Accelerated partial breast irradiation with multi-catheter brachytherapy:: Local control, side effects and cosmetic outcome for 274 patients.: Results of the German-Austrian multi-centre trial

被引:103
作者
Ott, Oliver J.
Hildebrandt, Guido
Poetter, Richard
Hammer, Josef
Lotter, Michael
Resch, Alexandra
Sauer, Rolf
Strnad, Vratislav
机构
[1] Univ Hosp Erlangen, Dept Radiat Oncol, D-91054 Erlangen, Germany
[2] Univ Hosp Leipzig, Dept Radiat Oncol, Leipzig, Germany
[3] Univ Hosp AKH Wien, Dept Radiotherapy & Radiobiol, Vienna, Austria
[4] Barmherzige Schwestern Hosp Linz, Dept Radiat Oncol, Linz, Austria
关键词
accelerated partial breast irradiation; multi-catheter brachytherapy; HDR; PDR;
D O I
10.1016/j.radonc.2006.08.028
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and purpose: To evaluate the safety and effectiveness of accelerated partial breast irradiation (APBI) with multi-catheter brachytherapy. Patients and methods: Between 11/2000 and 04/2005, 274 patients participated. Patients were eligible for APBI if they had histologically confirmed breast cancer, a tumour diameter <= 3 cm, complete resection with clear margins >= 2 mm, negative axillary lymph nodes or singular nodal micro-metastasis, no distant metastases, hormone receptor-positive tumours, and were >= 35 years. Patients were excluded if mammographically they showed a multicentric invasive growth pattern, poorly differentiated tumours, residual diffuse micro-calcifications, extensive intraductal component, or vessel invasion. Median follow-up was 32 months (range; 8-68). Results: The local control rate was 99.3% (272/274), the 3 year-local-recurrence-free survival probability, 99.6%. Perioperative complications occurred in 5.5% (15/274): 9 (3.3%) experienced implant infection and 6 (2.2%) hematoma. Acute toxicity (Grade 1/2 radio-dermatitis) was seen in 6.6% (18/274). Late side effects >= Grade 3 (fibrosis, telangiectasia) occurred in 1.8% (4/274). Cosmetic results were exceilent/good in 94% (253/274). Conclusions: This analysis underlined the safety and effectiveness of APBI in a carefully selected subgroup with favourable disease characteristics. Of course, longer follow-up and randomised trials are necessary to conclusively assess the potential of APBI. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:281 / 286
页数:6
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