Marcus Karen J, Goumnerova Liliana, Billett Amy L, Lavally Beverly, Scott R Michael, Bishop Karyn, Xu Rhongi, Young Poussaint Tina, Kieran Mark, Kooy Hanne, Pomeroy Scott L, Tarbell Nancy J
Children's Hospital, Boston, MA 02115, USA.
Int J Radiat Oncol Biol Phys. 2005 Feb 1;61(2):374-9. doi: 10.1016/j.ijrobp.2004.06.012.
To evaluate the efficacy of stereotactic radiotherapy (SRT) for small, localized, pediatric brain tumors and to determine the patterns of failure.
A total of 81 patients were enrolled in an institutional review board-approved prospective Dana-Farber Cancer Institute protocol between 1992 and 1998. Of the 81 patients, 50 had low-grade astrocytoma, 23 had residual or recurrent craniopharyngioma, 4 had posterior fossa ependymoma, and 4 had other histologic types. All patients underwent biopsy for diagnosis, with the exception of patients with neurofibromatosis and radiographic evidence of an optic system tumor. The neurocognitive outcome for all patients was also an endpoint of the study and will be reported separately. This report focused on the patients with low-grade gliomas only. Of the 50 patients, 26 were males and 24 females; the median age was 9 years (range, 2-26 years). The indications for treatment of patients with low-grade gliomas were progression during or after chemotherapy or progression after surgery alone. SRT was delivered using a dedicated 6-MV linear accelerator. Immobilization was accomplished with a removable head-frame. CT and MRI fusion was used for treatment planning. The target volume generally included the preoperative tumor plus a 2-mm margin for the planning target volume. The median collimator size was 47.25 mm (range, 30-60 mm). Three to nine arcs were used to deliver a mean total dose of 52.2 Gy in 1.8-Gy daily fractions.
With a median follow-up of 6.9 years (range, 0.9-10.2 years), the progression-free survival rate was 82.5% at 5 years and 65% at 8 years. The overall survival was 97.8% at 5 years and 82% at 8 years. Six patients had local progression. Two of the patients with local progression had pathologic progression to anaplastic astrocytoma 3 and 7 years after initial SRT. Five patients, all with optic system/hypothalamic primary tumors, developed central nervous system dissemination 1.0-7.4 years after SRT. One patient developed a presumed radiation-induced primitive neuroectodermal tumor 6 years after initial treatment. Six patients died, three of dissemination, two of progression to higher grade tumors, and one of a secondary radiation-induced tumor. All 6 cases of local progression were within the primary tumor bed at the time of progression and had received the full prescription dose. No marginal failures occurred.
Stereotactic radiotherapy provides excellent local control for children with small, localized low-grade glial tumors. Marginal failures have not been observed, supporting the use of limited margins to minimize late sequelae using stereotactic immobilization and planning techniques.
评估立体定向放射治疗(SRT)对小儿小的局限性脑肿瘤的疗效,并确定失败模式。
1992年至1998年期间,共有81例患者纳入了经机构审查委员会批准的达纳-法伯癌症研究所前瞻性方案。81例患者中,50例为低级别星形细胞瘤,23例为残留或复发性颅咽管瘤,4例为后颅窝室管膜瘤,4例为其他组织学类型。除患有神经纤维瘤病且有视神经系统肿瘤影像学证据的患者外,所有患者均接受活检以明确诊断。所有患者的神经认知结果也是该研究的一个终点,将另行报告。本报告仅关注低级别胶质瘤患者。50例患者中,男性26例,女性24例;中位年龄为9岁(范围2 - 26岁)。低级别胶质瘤患者的治疗指征为化疗期间或化疗后进展或仅手术后进展。使用专用的6兆伏直线加速器进行SRT。通过可移动头架实现固定。采用CT和MRI融合进行治疗计划。靶体积一般包括术前肿瘤加上计划靶体积的2毫米边界。中位准直器尺寸为47.25毫米(范围30 - 60毫米)。使用3至9个弧,以1.8 Gy的每日分次剂量给予平均总剂量52.2 Gy。
中位随访6.9年(范围0.9 - 10.2年),5年无进展生存率为82.5%,8年为65%。5年总生存率为97.8%,8年为82%。6例患者出现局部进展。2例局部进展患者在初始SRT后3年和7年病理进展为间变性星形细胞瘤。5例患者,均为视神经系统/下丘脑原发性肿瘤,在SRT后1.0 - 7.4年发生中枢神经系统播散。1例患者在初始治疗后6年发生疑似放射性诱发的原始神经外胚层肿瘤。6例患者死亡,3例死于播散,2例因进展为更高级别肿瘤死亡,1例死于继发性放射性诱发肿瘤。所有6例局部进展均发生在进展时的原发肿瘤床内,且已接受全部处方剂量。未发生边缘性失败。
立体定向放射治疗为患有小的局限性低级别胶质瘤的儿童提供了良好的局部控制。未观察到边缘性失败,支持使用有限边界以利用立体定向固定和计划技术将晚期后遗症降至最低。