Schwer Amanda L, Kavanagh Brian D, McCammon Robert, Gaspar Laurie E, Kleinschmidt-De Masters B K, Stuhr Kelly, Chen Changhu
Department of Radiation Oncology, University of Colorado Denver, Aurora, CO 80045-0508, USA.
Int J Radiat Oncol Biol Phys. 2009 Apr 1;73(5):1352-7. doi: 10.1016/j.ijrobp.2008.06.1919. Epub 2008 Nov 14.
To describe the radiographic and histopathologic changes after stereotactic radiosurgery (SRS) and epidermal growth factor receptor inhibition in patients with recurrent malignant gliomas.
A total of 15 patients with recurrent high-grade gliomas were treated on a prospective Phase I trial combining SRS and gefitinib. The SRS dose was escalated from 18 to 36 Gy in three fractions. The planning target volume was the T(1)-weighted contrast-enhancing (T(1)C) lesion plus 2 mm. Gefitinib was given at 250 mg daily. Serial brain magnetic resonance imaging scans were analyzed to characterize the volumetric changes in the T(1)C and T(2) abnormalities after treatment. Two patients underwent resection for suspected recurrence.
The median pretreatment magnetic resonance imaging T(1)C and T(2) volume was 40.9 and 184.1 cm(3), respectively. The median post-SRS percentage of increases in the T(1)C volume at 1, 2-4, and 5-7 months was 8.9%, 41.3%, and 99.6%, respectively. The median percentage increase in the T(2) volume likewise showed a trend upward after SRS, from 18.0% at 1 month to 37.8% at 5-7 months. For the 2 patients who underwent resection after SRS for an increasing T(1)C volume, the histopathologic analysis revealed therapy-induced vascular injury and necrosis. One patient with an asymptomatic increase in the T(1)C volume after SRS was treated conservatively. After a peak T(1)C volume increase at 9 months, the T(1)C volume had declined to 50% of the maximal volume at 15 months. The patients with the most dramatic increase in T(1)C volume experienced the longest overall survival.
Patients experienced a notable increase in magnetic resonance imaging T(1)C and T(2) volumes after the combination of SRS and epidermal growth factor receptor inhibition. The tissue changes were consistent with a potent treatment effect.
描述复发性恶性胶质瘤患者在立体定向放射外科治疗(SRS)和表皮生长因子受体抑制治疗后的影像学和组织病理学变化。
共有15例复发性高级别胶质瘤患者参加了一项将SRS与吉非替尼联合应用的前瞻性I期试验。SRS剂量分三次从18 Gy递增至36 Gy。计划靶体积为T1加权增强(T1C)病变加2 mm。吉非替尼每日剂量为250 mg。对系列脑磁共振成像扫描进行分析,以描述治疗后T1C和T2异常的体积变化。两名患者因怀疑复发而接受了手术切除。
治疗前磁共振成像T1C和T2体积的中位数分别为40.9 cm³和184.1 cm³。SRS后1个月、2 - 4个月和5 - 7个月T1C体积增加的中位数百分比分别为8.9%、41.3%和99.6%。T2体积增加的中位数百分比在SRS后同样呈上升趋势,从1个月时的18.0%升至5 - 7个月时的37.8%。对于SRS后因T1C体积增加而接受手术切除的2例患者,组织病理学分析显示治疗引起的血管损伤和坏死。1例SRS后T1C体积无症状增加的患者接受了保守治疗。在9个月时T1C体积增加达到峰值后,T1C体积在15个月时降至最大体积的50%。T1C体积增加最为显著的患者总生存期最长。
SRS与表皮生长因子受体抑制联合治疗后,患者磁共振成像T1C和T2体积显著增加。组织变化与强效治疗效果一致。