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间质高剂量率近距离放疗增敏:一种分次门诊治疗方案的可行性及美容效果

Interstitial high-dose-rate brachytherapy boost: the feasibility and cosmetic outcome of a fractionated outpatient delivery scheme.

作者信息

Manning M A, Arthur D W, Schmidt-Ullrich R K, Arnfield M R, Amir C, Zwicker R D

机构信息

Department of Radiation Oncology, Medical College of Virginia Hospitals of Virginia Commonwealth University, Richmond, Virginia 23298, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2000 Dec 1;48(5):1301-6. doi: 10.1016/s0360-3016(00)00792-6.

Abstract

PURPOSE

To evaluate the feasibility, potential toxicity, and cosmetic outcome of fractionated interstitial high dose rate (HDR) brachytherapy boost for the management of patients with breast cancer at increased risk for local recurrence.

METHODS AND MATERIALS

From 1994 to 1996, 18 women with early stage breast cancer underwent conventionally fractionated whole breast radiotherapy (50-50.4 Gy) followed by interstitial HDR brachytherapy boost. All were considered to be at high risk for local failure. Seventeen had pathologically confirmed final surgical margins of less than 2 mm or focally positive. Brachytherapy catheter placement and treatment delivery were conducted on an outpatient basis. Preplanning was used to determine optimal catheter positions to enhance dose homogeneity of dose delivery. The total HDR boost dose was 15 Gy delivered in 6 fractions of 2.5 Gy over 3 days. Local control, survival, late toxicities (LENT-SOMA), and cosmetic outcome were recorded in follow-up. In addition, factors potentially influencing cosmesis were analyzed by logistic regression analysis.

RESULTS

The minimum follow-up is 40 months with a median 50 months. Sixteen patients were alive without disease at last follow-up. There have been no in-breast failures observed. One patient died with brain metastases, and another died of unrelated causes without evidence of disease. Grade 1-2 late toxicities included 39% with hyperpigmentation, 56% with detectable fibrosis, 28% with occasional discomfort, and 11% with visible telangiectasias. Grade 3 toxicity was reported in one patient as persistent discomfort. Sixty-seven percent of patients were considered to have experienced good/excellent cosmetic outcomes. Factors with a direct relationship to adverse cosmetic outcome were extent of surgical defect (p = 0.00001), primary excision volume (p = 0.017), and total excision volume (p = 0.015).

CONCLUSIONS

For high risk patients who may benefit from increased doses, interstitial HDR brachytherapy provides a convenient outpatient method for boosting the lumpectomy cavity following conventional whole breast irradiation without overdosing normal tissues. The fractionation scheme of 15 Gy in 6 fractions over 3 days is well tolerated. The volume of tissue removed from the breast at lumpectomy appears to dominate cosmetic outcome in this group of patients.

摘要

目的

评估分割间质高剂量率(HDR)近距离放射治疗加量对局部复发风险增加的乳腺癌患者进行治疗的可行性、潜在毒性及美容效果。

方法与材料

1994年至1996年,18例早期乳腺癌女性患者接受了常规分割全乳放疗(50 - 50.4 Gy),随后进行间质HDR近距离放射治疗加量。所有患者均被认为局部失败风险高。17例患者病理证实手术切缘最终小于2 mm或局部阳性。近距离放射治疗导管放置和治疗均在门诊进行。采用预计划确定最佳导管位置以提高剂量分布的均匀性。HDR总加量剂量为15 Gy,分6次,每次2.5 Gy,在3天内完成。随访记录局部控制情况、生存率、晚期毒性(LENT - SOMA)及美容效果。此外,通过逻辑回归分析潜在影响美容效果的因素。

结果

最短随访时间为40个月,中位随访时间为50个月。16例患者在最后一次随访时无病存活。未观察到乳腺内复发。1例患者死于脑转移,另1例死于无关原因,无疾病证据。1 - 2级晚期毒性包括39%的患者有色素沉着,56%的患者有可检测到的纤维化,28%的患者偶尔有不适,11%的患者有可见的毛细血管扩张。1例患者报告有3级毒性,表现为持续不适。67%的患者被认为美容效果良好/优秀。与不良美容效果直接相关的因素有手术缺损范围(p = 0.00001)、初次切除体积(p = 0.017)和总切除体积(p = 0.015)。

结论

对于可能从增加剂量中获益的高危患者,间质HDR近距离放射治疗为常规全乳照射后对肿块切除腔进行加量提供了一种方便的门诊治疗方法,且不会使正常组织过量照射。3天内分6次给予15 Gy的分割方案耐受性良好。在这组患者中,肿块切除时从乳腺切除的组织体积似乎对美容效果起主导作用。

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