剂量去强化的 3 天光子、质子或近距离放射治疗:非随机对照部分乳腺照射试验。

IF 6.4 1区 医学 Q1 ONCOLOGY
Robert W Mutter, Michael A Golafshar, Matthew R Buras, Bryce P Comstock, Maddi Jacobson, Todd DeWees, Nicholas B Remmes, Leah N Francis, Judy C Boughey, Kathryn J Ruddy, Lisa A McGee, Arslan Afzal, Laura A Vallow, Keith M Furutani, Christopher L Deufel, Dean A Shumway, Haeyoung Kim, Minetta C Liu, Amy C Degnim, James W Jakub, Tamara Z Vern-Gross, William W Wong, Samir H Patel, Carlos E Vargas, Bradley J Stish, Mark R Waddle, Deanna H Pafundi, Michele Y Halyard, Kimberly S Corbin, Tina J Hieken, Sean S Park
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引用次数: 0

摘要

背景:乳腺部分照射(PBI)的最佳方法尚不清楚。我们对光子、质子和近距离放射治疗的新型去强化3分量PBI方案进行了研究:多中心非随机对照试验,主要结果为 3 年后与 PBI 前相比的不良外观。资格标准为年龄≥50岁,接受过保乳手术治疗的结节阴性雌激素受体阳性(ER+)浸润性乳腺癌或任何直径≤2.5厘米的原位导管癌(DCIS)。光子和质子 PBI 的 RBE 为 21.9 Gy,近距离放射治疗为 21 Gy,分 3 次进行。放疗技术和辅助内分泌治疗的使用由医生和患者自行决定:2015年6月17日至2017年7月13日期间,161名符合条件的患者接受了光子(56人)、质子(49人)或近距离放射治疗(56人)。患者年龄中位数为 66.8 岁。126人(78.3%)患有浸润性乳腺癌(均为ER+),35人(21.7%)患有DCIS(88.6%为ER+)。54.0%的浸润性乳腺癌患者和25.8%的ER+ DCIS患者开始并坚持接受规定的内分泌治疗。出现不良外观的患者比例(通过训练有素的护士评估)在基线时为 14.5%,3 年后为 2.3%(差异为 -12.2%,95% CI (-100%, -6.4%))。最后一次随访(中位随访时间为 5 年)时,护士评估的不良外观率为 5.7%,数字照片小组评估的不良外观率为 5.6%,患者自我报告的不良外观率为 5.2%。在患者报告的其他结果中,没有观察到有临床意义的变化,近距离治疗组仅发生了两起2级或以上的不良事件,均为2级。5年无局部复发生存率和无进展生存率分别为98.0%和95.5%。在60例Ki67≤13.25%的浸润性乳腺癌患者中,没有出现局部复发:结论:为期3天的去强化PBI能提供良好的疾病控制、耐受性和美容效果,符合预先设定的可接受性标准。这种方法对于小结节阴性ER+ BC和DCIS患者来说是一种有吸引力的选择:试验注册:ClinicalTrials.gov 识别码 NCT02453737。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dose Deintensified 3-Day Photon, Proton, or Brachytherapy: A Nonrandomized Controlled Partial Breast Irradiation Trial.

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.

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来源期刊
CiteScore
11.00
自引率
7.10%
发文量
2538
审稿时长
6.6 weeks
期刊介绍: International Journal of Radiation Oncology • Biology • Physics (IJROBP), known in the field as the Red Journal, publishes original laboratory and clinical investigations related to radiation oncology, radiation biology, medical physics, and both education and health policy as it relates to the field. This journal has a particular interest in original contributions of the following types: prospective clinical trials, outcomes research, and large database interrogation. In addition, it seeks reports of high-impact innovations in single or combined modality treatment, tumor sensitization, normal tissue protection (including both precision avoidance and pharmacologic means), brachytherapy, particle irradiation, and cancer imaging. Technical advances related to dosimetry and conformal radiation treatment planning are of interest, as are basic science studies investigating tumor physiology and the molecular biology underlying cancer and normal tissue radiation response.
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