Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, Ohio, USA.
Rose Ella Burkhardt Brain Tumor and Neuro-Oncology Center, Cleveland Clinic, Cleveland, Ohio, USA.
Neuro Oncol. 2024 Sep 5;26(9):1651-1659. doi: 10.1093/neuonc/noae076.
Single-session stereotactic radiosurgery (SRS) or surgical resection alone for brain metastases larger than 2 cm results in unsatisfactory local control. We conducted a phase I trial for brain metastases(>2 cm) to determine the safety of preoperative SRS at escalating doses.
Radiosurgery dose was escalated at 3 Gy increments for 3 cohorts based on maximum tumor dimension starting at: 18 Gy for >2-3 cm, 15 Gy for >3-4 cm, and 12 Gy for >4-6 cm. Dose-limiting toxicity was defined as grade III or greater acute toxicity.
A total of 35 patients/36 lesions were enrolled. For tumor size >2-3 cm, patients were enrolled up to the second dose level (21 Gy); for >3-4 cm and >4-6 cm cohorts the third dose level (21 and 18 Gy, respectively) was reached. There were 2 DLTs in the >3-4 cm arm at 21 Gy. The maximum tolerated dose of SRS for >2-3 cm was not reached; and was 18 Gy for both >3-4 cm arm and >4-6 cm arm. With a median follow-up of 64.0 months, the 6- and 12-month local control rates were 85.9% and 76.6%, respectively. One patient developed grade 3 radiation necrosis at 5 months. The 2-year rate of leptomeningeal disease (LMD) was 0%.
Preoperative SRS with dose escalation followed by surgical resection for brain metastases greater than 2 cm in size demonstrates acceptable acute toxicity. The phase II portion of the trial will be conducted at the maximum tolerated SRS doses.
单次立体定向放射外科(SRS)或单纯手术切除大于 2 厘米的脑转移瘤,局部控制效果不理想。我们进行了一项脑转移瘤(>2 厘米)的 I 期试验,以确定递增剂量术前 SRS 的安全性。
根据最大肿瘤尺寸,SRS 剂量递增 3 Gy,分为 3 个队列:>2-3 cm 起始剂量为 18 Gy,>3-4 cm 起始剂量为 15 Gy,>4-6 cm 起始剂量为 12 Gy。剂量限制性毒性定义为 3 级或更高级别的急性毒性。
共纳入 35 例患者/36 个病灶。对于肿瘤大小>2-3 cm,患者入组至第二剂量水平(21 Gy);对于>3-4 cm 和>4-6 cm 队列,达到第三剂量水平(分别为 21 和 18 Gy)。>3-4 cm 臂有 2 例 DLT 发生在 21 Gy。>2-3 cm 最大耐受 SRS 剂量未达到,对于>3-4 cm 臂和>4-6 cm 臂,最大耐受 SRS 剂量均为 18 Gy。中位随访 64.0 个月,6 个月和 12 个月的局部控制率分别为 85.9%和 76.6%。1 例患者在 5 个月时发生 3 级放射性坏死。2 年脑膜疾病(LMD)发生率为 0%。
对于大于 2 厘米的脑转移瘤,在手术切除前行递增剂量 SRS 治疗,具有可接受的急性毒性。试验的 II 期部分将在最大耐受 SRS 剂量下进行。