Makita Kenji, Hamamoto Yasushi, Kanzaki Hiromitsu, Nagasaki Kei, Takata Noriko, Tsuruoka Shintaro, Uwatsu Kotaro, Kido Teruhito
Department of Radiology, Ehime University Graduate School of Medicine, 454 Shitsukawa, Toon, Ehime, 791-0295, Japan.
Departments of Radiation Oncology, National Hospital Organization Shikoku Cancer Center, Kou-160, Minami-Umenomoto-Machi, Matsuyama, Ehime, 791-0280, Japan.
Discov Oncol. 2023 May 22;14(1):74. doi: 10.1007/s12672-023-00651-0.
This study aimed to evaluate the factors that affect the local control (LC) of bone metastases from radioresistant carcinomas (renal cell carcinoma, hepatocellular carcinoma [HCC], and colorectal carcinoma [CRC]) treated with palliative external-beam radiotherapy (EBRT).
Between January 2010 and December 2020, 211 bone metastases in 134 patients were treated with EBRT in two hospitals (a cancer center and university hospital). Based on follow-up CT, these cases were reviewed retrospectively to evaluate LC at the EBRT site.
The median EBRT dose (BED10) was 39.0 Gy (range, 14.4-66.3 Gy). The median follow-up time of the imaging studies was 6 months (range, 1-107 months). The 0.5-year overall survival and LC rates of the EBRT sites were 73% and 73%, respectively. Multivariate analysis revealed that the primary sites (HCC/CRC), low EBRT dose (BED10) (≤ 39.0 Gy), and non-administration of post-EBRT bone modifying agents (BMAs) and/or antineoplastic agents (ATs) were statistically significant factors that negatively affected the LC of EBRT sites. In the absence of BMAs or ATs, the EBRT dose (BED10) escalation from 39.0 Gy improved the LC of EBRT sites. Based on ATs administration, the LC of EBRT sites was significantly affected by tyrosine kinase inhibitors and/or immune checkpoint inhibitors.
Dose escalation improves LC in bone metastases from radioresistant carcinomas. Higher EBRT doses are needed to treat patients for whom few effective systemic therapies remain available.
本研究旨在评估影响接受姑息性外照射放疗(EBRT)的放射抗拒性癌(肾细胞癌、肝细胞癌[HCC]和结直肠癌[CRC])骨转移局部控制(LC)的因素。
2010年1月至2020年12月期间,两所医院(一家癌症中心和大学医院)对134例患者的211处骨转移灶进行了EBRT治疗。基于随访CT,对这些病例进行回顾性分析,以评估EBRT部位的LC情况。
EBRT中位剂量(BED10)为39.0 Gy(范围14.4 - 66.3 Gy)。影像学研究的中位随访时间为6个月(范围1 - 107个月)。EBRT部位的0.5年总生存率和LC率分别为73%和73%。多因素分析显示,原发部位(HCC/CRC)、低EBRT剂量(BED10)(≤39.0 Gy)以及未使用EBRT后骨改良剂(BMA)和/或抗肿瘤药物(AT)是对EBRT部位LC产生负面影响的统计学显著因素。在未使用BMA或AT的情况下,EBRT剂量(BED10)从39.0 Gy增加可改善EBRT部位的LC。基于AT的使用情况,EBRT部位的LC受酪氨酸激酶抑制剂和/或免疫检查点抑制剂的显著影响。
剂量增加可改善放射抗拒性癌骨转移的LC。对于几乎没有有效全身治疗方案的患者,需要更高的EBRT剂量进行治疗。