PREDICTORS OF ANDROGEN DEPRIVATION THERAPY EFFICACY COMBINED WITH PROSTATIC IRRADIATION: THE CENTRAL ROLE OF TUMOR STAGE AND RADIATION DOSE

被引:13
|
作者
Williams, Scott [1 ,2 ]
Buyyounouski, Mark [3 ]
Kestin, Larry [4 ]
Duchesne, Gillian [2 ]
Pickles, Tom [5 ]
机构
[1] Peter MacCallum Canc Ctr, Div Radiat Oncol, Melbourne, Vic 8006, Australia
[2] Univ Melbourne, Melbourne, Vic, Australia
[3] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[4] William Beaumont Hosp, Royal Oak, MI 48072 USA
[5] British Columbia Canc Agcy, Vancouver, BC V5Z 4E6, Canada
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2011年 / 79卷 / 03期
关键词
Prostate cancer; Radiotherapy; Androgen deprivation; Outcomes; RANDOMIZED CONTROLLED-TRIAL; PHASE-III TRIAL; DEFINING BIOCHEMICAL FAILURE; LOCALLY ADVANCED-CARCINOMA; QUALITY-OF-LIFE; HORMONAL-THERAPY; CLINICAL-TRIALS; CANCER; RADIOTHERAPY; MEN;
D O I
10.1016/j.ijrobp.2009.11.044
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To evaluate the response of clinically localized prostate cancer to various durations of planned androgen deprivation therapy (ADT) and to investigate subgroups predicting response. Methods and Materials: Data of 3,666 prostate cancer patients treated with either combined ADT and external beam radiotherapy (EBRT) or EBRT alone at four institutions were examined. ADT consisted of neoadjuvant, concurrent, or adjuvant ADT or combinations of these regimens. The primary endpoint was time to biochemical failure (nadir plus 2 ng/ml), assessed from the end of therapy. Factors predictive for the need for ADT were examined with interaction analyses. Results: The impact of increasing ADT duration was nonlinear with, on average, 6 months of adjuvant ADT resulting in a reduction of the risk of biochemical failure by 38% (95% confidence interval [CI], 29%-46%), while 12, 24, and 36 months of ADT resulted in a 58% (95% Cl, 47%-67%), 66% (95% CI, 55%-75%), and 66% (95% CI, 51%-77%) relative failure reduction, respectively. Patients with higher T stage cancers and those treated with lower radiation doses had a significantly greater benefit for increasing ADT duration (interaction, p = 0.016 and p = 0.007, respectively). Pretreatment prostate-specific antigen values, Gleason score, age, and risk group did not modify the response to ADT. Conclusions: The known ADT efficacy derived from randomized studies can be generalized to patients with different features, and individual predictions of potential benefit from ADT use and duration may be calculated to aid patient and physician decision making. Tumor stage and radiation dose variations were related to significantly different ADT duration effects. The validity of these predictive factors requires prospective evaluation. (C) 2011 Elsevier Inc.
引用
收藏
页码:724 / 731
页数:8
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