Kyrgias George, Zygogianni Anna, Theodorou Kiki, Koukourakis Michael, Oikonomou Anastasia, Kouvaris John, Kouloulias Vassilios
Departments of *Radiotherapy §Medical Physics, School of Health Sciences, Faculty of Medicine, University of Thessaly †Department of Radiation Oncology, University Hospital of Larissa, Larissa, Thessaly ‡1st Department of Radiology-Radiotherapy Unit #2nd Department of Radiology-Radiotherapy Unit, School of Medicine, Kapodistrian University of Athens ¶2nd Department of Surgery, St Savvas Anticancer Hospital of Athens, Athens ∥Department of Radiotherapy-Oncology, Democritus University of Thrace-Medical School, Alexandroupolis, Greece.
Am J Clin Oncol. 2015 Aug;38(4):358-63. doi: 10.1097/COC.0b013e3182a46740.
The aim of this study is to evaluate the feasibility and the related toxicity of hypofractionated whole-breast irradiation with a concomitant daily boost in early breast cancer women not eligible for accelerated partial-breast irradiation.
Twenty-seven patients received 46 Gy to the whole breast in 20 fractions/4 weeks with 2.3 Gy/fraction plus an additional concomitant daily boost of 0.4 Gy to the tumor bed, giving a total dose of 54 Gy (EQD2=60 Gy). The cosmetic outcome was assessed according to the European Organization for Research and Treatment of Cancer and Radiation Therapy Oncology Group grading system.
Three months after the end of radiotherapy, 59.2% and 40.7% of patients showed grade 0 skin toxicity and grade 1 skin toxicity, respectively. After 6 months, 70.4% and 29.6% of patients showed grade 0 and grade 1 skin toxicity. After 1 year, grade 0 skin toxicity was found in 77.7% of the patients and grade 1 skin toxicity in 22.2% of the patients. After 18 months, grade 0 skin toxicity was found in 92.6% and grade 1 skin toxicity in 7.4% of the patients. After a median follow-up of 24 months, all patients showed excellent cosmetic results with minimal breast edema and minimal skin changes. There have been no local relapses to date.
The accelerated hypofractionated schedule with a concomitant boost appears to be an acceptable alternative to the traditional longer schedule, with low local toxicity and excellent to good short-term cosmetic results, although a much longer follow-up is needed to assess the local control rate.
本研究旨在评估在不符合加速部分乳腺照射条件的早期乳腺癌女性中,采用超分割全乳照射并每日同步加量照射的可行性及相关毒性。
27例患者接受全乳46 Gy照射,分20次/4周,每次2.3 Gy,同时对瘤床每日额外同步加量0.4 Gy,总剂量达54 Gy(等效剂量2=60 Gy)。根据欧洲癌症研究与治疗组织及放射治疗肿瘤学组的分级系统评估美容效果。
放疗结束3个月后,分别有59.2%和40.7%的患者出现0级和1级皮肤毒性。6个月后,70.4%和29.6%的患者出现0级和1级皮肤毒性。1年后,77.7%的患者出现0级皮肤毒性,22.2%的患者出现1级皮肤毒性。18个月后,92.6%的患者出现0级皮肤毒性,7.4%的患者出现1级皮肤毒性。中位随访24个月后,所有患者均获得了极佳的美容效果,乳房水肿轻微,皮肤变化极小。迄今为止未出现局部复发。
同步加量的加速超分割方案似乎是传统较长疗程的可接受替代方案,局部毒性低,短期美容效果良好至极佳,不过需要更长时间的随访来评估局部控制率。