Thermal Boost Combined with Interstitial Brachytherapy in Early Breast Cancer Conserving Therapy-Initial Group Long-Term Clinical Results and Late Toxicity

被引:4
作者
Chichel, Adam [1 ]
Burchardt, Wojciech [1 ,2 ]
Chyrek, Artur J. [1 ]
Bieleda, Grzegorz [2 ,3 ]
机构
[1] Greater Poland Canc Ctr, Dept Brachytherapy, PL-61866 Poznan, Poland
[2] Poznan Univ Med Sci, Dept Electroradiol, PL-61866 Poznan, Poland
[3] Greater Poland Canc Ctr, Dept Med Phys, PL-61866 Poznan, Poland
关键词
thermal boost; hyperthermia; breast cancer; interstitial brachytherapy; conserving therapy; DOSE-RATE BRACHYTHERAPY; PHASED-ARRAY THERMOTHERAPY; 20-YEAR FOLLOW-UP; RADIATION-THERAPY; LOCAL-CONTROL; CONSERVATIVE TREATMENT; CHEST-WALL; STAGE-I; HYPERTHERMIA; RADIOTHERAPY;
D O I
10.3390/jpm12091382
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
(1) In breast-conserving therapy (BCT), adjuvant radiation, including tumor bed boost, is mandatory. Safely delivered thermal boost (TB) based on radio-sensitizing interstitial microwave hyperthermia (MWHT) preceding standard high-dose-rate (HDR) brachytherapy (BT) boost has the potential for local control (LC) improvement. The study is to report the long-term results regarding LC, disease-free survival (DFS), overall survival (OS), toxicity, and cosmetic outcome (CO) of HDR-BT boost +/- MWHT for early breast cancer (BC) patients treated with BCT. (2) In the years 2006 and 2007, 57 diverse stages and risk (IA-IIIA) BC patients were treated with BCT +/- adjuvant chemotherapy followed by 42.5-50.0 Gy whole breast irradiation (WBI) and 10 Gy HDR-BT boost. Overall, 25 patients (group A; 43.9%) had a BT boost, and 32 (group B; 56.1%) had an additional pre-BT single session of interstitial MWHT on a tumor bed. Long-term LC, DFS, OS, CO, and late toxicity were evaluated. (3) Median follow-up was 94.8 months (range 1.1-185.5). LC was 55/57, or 96.5% (1 LR in each group). DFS was 48/57, or 84.2% (4 failures in group A, 5 in B). OS was 46/57, or 80.7% (6 deaths in group A, 5 in B). CO was excellent in 60%, good in 36%, and satisfactory in 4% (A), and in 53.1%, 34.4%, and 9.4% (B), respectively. One poor outcome was noted (B). Late toxicity as tumor bed hardening occurred in 19/57, or 33.3% of patients (9 in A, 10 in B). In one patient, grade 2 telangiectasia occurred (group A). All differences were statistically insignificant. (4) HDR-BT boost +/- TB was feasible, well-tolerated, and highly locally effective. LC, DFS, and OS were equally distributed between the groups. Pre-BT MWHT did not increase rare late toxicity.
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页数:12
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