Single-Institution Phase 1/2 Prospective Clinical Trial of Single-Fraction, High-Gradient Adjuvant Partial-Breast Irradiation for Hormone Sensitive Stage 0-I Breast Cancer

被引:17
|
作者
Kennedy, William R. [1 ]
Thomas, Maria A. [1 ]
Stanley, Jennifer A. [1 ]
Luo, Jingqin [2 ]
Ochoa, Laura L. [1 ]
Clifton, Katherine K. [3 ]
Cyr, Amy E. [4 ]
Margenthaler, Julie A. [4 ]
DeWees, Todd A. [5 ]
Price, Alex [1 ]
Kashani, Rojano [6 ]
Green, Olga [1 ]
Zoberi, Imran [1 ]
机构
[1] Washington Univ, Sch Med, Dept Radiat Oncol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Surg, Siteman Canc Ctr Biostat Core, St Louis, MO USA
[3] Washington Univ, Sch Med, Div Oncol, St Louis, MO USA
[4] Washington Univ, Sch Med, Dept Surg, St Louis, MO USA
[5] Mayo Clin, Dept Biomed Stat & Informat, Scottsdale, AZ USA
[6] Univ Michigan, Dept Radiat Oncol, Ann Arbor, MI 48109 USA
关键词
SOCIETY CONSENSUS STATEMENT; RADIATION-THERAPY; CONSERVING SURGERY; RANDOMIZED-TRIAL; FOLLOW-UP; IN-SITU; BRACHYTHERAPY; RADIOTHERAPY; WOMEN; LUMPECTOMY;
D O I
10.1016/j.ijrobp.2020.02.021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We sought to evaluate the feasibility and tolerability of a novel accelerated partial breast irradiation regimen delivered in a single fraction postoperatively. Methods and Materials: We enrolled 50 patients with low-risk, hormone-sensitive breast cancer from 2015 to 2018 on a prospective phase 1/2 trial to receive single-fraction, high-gradient partial-breast irradiation (SFHGPBI) 2 to 8 weeks after lumpectomy for node-negative, invasive, or in situ breast cancer. The high gradient was achieved by prescribing 20 Gy to the surgical bed and 5 Gy to the breast tissue within 1 cm of the surgical bed simultaneously in 1 fraction using external beam. Results: The median age was 65 (range, 52-84). Ten patients (20%) had small-volume ductal carcinoma in situ while the remainder had stage I disease. At a median follow-up of 25 months, we evaluated toxicity, patient- and physician-reported cosmesis, patient-reported quality of life (QOL), and initial tumor control. There was no Common Terminology Criteria for Adverse Events v4.0 grade 3+ toxicity. Only 34% of patients experienced grade 1 erythema. Good-to-excellent pretreatment cosmesis was present in 100% and 98% per physicians and patients, respectively, and did not change post-SFHGPBI. Quantitative cosmesis by percentage of breast retraction assessment significantly improved over time during the post-SFHGPBI period per mixed repeated measures modeling (P = .0026). QOL per European Organization for Research and Treatment of Cancer QOL Questionnaires C30 and BR-23 did not decline other than temporarily in the systemic therapy effects and hair loss domains, both of which returned to pretreatment values. There was 1 noninvasive in-breast recurrence in a separate untreated quadrant 18 months post-SFHGPBI and 1 isolated axillary recurrence 30 months post-SFHGPBI, both salvaged successfully. There were no distant recurrences or cancer-related deaths observed. Conclusions: Accelerated partial-breast irradiation delivered in a single fraction post-operatively using external beam techniques is a novel, feasible, well-tolerated regimen. SFHGPBI does not adversely affect cosmesis or QOL as reported by both physicians and patients. Initial tumor control rates are excellent, with longer follow-up required to confirm efficacy. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:344 / 352
页数:9
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