Outcomes of Asian patients with localized prostate cancer treated with combined intensity modulated radiation therapy (IMRT) and high dose rate (HDR) brachytherapy: A single institution experience

被引:5
作者
Ng, Ivy Wei Shan [1 ]
Tey, Jeremy Chee Seong [1 ]
Soon, Yu Yang [1 ]
Tseng, Michelle Shu Fen [1 ]
Chen, Desiree [1 ]
Lim, Keith Hsiu Chin [1 ]
机构
[1] Natl Univ Hlth Syst, Dept Radiat Oncol, Natl Canc Inst, Natl Univ Hosp, Singapore, Singapore
关键词
brachytherapy; high dose rate; intensity modulated radiotherapy; prostate cancer; radiotherapy; EXTERNAL-BEAM RADIOTHERAPY; RANDOMIZED-TRIAL; BOOST; RISK; MEN; RECOMMENDATIONS; INTERMEDIATE;
D O I
10.1111/ajco.12819
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
AimExternal beam radiotherapy (EBRT) followed by high dose rate (HDR) brachytherapy boost has demonstrated minimal toxicities and improved disease control rate compared with EBRT alone in observational and randomized studies with predominantly Caucasian patients. This study aims to report the outcomes of patients treated with this approach in our predominantly Asian population. MethodsMedical records for patients with localized prostate cancer who received combined EBRT delivered via intensity modulated radiotherapy (IMRT) technique followed by HDR brachytherapy boost were retrospectively reviewed. Outcomes evaluated included 5-year biochemical recurrence-free survival (per Phoenix definition), overall survival and treatment toxicities. ResultsFrom June 2009 to March 2015, 75 patients were treated with IMRT followed by HDR brachytherapy boost. Twenty patients (27%) had intermediate risk, 55 (74%) had high-risk disease. Median follow up was 64 months. All patients received IMRT to a median dose of 45 Gy to the pelvis followed by HDR brachytherapy boost. Sixty, 10 and 5 patients received boost of 21 Gy in two fractions, 19 Gy in two fractions and 15 Gy in a single fraction, respectively. All patients met the planning criteria adapted from RTOG 0815. The 5-year prostate-specific antigen (PSA) control was 85.2% (80.3% and 100% for high-risk and intermediate-risk group, respectively). Cancer-specific survival and overall survival are 97.3% and 92.0%, respectively. Eleven (15%) patients developed biochemical failure, six of which had distant metastasis. Three (4%) developed grade 3 genitourinary toxicity (urethral stricture and/or cystitis) and none developed grade 3 radiation proctitis. ConclusionOur outcomes are comparable to internationally published data and demonstrate reproducibility of this approach in our population.
引用
收藏
页码:e386 / e391
页数:6
相关论文
共 32 条
[1]   Moderate dose escalation with single-fraction high-dose-rate brachytherapy boost for clinically localized intermediate- and high-risk prostate cancer: 5-year outcome of the first 100 consecutively treated patients [J].
Agoston, Peter ;
Major, Tibor ;
Froehlich, Georgina ;
Szabo, Zoltan ;
Loevey, Jozsef ;
Fodor, Janos ;
Kasler, Miklos ;
Polgar, Csaba .
BRACHYTHERAPY, 2011, 10 (05) :376-384
[2]  
[Anonymous], 2012, FACT SHEETS CANC
[3]  
[Anonymous], 2017, PROST PELV LYMPH NOD
[4]  
[Anonymous], 2015, 0815 RTOG
[5]  
[Anonymous], 2014, World Cancer Report 2014
[6]  
[Anonymous], 2015, PROST CANC UR
[7]  
Brenner DJ, 2002, INT J RADIAT ONCOL, V52, P6
[8]   High-dose-rate brachytherapy plus external beam radiotherapy for T1 to T3 prostate cancer: An experience in Taiwan [J].
Chen, Yen-Chao ;
Chuang, Cheng-Keng ;
Hsieh, Ming-Li ;
Chen, Wen-Cheng ;
Fan, Kang-Hsing ;
Yeh, Chie-Yi ;
Lee, Chung-Chi ;
Hong, Ji-Hong .
UROLOGY, 2007, 70 (01) :101-105
[9]   Biochemical outcome after radical prostatectomy, external beam radiation therapy, or interstitial radiation therapy for clinically localized prostate cancer [J].
D'Amico, AV ;
Whittington, R ;
Malkowicz, SB ;
Schultz, D ;
Blank, K ;
Broderick, GA ;
Tomaszewski, JE ;
Renshaw, AA ;
Kaplan, I ;
Beard, CJ ;
Wein, A .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 280 (11) :969-974
[10]   Excellent Results From High Dose Rate Brachytherapy and External Beam for Prostate Cancer are Not Improved by Androgen Deprivation [J].
Demanes, D. Jeffrey ;
Brandt, David ;
Schour, Lionel ;
Hill, Dennis R. .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2009, 32 (04) :342-347