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Posttreatment prostate specific antigen nadir predicts prostate cancer specific and all cause mortality

机译:治疗后前列腺特异性抗原最低点预示着前列腺癌特异性,所有原因均导致死亡

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Purpose: We investigated whether the prostate specific antigen nadir predicts prostate cancer specific and all cause mortality in men treated in a randomized trial of radiation with or without 6 months of androgen deprivation therapy. Materials and Methods: The study included 204 men with cT1b-T2bN0M0 prostate adenocarcinoma and at least 1 unfavorable factor, including prostate specific antigen less than 10 to 40 ng/ml, Gleason 7 or greater, or T3 on magnetic resonance imaging. We performed Fine and Gray regression, and Cox multivariable analysis to determine whether an increasing prostate specific antigen nadir was associated with prostate cancer specific and all cause mortality, adjusting for treatment, age, Adult Comorbidity Evaluation 27 score and cancer prognostic factors. Results: At a 6.9-year median followup median prostate specific antigen nadir was 0.7 ng/ml for radiation alone and 0.1 ng/ml for radiation plus androgen deprivation therapy. The prostate specific antigen nadir (adjusted HR 1.18g/ml increase, 95% CI 1.07-1.31, p = 0.001) and Gleason 8 or greater (adjusted HR 8.05, 95% CI 1.01-64.05, p = 0.049) significantly predicted increased prostate cancer specific mortality. Moderate/severe comorbidity carried a decreased risk (adjusted HR 0.13, 95% CI 0.02-0.96, p = 0.045). Higher prostate specific antigen nadir (adjusted HR 1.10g/ml increase, 95% CI 1.04-1.17), older age (adjusted HR 1.10/year, 95% CI 1.04-1.15) and interaction between comorbidity score and randomization arm (each p <0.001) increased the all cause mortality risk. Men who achieved a prostate specific antigen nadir of the median value or less had lower estimated prostate cancer specific and all cause mortality at 7 years (3.7% vs 18.3%, p = 0.0005 and 31.5% vs 55.0%, p = 0.002). Conclusions: Posttreatment prostate specific antigen nadir is significantly associated with the risk of prostate cancer specific and all cause mortality after radiation with or without androgen deprivation therapy. A suboptimal prostate specific antigen nadir may identify candidates for earlier intervention to prolong survival.
机译:目的:我们调查了在接受或不接受6个月雄激素剥夺治疗的放射线随机试验中,前列腺特异性抗原最低点是否预示着前列腺癌特异性和所有原因均导致了死亡率。材料和方法:该研究包括204名患有cT1b-T2bN0M0前列腺腺癌和至少1种不利因素的男性,包括前列腺特异性抗原低于10至40 ng / ml,格里森7或更高或磁共振成像中的T3。我们进行了Fine和Gray回归分析,以及Cox多变量分析,以确定增加的前列腺特异性抗原最低点是否与前列腺癌特异性和所有原因相关,并根据治疗,年龄,成人合并症评估27得分和癌症预后因素进行调整。结果:在6.9年的中位随访中,仅放疗的前列腺特异性抗原最低点为0.7 ng / ml,放疗加雄激素剥夺疗法的中位前列腺特异性抗原最低点为0.1 ng / ml。前列腺特异性抗原最低点(调整后的HR 1.18 / ng / ml,95%CI 1.07-1.31,p = 0.001)和Gleason 8或更高水平(调整后的HR 8.05,95%CI 1.01-64.05,p = 0.049)显着预计会增加前列腺癌的特定死亡率。中度/重度合并症降低了风险(校正后的HR 0.13,95%CI 0.02-0.96,p = 0.045)。较高的前列腺特异性抗原最低点(调整后的HR 1.10 / ng / ml,95%CI 1.04-1.17),老年(调整后的HR 1.10 / year,95%CI 1.04-1.15)以及合并症评分与随机分组之间的相互作用(每个p <0.001)增加了所有原因导致的死亡风险。达到前列腺特异性抗原最低值或中位数以下的男性的前列腺癌特异性估计值较低,并且所有人均导致7岁的死亡率(3.7%比18.3%,p = 0.0005和31.5%vs 55.0%,p = 0.002)。结论:治疗后前列腺特异性抗原最低点与特异性前列腺癌的风险显着相关,并且在有或没有雄激素剥夺治疗的情况下,所有这些因素都会导致放射后死亡。次佳的前列腺特异性抗原最低值可能会识别出较早干预以延长生存期的候选药物。

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