Ott Oliver J, Lotter Michael, Sauer Rolf, Strnad Vratislav
Department of Radiation Oncology, University Hospital Erlangen, Erlangen, Germany.
Strahlenther Onkol. 2007 Aug;183(8):426-31. doi: 10.1007/s00066-007-1738-6.
To describe relative skin dose estimations and their impact on cosmetic outcome in interstitial multicatheter accelerated partial-breast irradiation (APBI).
Between April 2001 and January 2005, 105 consecutive patients with early breast cancer were recruited in Erlangen, Germany, for this substudy of the German-Austrian APBI phase II trial. 51% (54/105) received pulsed-dose-rate (PDR), and 49% (51/105) high-dose-rate (HDR) brachytherapy. Prescribed reference dose for HDR brachytherapy was 32 Gy in eight fractions of 4 Gy, twice daily. Prescribed reference dose in PDR brachytherapy was 49.8 Gy in 83 consecutive fractions of 0.6 Gy every hour. Total treatment time was 3-4 days. With a wire cross on the skin surface during the brachytherapy-planning procedure the minimal, mean and maximal relative skin doses (SD(min%), SD(max%), SD(mean%)) were recorded. Endpoint of this evaluation was the cosmetic outcome in relation to the relative skin doses.
Median follow-up time was 38 months (range, 19-65 months). Cosmetic results for all patients were excellent in 57% (60/105), good in 36% (38/105), and fair in 7% (7/105). The SD(min%) (27.0% vs. 31.7%; p = 0.032), SD(mean%) (34.2% vs. 38.1%; p = 0.008), and SD(max%) (38.2% vs. 46.4%; p = 0.003) were significantly lower for patients with excellent cosmetic outcome compared to patients with a suboptimal outcome. SD(mean%) (37.6% vs. 34.2%; p = 0.026) and SD(max%) (45.4% vs. 38.2%; p = 0.008) were significantly higher for patients with good cosmetic outcome compared with the patients with excellent results.
The appraisal of skin doses has been shown to be relevant to the achievement of excellent cosmetic outcome. Further investigations are necessary, especially on the basis of CT-based brachytherapy planning, to further improve the treatment results of multicatheter APBI.
描述间质多导管加速部分乳腺照射(APBI)中相对皮肤剂量估计及其对美容效果的影响。
2001年4月至2005年1月期间,德国埃尔朗根连续招募了105例早期乳腺癌患者参与德奥APBI II期试验的这项子研究。51%(54/105)接受了脉冲剂量率(PDR)近距离放疗,49%(51/105)接受了高剂量率(HDR)近距离放疗。HDR近距离放疗的规定参考剂量为32 Gy,分8次,每次4 Gy,每天2次。PDR近距离放疗的规定参考剂量为49.8 Gy,连续83次,每小时0.6 Gy。总治疗时间为3 - 4天。在近距离放疗计划过程中,通过皮肤表面的金属丝交叉记录最小、平均和最大相对皮肤剂量(SD(min%)、SD(max%)、SD(mean%))。该评估的终点是与相对皮肤剂量相关的美容效果。
中位随访时间为38个月(范围19 - 65个月)。所有患者的美容效果为优的占57%(60/105),良的占36%(38/105),差的占7%(7/105)。美容效果优的患者的SD(min%)(27.0%对31.7%;p = 0.032)、SD(mean%)(34.2%对38.1%;p = 0.008)和SD(max%)(38.2%对46.4%;p = 0.003)显著低于美容效果欠佳的患者。美容效果良的患者的SD(mean%)(37.6%对34.2%;p = 0.026)和SD(max%)(45.4%对38.2%;p = 0.008)显著高于美容效果优的患者。
已表明皮肤剂量评估与实现优异的美容效果相关。有必要进一步开展研究,尤其是基于CT的近距离放疗计划,以进一步改善多导管APBI的治疗效果。