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每日一次加速部分乳腺照射的长期结果:2 期试验结果。

Long-Term Outcomes of Once-Daily Accelerated Partial-Breast Irradiation With Tomotherapy: Results of a Phase 2 Trial.

机构信息

Radioterapia Oncologica, Ospedale San Giovanni Addolorata, Rome, Italy.

Radioterapia, Dipartimento di Biomedicina e Prevenzione, Università degli Studi di Roma Tor Vergata, Rome, Italy.

出版信息

Int J Radiat Oncol Biol Phys. 2021 Mar 1;109(3):678-687. doi: 10.1016/j.ijrobp.2020.10.009. Epub 2020 Oct 21.

Abstract

PURPOSE

We report long-term outcomes of phase 2 trial on patients with invasive breast cancer treated with accelerated partial-breast irradiation (APBI) using tomotherapy after breast conservative surgery.

METHODS AND MATERIALS

From December 2010 to December 2018, we treated 338 women with APBI-tomotherapy: 38.5 Gy in 10 once-daily fractions. Patients selected were age ≥50 years old, with ≤3 cm in size unifocal tumor and at least 2 mm of clear margins. Disease outcomes were analyzed by clinicopathologic characteristics, molecular phenotypes, and American Society for Radiation Oncology (ASTRO) 2017 updated consensus groupings.

RESULTS

The median age was 65 years (range, 50-86). The invasive ductal (87.5%) and the luminal A-like molecular phenotype (70%) were the most common tumors. Overall 242 patients (71.6%) were considered "suitable" for enrollment in APBI according to the eligibility criteria of the ASTRO-2017 consensus statement. With a median follow-up of 76 months (range, 17-113), 2 patients (0.6%) had an invasive ipsilateral breast tumor recurrence (IBTR), and 2 patients (0.6%) had an axillary ipsilateral failure. The rate of local control in terms of free of IBTR was 99.4% and locoregional control (no recurrence in ipsilateral breast as well as in regional nodes) was 98.8%. Progression-free survival was 98.4% and 92% at 5 and 10 years, respectively. Acute and late skin toxicity, graded according to the Common Terminology Criteria for Adverse Events, were 7.7% (G1) and 0.6% (G2) and 4.4% (G1) and 1.1% (G2), respectively. There were no grade 3/4 toxicities, however. Very few patients (2%) or physicians (2%) assessed cosmetic outcome as fair or poor at the 2-year follow-up.

CONCLUSIONS

This phase 2 trial on APBI-tomotherapy shows excellent long-term results. Once-daily fractionation schedule was well tolerated with a low rate of adverse events and worse cosmetic outcome. In this series, even among those deemed cautionary or unsuitable for APBI by ASTRO criteria, we demonstrated a low rate of IBTR.

摘要

目的

我们报告了一项针对接受保乳手术后接受适形调强放疗(APBI)的浸润性乳腺癌患者的 2 期临床试验的长期结果。

方法和材料

从 2010 年 12 月至 2018 年 12 月,我们对 338 名接受 APBI-调强放疗的女性患者进行了治疗:38.5Gy,分 10 次,每日 1 次。入选患者年龄≥50 岁,肿瘤最大径≤3cm,切缘至少 2mm 无肿瘤。根据临床病理特征、分子表型和美国放射肿瘤学会(ASTRO)2017 年更新的共识分组对疾病结局进行分析。

结果

中位年龄为 65 岁(范围 50-86 岁)。最常见的肿瘤为浸润性导管癌(87.5%)和 luminal A 样分子表型(70%)。根据 ASTRO-2017 共识声明的入选标准,242 例患者(71.6%)被认为“适合”接受 APBI。中位随访时间为 76 个月(范围 17-113 个月),2 例患者(0.6%)发生同侧乳腺浸润性肿瘤复发(IBTR),2 例患者(0.6%)发生同侧腋窝淋巴结失败。无同侧 IBTR 的局部控制率为 99.4%,无同侧乳房和区域淋巴结复发的局部区域控制率为 98.8%。无进展生存率分别为 98.4%和 92%,5 年和 10 年时分别为 98.4%和 92%。根据常见不良事件术语标准(CTCAE),急性和晚期皮肤毒性分别为 7.7%(G1)和 0.6%(G2)、4.4%(G1)和 1.1%(G2)。无 3/4 级毒性。少数患者(2%)或医生(2%)在 2 年随访时将美容效果评估为一般或差。

结论

这项关于 APBI-调强放疗的 2 期试验显示出优异的长期结果。每日 1 次分割方案耐受性良好,不良反应发生率低,美容效果较差。在本系列中,即使根据 ASTRO 标准,有些患者被认为是谨慎的或不适合接受 APBI,但我们仍显示出较低的 IBTR 发生率。

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