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单机构、1/2 期前瞻性临床试验:单剂量、高梯度辅助部分乳房照射治疗激素敏感 0 期-I 期乳腺癌。

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.

机构信息

Department of Radiation Oncology, Washington University School of Medicine, St Louis, Missouri.

Department of Surgery, Siteman Cancer Center Biostatistics Core, Washington University School of Medicine, St Louis, Missouri.

出版信息

Int J Radiat Oncol Biol Phys. 2020 Jun 1;107(2):344-352. doi: 10.1016/j.ijrobp.2020.02.021. Epub 2020 Feb 19.

Abstract

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 postoperatively 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.

摘要

目的

我们旨在评估在术后单次分割的情况下,一种新的加速部分乳腺照射方案的可行性和耐受性。

方法和材料

我们从 2015 年至 2018 年,在一项前瞻性的 1/2 期试验中,招募了 50 例低危、激素敏感型乳腺癌患者,这些患者在接受保乳手术后 2 至 8 周,接受单次分割、高梯度部分乳腺照射(SFHGPBI)。通过外部束同时给予手术床 20 Gy 和手术床周围 1 cm 内的乳腺组织 5 Gy,实现高梯度。

结果

中位年龄为 65 岁(范围 52-84 岁)。10 例(20%)患者有小体积导管原位癌,其余患者均为 I 期疾病。在中位随访 25 个月时,我们评估了毒性、患者和医生报告的美容效果、患者报告的生活质量(QOL)以及初始肿瘤控制情况。无 CTCAE v4.0 分级 3+毒性。只有 34%的患者出现 1 级红斑。术前美容效果良好至优秀,医生和患者的比例分别为 100%和 98%,且在接受 SFHGPBI 后未发生变化。通过混合重复测量模型(P =.0026)评估的乳腺回缩百分比定量美容效果在 SFHGPBI 后期间显著改善。欧洲癌症研究与治疗组织(EORTC)的 QLQ-C30 和 BR-23 问卷评估的 QOL 没有下降,除了在系统治疗效果和脱发两个方面暂时下降,这两个方面都恢复到了术前水平。在接受 SFHGPBI 后 18 个月,在另一个未接受治疗的象限中出现 1 例非侵袭性乳腺内复发,在接受 SFHGPBI 后 30 个月,出现 1 例孤立性腋窝复发,均成功挽救。未观察到远处复发或癌症相关死亡。

结论

使用外部束技术在术后单次分割中进行加速部分乳腺照射是一种新的、可行的、耐受良好的方案。SFHGPBI 不会对医生和患者报告的美容效果或 QOL 产生不利影响。初始肿瘤控制率非常高,需要更长的随访时间来确认疗效。

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