Long-term outcomes from dose-escalated image-guided intensity-modulated radiotherapy with androgen deprivation: encouraging results for intermediate- and high-risk prostate cancer

被引:24
作者
Wilcox, Shea W. [1 ,4 ]
Aherne, Noel J. [2 ,4 ]
Benjamin, Linus C. [1 ]
Wu, Bosco [1 ]
Silva, Thomaz de Campos [3 ]
McLachlan, Craig S. [4 ]
Mckay, Michael J. [3 ,5 ]
Last, Andrew J. [1 ]
Shakespeare, Thomas P. [1 ,2 ,3 ,4 ]
机构
[1] North Coast Canc Inst, Port Macquarie, NSW 2444, Australia
[2] North Coast Canc Inst, Coffs Harbour, NSW, Australia
[3] North Coast Canc Inst, Lismore, NSW, Australia
[4] Univ New S Wales, Rural Clin Sch, Sydney, NSW, Australia
[5] Univ Sydney, Sydney, NSW 2006, Australia
关键词
dose-escalation; image-guided radiotherapy; treatment related toxicity; biochemical disease-free survival; III RANDOMIZED-TRIAL; RADIATION-THERAPY; RADICAL PROSTATECTOMY; 78; GY; ADJUVANT; SUPPRESSION; CARCINOMA; TOXICITY; DISEASE;
D O I
10.2147/OTT.S65238
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Purpose: Dose-escalated (DE) radiotherapy in the setting of localized prostate cancer has been shown to improve biochemical disease-free survival (bDFS) in several studies. In the same group of patients, androgen deprivation therapy (ADT) has been shown to confer a survival benefit when combined with radiotherapy doses of up to 70 Gy; however, there is currently little long-term data on patients who have received high-dose intensity-modulated radiotherapy (IMRT) with ADT. We report the long-term outcomes in a large cohort of patients treated with the combination of DE image-guided IMRT (IG-IMRT) and ADT. Methods and materials: Patients with localized prostate cancer were identified from a centralized database across an integrated cancer center. All patients received DE IG-IMRT, combined with ADT, and had a minimum follow up of 12 months post-radiotherapy. All relapse and toxicity data were collected prospectively. Actuarial bDFS, metastasis-free survival, prostate cancer-specific survival, and multivariate analyses were calculated using the SPSS v20.0 statistical package. Results: Seven hundred and eighty-two eligible patients were identified with a median follow up of 46 months. Overall, 4.3% of patients relapsed, 2.0% developed distant metastases, and 0.6% died from metastatic prostate cancer. At 5-years, bDFS was 88%, metastasis-free survival was 95%, and prostate cancer-specific survival was 98%. Five-year grade 2 genitourinary and gastrointestinal toxicity was 2.1% and 3.4%, respectively. No grade 3 or 4 late toxicities were reported. Pretreatment prostate specific antigen (P=0.001) and Gleason score (P=0.03) were significant in predicting biochemical failure on multivariate analysis. Conclusion: There is a high probability of tumor control with DE IG-IMRT combined with androgen deprivation, and this is a technique with a low probability of significant late toxicity. Our long term results corroborate the safety and efficacy of treating with IG-IMRT to high doses and compares favorably with published series for the treatment of prostate cancer.
引用
收藏
页码:1519 / 1523
页数:5
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