University of Michigan, Department of Radiation Oncology, United States.
University of California San Francisco, Department of Radiation Oncology, United States.
Radiother Oncol. 2019 Dec;141:101-107. doi: 10.1016/j.radonc.2019.07.027. Epub 2019 Aug 17.
Patients with hepatocellular carcinoma (HCC) commonly have underlying liver dysfunction with variable tolerance to liver stereotactic body radiation therapy (SBRT). We hypothesized that insertion of a 1-month mid-treatment break would allow us to adapt treatment to the individual patient response, thereby reducing toxicity without compromising local control (LC).
We analyzed HCC patients receiving 3-5 fraction SBRT at our institution from 2005 to 2017. Over this time, patients were offered enrollment on prospective trials assessing individualized adaptive SBRT. Based on normal tissue complication probability and modeling of changes in liver function following a 1-month treatment break between fractions 3 and 4, patients could receive a total of 3 or 5 fractions. Patients not on trial received 3 or 5 fractions without a break. Toxicity was defined as a ≥2 point rise in Child-Pugh (CP) score within 6 months of SBRT.
178 patients were treated with SBRT to 263 HCCs. Median follow-up was 23 months. 86 treatments had a 1-month break. 1-Year LC was 95.4%; this was not different between patients treated with or without a break (p = 0.14). Controlling for tumor size and dose a break was not associated with inferior LC (HR: 0.58, 95%CI: 0.1-3.34, p = 0.54). 54 patients experienced a ≥2 point rise in CP score. Controlling for the number of prior liver directed therapies and mean liver dose, a treatment break reduced the odds of toxicity (OR: 0.42, 95% CI: 0.17-1.03, p = 0.06).
A one-month mid-treatment break and reassessment may reduce the odds of treatment related toxicity without compromising LC.
肝细胞癌(HCC)患者常伴有肝功能不全,对肝脏立体定向体部放射治疗(SBRT)的耐受程度不同。我们假设在治疗过程中插入一个 1 个月的中期休息期,可以使我们根据个体患者的反应来调整治疗方案,从而降低毒性而不影响局部控制(LC)。
我们分析了 2005 年至 2017 年期间在我们机构接受 3-5 次分割 SBRT 的 HCC 患者。在此期间,患者可以选择参加评估个体化适应性 SBRT 的前瞻性试验。根据正常组织并发症概率和在第 3 次和第 4 次分割之间的 1 个月治疗休息期间肝功能变化的建模,患者可以接受总共 3 次或 5 次分割。未参加试验的患者则接受 3 次或 5 次分割而没有休息期。毒性定义为 SBRT 后 6 个月内 Child-Pugh(CP)评分升高≥2 分。
178 例 HCC 患者接受了 263 次 SBRT。中位随访时间为 23 个月。86 次治疗有 1 个月的休息期。1 年 LC 为 95.4%;有或没有休息期的患者之间没有差异(p=0.14)。在控制肿瘤大小和剂量的情况下,休息期与较低的 LC 无关(HR:0.58,95%CI:0.1-3.34,p=0.54)。54 例患者 CP 评分升高≥2 分。在控制先前肝定向治疗次数和平均肝剂量的情况下,治疗休息期降低了毒性的可能性(OR:0.42,95%CI:0.17-1.03,p=0.06)。
在治疗过程中插入一个 1 个月的中期休息期和重新评估可能会降低与治疗相关的毒性的可能性,而不影响 LC。