质子超分割加速放疗治疗乳腺血管肉瘤

IF 2.1 Q3 ONCOLOGY
W. S. Looi, J. Bradley, Xiaoying Liang, Christiana M. Shaw, Mark M. Leyngold, R. M. Mailhot Vega, E. Brooks, M. Rutenberg, L. Spiguel, F. Giap, N. Mendenhall
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Toxicity was recorded prospectively by using the Common Terminology Criteria for Adverse Events, version 4.0. Results The median follow-up duration was 1.5 (range, 0.25-2.9) years. The median age at RAAS diagnosis was 73 (range, 60-83) years with a median latency of 8.9 (range, 5-14) years between radiation therapy completion and RAAS diagnosis. The median mean heart dose was 2.2 (range, 0.1-4.96) Gy. HART was delivered postoperatively (n = 1), preoperatively (n = 3), preoperatively for local recurrence after initial management with mastectomy (n = 1), and as definitive treatment (n = 1). All patients had local control of disease throughout follow-up. Three of 4 patients treated preoperatively had a pathologic complete response. The patient treated definitively had a complete metabolic response on her posttreatment PET/CT (positron emission tomography–computed tomography) scan. Two patients developed distant metastatic disease despite local control and died of their disease. 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引用次数: 0

摘要

目的放射相关性血管肉瘤(RAAS)是癌症放射治疗中罕见的并发症。超分割加速再照射(HART)可改善术后局部控制。质子治疗可以通过减轻潜在毒性来进一步提高治疗率。材料和方法在2015年至2021年间,6名参与前瞻性登记的局部RAAS患者接受了HART质子治疗。HART每天递送两次或三次,其粒径分别为1.5或1.0 Gy。所有患者都接受了45 Gy的大选择性剂量治疗,然后增加到65 Gy(范围60-75)的中位剂量。使用4.0版不良事件通用术语标准前瞻性记录毒性。结果中位随访时间为1.5年(0.25~2.9年)。RAAS诊断的中位年龄为73岁(范围60-83),放射治疗完成和RAAS诊断之间的中位潜伏期为8.9年(范围5-14)。平均心脏剂量中位数为2.2(0.1-4.96)Gy。术后给予HART(n = 1) ,术前(n = 3) ,术前乳房切除术后局部复发(n = 1) 和作为最终治疗(n = 1) 。所有患者在整个随访过程中都得到了局部疾病控制。术前接受治疗的4例患者中,有3例出现病理学完全缓解。接受治疗的患者在治疗后的PET/CT(正电子发射断层扫描-计算机断层扫描)扫描中有完全的代谢反应。两名患者尽管得到了局部控制,但仍发展为远处转移性疾病,并死于疾病。3名患者出现急性3级毒性:2名术前接受HART治疗的患者出现伤口裂开,1名术后出现3级伤口感染,症状得到缓解。结论HART联合质子治疗局部控制RAAS疗效确切,病理完全缓解率高,至今无局部复发。然而,应该对远处转移进行警惕性监测。毒性与光子/电子系列相当。在这种大容量再照射环境中,RAAS的质子治疗可以最大限度地保留正常组织。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hyperfractionated-Accelerated Reirradiation with Proton Therapy for Radiation-Associated Breast Angiosarcoma
Purpose Radiation-associated angiosarcoma (RAAS) is a rare complication among patients treated with radiation therapy for breast cancer. Hyperfractionated-accelerated reirradiation (HART) improves local control after surgery. Proton therapy may further improve the therapeutic ratio by mitigating potential toxicity. Materials and Methods Six patients enrolled in a prospective registry with localized RAAS received HART with proton therapy between 2015 and 2021. HART was delivered twice or thrice daily in fraction sizes of 1.5 or 1.0 Gy, respectively. All patients received 45 Gy to a large elective volume followed by boosts to a median dose of 65 (range, 60-75) Gy. Toxicity was recorded prospectively by using the Common Terminology Criteria for Adverse Events, version 4.0. Results The median follow-up duration was 1.5 (range, 0.25-2.9) years. The median age at RAAS diagnosis was 73 (range, 60-83) years with a median latency of 8.9 (range, 5-14) years between radiation therapy completion and RAAS diagnosis. The median mean heart dose was 2.2 (range, 0.1-4.96) Gy. HART was delivered postoperatively (n = 1), preoperatively (n = 3), preoperatively for local recurrence after initial management with mastectomy (n = 1), and as definitive treatment (n = 1). All patients had local control of disease throughout follow-up. Three of 4 patients treated preoperatively had a pathologic complete response. The patient treated definitively had a complete metabolic response on her posttreatment PET/CT (positron emission tomography–computed tomography) scan. Two patients developed distant metastatic disease despite local control and died of their disease. Acute grade 3 toxicity occurred in 3 patients: 2 patients undergoing preoperative HART experienced wound dehiscence and 1 postoperatively developed grade 3 wound infection, which resolved. Conclusion HART with proton therapy appears effective for local control of RAAS with a high rate of pathologic complete response and no local recurrences to date. However, vigilant surveillance for distant metastasis should occur. Toxicity is comparable to that in photon/electron series. Proton therapy for RAAS may maximize normal tissue sparing in this large-volume reirradiation setting.
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来源期刊
International Journal of Particle Therapy
International Journal of Particle Therapy Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
3.70
自引率
5.90%
发文量
23
审稿时长
20 weeks
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