Mayadev Jyoti, Viswanathan Akila, Liu Yu, Li Chin-Shang, Albuquerque Kevin, Damato Antonio L, Beriwal Sushil, Erickson Beth
Department of Radiation Oncology, Davis Medical Center, University of California, Sacramento, CA.
Department of Radiation Oncology, Brigham & Women's Hospital, Harvard Medical School, Boston, MA.
Brachytherapy. 2017 Jan-Feb;16(1):22-43. doi: 10.1016/j.brachy.2016.03.008.
Advanced imaging used in combination with brachytherapy (BT) has revolutionized the treatment of patients with cervical cancer. We present a comprehensive review of the literature for definitive radiation with high-dose-rate (HDR) BT. In addition, we investigate potential outcome improvement with image-based brachytherapy (IBBT) compared to studies using traditional Point A dosing. This review extensively investigates acute and late toxicities.
This study reviews the literature from 2000 to 2015 with an emphasis on modern approaches including concurrent chemotherapy (chemoRT), radiation, and HDR BT and IBBT. Descriptive statistics and pelvic control (PC), disease-free survival (DFS), and overall survival (OS) outcomes were calculated using weighted means to report pooled analysis of outcomes.
Literature search yielded 16 prospective, 51 retrospective studies that reported survival outcomes, and 13 retrospective studies that focused on acute and late toxicity outcomes regardless of applicator type. There are 57 studies that report Point A dose specification with 33 having chemoRT, and 10 studies that use IBBT, 8 with chemoRT. Patients receiving radiation and chemoRT with HDR BT in the prospective studies, with >24 months followup, rates of PC were: for RT: 73%, SD: 11; CRT: 82%, SD: 8; DFS-RT: 55%, SD: 10; CRT: 65%, SD: 7; OS-RT: 66%, SD: 7; CRT: 70%, SD: 11. In the retrospective studies, the PC rates (weighted means) for the radiation and chemoradiation outcomes are 75% vs. 80%, and for DFS, the values were 55% vs. 63%, respectively. Comparing patients receiving chemoRT and IBBT to traditional Point A dose specification, there is a significant improvement in PC (p < 0.01) and DFS (p < 0.01) with IBBT. The range of genitourinary late toxicity reported for radiation was Grade 3: 1-6% and for chemoRT 2-20%. The range of late gastrointestinal toxicity for radiation was Grade 3: 4-11% and for chemoRT, 1-11%. For the late gynecologic toxicity, only 1 of the 16 prospective trials report a Grade 1-2 of 17% for radiation and 9% for chemoRT effects.
We present concise outcomes of PC, DFS, OS, and toxicity for cervical cancer patients treated with chemoradiation and HDR BT. Our data suggest an improvement in outcomes with the use of IBBT compared with traditional Point A dose prescriptions. In conclusion, HDR BT is a safe, effective modality when combined with IBBT.
与近距离放射治疗(BT)联合使用的先进成像技术彻底改变了宫颈癌患者的治疗方式。我们对高剂量率(HDR)BT确定性放疗的文献进行了全面综述。此外,与使用传统A点剂量法的研究相比,我们研究了基于图像的近距离放射治疗(IBBT)在改善治疗结果方面的潜力。本综述广泛研究了急性和晚期毒性。
本研究回顾了2000年至2015年的文献,重点关注现代治疗方法,包括同步化疗(放化疗)、放疗以及HDR BT和IBBT。使用加权均值计算描述性统计数据以及盆腔控制(PC)、无病生存期(DFS)和总生存期(OS)结果,以报告结果的汇总分析。
文献检索得到16项前瞻性研究、51项报告生存结果的回顾性研究以及13项关注急性和晚期毒性结果(无论施源器类型)的回顾性研究。有57项研究报告了A点剂量规范,其中33项采用放化疗,10项采用IBBT,8项采用放化疗。在前瞻性研究中接受放疗和HDR BT同步放化疗且随访时间>24个月的患者,PC率为:单纯放疗:73%,标准差:11;同步放化疗:82%,标准差:8;DFS-放疗:55%,标准差:10;同步放化疗:65%,标准差:7;OS-放疗:66%,标准差:7;同步放化疗:70%,标准差:11。在回顾性研究中,放疗和放化疗结果的PC率(加权均值)分别为75%和80%,DFS值分别为55%和63%。将接受同步放化疗和IBBT的患者与传统A点剂量规范进行比较,IBBT在PC(p<0.01)和DFS(p<0.01)方面有显著改善。报告的放疗泌尿生殖系统晚期毒性范围为3级:1%-6%,同步放化疗为2%-20%。放疗胃肠道晚期毒性范围为3级:4%-11%,同步放化疗为1%-11%。对于晚期妇科毒性,16项前瞻性试验中只有1项报告放疗的1-2级发生率为17%,同步放化疗为9%。
我们给出了接受放化疗和HDR BT治疗的宫颈癌患者的PC、DFS、OS和毒性的简要结果。我们的数据表明,与传统A点剂量处方相比,使用IBBT可改善治疗结果。总之,HDR BT与IBBT联合使用时是一种安全有效的治疗方式。