Department of Radiation Oncology, Tata Memorial Hospital, Parel, Mumbai-12, India.
Int J Gynecol Cancer. 2011 Aug;21(6):1110-6. doi: 10.1097/IGC.0b013e31821caa55.
The objectives are to report the dosimetric analysis, preliminary clinical outcome, and comparison with published data of 3-dimensional magnetic resonance-based high dose rate brachytherapy (BT) in cervical cancer.
The data set of 24 patients with cervical cancer treated with high dose-rate brachytherapy applications was analyzed. All patients received radiation with or without chemotherapy (10 patients received concomitant chemoradiation). Point A, International Commission on Radiation Units and Measurement (ICRU) point doses, and Groupe Europeen de Curietherapie-European Society for Therapeutic Radiology and Oncology dose volume parameters, namely, high-risk clinical target volume (HR-CTV), D90 and D100 doses, and dose to D0.1cc and D2cc, for rectum, bladder, and sigmoid, were calculated and correlated.
Mean ± SD HR-CTV was 45.2 ± 15.8 cc. The mean ± SD point A dose was 73.4 ± 4.5 Gy (median, 74.3 Gy) total biologically equivalent dose in 2 Gy per fraction (EQD2), whereas mean ± SD D90 doses were 70.9 ± 10.6 GyEQD2 (median, 68). The mean ± SD ICRU rectal and bladder points were 63.5 ± 8.1 and 80.4 ± 34.4 GyEQD2, respectively. The D0.1cc and D2cc for rectum were 66.0 ± 9.9 GyEQD2 (median, 64.5) and 57.8 ± 7.7 GyEQD2 (median, 58.8), for bladder 139.1 ± 54.7 GyEQD2 (median, 131.9) and 93.4 ± 24.6 GyEQD2 (median, 91), and sigmoid were 109.4 ± 45.2 GyEQD2 (median, 91) and 74.6 ± 19.6 GyEQD2 (median, 69.6). With a median follow-up of 24 months, 3 patients had local nodal failure, 1 had right external iliac nodal failure, and 1 had left supraclavicular nodal failure.
The 3-D magnetic resonance image-based high dose-rate brachytherapy approach in cervical cancers is feasible. In our experience, the HR-CTV volumes are large, and D0.1cc and D2cc doses to bladder and sigmoid are higher than published literature so far.
报告宫颈癌三维磁共振引导高剂量率近距离放疗(BT)的剂量学分析、初步临床结果,并与已发表数据进行比较。
分析了 24 例宫颈癌患者接受高剂量率 BT 治疗的数据。所有患者均接受放疗联合或不联合化疗(10 例接受同期放化疗)。计算并比较了国际辐射单位和测量委员会(ICRU)点剂量、欧洲近距离治疗协作组-欧洲肿瘤放射治疗学会(Groupe Europeen de Curietherapie-European Society for Therapeutic Radiology and Oncology)剂量体积参数,即高危临床靶区(HR-CTV)、D90 和 D100 剂量以及直肠、膀胱和乙状结肠的 D0.1cc 和 D2cc 剂量,包括点 A、剂量和剂量体积参数。
HR-CTV 的平均(SD)为 45.2(15.8)cc。点 A 剂量的平均(SD)为 73.4(4.5)Gy,即 2 Gy 分次数(EQD2)总生物等效剂量为 74.3 Gy,而 D90 剂量的平均(SD)为 70.9(10.6)GyEQD2(中位数为 68Gy)。ICRU 直肠和膀胱点的平均(SD)分别为 63.5(8.1)和 80.4(34.4)GyEQD2。直肠的 D0.1cc 和 D2cc 分别为 66.0(9.9)GyEQD2(中位数为 64.5Gy)和 57.8(7.7)GyEQD2(中位数为 58.8Gy),膀胱的 D0.1cc 和 D2cc 分别为 139.1(54.7)GyEQD2(中位数为 131.9Gy)和 93.4(24.6)GyEQD2(中位数为 91Gy),乙状结肠的 D0.1cc 和 D2cc 分别为 109.4(45.2)GyEQD2(中位数为 91Gy)和 74.6(19.6)GyEQD2(中位数为 69.6Gy)。中位随访 24 个月时,3 例患者发生局部淋巴结失败,1 例发生右髂外淋巴结失败,1 例发生左锁骨上淋巴结失败。
宫颈癌的三维磁共振图像引导高剂量率近距离放疗方法是可行的。根据我们的经验,HR-CTV 体积较大,膀胱和乙状结肠的 D0.1cc 和 D2cc 剂量高于目前已发表的文献。