Radiation Dose Predicts for Biochemical Control in Intermediate-Risk Prostate Cancer Patients Treated With Low-Dose-Rate Brachytherapy Journal Article


Authors: Ho, A. Y.; Burri, R. J.; Cesaretti, J. A.; Stone, N. N.; Stock, R. G.
Article Title: Radiation Dose Predicts for Biochemical Control in Intermediate-Risk Prostate Cancer Patients Treated With Low-Dose-Rate Brachytherapy
Abstract: Purpose: To evaluate the influence of patient- and treatment-related factors on freedom from biochemical failure (FFbF) in patients with intermediate-risk prostate cancer. Methods and Materials: From a prospectively collected database of 2250 men treated at Mount Sinai Hospital from 1990 to 2004 with low-dose-rate brachytherapy for prostate cancer, 558 men with either one or more intermediate-risk features (prostate-specific antigen [PSA] level 10-20 ng/mL, Gleason score 7, or Stage T2b) were identified who had a minimum follow-up of 24 months and postimplant CT-based dosimetric analysis. Biologically effective dose (BED) values were calculated to compare doses from different isotopes and treatment regimens. Patients were treated with brachytherapy with or without hormone therapy and/or external-beam radiotherapy. Patient- and treatment-related factors were analyzed with respect to FFbF. The median follow-up was 60 months (range, 24-167 months). Biochemical failure was defined according to the Phoenix definition. Univariate analyses were used to determine whether any variable was predictive of FFbF. A two-sided p value of &lt;0.05 was considered significant. Results: Overall, the actuarial FFbF at 10 years was 86%. Dose (BED &lt;150 Gy<sub>2</sub> vs. ≥150 Gy<sub>2</sub>) was the only significant predictor of FFbF (p &lt; 0.001). None of the other variables (PSA, external-beam radiotherapy, Gleason score, treatment type, hormones, stage, and number of risk factors) was found to be a statistically significant predictor of 10-year FFbF. Conclusions: Radiation dose is an important predictor of FFbF in intermediate-risk prostate cancer. Treatment should continue to be individualized according to presenting disease characteristics until results from Radiation Therapy Oncology Group trial 0232 become available. © 2009 Elsevier Inc. All rights reserved.
Keywords: cancer chemotherapy; controlled study; human tissue; treatment failure; major clinical study; cancer risk; cancer radiotherapy; radiation dose; cancer staging; follow-up studies; isotopes; prostate specific antigen; computer assisted tomography; radiotherapy dosage; radiotherapy; risk factors; patient monitoring; biopsy; prostate cancer; prostate-specific antigen; prostatic neoplasms; goserelin; leuprorelin; prostate; iodine 125; iodine radioisotopes; dosimetry; biochemical failure; androgen antagonists; brachytherapy; gleason scores; hormonal therapy; relative biological effectiveness; external beam radiotherapy; flutamide; antineoplastic agents, hormonal; univariate analysis; analysis of variance; radioisotopes; leuprolide; intermediate risk; biochemical control; biologically effective dose; freedom from biochemical failures; hormone therapy; low dose rate brachytherapy; p-values; prostate cancers; radiation therapy oncology groups; peeling; risk analysis; diseases; isotope; palladium 103; anilides; nitriles; palladium; tosyl compounds
Journal Title: International Journal of Radiation Oncology, Biology, Physics
Volume: 75
Issue: 1
ISSN: 0360-3016
Publisher: Elsevier Inc.  
Date Published: 2009-09-01
Start Page: 16
End Page: 22
Language: English
DOI: 10.1016/j.ijrobp.2008.10.071
PUBMED: 19289266
PROVIDER: scopus
DOI/URL:
Notes: --- - "Cited By (since 1996): 6" - "Export Date: 30 November 2010" - "CODEN: IOBPD" - "Source: Scopus"
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  1. Alice Yoosun Ho
    122 Ho