High-Dose-Rate Brachytherapy for the Treatment of Vaginal Intraepithelial Neoplasia

被引:20
作者
Song, Jin Ho [1 ]
Lee, Joo Hwan [1 ]
Lee, Jong Hoon [2 ]
Park, Jong Sup [3 ]
Hong, Sook Hee [4 ]
Jang, Hong Seok [1 ]
Kim, Yeon Sil [1 ]
Choi, Byung Ock [1 ]
Yoon, Sei Chul [5 ]
机构
[1] Catholic Univ Korea, Coll Med, Seoul St Marys Hosp, Dept Radiat Oncol, Seoul, South Korea
[2] Catholic Univ Korea, Coll Med, St Vincents Hosp, Dept Radiat Oncol, Suwon, South Korea
[3] Catholic Univ Korea, Coll Med, Seoul St Marys Hosp, Dept Obstet & Gynecol, Seoul, South Korea
[4] Catholic Univ Korea, Coll Med, Seoul St Marys Hosp, Dept Med Oncol, Seoul, South Korea
[5] Catholic Univ Korea, Bucheon St Marys Hosp, Dept Radiat Oncol, Coll Med, Puchon 420717, South Korea
来源
CANCER RESEARCH AND TREATMENT | 2014年 / 46卷 / 01期
关键词
Vaginal neoplasms; Carcinoma in situ; Radiotherapy; Brachytherapy; RATE INTRACAVITARY BRACHYTHERAPY; MANAGEMENT; HYSTERECTOMY;
D O I
10.4143/crt.2014.46.1.74
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Vaginal intraepithelial neoplasia (VAIN), a rare premalignant condition, is difficult to eradicate. We assess the effectiveness of high-dose rate intracavitary brachytherapy (HDR-ICR) in patients with VAIN or carcinoma in situ (CIS) of the vagina after hysterectomy. Materials and Methods We reviewed 34 patients treated for posthysterectomy VAIN or CIS of the vagina by brachytherapy as the sole treatment. All patients underwent a coloposcopic-directed punch biopsy or had abnormal cytology, at least 3 consecutive times. All patients were treated with a vaginal cylinder applicator. The total radiation dose was mainly 40 Gy in 8 fractions during the periods of 4 weeks at a prescription point of the median 0.2 cm (range, 0 to 0.5 cm) depth from the surface of the vaginal mucosa. Results Acute toxicity was minimal. Seven patients had grade 1/2 acute urinary and rectal complications. There were 15 cases of late toxicity, predominantly vaginal mucosal reaction in 12 patients. Of these patients, two patients suffered from grade 3 vaginal stricture and dyspareunia continuously. After a median follow-up time of 48 months (range, 4 to 122 months), there were 2 recurrences and 2 persistent diseases, in which a second-line therapy was needed. The success rate was 88.2%. The average prescription point in failure patients was 1.1 mm from the surface of the vagina compared to an average of 2.6 mm in non-recurrent patients (p=0.097). Conclusion HDR-ICR is an effective treatment method in VAIN patients. In spite of high cure rates, we should consider issues regarding vaginal toxicity and radiation techniques to reduce the occurrence of failure and toxicity.
引用
收藏
页码:74 / 80
页数:7
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