Radioterapia Oncologica, Ospedale San Giovanni Addolorata, Rome, Italy.
Radioterapia, Dipartimento di Biomedicina e Prevenzione, Università degli Studi di Roma Tor Vergata, Rome, Italy.
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.
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.
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.
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.
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.
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。
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。
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。
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。