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剂量降低的3天光子、质子或近距离放射治疗:一项非随机对照部分乳腺照射试验。

Dose Deintensified 3-Day Photon, Proton, or Brachytherapy: A Nonrandomized Controlled Partial Breast Irradiation Trial.

作者信息

Mutter Robert W, Golafshar Michael A, Buras Matthew R, Comstock Bryce P, Jacobson Maddi, DeWees Todd, Remmes Nicholas B, Francis Leah N, Boughey Judy C, Ruddy Kathryn J, McGee Lisa A, Afzal Arslan, Vallow Laura A, Furutani Keith M, Deufel Christopher L, Shumway Dean A, Kim Haeyoung, Liu Minetta C, Degnim Amy C, Jakub James W, Vern-Gross Tamara Z, Wong William W, Patel Samir H, Vargas Carlos E, Stish Bradley J, Waddle Mark R, Pafundi Deanna H, Halyard Michele Y, Corbin Kimberly S, Hieken Tina J, Park Sean S

机构信息

Department of Radiation Oncology, Mayo Clinic, Rochester, Minnesota; Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota.

Division of Biostatistics and Clinical Trials, Department of Quantitative Health Sciences, Mayo Clinic, Phoenix, Arizona.

出版信息

Int J Radiat Oncol Biol Phys. 2025 Feb 1;121(2):352-364. doi: 10.1016/j.ijrobp.2024.09.019. Epub 2024 Sep 17.

Abstract

PURPOSE

The optimal approach for partial breast irradiation (PBI) is unknown. We investigated a novel de-intensified 3-fraction PBI regimen for photons, protons, and brachytherapy.

METHODS AND MATERIALS

A multicenter nonrandomized controlled trial with the primary outcome of adverse cosmesis at 3 years versus before PBI. Eligibility criteria were age ≥50 years treated with breast-conserving surgery for node-negative estrogen receptor-positive (ER+) invasive breast cancer or any ductal carcinoma in situ (DCIS) measuring ≤2.5 cm. Photon and proton PBI were prescribed 21.9 Gy (relative biological effectiveness) and brachytherapy 21 Gy in 3 fractions. Radiation therapy technique and adjuvant endocrine therapy were selected at physician and patient discretion.

RESULTS

Between June 17, 2015, and July 13, 2017, 161 eligible patients were treated with photons (56), protons (49), or brachytherapy (56). Median patient age was 66.8 years. One hundred twenty-six (78.3%) had invasive breast cancer (all ER+) and 35 (21.7%) had DCIS (88.6% ER+). Fifty-four percent of patients with invasive breast cancer and 25.8% of patients with ER+ DCIS initiated and adhered to the prescribed endocrine therapy. The proportion of patients with adverse cosmesis (by trained nurse assessment) was 14.5% at baseline and 2.3% at 3 years (difference, -12.2%; 95% CI, -100% to -6.4%). Adverse cosmesis at the last follow-up, with a median follow-up of 5 years, was 5.7% by nurse assessment, 5.6% by panel assessment of digital photographs, and 5.2% by patient self-report. There were no observed clinically meaningful changes in other patient-reported outcomes, and just 2 grade 2 or higher adverse events, both grade 2, in the brachytherapy cohort. Five-year local recurrence-free survival and progression-free survival were 98.0% and 95.5%, respectively. There were no local recurrences among 60 patients with invasive breast cancer and Ki67 ≤13.25%.

CONCLUSIONS

Deintensified 3-day PBI provided favorable disease control, tolerability, and cosmetic outcomes, meeting the prespecified criteria for acceptability. This approach is an attractive option for patients with small node-negative ER+ breast cancer and DCIS.

摘要

目的

部分乳腺照射(PBI)的最佳方法尚不清楚。我们研究了一种新的低分割3次照射的PBI方案,用于光子、质子和近距离放射治疗。

方法和材料

一项多中心非随机对照试验,主要结局是3年时与PBI前相比的不良美容效果。纳入标准为年龄≥50岁,接受保乳手术治疗的淋巴结阴性雌激素受体阳性(ER+)浸润性乳腺癌或任何最大径≤2.5 cm的导管原位癌(DCIS)。光子和质子PBI的处方剂量为21.9 Gy(相对生物效应),近距离放射治疗为21 Gy,分3次照射。放射治疗技术和辅助内分泌治疗由医生和患者自行决定。

结果

2015年6月17日至2017年7月13日期间,161例符合条件的患者接受了光子治疗(56例)、质子治疗(49例)或近距离放射治疗(56例)。患者中位年龄为66.8岁。126例(78.3%)为浸润性乳腺癌(均为ER+),35例(21.7%)为DCIS(88.6%为ER+)。54%的浸润性乳腺癌患者和25.8%的ER+ DCIS患者开始并坚持了规定的内分泌治疗。基线时不良美容效果(由经过培训的护士评估)的患者比例为14.5%,3年时为2.3%(差异为-12.2%;95% CI,-100%至-6.4%)。在中位随访5年的最后一次随访中,护士评估的不良美容效果为5.7%,数码照片小组评估为5.6%,患者自我报告为5.2%。在其他患者报告的结局中未观察到有临床意义的变化,近距离放射治疗队列中仅出现2例2级或更高等级的不良事件,均为2级。5年局部无复发生存率和无进展生存率分别为98.0%和95.5%。60例Ki67≤13.25%的浸润性乳腺癌患者中无局部复发。

结论

低分割3日PBI提供了良好的疾病控制、耐受性和美容效果,符合预先设定的可接受标准。这种方法对于小的淋巴结阴性ER+乳腺癌和DCIS患者是一个有吸引力的选择。

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