Department of Oncology, Aarhus University Hospital, Denmark.
Department of Radiation Oncology, Christian Doppler Laboratory for Medical Radiation Research for Radiation Oncology, Medical University of Vienna, Austria.
Int J Radiat Oncol Biol Phys. 2019 Jul 15;104(4):885-894. doi: 10.1016/j.ijrobp.2019.03.020. Epub 2019 Mar 21.
To describe the evolution of external beam radiation therapy (EBRT) from EMBRACE-I (general guidelines for EBRT) to the initial phase of the EMBRACE-II study (detailed protocol for EBRT).
EMBRACE-I enrolled 1416 locally advanced cervical cancer patients treated with chemoradiation including image-guided adaptive brachytherapy during 2008 to 2015. From March 2016 until March 2018, 153 patients were enrolled in the ongoing EMBRACE-II study, which involves a comprehensive detailed strategy and accreditation procedure for EBRT target contouring, treatment planning, and image guidance. EBRT planning target volumes (PTVs), treated volumes (V43 Gy), and conformity index (CI; V43 Gy/PTV) were evaluated in both studies and compared.
For EMBRACE-I, conformal radiation therapy (60% of patients) or intensity-modulated radiation therapy (IMRT) and volumetric arc therapy (VMAT; 40%) was applied with 45 to 50 Gy over 25 to 30 fractions to the elective clinical target volume (CTV). For pelvic CTVs (82%), median PTV and V43 Gy volumes were 1549 and 2390 mL, respectively, and CI was 1.54. For pelvic plus paraortic nodal (PAN) CTVs (15%), median PTV and V43 Gy volumes were 1921 and 2895 mL, and CI was 1.51. For pelvic CTVs treated with 45 to 46 Gy, the use of conformal radiation therapy was associated with a median V43 Gy volume that was 546 mL larger than with IMRT/VMAT. For pelvic CTVs treated with IMRT, the use of a dose prescription ≥48 Gy was associated with a median V43 Gy volumes that was 428 mL larger than with a dose prescription of 45 to 46 Gy. For EMBRACE-II, all patients were treated with: IMRT/VMAT, daily IGRT, 45 Gy over 25 fractions for the elective CTV, and simultaneously integrated boost for pathologic lymph nodes. For pelvic CTVs (61%), median PTV and V43 Gy volumes were 1388 and 1418 mL, and CI was 1.02. For pelvic plus PAN CTVs (32%), median PTV and V43 Gy volumes were 1720 and 1765 mL, and CI was 1.03. From EMBRACE-I to initial II, median V43 Gy was decreased by 972 mL (41%) and 1130 mL (39%), and median CI decreased from 1.54 to 1.02 and 1.51 to 1.03 for pelvic and pelvic plus PAN irradiation, respectively.
Application of IMRT/VMAT, IGRT, and a 45-Gy dose provides the potential of higher conformality inducing significant reduction of treated volume. Adherence to a detailed protocol including comprehensive accreditation, as in EMBRACE-II, reduces considerably V43 Gy and V50 Gy and improves conformality and interinstitutional consistency.
描述从 EMBRACE-I(EBRT 一般指南)到 EMBRACE-II 研究初始阶段的外部束放射治疗(EBRT)的演变过程(EBRT 详细方案)。
EMBRACE-I 纳入了 1416 例局部晚期宫颈癌患者,这些患者在 2008 年至 2015 年间接受了放化疗,包括图像引导自适应近距离放射治疗。从 2016 年 3 月至 2018 年 3 月,153 例患者入组了正在进行的 EMBRACE-II 研究,该研究涉及 EBRT 靶区勾画、治疗计划和图像引导的综合详细策略和认证程序。在两项研究中评估了 EBRT 计划靶区(PTV)、治疗体积(V43Gy)和适形指数(CI;V43Gy/PTV),并进行了比较。
对于 EMBRACE-I,采用了适形放疗(60%的患者)或调强放疗(IMRT)和容积弧形治疗(VMAT;40%),45 至 50Gy 共 25 至 30 次,用于选择性临床靶区(CTV)。对于盆腔 CTV(82%),中位 PTV 和 V43Gy 体积分别为 1549 和 2390mL,CI 为 1.54。对于盆腔加旁主动脉淋巴结(PAN)CTV(15%),中位 PTV 和 V43Gy 体积分别为 1921 和 2895mL,CI 为 1.51。对于接受 45 至 46Gy 治疗的盆腔 CTV,与 IMRT/VMAT 相比,采用适形放疗时,中位 V43Gy 体积增加了 546mL。对于接受 IMRT 治疗的盆腔 CTV,与 45 至 46Gy 剂量处方相比,使用剂量处方≥48Gy 与中位 V43Gy 体积增加了 428mL。对于 EMBRACE-II,所有患者均接受了以下治疗:IMRT/VMAT、每日 IGRT、45Gy 共 25 次用于选择性 CTV,同时对病理淋巴结进行同步整合增敏。对于盆腔 CTV(61%),中位 PTV 和 V43Gy 体积分别为 1388 和 1418mL,CI 为 1.02。对于盆腔加 PAN CTV(32%),中位 PTV 和 V43Gy 体积分别为 1720 和 1765mL,CI 为 1.03。从 EMBRACE-I 到 EMBRACE-II,中位 V43Gy 分别减少了 972mL(41%)和 1130mL(39%),中位 CI 分别从 1.54 降至 1.02 和 1.51 降至 1.03,用于盆腔和盆腔加 PAN 照射。
应用 IMRT/VMAT、IGRT 和 45Gy 剂量有可能提高适形度,显著减少治疗体积。遵循包括全面认证在内的详细方案,如 EMBRACE-II,可显著降低 V43Gy 和 V50Gy,并提高适形度和机构间一致性。