Gill Beant S, Kim Hayeon, Houser Christopher J, Kelley Joseph L, Sukumvanich Paniti, Edwards Robert P, Comerci John T, Olawaiye Alexander B, Huang Marilyn, Courtney-Brooks Madeleine, Beriwal Sushil
Department of Radiation Oncology, Magee-Womens Hospital of University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.
Department of Gynecologic Oncology, Magee-Womens Hospital of University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.
Int J Radiat Oncol Biol Phys. 2015 Mar 1;91(3):540-7. doi: 10.1016/j.ijrobp.2014.10.053. Epub 2015 Jan 30.
Image-based brachytherapy is increasingly used for gynecologic malignancies. We report early outcomes of magnetic resonance imaging (MRI)-guided brachytherapy.
Consecutive patient cases with FIGO stage IB1 to IVA cervical cancer treated at a single institution were retrospectively reviewed. All patients received concurrent cisplatin with external beam radiation therapy along with interdigitated high-dose-rate intracavitary brachytherapy. Computed tomography or MRI was completed after each application, the latter acquired for at least 1 fraction. High-risk clinical target volume (HRCTV) and organs at risk were identified by Groupe Européen de Curiethérapie and European SocieTy for Radiotherapy and Oncology guidelines. Doses were converted to equivalent 2-Gy doses (EQD2) with planned HRCTV doses of 75 to 85 Gy.
From 2007 to 2013, 128 patients, median 52 years of age, were treated. Predominant characteristics included stage IIB disease (58.6%) with a median tumor size of 5 cm, squamous histology (82.8%), and no radiographic nodal involvement (53.1%). Most patients (67.2%) received intensity modulated radiation therapy (IMRT) at a median dose of 45 Gy, followed by a median brachytherapy dose of 27.5 Gy (range, 25-30 Gy) in 5 fractions. At a median follow up of 24.4 months (range, 2.1-77.2 months), estimated 2-year local control, disease-free survival, and cancer-specific survival rates were 91.6%, 81.8%, and 87.6%, respectively. Predictors of local failure included adenocarcinoma histology (P<.01) and clinical response at 3 months (P<.01). Among the adenocarcinoma subset, receiving HRCTV D90 EQD2 ≥84 Gy was associated with improved local control (2-year local control rate 100% vs 54.5%, P=.03). Grade 3 or greater gastrointestinal or genitourinary late toxicity occurred at a 2-year actuarial rate of 0.9%.
This study constitutes one of the largest reported series of MRI-guided brachytherapy in North America, demonstrating excellent local control with acceptable morbidity. Dose escalation may be warranted when feasible for adenocarcinomas to offset the risk of local failure.
基于图像的近距离放射治疗越来越多地用于妇科恶性肿瘤。我们报告磁共振成像(MRI)引导下近距离放射治疗的早期结果。
回顾性分析在单一机构接受治疗的FIGO分期为IB1至IVA期宫颈癌的连续患者病例。所有患者均接受顺铂同步外照射放疗以及交叉指型高剂量率腔内近距离放射治疗。每次治疗后完成计算机断层扫描或MRI,后者至少获取1个分次的数据。根据欧洲近距离治疗协作组和欧洲放射治疗与肿瘤学会指南确定高危临床靶区(HRCTV)和危及器官。剂量转换为等效2 Gy剂量(EQD2),计划HRCTV剂量为75至85 Gy。
2007年至2013年,共治疗128例患者,中位年龄52岁。主要特征包括IIB期疾病(58.6%),中位肿瘤大小5 cm,鳞状组织学(82.8%),无影像学淋巴结受累(53.1%)。大多数患者(67.2%)接受调强放射治疗(IMRT),中位剂量45 Gy,随后进行中位近距离放射治疗剂量27.5 Gy(范围25 - 30 Gy),分5次给予。中位随访24.4个月(范围2.1 - 77.2个月),估计2年局部控制率、无病生存率和癌症特异性生存率分别为91.6%、81.8%和87.6%。局部失败的预测因素包括腺癌组织学(P <.01)和3个月时的临床反应(P <.01)。在腺癌亚组中,HRCTV D90 EQD2≥84 Gy与局部控制改善相关(2年局部控制率100%对54.5%,P =.03)。2年精算3级或更高级别的胃肠道或泌尿生殖系统晚期毒性发生率为0.9%。
本研究是北美报道的最大系列MRI引导下近距离放射治疗之一,显示出良好的局部控制且并发症可接受。对于腺癌,在可行时可能需要增加剂量以抵消局部失败的风险。