Two-fraction high-dose-rate brachytherapy within a single day combined with external beam radiotherapy for prostate cancer: single institution experience and outcomes

被引:10
|
作者
Liu, Junyang [1 ]
Kaidu, Motoki [1 ]
Sasamoto, Ryuta [2 ]
Ayukawa, Fumio [1 ]
Yamana, Nobuko [1 ]
Sato, Hiraku [1 ]
Tanaka, Kensuke [1 ]
Kawaguchi, Gen [1 ]
Ohta, Atsushi [1 ]
Maruyama, Katsuya [1 ]
Abe, Eisuke [1 ]
Kasahara, Takashi [3 ]
Nishiyama, Tsutomu [3 ]
Tomita, Yoshihiko [3 ]
Aoyama, Hidefumi [1 ]
机构
[1] Niigata Univ, Grad Sch Med & Dent Sci, Dept Radiol & Radiat Oncol, Chuo Ku, 1-757 Asahimachi Dori, Niigata 9518510, Japan
[2] Niigata Univ, Sch Hlth Sci, Chuo Ku, 1-757 Asahimachi Dori, Niigata 9518510, Japan
[3] Niigata Univ, Grad Sch Med & Dent Sci, Urol Dept, Chuo Ku, 1-757 Asahimachi Dori, Niigata 9518510, Japan
关键词
high-dose-rate; brachytherapy; HDR-BT; radiotherapy; prostate cancer; toxicity; MODULATED RADIATION-THERAPY; ANDROGEN DEPRIVATION THERAPY; RADICAL PROSTATECTOMY; HIGH-RISK; HDR BRACHYTHERAPY; HORMONAL-THERAPY; BOOST; MONOTHERAPY; TOXICITY; RECOMMENDATIONS;
D O I
10.1093/jrr/rrw003
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We investigated the outcomes of treatment for patients with localized prostate cancer (PCa) treated with 3D conformal radiation therapy (3D-CRT) followed by two-fraction high-dose-rate brachytherapy within a single day (2-fr.-HDR-BT/day) at a single institution. A total of 156 consecutive Asian males (median age, 67 years) were enrolled. To compare our findings with those of other studies, we analyzed our results using the D'Amico classification, assigning the patients to low-(n = 5; 3.2%), intermediate-(n = 36; 23.1%) and high-risk (n = 115; 73.7%) groups (Stage T3 PCa patients were classified as high-risk). One patient in the D'Amico low-risk group (20%), 13 intermediate-risk patients (36.1%) and 99 high-risk patients (86.1%) underwent androgen deprivation therapy. We administered a prescription dose of 39 Gy in 13 fractions of 3D-CRT combined with 18 Gy of HDR-BT in two 9-Gy fractions delivered within a single day. We did not distinguish between risk groups in determining the prescription dose. The median follow-up period was 38 months. Of the 156 patients, one died from primary disease and five died from other diseases. The 3-year overall survival (OS) rates were 100%, 100% and 93.7%, and the 3-year 'biochemical no evidence of disease (bNED)' rates were 100%, 100% and 96.9% for the D'Amico low-, intermediate-and high-risk groups, respectively. No patient developed >= Grade 3 early toxicity. The Grade 3 late genitourinary toxicity rate was 2.6%, and no >= Grade 3 late gastrointestinal toxicity occurred. The efficacy and safety of this study were satisfactory, and longer-term follow-up is necessary.
引用
收藏
页码:280 / 287
页数:8
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