Department of Radiation Oncology, Leiden University Medical Center, Leiden, The Netherlands.
Department of Radiation Oncology, Haaglanden Medical Center, The Hague, The Netherlands.
Breast Cancer Res Treat. 2018 Jun;169(3):549-559. doi: 10.1007/s10549-018-4712-3. Epub 2018 Feb 19.
We investigated the acute toxicity of accelerated partial breast irradiation using external beam (EB-APBI) or intraoperative radiotherapy (IORT) techniques in elderly breast cancer patients.
Women ≥ 60 years with unifocal breast tumors of ≤ 30 mm were eligible for this prospective multi-center cohort study. IORT was applied with electrons following lumpectomy (23.3 Gy). EB-APBI was delivered using 3D-CRT or IMRT in 10 daily fractions of 3.85 Gy within 6 weeks after surgery. Acute toxicity was scored using the CTCAE v3.0 at 3 months after treatment. Patient-reported symptoms were analyzed using visual analogue scales (VAS) for pain and fatigue (scale 0-10), and single items from the EORTC QLQ-C30 and Breast Cancer questionnaires.
In total, 267 (IORT) and 206 (EB-APBI) patients were available for toxicity analysis. More patients experienced ≥ grade 2 CTCAE acute toxicity in the IORT group (10.4% IORT and 4.9% EB-APBI; p = 0.03); grade 3 toxicity was low (3.3% IORT and 1.5% EB-APBI; ns); and no grade 4 toxicity occurred. EB-APBI patients experienced less fatigue direct postoperatively (EORTC p < 0.00, VAS p < 0.00). After 3 months only pain, according to the VAS scale, was significantly worse in the EB-APBI group (p < 0.00).
Acute toxicity after IORT and EB-APBI treatment is acceptable.
我们研究了使用外部束(EB-APBI)或术中放疗(IORT)技术对老年乳腺癌患者进行加速部分乳房照射的急性毒性。
年龄≥60 岁且乳房单病灶肿瘤直径≤30mm的女性符合本前瞻性多中心队列研究的纳入标准。IORT 在乳房肿瘤切除术(23.3Gy)后采用电子束进行。EB-APBI 在手术后 6 周内采用 3D-CRT 或 IMRT,每天 10 次,每次 3.85Gy,共 10 次。在治疗后 3 个月使用 CTCAE v3.0 对急性毒性进行评分。采用视觉模拟量表(VAS)对疼痛和疲劳(0-10 分)以及 EORTC QLQ-C30 和乳腺癌问卷的单项进行患者报告症状分析。
共有 267 例(IORT)和 206 例(EB-APBI)患者可进行毒性分析。IORT 组更多患者出现≥2 级 CTCAE 急性毒性(10.4% IORT 和 4.9% EB-APBI;p=0.03);3 级毒性较低(3.3% IORT 和 1.5% EB-APBI;无统计学差异);无 4 级毒性。EB-APBI 患者术后直接疲劳程度较轻(EORTC p<0.00,VAS p<0.00)。仅在 3 个月时,EB-APBI 组的疼痛(VAS 评分)明显更严重(p<0.00)。
IORT 和 EB-APBI 治疗后的急性毒性是可接受的。