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老年乳腺癌患者术中放疗和外照射加速部分乳腺照射的急性毒性。

Acute toxicity of intraoperative radiotherapy and external beam-accelerated partial breast irradiation in elderly breast cancer patients.

机构信息

Department of Radiation Oncology, Leiden University Medical Center, Leiden, The Netherlands.

Department of Radiation Oncology, Haaglanden Medical Center, The Hague, The Netherlands.

出版信息

Breast Cancer Res Treat. 2018 Jun;169(3):549-559. doi: 10.1007/s10549-018-4712-3. Epub 2018 Feb 19.

Abstract

BACKGROUND AND PURPOSE

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.

MATERIALS AND METHODS

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.

RESULTS

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).

CONCLUSION

Acute toxicity after IORT and EB-APBI treatment is acceptable.

摘要

背景与目的

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。

材料与方法

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。

结果

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)。

结论

IORT 和 EB-APBI 治疗后的急性毒性是可接受的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef32/5953978/04da63e1f7a6/10549_2018_4712_Fig1_HTML.jpg

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