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ASTRO 共识声明中关于加速部分乳腺照射应用的指南如何适应术中放射治疗?欧洲肿瘤研究所治疗患者的回顾性分析。

How do the ASTRO consensus statement guidelines for the application of accelerated partial breast irradiation fit intraoperative radiotherapy? A retrospective analysis of patients treated at the European Institute of Oncology.

机构信息

Division of Radiation Oncology, European Institute of Oncology, Milan, Italy.

出版信息

Int J Radiat Oncol Biol Phys. 2012 Jul 1;83(3):806-13. doi: 10.1016/j.ijrobp.2011.08.014. Epub 2012 Jan 13.

Abstract

PURPOSE

To verify how the classification according to the American Society for Therapeutic Radiation Oncology (ASTRO) consensus statement (CS) for the application of accelerated partial breast irradiation (APBI) fits patients treated with intraoperative radiotherapy with electrons (ELIOT) at a single institution.

METHODS AND MATERIALS

The study included 1,822 patients treated with ELIOT as the sole radiation modality outside of a clinical trial at the European Institute of Oncology after breast-conserving surgery for invasive breast cancer, who were classified into CS groups of suitable, cautionary, and unsuitable. The outcome in terms of ipsilateral breast recurrence, regional node relapse, distant metastases, progression free-survival, cause-specific survival, and overall survival were assessed.

RESULTS

All the 1,822 cases except for 25 could be classified according to ASTRO CS: 294 patients met the criteria for inclusion into the suitable group, 691 patients into the cautionary group, and 812 patients into the unsuitable group. The 5-year rate of ipsilateral breast recurrence for suitable, cautionary, and unsuitable groups were 1.5%, 4.4%, and 8.8%, respectively (p = 0.0003). Whereas the regional node relapse showed no difference, the rate of distant metastases was significantly different in the unsuitable group compared with the suitable and cautionary groups, having a significant impact on survival.

CONCLUSION

In the context of patients treated with ELIOT, the ASTRO guidelines identify well the groups for whom APBI might be considered as an effective alternative to whole breast radiotherapy and also identify groups for whom APBI is not indicated.

摘要

目的

验证根据美国放射肿瘤学会(ASTRO)加速部分乳房照射(APBI)应用共识声明(CS)对患者进行分类,与在单一机构接受电子术中放射治疗(ELIOT)的患者是否相符。

方法和材料

这项研究纳入了 1822 例在欧洲肿瘤研究所行保乳手术后接受 ELIOT 作为单一放射治疗方案、且未参加临床试验的浸润性乳腺癌患者,根据 CS 将其分为适宜、谨慎和不适宜组。评估了同侧乳房复发、区域淋巴结复发、远处转移、无进展生存率、无病生存率和总生存率的结果。

结果

除 25 例外,所有 1822 例患者均能根据 ASTRO CS 进行分类:294 例患者符合纳入适宜组的标准,691 例患者符合纳入谨慎组的标准,812 例患者符合纳入不适宜组的标准。适宜、谨慎和不适宜组的 5 年同侧乳房复发率分别为 1.5%、4.4%和 8.8%(p=0.0003)。虽然区域淋巴结复发无差异,但不适宜组远处转移率明显高于适宜组和谨慎组,对生存率有显著影响。

结论

在接受 ELIOT 治疗的患者中,ASTRO 指南很好地识别了哪些患者可能适合将 APBI 作为全乳放疗的有效替代,以及哪些患者不适合使用 APBI。

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