Department of Radiation Oncology, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Canada.
Department of Radiation Oncology, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Canada.
Int J Radiat Oncol Biol Phys. 2018 Nov 1;102(3):499-507. doi: 10.1016/j.ijrobp.2018.06.047. Epub 2018 Jul 10.
We report mature outcomes for a cohort of patients with no prior radiation (de novo) to the spine treated with 24 Gy in 2 daily fractions for metastases, which represents the same stereotactic body radiation therapy (SBRT) regimen under evaluation in the current Symptom Control-24 phase 3 randomized trial (NCT02512965).
The cohort consisted of 279 de novo spinal metastases in 145 consecutive patients treated with 24 Gy in 2 SBRT fractions, identified from a prospective single-institution database. The endpoints were overall survival (OS), imaging-based local failure (LF), and cumulative risk of vertebral compression fractures (VCF).
The median follow-up per treated metastasis was 15.0 months (range, 0.1-71.6). The 1-year and 2-year OS rates were 73.1% and 60.7%, respectively. Presence of epidural disease (P < .0001), lung (P = .0415), and renal cell (P < .0001) primary histologies and baseline diffuse metastases (P = .0034) were significant prognostic factors for OS. The 1-year and 2-year LF rates were 9.7% and 17.6%, respectively, and the median time to LF was 9.2 month (range, 0.4-31.3 months). Only the presence of epidural disease predicted for LF (P < .0001). The cumulative risk of VCF at 1 and 2 years was 8.5% and 13.8%, respectively. Lytic (P = .0143) or mixed lytic/blastic (P = .0214) lesions, spinal malalignment (P = .0121), and the dose to 90% of the planning target volume (P = .0085) were significant predictors for VCF.
Twenty-four Gray in 2 daily fractions is safe and effective in achieving high tumor control rates for de novo spinal metastases. These outcomes will serve as a benchmark for the ongoing Symptom Control-24 randomized trial comparing 24 Gy in 2 SBRT fractions to 20 Gy delivered in 5 daily conventional fractions.
我们报告了一组未经放射治疗(初发)的脊柱转移瘤患者的成熟结果,这些患者接受了 24 Gy 分 2 次每日分割的立体定向体部放射治疗(SBRT),这与目前正在进行的 Symptom Control-24 期 3 随机试验(NCT02512965)中评估的相同 SBRT 方案相同。
该队列由 145 例连续患者的 279 例初发脊柱转移瘤组成,这些患者接受了 24 Gy 的 2 次 SBRT 分割治疗,这些患者是从一个前瞻性的单机构数据库中确定的。终点是总生存期(OS)、基于影像学的局部失败(LF)和累积椎体压缩性骨折(VCF)风险。
每例治疗转移瘤的中位随访时间为 15.0 个月(范围,0.1-71.6)。1 年和 2 年 OS 率分别为 73.1%和 60.7%。硬膜外疾病(P<.0001)、肺(P=.0415)和肾细胞(P<.0001)原发性组织学和基线弥漫性转移(P=.0034)是 OS 的显著预后因素。1 年和 2 年 LF 率分别为 9.7%和 17.6%,中位 LF 时间为 9.2 个月(范围,0.4-31.3 个月)。只有硬膜外疾病与 LF 相关(P<.0001)。1 年和 2 年 VCF 的累积风险分别为 8.5%和 13.8%。溶骨性(P=.0143)或混合溶骨性/成骨性(P=.0214)病变、脊柱失稳(P=.0121)和计划靶区 90%的剂量(P=.0085)是 VCF 的显著预测因素。
24 Gy 分 2 次每日分割在实现初发脊柱转移瘤高肿瘤控制率方面是安全有效的。这些结果将作为正在进行的 Symptom Control-24 随机试验的基准,该试验比较了 24 Gy 分 2 次 SBRT 分割与 20 Gy 分 5 次常规分割的疗效。