Facondo Giuseppe, Vullo Gianluca, DE Sanctis Vitaliana, Valeriani Maurizio, Ascolese Anna Maria, Massaro Maria, Anzellini Dimitri, Osti Mattia Falchetto
Department of Medicine and Surgery and Translational Medicine,Sapienza University of Rome, Radiotherapy Oncology, St. Andrea Hospital, Rome, Italy.
Cancer Diagn Progn. 2021 May 3;1(2):53-60. doi: 10.21873/cdp.10008. eCollection 2021 May-Jun.
Standard treatment for locally advanced cervical cancer is external beam radiotherapy followed by brachytherapy (BT). Stereotactic body radiation therapy (SBRT) is a possible option for treating patients ineligible for BT.
From October 2012 to July 2020, nine women with cervical cancer received SBRT to high-risk volumes. The Kaplan-Meier method was used to estimate the rates of overall and disease-free survival.
The median age was 52 years; 88% of patients had squamous carcinoma. Reasons for forgoing BT were cervical canal stenosis, treatment refusal and hematological disease. The median boost dose was 18 Gy and the median dose per fraction was 6 Gy. Median follow-up was 16 months. The median survival was 24 months, the actuarial 2-year OS rate was 70%, and median disease-free survival was 11 months. One grade 3 late vaginal toxicity was reported. No acute nor late grade 4 toxicities were observed.
SBRT boost in patients with cervical cancer ineligible for BT led to acceptable survival outcomes and a safe toxicity profile.
局部晚期宫颈癌的标准治疗是外照射放疗后行近距离放疗(BT)。立体定向体部放疗(SBRT)是治疗不适合BT的患者的一种可能选择。
2012年10月至2020年7月,9例宫颈癌患者接受了针对高危靶区的SBRT。采用Kaplan-Meier法估计总生存率和无病生存率。
中位年龄为52岁;88%的患者为鳞状细胞癌。放弃BT的原因包括宫颈管狭窄、拒绝治疗和血液系统疾病。中位追加剂量为18 Gy,中位分次剂量为6 Gy。中位随访时间为16个月。中位生存期为24个月,2年总生存率为70%,中位无病生存期为11个月。报告了1例3级晚期阴道毒性反应。未观察到急性或晚期4级毒性反应。
对不适合BT的宫颈癌患者行SBRT追加放疗可带来可接受的生存结果和安全的毒性反应。