Endoluminal high-dose-rate brachytherapy for locally recurrent or persistent esophageal cancer

被引:10
|
作者
Taggar, Amandeep S. [1 ,2 ]
Pitter, Kenneth L. [1 ]
Cohen, Gil'ad N. [3 ]
Schattner, Mark [4 ]
Gerdes, Hans [4 ]
Markowitz, Arnold J. [4 ]
Ilson, David [5 ]
Brady, Paul [1 ]
Cuaron, John J. [1 ]
Goodman, Karyn A. [6 ]
Wu, Abraham J. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, 1275 York Ave, New York, NY 10021 USA
[2] Sunnybrook Odette Canc Ctr, Dept Radiat Oncol, Toronto, ON, Canada
[3] Mem Sloan Kettering Canc Ctr, Dept Med Phys, New York, NY 10021 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Gastroenterol & Nutr, 1275 York Ave, New York, NY 10021 USA
[5] Mem Sloan Kettering Canc Ctr, Dept Med Oncol, 1275 York Ave, New York, NY 10021 USA
[6] Univ Denver, Dept Radiat Oncol, Aurora, CO USA
关键词
Early stage; Recurrent; Esophageal cancer; Brachytherapy; High-dose-rate; INTRALUMINAL BRACHYTHERAPY; RADIATION-THERAPY; CARCINOMA; PALLIATION; SURGERY;
D O I
10.1016/j.brachy.2018.01.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE: Management of locally recurrent or persistent esophageal cancer (EC) after standard chemoradiation is challenging. This study updates our experience of treating medically inoperable EC patients with endoluminal high-dose-rate brachytherapy (EHDRBT) including the patients treated with a novel multiballoon channel centering esophageal applicator. METHODS AND MATERIALS: Thirty-three consecutive patients with early-stage primary (n = 7), posttreatment persistent (n = 7), and recurrent (n = 19) EC treated with EHDRBT at our institution were included. Median dose and treatment lengths were 14 Gy (range 10-17.5 Gy) and 6 cm (3.5-9.0 cm), respectively. Endoscopy and biopsy were performed 3 months after EHDRBT and then every 3-6 months thereafter. RESULTS: Median followup was 17.4 months (range 5.0-88.3). Grade 1 and 2 toxicities were observed in 13 (44.8%) and 11 (37.9%) patients, respectively. Grade 3 toxicity (tracheoesophageal fistula) was observed in 1 patient who had previously received two courses of external beam radiotherapy as well as a stent insertion. Median overall survival (OS) for entire cohort was 20.9 months, and 1-year OS was 78%. Complete response was achieved in 58.6% of patients with median time to failure and 1-year disease-free survival of 10.3 months (range 5.4-28.2) and 27%, respectively. CONCLUSIONS: For medically inoperable patients with early-stage primary or local posttreatment residual or recurrent EC, EHDRBT is a well-tolerated treatment option with minimal Grade >= 3 toxicity. Brachytherapy in our hands continues to be a safe treatment option. Although 58.6% of patients achieved a complete response and the OS of this cohort is relatively good, long-term local control and cure remains a challenge. (C) 2018 American Brachytherapy Society. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:621 / 627
页数:7
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