Department of Radiation Oncology, Gustave Roussy Cancer Campus, 114 Rue Edouard Vaillant, 94800 Villejuif, France.
Department of Public Health, Lucien Neuwirth Cancer Institute, 108 bis avenue Albert Raimond, BP60008, 42271 Saint-Priest-en-Jarez, France.
Gynecol Oncol. 2020 Aug;158(2):323-330. doi: 10.1016/j.ygyno.2020.05.032. Epub 2020 May 29.
This study assessed outcomes of inoperable endometrial cancer (IEC) patients treated with definitive external beam radiation therapy (EBRT) followed by a 3D image-guided brachytherapy boost.
All consecutive patients treated with EBRT followed by 3D image-guided brachytherapy for IEC were retrospectively included. EBRT delivered a dose of 45Gy. Then, patients had an uterovaginal brachytherapy guided by 3D imaging. Clinical target volume (CTV) included the whole uterus and the initial disease extent. Gross tumour volume (GTV) included the residual disease at time of brachytherapy.
Twenty-seven patients were identified. Causes of inoperability were comorbidities (37%) or tumour loco regional extent (63%). Including EBRT and brachytherapy, the median D (minimal dose delivered to 90% of the volume) was 60.7 Gy (IQR = 56.4-64.2) for the CTV, and was 73.6 Gy (IQR = 64.1-83.7) for the GTV. The median overall treatment time was 50 days (IQR = 46-54). The mean follow-up was 36.5 months (SD = 30.2). The cumulative incidence of local, pelvic and distant failures was 19% (n = 5), 7% (n = 2) and 26% (n = 7), respectively. Five-year overall survival was 63% (95% CI = 43-91). Late urinary and gastro intestinal toxicities ≥ grade 2 were reported in four (15%) and two patients (7%) respectively. No vaginal toxicity ≥ grade 2 was reported.
EBRT followed by intracavitary brachytherapy seems to be an effective option for IEC. The implementation of 3D concepts at time of brachytherapy may contribute to high local control probability and low toxicity profile. Large scale retrospective or prospective data are needed to confirm these early data.
本研究评估了无法手术的子宫内膜癌(IEC)患者接受根治性外照射放疗(EBRT)后,再行三维图像引导近距离放疗加量的治疗结果。
回顾性纳入所有接受 EBRT 后行三维图像引导近距离放疗治疗 IEC 的连续患者。EBRT 给予 45Gy 剂量。然后,患者行阴道三维成像引导的腔内近距离放疗。临床靶区(CTV)包括整个子宫和初始疾病范围。大体肿瘤体积(GTV)包括近距离放疗时残留的疾病。
共确定 27 例患者。无法手术的原因是合并症(37%)或肿瘤局部范围(63%)。包括 EBRT 和近距离放疗,CTV 的中位 D(最小剂量达到 90%体积)为 60.7Gy(IQR=56.4-64.2),GTV 为 73.6Gy(IQR=64.1-83.7)。中位总治疗时间为 50 天(IQR=46-54)。平均随访 36.5 个月(SD=30.2)。局部、盆部和远处失败的累积发生率分别为 19%(n=5)、7%(n=2)和 26%(n=7)。5 年总生存率为 63%(95%CI=43-91)。4 例(15%)和 2 例(7%)患者分别报告有≥2 级迟发性尿和胃肠道毒性。无阴道≥2 级毒性。
EBRT 后行腔内近距离放疗似乎是 IEC 的有效选择。在近距离放疗时实施三维概念可能有助于提高局部控制率和降低毒性谱。需要大样本回顾性或前瞻性数据来证实这些早期数据。