Role of Isotope Selection in Long-term Outcomes in Patients With Intermediate-risk Prostate Cancer Treated With a Combination of External Beam Radiotherapy and Low-dose-rate Interstitial Brachytherapy

被引:6
作者
Wernicke, A. Gabriella [1 ]
Shamis, Michael
Yan, Weisi
Trichter, Samuel
Sabbas, Albert M.
Goltser, Yevgenia
Christos, Paul J.
Brennan, Jennifer S.
Parashar, Bhupesh
Nori, Dattatreyudu
机构
[1] Weil Med Coll Cornell Univ, Dept Radiat Oncol, New York, NY 10065 USA
关键词
RELAPSE-FREE SURVIVAL; DISEASE-FREE SURVIVAL; RADIATION-THERAPY; CONFORMAL RADIOTHERAPY; SEATTLE EXPERIENCE; HORMONAL-THERAPY; CARCINOMA; IMPLANTATION; IRRADIATION; I-125;
D O I
10.1016/j.urology.2012.01.043
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE To examine the rates of long-term biochemical recurrence-free survival (BRFS) with respect to isotope in intermediate-risk prostate cancer treated with external beam radiotherapy (EBRT) and brachytherapy. METHODS A total of 242 consecutive patients with intermediate-risk prostate cancer were treated with iodine-125 (I-125) or palladium-103 (Pd-103) implants after EBRT (range 45.0-50.4 Gy) from 1996 to 2002. Of the 242 patients, 119 (49.2%) were treated with I-125 and 123 (50.8%) with Pd-103. Multivariate Cox regression analysis was used to analyze BRFS, defined according to the Phoenix definition (prostate-specific antigen nadir plus 2 ng/mL) with respect to Gleason score, stage, pretreatment prostate-specific antigen level, and source selection. Late genitourinary/gastrointestinal toxicities were assessed using the Radiation Therapy Oncology Group/European Organization for Research and Treatment of Cancer scale. RESULTS At a median follow-up of 10 years, the BRFS rate was 77.3%. A statistically significant difference was found in the 10-year BRFS rate between the I-125- and Pd-103-treated groups (82.7% and 70.6%, respectively; P = .001). The addition of hormonal therapy did not improve the 10-year BRFS rate (77.6%) compared with RT alone (77.1%; P = .22). However, a statistically significant difference in the BRFS rate was found with the addition of hormonal therapy to Pd-103, improving the 10-year BRFS rate for (73.8%) compared with Pd-103 alone (69.1%; P = .008). On multivariate analysis, isotope type (Pd-103 vs I-125), pretreatment prostate-specific antigen level > 10 ng/mL, and greater tumor stage increased the risk of recurrence by 2.6-fold (P = .007), 5.9-fold (P < .0001), and 1.7-fold (P = .14), respectively. CONCLUSION I-125 renders a superior rate of BRFS compared with Pd-103 when used with EBRT. Hormonal therapy does not provide additional benefit in patients with intermediate-risk prostate cancer treated with a combination of EBRT and brachytherapy, except for the addition of hormonal therapy to Pd-103. UROLOGY 79: 1098-1104, 2012. (C) 2012 Elsevier Inc.
引用
收藏
页码:1098 / 1104
页数:7
相关论文
共 31 条
[1]  
[Anonymous], CANC STAG MAN
[2]   10-year disease-free survival rates after simultaneous irradiation for prostate cancer with a focus on calculation methodology [J].
Critz, FA ;
Levinson, K .
JOURNAL OF UROLOGY, 2004, 172 (06) :2232-2238
[3]  
Critz FA, 1998, CANCER J SCI AM, V4, P359
[4]   Pd-103 brachytherapy and external beam irradiation for clinically localized, high-risk prostatic carcinoma [J].
Dattoli, M ;
Wallner, K ;
Sorace, R ;
Koval, J ;
Cash, J ;
Acosta, R ;
Brown, C ;
Etheridge, J ;
Binder, M ;
Brunelle, R ;
Kirwan, N ;
Sanchez, S ;
Stein, D ;
Wasserman, S .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1996, 35 (05) :875-879
[5]   Long-term outcomes after treatment with brachytherapy and supplemental conformal radiation for prostate cancer patients having intermediate and high-risk features [J].
Dattoli, Michael ;
Wallner, Kent ;
True, Lawrence ;
Cash, Jennifer ;
Sorace, Richard .
CANCER, 2007, 110 (03) :551-555
[6]   Actuarial disease-free survival after prostate cancer brachytherapy using interactive techniques with biplane ultrasound and fluoroscopic guidance [J].
Grado, GL ;
Larson, TR ;
Balch, CS ;
Grado, MM ;
Collins, JM ;
Kriegshauser, JS ;
Swanson, GP ;
Navickis, RJ ;
Wilkes, MM .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1998, 42 (02) :289-298
[7]  
Grimm PD, 1994, UROL CLIN N AM, V2, P113
[8]   Role of external beam radiotherapy with low-dose-rate brachytherapy in treatment of prostate cancer [J].
Jani, AB ;
Feinstein, JM ;
Pasciak, R ;
Krengel, S ;
Weichselbaum, RR .
UROLOGY, 2006, 67 (05) :1007-1011
[9]   Late toxicity and biochemical recurrence after external-beam radiotherapy combined with permanent-source prostate brachytherapy - Analysis of radiation therapy oncology group study 0019 [J].
Lee, W. Robert ;
Bae, Kyoungwha ;
Lawton, Colleen ;
Gillin, Michael ;
Morton, Gerard ;
Firat, Selim ;
Baikadi, Madhava ;
Kuettel, Michael ;
Greven, Kathryn ;
Sandler, Howard .
CANCER, 2007, 109 (08) :1506-1512
[10]   A phase II study of external beam radiotherapy combined with permanent source brachytherapy for intermediate-risk, clinically localized adenocarcinoma of the prostate: Preliminary results of RTOG P-0019 [J].
Lee, WR ;
DeSilvio, M ;
Lawton, C ;
Gillin, M ;
Morton, G ;
Firat, S ;
Baikadi, M ;
Kuettel, M ;
Greven, K ;
Sandler, H .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2006, 64 (03) :804-809