Zelefsky Michael J, Kuban Deborah A, Levy Larry B, Potters Louis, Beyer David C, Blasko John C, Moran Brian J, Ciezki Jay P, Zietman Anthony L, Pisansky Thomas M, Elshaikh Mohamed, Horwitz Eric M
Department of Radiation Oncology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Int J Radiat Oncol Biol Phys. 2007 Feb 1;67(2):327-33. doi: 10.1016/j.ijrobp.2006.08.056. Epub 2006 Nov 2.
To assess long-term prostate-specific antigen (PSA) outcome after permanent prostate brachytherapy (BT) and identify predictors of improved disease-free survival.
Eleven institutions combined data on 2,693 patients treated with permanent interstitial BT monotherapy for T1-T2 prostate cancer. Of these patients, 1,831 (68%) were treated with I-125 (median dose, 144 Gy) and 862 (32%) were treated with Pd-103 (median dose, 130 Gy). Criteria for inclusion were: available pre-BT PSA, BT > or =5 years before data submission, BT between 1988-1998, and no androgen deprivation before failure. The median follow-up was 63 months.
Among patients where the I-125 dose to 90% of the prostate (D90) was > or =130 Gy, the 8-year PSA relapse-free survival (PRFS) was 93% compared with 76% for those with lower D90 dose levels (p < 0.001). A multivariable analysis identified tumor stage (p = 0.002), Gleason score (p < 0.001), pretreatment PSA level (p < 0.001), treatment year (p = 0.001), and the isotope used (p = 0.004) as pretreatment and treatment variables associated with PRFS. When restricted to patients with available postimplantation dosimetric information, D90 emerged as a significant predictor of biochemical outcome (p = 0.01), and isotope was not significant. The 8-year PRFS was 92%, 86%, 79%, and 67%, respectively, for patients with PSA nadir values of 0-0.49, 0.5-0.99, 1.0-1.99, and >2.0 ng/mL (p < 0.001). Among patients free of biochemical relapse at 8 years, the median nadir level was 0.1 ng/mL, and 90% of these patients achieved a nadir PSA level <0.6 ng/mL.
Outcome after permanent BT for prostatic cancer relates to tumor stage, Gleason score, pretreatment PSA, BT year, and post-BT dosimetric quality. PSA nadir < or =0.5 ng/mL was particularly associated with durable long-term PSA disease-free survival. The only controllable factor to impact on long-term outcome was the D90 which is a reflection of implant quality.
评估永久性前列腺近距离放射治疗(BT)后的长期前列腺特异性抗原(PSA)结果,并确定无病生存改善的预测因素。
11家机构汇总了2693例接受永久性间质BT单药治疗T1-T2期前列腺癌患者的数据。其中,1831例(68%)接受I-125治疗(中位剂量144Gy),862例(32%)接受Pd-103治疗(中位剂量130Gy)。纳入标准为:有BT前可用的PSA,在提交数据前BT≥5年,BT时间在1988-1998年之间,且在疾病进展前未接受雄激素剥夺治疗。中位随访时间为63个月。
在前列腺90%体积接受的I-125剂量(D90)≥130Gy的患者中,8年PSA无复发生存率(PRFS)为93%,而D90剂量水平较低的患者为76%(p<0.001)。多变量分析确定肿瘤分期(p=0.002)、Gleason评分(p<0.001)、治疗前PSA水平(p<0.001)、治疗年份(p=0.001)以及所用同位素(p=0.004)为与PRFS相关的治疗前和治疗变量。当仅限于有植入后剂量测定信息的患者时,D90成为生化结果的显著预测因素(p=0.01),而同位素不显著。PSA最低点值为0-0.49、0.5-0.99、1.0-1.99和>2.0ng/mL的患者8年PRFS分别为92%、86%、79%和67%(p<0.001)。在8年时无生化复发的患者中,最低点水平的中位数为0.1ng/mL,其中90%的患者最低点PSA水平<0.6ng/mL。
前列腺癌永久性BT后的结果与肿瘤分期、Gleason评分、治疗前PSA、BT年份以及BT后剂量测定质量有关。PSA最低点≤0.5ng/mL尤其与持久的长期PSA无病生存相关。影响长期结果的唯一可控因素是D90,它反映了植入质量。