1995. Those patients considered at high risk for progression were offered radical intervention. The remaining patients were closely monitored and formed the cohort for this study. We calculated the proportion and frequency of patients who had a trigger for treatment based on the various prostate specific antigen triggers (prostate specific antigen doubling time, prostate specific antigen velocity, prostate specific antigen threshold). RESULTS: Of 450 patients followed on surveillance 305 remained on active surveillance without definitive intervention. None of these 305 patients have died of prostate cancer or have had symptomatic metastatic disease develop. Median followup was 6.8 years. The proportion of patients who would have had a trigger for treatment ranged from 14% to 42% for the threshold triggers, 37% to 50% for the prostate specific antigen doubling time triggers and 42% to 84% for the velocity triggers. CONCLUSIONS: Almost all of the prostate specific antigen triggers examined in this study would have led to high rates of trigger for treatment. More work is needed to identify a trigger that better strikes the balance between recommending treatment for patients at high risk for progression and minimizing treatment for those at low risk for progression.
机译:目的:我们确定了在积极监测下患有非进行性前列腺癌的男性比例,这些男性使用各种前列腺特异性抗原动力学指标来触发治疗。材料与方法:1995年开始对具有良好临床参数(T1b-T2b N0M0期,Gleason总和为7以下,前列腺特异性抗原为15 ng / ml以下)的患者进行前瞻性II期研究。进行干预的高风险者得到了治疗。其余患者受到密切监测,并组成了该研究的队列。我们根据各种前列腺特异性抗原触发因素(前列腺特异性抗原加倍时间,前列腺特异性抗原速度,前列腺特异性抗原阈值)计算出具有治疗触发因素的患者比例和发生频率。结果:在接受监测的450例患者中,有305例仍接受了主动监测,没有明确的干预措施。这305名患者均未死于前列腺癌或发生症状性转移性疾病。中位随访时间为6.8年。触发阈值的患者比例为14%至42%,前列腺特异性抗原加倍时间触发的患者比例为37%至50%,速度触发的患者比例为42%至84%。结论:在这项研究中检查的几乎所有前列腺特异性抗原触发物都会导致高触发率的治疗。需要做更多的工作来确定一个触发因素,以便更好地在为进展风险高的患者推荐治疗与最小化进展风险低的治疗之间取得平衡。

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