Department of Radiation Oncology, Stanford University, Stanford, California, USA.
Cancer. 2011 Sep 1;117(17):4060-9. doi: 10.1002/cncr.25997. Epub 2011 Mar 22.
This study was undertaken to determine outcomes of stereotactic body radiotherapy for colorectal liver metastases in a pooled patient cohort.
Patients with colorectal liver metastases from 3 institutions were included if they had 1 to 4 lesions, received 1 to 6 fractions of stereotactic body radiotherapy, and had radiologic imaging ≥ 3 months post-treatment. Sixty-five patients with 102 lesions treated from August 2003 to May 2009 were retrospectively analyzed. A tumor control probability (TCP) model was used to estimate the 3-fraction dose required for > 90% local control after converting the schedule into biologically equivalent dose (BED), single-fraction equivalent dose, or linear quadratic model-based single-fraction dose.
Forty-seven (72%) patients had ≥ 1 chemotherapy regimen before stereotactic body radiotherapy, and 27 (42%) patients had ≥ 2 regimens. The median follow-up was 1.2 years (range, 0.3-5.2 years). The median dose was 42 gray (Gy; range, 22-60 Gy). When evaluated separately by multivariate analysis, total dose (P = .0015), dose/fraction (P = .003), and BED (P = .004) all correlated with local control by lesion. On multivariate analysis, nonactive extrahepatic disease was associated with overall survival (OS; P = .046), and sustained local control was closely correlated (P = .06). By using single-fraction equivalent dose, BED, or linear quadratic model-based single-fraction dose in the TCP model, the estimated dose range needed for 1-year local control > 90% is 46 to 52 Gy in 3 fractions.
Liver stereotactic body radiotherapy is well tolerated and effective for colorectal liver metastases. The strong correlation between local control and OS supports controlling hepatic disease even for heavily pretreated patients. For a 3-fraction regimen of stereotactic body radiotherapy, a prescription dose of ≥ 48 Gy should be considered, if normal tissue constraints allow.
本研究旨在确定立体定向体部放疗在结直肠癌肝转移患者中的应用效果,研究纳入了来自 3 家机构的患者,他们有 1-4 个病灶,接受了 1-6 次立体定向体部放疗,并且在治疗后 3 个月以上有影像学检查。回顾性分析了 2003 年 8 月至 2009 年 5 月期间收治的 65 例患者的 102 个病灶。使用肿瘤控制概率(TCP)模型将方案转换为生物等效剂量(BED)、单次剂量等效或线性二次模型单次剂量后,估算 3 次分割所需的剂量,以获得 > 90%的局部控制率。
47 例(72%)患者在接受立体定向体部放疗前接受了≥1 种化疗方案,27 例(42%)患者接受了≥2 种化疗方案。中位随访时间为 1.2 年(范围:0.3-5.2 年)。中位剂量为 42 戈瑞(Gy;范围:22-60 Gy)。多变量分析时,单独评估总剂量(P=0.0015)、剂量/分割(P=0.003)和 BED(P=0.004)与肿瘤局部控制相关。多变量分析时,非活动性肝外疾病与总生存(OS;P=0.046)相关,且与持续局部控制密切相关(P=0.06)。使用 TCP 模型中的单次剂量等效、BED 或线性二次模型的单次剂量,估算出 1 年局部控制率>90%所需的剂量范围为 3 次分割 46-52 Gy。
肝脏立体定向体部放疗对结直肠癌肝转移是一种耐受良好且有效的治疗方法。局部控制与 OS 之间的强烈相关性支持即使对接受过大量治疗的患者也应控制肝内疾病。对于 3 次分割的立体定向体部放疗方案,如果允许的话,应考虑≥48 Gy 的处方剂量。