Department of Human Oncology, University of Wisconsin School of Medicine and Public Health, 600 Highland Ave, K4/B100, Madison, WI 53792, USA.
J Neurooncol. 2011 Nov;105(2):301-8. doi: 10.1007/s11060-011-0590-9. Epub 2011 Apr 27.
To determine the safety, tolerability, and report on secondary efficacy endpoints of motexafin gadolinium (MGd) in combination with whole-brain radiotherapy (WBRT) and stereotactic radiosurgery (SRS) for patients with ≤ 6 brain metastases. We conducted an international study of WBRT (37.5 Gy in 15 fractions) and SRS (15-21 Gy) with the addition of MGd (5 mg/kg preceding each fraction beginning week 2). The primary endpoint was to evaluate the rate of irreversible grade 3 or any grade ≥ 4 neurotoxicity and establish feasibility in preparation for a phase III trial. Sixty-five patients were enrolled from 14 institutions, of which 45 (69%) received SRS with MGd as intended and were available for evaluation. Grade ≥ 3 neurotoxicity attributable to radiation therapy within 3 months of SRS was seen in 2 patients (4.4%), including generalized weakness and radionecrosis requiring surgical management. Immediately following the course of MGd plus WBRT, new brain metastases were detected in 11 patients (24.4%) at the time of the SRS treatment planning MRI. The actuarial incidence of neurologic progression at 6 months and 1 year was 17 and 20%, respectively. The median investigator-determined neurologic progression free survival and overall survival times were 8 (95% CI: 5-14) and 9 months (95% CI: 6-not reached), respectively. We observed a low rate of neurotoxicity, demonstrating that the addition of MGd does not increase the incidence or severity of neurologic complications from WBRT with SRS boost.
为了确定≤6 个脑转移瘤患者联合使用莫替沙芬钆(MGd)与全脑放疗(WBRT)和立体定向放射外科(SRS)的安全性、耐受性,并报告次要疗效终点的情况。我们开展了一项国际研究,对 WBRT(37.5Gy 分 15 次给予)和 SRS(15-21Gy)进行了研究,在此基础上加用 MGd(第 2 周开始,每次剂量前给予 5mg/kg)。主要终点是评估不可逆性 3 级或任何等级≥4 级神经毒性的发生率,并为 III 期试验做准备,评估可行性。这项研究共纳入了来自 14 家机构的 65 例患者,其中 45 例(69%)按计划接受了 SRS 联合 MGd 治疗,可用于评估。SRS 后 3 个月内,有 2 例(4.4%)患者出现归因于放疗的 3 级以上神经毒性,包括全身无力和放射性坏死,需要手术治疗。在 WBRT 加 MGd 治疗后立即进行 SRS 治疗计划 MRI 检查时,11 例(24.4%)患者发现新的脑转移灶。6 个月和 1 年时的神经进展累积发生率分别为 17%和 20%。研究者确定的神经进展无进展生存期和总生存期中位数分别为 8 个月(95%CI:5-14)和 9 个月(95%CI:6-未达到)。我们观察到神经毒性发生率较低,表明与 SRS 加 WBRT 相比,MGd 的加入并未增加神经并发症的发生率或严重程度。