Fondazione "Giovanni Paolo II," Unità Operativa di Radioterapia, Università Cattolica del Sacro Cuore, Campobasso, Italy.
Division of Radiotherapy, IEO European Institute of Oncology, IRCCS, Milan, Italy.
Oncologist. 2020 Feb;25(2):e311-e320. doi: 10.1634/theoncologist.2019-0309. Epub 2019 Oct 10.
Recent studies have reported improvement of outcomes (progression-free survival, overall survival, and prolongation of androgen deprivation treatment-free survival) with stereotactic body radiotherapy (SBRT) in non-small cell lung cancer and prostate cancer. The aim of this retrospective, multicenter study (MITO RT-01) was to define activity and safety of SBRT in a very large, real-world data set of patients with metastatic, persistent, and recurrent ovarian cancer (MPR-OC).
The endpoints of the study were the rate of complete response (CR) to SBRT and the 24-month actuarial local control (LC) rate on "per-lesion" basis. The secondary endpoints were acute and late toxicities and the 24-month actuarial late toxicity-free survival. Objective response rate (ORR) included CR and partial response (PR). Clinical benefit (CB) included ORR and stable disease (SD). Toxicity was evaluated by the Radiation Therapy Oncology Group (RTOG) and the European Organization for Research and Treatment of Cancer (EORTC) and Common Terminology Criteria for Adverse Events (CTCAE) scales, according to center policy. Logistic and Cox regression were used for the uni- and multivariate analysis of factors predicting clinical CR and actuarial outcomes.
CR, PR, and SD were observed in 291 (65.2%), 106 (23.8%), and 33 (7.4%) lesions, giving a rate of CB of 96.4%. Patient aged ≤60 years, planning target volume (PTV) ≤18 cm , lymph node disease, and biologically effective dose α/β10 > 70 Gy were associated with higher chance of CR in the multivariate analysis. With a median follow-up of 22 months (range, 3-120), the 24-month actuarial LC rate was 81.9%. Achievement of CR and total dose >25 Gy were associated with better LC rate in the multivariate analysis. Mild toxicity was experienced in 54 (20.7%) patients; of 63 side effects, 48 were grade 1, and 15 were grade 2. The 24-month late toxicity-free survival rate was 95.1%.
This study confirms the activity and safety of SBRT in patients with MPR-OC and identifies clinical and treatment parameters able to predict CR and LC rate.
This study aimed to define activity and safety of stereotactic body radiotherapy (SBRT) in a very large, real life data set of patients with metastatic, persistent, recurrent ovarian cancer (MPR-OC). Patient age <60 years, PTV <18 cm , lymph node disease, and biologically effective dose α/β10 >70 Gy were associated with higher chance of complete response (CR). Achievement of CR and total dose >25 Gy were associated with better local control (LC) rate. Mild toxicity was experienced in 20.7% of patients. In conclusion, this study confirms the activity and safety of SBRT in MPR-OC patients and identifies clinical and treatment parameters able to predict CR and LC rate.
最近的研究报告称,立体定向体放射治疗(SBRT)可改善非小细胞肺癌和前列腺癌患者的无进展生存期、总生存期和雄激素剥夺治疗无进展生存期。本回顾性多中心 MITO RT-01 研究旨在确定 SBRT 在转移性、持续性和复发性卵巢癌(MPR-OC)患者的大型真实世界数据集中的疗效和安全性。
本研究的终点是 SBRT 的完全缓解(CR)率和基于“每病灶”的 24 个月局部控制(LC)的 24 个月 actuarial 率。次要终点是急性和迟发性毒性以及 24 个月 actuarial 迟发性毒性无生存。客观缓解率(ORR)包括 CR 和部分缓解(PR)。临床获益(CB)包括 ORR 和稳定疾病(SD)。毒性按照中心政策通过放射治疗肿瘤学组(RTOG)和欧洲癌症研究与治疗组织(EORTC)和不良事件通用术语标准(CTCAE)量表进行评估。逻辑和 Cox 回归用于单变量和多变量分析预测临床 CR 和 actuarial 结果的因素。
291 个病灶(65.2%)观察到 CR、PR 和 SD,CB 率为 96.4%。在多变量分析中,患者年龄≤60 岁、计划靶区(PTV)≤18 cm、淋巴结疾病和生物有效剂量α/β10>70 Gy 与更高的 CR 机会相关。中位随访时间为 22 个月(范围 3-120),24 个月的 actuarial LC 率为 81.9%。在多变量分析中,CR 和总剂量>25 Gy 与更好的 LC 率相关。54 例(20.7%)患者出现轻度毒性;63 种副作用中,48 种为 1 级,15 种为 2 级。24 个月的迟发性毒性无生存概率为 95.1%。
本研究证实了 SBRT 在 MPR-OC 患者中的疗效和安全性,并确定了能够预测 CR 和 LC 率的临床和治疗参数。
本研究旨在确定立体定向体放射治疗(SBRT)在大量真实世界转移性、持续性、复发性卵巢癌(MPR-OC)患者中的疗效和安全性。患者年龄<60 岁、PTV<18 cm、淋巴结疾病和生物有效剂量α/β10>70 Gy 与更高的完全缓解(CR)机会相关。达到 CR 和总剂量>25 Gy 与更好的局部控制(LC)率相关。20.7%的患者出现轻度毒性。总之,本研究证实了 SBRT 在 MPR-OC 患者中的疗效和安全性,并确定了能够预测 CR 和 LC 率的临床和治疗参数。