Intensity-modulated radiation therapy with the central shielding technique for patients with uterine cervical cancer†

被引:0
|
作者
Torii, Akira [1 ]
Tomita, Natsuo [1 ]
Kuno, Mayu [2 ]
Nishio, Masahiro [3 ]
Yamada, Yuki [4 ]
Takaoka, Taiki [1 ]
Okazaki, Dai [1 ]
Niwa, Masanari [1 ]
Kita, Nozomi [1 ]
Takano, Seiya [1 ]
Murao, Takayuki [2 ]
Ogawa, Yasutaka [3 ]
Hiwatashi, Akio [1 ]
机构
[1] Nagoya City Univ Hosp, Dept Radiat Oncol, 1 Kawasumi,Mizuho Cho,Mizuho Ku, Nagoya, Aichi 4678601, Japan
[2] Ichinomiya Municipal Hosp, Dept Radiat Oncol, 2-2-22 Bunkyo, Ichinomiya, Aichi 4918558, Japan
[3] Kasugai Municipal Hosp, Dept Radiat Oncol, 1-1-1 Takaki Cho, Kasugai, Aichi 4868510, Japan
[4] Konan Kosei Hosp, Dept Radiat Oncol, 137 Ohmatsubara,Takaya Cho, Konan, Aichi 4838704, Japan
关键词
uterine cervical cancer; intensity-modulated radiotherapy; helical tomotherapy; adverse effects; treatment outcome; EXTERNAL-BEAM RADIOTHERAPY; CLINICAL TARGET VOLUME; CANCER; BRACHYTHERAPY; CARCINOMA; OUTCOMES; PATTERN; NODES;
D O I
10.1093/jrr/rrad039
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We aimed to examine outcomes and toxicities of intensity-modulated radiation therapy (IMRT) with the central shielding (CS) technique for patients with uterine cervical cancer. This retrospective study included 54 patients with International Federation of Gynecology and Obstetrics IB-IVA cancer. Whole pelvic radiotherapy or extended-field radiotherapy were performed at the dose of 50.4 Gy in 28 fractions with helical tomotherapy (HT). Six patients had para-aortic lymph node metastases. The CS technique with HT was utilized after a total dose of 28.8-41.4 Gy to reduce doses to the rectum and bladder. The prescribed dose of intracavitary brachytherapy was mainly 18-24 Gy in three or four fractions at point A. Concurrent chemotherapy was used for 47 patients (87%). Median follow-up time was 56 months. Seventeen patients (31%) developed recurrence. The recurrence of the cervix was observed in two patients (4%). The 5-year rates of the locoregional control, progression-free survival (PFS) and overall survival were 79, 66 and 82%, respectively. Among several factors evaluated, histological type of adenocarcinoma was only a significantly worse prognostic factor for PFS by multivariate analysis (hazard ratio, 4.9 [95% confidence interval, 1.3-18], P = 0.018). Grade 2 or higher late toxicities were observed in nine patients (17%). Two patients (4%) each had grade 3 proctitis and grade 3 ileus, respectively. No grade 4 toxicity or treatment-related death was observed. The results suggest that IMRT with the CS technique allows a high local control without increasing the risk of complications for cervical cancer patients.
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页码:720 / 727
页数:8
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