Department of Radiology, Ehime University Graduate School of Medicine, 454 Shitsukawa, Toon, Ehime, 791-0295, Japan.
Department of Radiation Oncology, National Hospital Organization Shikoku Cancer Center, Kou-160, Minami-Umenomoto-Machi, Matsuyama, Ehime, 791-0280, Japan.
Radiat Oncol. 2021 Nov 20;16(1):225. doi: 10.1186/s13014-021-01940-0.
Over the past decades, remarkable advancements in systemic drug therapy have improved the prognosis of patients with bone metastases. Individualization is required in external beam radiotherapy (EBRT) for bone metastases according to the patient's prognosis. To establish individualized EBRT for bone metastases, we investigated factors that affect the local control (LC) of bone metastases.
Between January 2010 and December 2019, 536 patients received EBRT for 751 predominantly osteolytic bone metastases. LC at EBRT sites was evaluated with a follow-up computed tomography. The median EBRT dose was biologically effective dose (BED) (39.0) (range of BED: 14.4-71.7 Gy).
The median follow-up time and median time of computed tomography follow-up were 11 (range 1-123) months and 6 (range 1-119) months, respectively. The 0.5- and 1-year overall survival rates were 73% and 54%, respectively. The 0.5- and 1-year LC rates were 83% and 79%, respectively. In multivariate analysis, higher age (≥ 70 years), non-vertebral bone metastases, unfavorable primary tumor sites (esophageal cancer, colorectal cancer, hepatobiliary/pancreatic cancer, renal/ureter cancer, sarcoma, melanoma, and mesothelioma), lower EBRT dose (BED < 39.0 Gy), and non-administration of bone-modifying agents (BMAs)/antineoplastic agents after EBRT were significantly unfavorable factors for LC of bone metastases. There was no statistically significant difference in the LC between BED = 39.0 and BED > 39.0 Gy.
Regarding tumor-related factors, primary tumor sites and the sites of bone metastases were significant for the LC. As for treatment-related factors, lower EBRT doses (BED < 39.0 Gy) and non-administration of BMAs/antineoplastic agents after EBRT were associated with poor LC. Dose escalation from BED = 39.0 Gy did not necessarily improve LC.
在过去的几十年中,全身性药物治疗的显著进步改善了骨转移患者的预后。根据患者的预后,骨转移的外照射放疗(EBRT)需要个体化。为了为骨转移建立个体化的 EBRT,我们研究了影响骨转移局部控制(LC)的因素。
2010 年 1 月至 2019 年 12 月,536 例患者接受了 751 例主要为溶骨性骨转移的 EBRT。用随访 CT 评估 EBRT 部位的 LC。中位 EBRT 剂量为生物有效剂量(BED)(39.0)(BED 范围:14.4-71.7 Gy)。
中位随访时间和中位 CT 随访时间分别为 11 个月(范围 1-123 个月)和 6 个月(范围 1-119 个月)。0.5 年和 1 年总生存率分别为 73%和 54%。0.5 年和 1 年的 LC 率分别为 83%和 79%。多变量分析显示,年龄较大(≥70 岁)、非脊柱骨转移、原发肿瘤部位不良(食管癌、结直肠癌、肝胆胰癌、肾/输尿管癌、肉瘤、黑色素瘤和间皮瘤)、EBRT 剂量较低(BED<39.0 Gy)和 EBRT 后未使用骨修饰剂(BMAs)/抗肿瘤药物是骨转移 LC 的不利因素。BED=39.0 Gy 和 BED>39.0 Gy 之间的 LC 没有统计学上的显著差异。
就肿瘤相关因素而言,原发肿瘤部位和骨转移部位对 LC 有重要意义。至于治疗相关因素,较低的 EBRT 剂量(BED<39.0 Gy)和 EBRT 后未使用 BMAs/抗肿瘤药物与较差的 LC 相关。从 BED=39.0 Gy 增加剂量不一定能提高 LC。