Kaidar-Person Orit, Abdah-Bortnyak Roxolyana, Amit Amnon, Nevelsky Alexander, Berniger Alison, Bar-Deroma Raquel, Ben-Yosef Rahamim, Kuten Abraham
Division of Oncology, Rambam Health Care Campus, Haifa, Israel.
Gyneco-Oncology Unit, Rambam Health Care Campus, Haifa, Israel.
Rep Pract Oncol Radiother. 2013 Oct 16;19(1):56-61. doi: 10.1016/j.rpor.2013.09.005. eCollection 2014 Jan.
AIM/BACKGROUND: We sought to determine the tolerance level and complication rates of the vaginal vault to combined high-dose-rate intra-cavitary brachytherapy with concomitant chemo-radiotherapy.
A retrospective review of medical records of all the patients who received definitive chemo-radiotherapy for cervical cancer between 1998 and 2002 was undertaken. The records were reviewed for doses and for radiation-associated early and late sequelae of the vagina, rectum and bladder. Cumulative biological effective dose was calculated for two reference vaginal surface points.
Fifty patients were included. Average age at diagnosis was 54 years. Median follow-up was 59 months. There were no recorded instances of acute grade IV toxicity. Maximal high-dose-rate vaginal surface dose (upper central point) was 103 Gy, and maximal brachytherapy lateral surface dose was 70 Gy. Maximal cumulative biological effective dose for the lateral surface reference point was 465.5 Gy3, and the maximal cumulative biological effective dose for the superior reference point was 878.6 Gy3. There were no cases of vaginal necrosis or fistulas, and no cases of grade IV late vaginal, rectal or bladder toxicity. No correlation was found between the maximal vaginal surface dose and vaginal, rectal or bladder toxicity.
The maximal surface HDR brachytherapy dose of 103 Gy and the maximal cBED of 878.6 Gy3 were not associated with fistula or necrosis or other grade 3-4 vaginal complications. Concomitant chemo-radiotherapy, including pelvic radiotherapy and high-dose-rate intracavitary brachytherapy, is relatively safe for cervical cancer patients.
目的/背景:我们试图确定阴道穹窿对高剂量率腔内近距离放疗联合同步放化疗的耐受水平和并发症发生率。
对1998年至2002年间接受宫颈癌根治性放化疗的所有患者的病历进行回顾性研究。对阴道、直肠和膀胱的剂量以及与放疗相关的早期和晚期后遗症进行记录审查。计算两个参考阴道表面点的累积生物等效剂量。
纳入50例患者。诊断时的平均年龄为54岁。中位随访时间为59个月。无急性IV级毒性记录实例。阴道表面最大高剂量率(上中心点)为103 Gy,近距离放疗侧面最大剂量为70 Gy。侧面参考点的最大累积生物等效剂量为465.5 Gy³,上方参考点的最大累积生物等效剂量为878.6 Gy³。无阴道坏死或瘘管病例,无IV级晚期阴道、直肠或膀胱毒性病例。未发现阴道表面最大剂量与阴道、直肠或膀胱毒性之间存在相关性。
103 Gy的最大表面高剂量率近距离放疗剂量和878.6 Gy³的最大累积生物等效剂量与瘘管、坏死或其他3 - 4级阴道并发症无关。包括盆腔放疗和高剂量率腔内近距离放疗在内的同步放化疗对宫颈癌患者相对安全。