Department of Radiotherapy, Ghent University Hospital, Belgium.
Radiother Oncol. 2011 Dec;101(3):351-5. doi: 10.1016/j.radonc.2011.06.020.
To determine the maximum tolerated dose (MTD) in a phase I trial on adaptive dose-painting-by-numbers (DPBN) for non-metastatic head and neck cancer.
Adaptive intensity-modulated radiotherapy was based on voxel intensity of pre-treatment and per-treatment [(18)F]fluoro-2-deoxy-d-glucose positron emission tomography ((18)F-FDG-PET) scans. Dose was escalated to a median total dose of 80.9 Gy in the high-dose clinical target volume (dose level I) and 85.9 Gy in the gross tumor volume (dose level II). The MTD would be reached, if ≥ 33% of patients developed any grade ≥ 4 toxicity (DLT) up to 3 months follow-up.
Between February 2007 and August 2009, seven patients at dose level I and 14 at dose level II were treated. All patients completed treatment without interruption. At a median follow-up for surviving patients of 38 (dose level I) and 22 months (dose level II) there was no grade ≥ 4 toxicity during treatment and follow-up but six cases of mucosal ulcers at latency of 4-10 months, of which five (36%) were observed at dose level II. Mucosal ulcers healed spontaneously in four patients.
Considering late mucosal ulcers as DLT, the MTD of a median dose of 80.9 Gy has been reached in our trial.
在一项针对非转移性头颈部癌症的自适应剂量绘制(DPBN)的 I 期试验中确定最大耐受剂量(MTD)。
自适应调强放疗基于治疗前和治疗期间 [(18)F]氟-2-脱氧-d-葡萄糖正电子发射断层扫描((18)F-FDG-PET)扫描的体素强度。在高剂量临床靶区(剂量水平 I)中,剂量递增至 80.9 Gy 的中位数总剂量,在大体肿瘤体积(剂量水平 II)中递增至 85.9 Gy。如果在 3 个月随访时,≥ 33%的患者发生任何≥ 4 级毒性(DLT),则达到 MTD。
2007 年 2 月至 2009 年 8 月,在剂量水平 I 治疗了 7 例患者,在剂量水平 II 治疗了 14 例患者。所有患者均无中断完成治疗。在存活患者的中位随访时间为 38(剂量水平 I)和 22 个月(剂量水平 II)时,在治疗和随访期间没有发生任何≥ 4 级毒性,但有 6 例黏膜溃疡在潜伏期 4-10 个月,其中 5 例(36%)发生在剂量水平 II。四名患者的黏膜溃疡自发愈合。
考虑到晚期黏膜溃疡作为 DLT,本试验中已达到中位数剂量 80.9 Gy 的 MTD。