Department of Radiation Oncology, Alfred Health and Monash University, Melbourne, VIC, Australia.
Int J Radiat Oncol Biol Phys. 2011 Jan 1;79(1):179-87. doi: 10.1016/j.ijrobp.2009.10.016. Epub 2010 Apr 6.
To report on prostate-specific antigen (PSA) "bounces" after (125)I prostate brachytherapy to review the relationship to biochemical control and correlate both clinical and dosimetric variables.
We analyzed 194 hormone-naive patients with a follow-up of ≥ 3 years. Four bounce definitions were applied: an increase of ≥ 0.2 ng/mL (definition I), ≥ 0.4 ng/mL (definition II), ≥ 15% (definition III), and ≥ 35% (definition IV) of a previous value with spontaneous return to the prebounce level or lower.
Using definition I, II, III, and IV, a bounce was detected in 50%, 34%, 11%, and 9% of patients, respectively. The median time to onset was 14-16 months, the duration was 12-21.5 months, and the magnitude of the increase was 0.5-2 ng/mL. A magnitude of >2 ng/mL, fulfilling the criteria for biochemical failure (BF) according to the American Society for Therapeutic Radiology and Oncology Phoenix definition, was detected in 11.3%, 16.9%, 47.6%, and 50% using definitions I, II, III, and IV, respectively; 11 patients (5.7%) had true BF. The PSA bounces occurred earlier than BF (p < 0.001). The prediction of BF remains controversial and is probably unrelated to biochemical control. The only statistically significant factor predictive of a PSA bounce was younger age (definitions I and II).
PSA bounces are common after brachytherapy. All definitions resulted in a high number of false-positive calls for BF during the first 2 years. The definition of an increase of ≥ 0.2 ng/mL should be preferred because of the lowest number of false-positive results for BF. Patients experiencing a PSA bounce during the first 2 years after brachytherapy should undergo surveillance every 3-6 months. Additional investigations are recommended for elevated postimplant PSA levels that have not corrected by 3 years of follow-up.
报告前列腺特异性抗原(PSA)在(125)I 前列腺近距离放射治疗后的“反弹”,以探讨其与生化控制的关系,并对临床和剂量学变量进行相关分析。
我们分析了 194 例激素初治、随访时间≥3 年的患者。采用了 4 种 PSA 反弹定义:较前值升高≥0.2ng/ml(定义 I)、≥0.4ng/ml(定义 II)、≥15%(定义 III)和≥35%(定义 IV),且自发降至反弹前水平或更低。
使用定义 I、II、III 和 IV,分别有 50%、34%、11%和 9%的患者出现反弹。中位反弹时间为 14-16 个月,持续时间为 12-21.5 个月,PSA 增加幅度为 0.5-2ng/ml。满足美国放射治疗肿瘤学会凤凰定义的生化失败(BF)标准的 PSA 反弹幅度>2ng/ml,分别在定义 I、II、III 和 IV 中占 11.3%、16.9%、47.6%和 50%;11 例(5.7%)患者发生了真正的 BF。PSA 反弹发生时间早于 BF(p<0.001)。BF 的预测仍存在争议,可能与生化控制无关。唯一具有统计学意义的 BF 预测因素是年龄较轻(定义 I 和 II)。
PSA 反弹在近距离放射治疗后很常见。所有定义在前 2 年都导致了大量 BF 的假阳性结果。由于对 BF 的假阳性结果数量最低,因此应首选 PSA 升高≥0.2ng/ml 的定义。近距离放射治疗后 2 年内出现 PSA 反弹的患者应每 3-6 个月进行一次随访。对于植入后 PSA 水平升高且随访 3 年仍未纠正的患者,建议进行额外的检查。