Accelerated partial breast irradiation in a single 18 Gy fraction with high-dose-rate brachytherapy: preliminary results

被引:27
作者
Anchuelo Latorre, Javier [1 ]
Galdos, Piedad [1 ]
Alonso Buznego, Lucia [2 ]
Garcia Blanco, Ana [1 ]
Cardenal, Juan [1 ]
Ferri, Maria [1 ]
Diaz de Cerio, Ivan [1 ]
Arrojo, Elisabet [1 ]
Sierrasesumaga, Nicolas [1 ]
Gonzalez Noriega, Monica [3 ]
De Juan Ferre, Ana [2 ]
Fabregat, Rosa [4 ]
Ruiz, Samuel [4 ]
Prada, Pedro J. [1 ]
机构
[1] Hosp Univ Marques de Valdecilla, Dept Radiat Oncol, C Avd Valdecilla S-N, Santander 39008, Cantabria, Spain
[2] Hosp Univ Marques de Valdecilla, Dept Med Oncol, Santander, Cantabria, Spain
[3] Hosp Univ Marques de Valdecilla, Dept Surg, Santander, Cantabria, Spain
[4] Hosp Univ Marques de Valdecilla, Dept Radiat Phys, Santander, Cantabria, Spain
关键词
APBI; brachytherapy; breast cancer; morbidity; INTERSTITIAL MULTICATHETER BRACHYTHERAPY; 20-YEAR FOLLOW-UP; RADIATION-THERAPY; RANDOMIZED-TRIAL; INTRAOPERATIVE RADIOTHERAPY; EXTERNAL RADIOTHERAPY; CONSERVING SURGERY; PHASE-3; TRIAL; VS; APBI; I-II;
D O I
10.5114/jcb.2018.73994
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To evaluate the feasibility of acute and chronic toxicity in patients suitable for accelerated partial breast irradiation (APBI) in a single 18 Gy fraction with multicatheter high-dose-rate (HDR) brachytherapy, as well as cosmetic and oncological outcomes. Material and methods: Between September 2014 and March 2016, twenty consecutive patients with low-risk invasive and ductal carcinoma in situ were treated with interstitial multicatheter HDR brachytherapy in a single 18 Gy fraction. Results: Median age was 63.5 years (range, 51-79). Acute toxicity was observed in seven patients, while the pain during following days and hematoma were seen in four patients. With a median follow-up of 24 months, late toxicity was found in one patient with fat necrosis g2 and fibrosis g2 in another patient. The overall survival (OS) and locoregional control (LC) was 100%. Disease-free survival (DFS) and distant control was 95%. Good to excellent cosmetic outcomes were noted in 80% of patients and fair in 4 patients (20%). Conclusions: This is the first report in the medical literature that focuses on feasibility and acute and chronic toxicity, with a median follow-up of 24 months (range, 20-40). The protocol is viable and convenient. However, a longer follow-up is needed to know chronic toxicity and oncologic outcomes.
引用
收藏
页码:58 / 63
页数:6
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