Méndez Romero Alejandra, Keskin-Cambay Fatma, van Os Rob M, Nuyttens Joost J, Heijmen Ben J M, IJzermans Jan N M, Verhoef Cornelis
Department of Radiation Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Department of Radiation Oncology, Academic Medical Center, Amsterdam, The Netherlands.
Rep Pract Oncol Radiother. 2017 Mar-Apr;22(2):126-131. doi: 10.1016/j.rpor.2016.10.003. Epub 2016 Dec 2.
To investigate whether the impact of dose escalation in our patient population represented an improvement in local control without increasing treatment related toxicity.
A cohort of consecutive patients with colorectal liver metastases treated with stereotactic body radiation therapy (SBRT) between December 2002 and December 2013 were eligible for this study. Inclusion criteria were a Karnofsky performance status ≥80% and, according to the multidisciplinary tumor board, ineligibility for surgery or radiofrequency ablation. Exclusion criteria were a lesion size >6 cm, more than 3 metastases, and treatment delivered with other fractionation scheme than 3 times 12.5 Gy or 16.75 Gy prescribed at the 65-67% isodose. To analyze local control, CT or MRI scans were acquired during follow-up. Toxicity was scored using the Common Toxicity Criteria Adverse Events v4.0.
A total of 40 patients with 55 colorectal liver metastases were included in this study. We delivered 37.5 Gy to 32 lesions, and 50.25 Gy to 23 lesions. Median follow-up was 26 and 25 months for these two groups. Local control at 2 and 3 years was 74 and 66% in the low dose group while 90 and 81% was reached in the high dose group. No significant difference in local control between the two dose fractionation schemes could be found. Grade 3 toxicity was limited and was not increased in the high dose group.
SBRT for colorectal liver metastases offers a high chance of local control at long term. High irradiation doses may contribute to enhance this effect without increasing toxicity.
研究在我们的患者群体中剂量递增是否代表在不增加治疗相关毒性的情况下局部控制得到改善。
2002年12月至2013年12月期间接受立体定向体部放射治疗(SBRT)的连续结直肠肝转移患者队列符合本研究条件。纳入标准为卡氏评分≥80%,且根据多学科肿瘤委员会评估,不适合手术或射频消融。排除标准为病灶大小>6 cm、转移灶超过3个,以及采用除65 - 67%等剂量线处规定的3次12.5 Gy或16.75 Gy以外的其他分割方案进行治疗。为分析局部控制情况,随访期间进行CT或MRI扫描。使用《常见毒性标准不良事件v4.0》对毒性进行评分。
本研究共纳入40例患者,有55个结直肠肝转移灶。我们对32个病灶给予37.5 Gy照射,对23个病灶给予50.25 Gy照射。这两组的中位随访时间分别为26个月和25个月。低剂量组2年和3年的局部控制率分别为74%和66%,而高剂量组分别达到90%和81%。两种剂量分割方案之间的局部控制无显著差异。3级毒性有限,高剂量组未增加。
SBRT治疗结直肠肝转移长期局部控制机会高。高照射剂量可能有助于增强这种效果而不增加毒性。