Multi-institutional analysis of long-term outcome for stages T1-T2 prostate cancer treated with permanent seed implantation

被引:367
作者
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.
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, New York, NY 10021 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX 77030 USA
[3] Arizona Oncol Serv, Scottsdale, AZ USA
[4] New York Prostate Inst, Oceanside, NY USA
[5] Seattle Prostate Inst, Seattle, WA USA
[6] Chicago Prostate Canc Ctr, Chicago, IL USA
[7] Cleveland Clin Fdn, Dept Radiat Oncol, Cleveland, OH 44195 USA
[8] Massachusetts Gen Hosp, Dept Radiat Oncol, Boston, MA 02114 USA
[9] Mayo Clin & Mayo Fdn, Dept Radiat Oncol, Rochester, MN 55905 USA
[10] Univ Michigan, Sch Med, Dept Radiat Oncol, Ann Arbor, MI 48109 USA
[11] Fox Chase Canc Ctr, Dept Radiat Oncol, Philadelphia, PA 19111 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2007年 / 67卷 / 02期
关键词
brachytherapy; prostate cancer; prostate-specific antigen; isotope; dose;
D O I
10.1016/j.ijrobp.2006.08.056
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To assess long-term prostate-specific antigen (PSA) outcome after permanent prostate brachytherapy (BT) and identify predictors of improved disease-free survival. Methods and Materials: 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 >= 5 years before data submission, BT between 1988-1998, and no androgen deprivation before failure. The median follow-up was 63 months. Results: Among patients where the I-125 dose to 90% of the prostate (D90) was >= 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. Conclusions: Outcome after permanent BT for prostatic cancer relates to tumor stage, Gleason score, pretreatment PSA, BT year, and post-BT dosimetric quality. PSA nadir <= 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. (c) 2007 Elsevier Inc.
引用
收藏
页码:327 / 333
页数:7
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