Division of Radiation Therapy, Radiation and Proton Therapy Center, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka, 411-8777, Japan.
Department of Radiation Oncology, Juntendo University Graduate School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan.
J Radiat Res. 2024 Sep 24;65(5):701-711. doi: 10.1093/jrr/rrae060.
Purpose of this study is to evaluate patient characteristics, treatments and outcomes in bone metastasis radiotherapy practice. Patients for whom radiotherapy for bone metastasis was planned at 26 institutions in Japan between December 2020 and March 2021 were consecutively registered in this prospective, observational study. Study measures included patient characteristics, pain relief, skeletal-related events (SREs), overall survival and incidence of radiation-related adverse events. Pain was evaluated using a numerical rating scale (NRS) from 0 to 10. Irradiated dose was analyzed by the biologically effective dose (BED) assuming α/β = 10. Overall, 232 patients were registered; 224 patients and 302 lesions were fully analyzed. Eastern Cooperative Oncology Group Performance Status was 0/1/2/3/4 in 23%/38%/22%/13%/4%; 59% of patients had spinal metastases and 84% had painful lesions (NRS ≥ 2). BED was <20 Gy (in 27%), 20-30 Gy (24%), 30-40 Gy (36%) and ≥ 40 Gy (13%); 9% of patients were treated by stereotactic body radiotherapy. Grade 3 adverse events occurred in 4% and no grade 4-5 toxicity was reported. Pain relief was achieved in 52% at 2 months. BED is not related to pain relief. The cumulative incidence of SREs was 6.5% (95% confidence interval (CI) 3.1-9.9) at 6 months; no factors were significantly associated with SREs. With spinal lesions, 18% of patients were not ambulatory at baseline and 50% of evaluable patients in this group could walk at 2 months. The 6-month overall survival rate was 70.2% (95% CI 64.2-76.9%). In conclusion, we report real-world details of radiotherapy in bone metastasis.
本研究旨在评估骨转移放疗实践中的患者特征、治疗方法和结局。2020 年 12 月至 2021 年 3 月期间,日本 26 家机构计划对骨转移患者进行放疗,连续注册入组本前瞻性观察性研究。研究措施包括患者特征、疼痛缓解、骨骼相关事件(SREs)、总生存和放射性不良反应发生率。疼痛使用数字评分量表(NRS)从 0 到 10 进行评估。照射剂量通过假设 α/β=10 的生物有效剂量(BED)进行分析。共登记了 232 例患者;224 例患者和 302 个病灶进行了全分析。东部肿瘤协作组表现状态为 0/1/2/3/4 的患者分别占 23%/38%/22%/13%/4%;59%的患者有脊柱转移,84%的患者有疼痛性病变(NRS≥2)。BED<20 Gy(占 27%)、20-30 Gy(24%)、30-40 Gy(36%)和≥40 Gy(13%);9%的患者接受立体定向体部放疗。发生 3 级不良反应的患者占 4%,未报告 4-5 级毒性。2 个月时疼痛缓解率为 52%。BED 与疼痛缓解无关。6 个月时 SRE 的累积发生率为 6.5%(95%可信区间 3.1-9.9);无因素与 SRE 显著相关。脊柱病变患者中,18%的患者基线时不能行走,该组中 50%的可评估患者在 2 个月时可以行走。6 个月的总生存率为 70.2%(95%可信区间 64.2-76.9%)。总之,我们报告了骨转移放疗的真实世界细节。