Department of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.
Int J Radiat Oncol Biol Phys. 2012 May 1;83(1):107-12. doi: 10.1016/j.ijrobp.2011.05.038. Epub 2011 Oct 20.
To report the outcomes in patients with recurrent or unresectable pilocytic astrocytoma (PA) treated with Gamma Knife stereotactic radiosurgery (SRS).
Retrospective review of 18 patients (20 lesions) with biopsy-confirmed PA having SRS at our institution from 1992 through 2005.
The median patient age at SRS was 23 years (range, 4-56). Thirteen patients (72%) had undergone one or more previous surgical resections, and 10 (56%) had previously received external-beam radiation therapy (EBRT). The median SRS treatment volume was 9.1 cm(3) (range, 0.7-26.7). The median tumor margin dose was 15 Gy (range, 12-20). The median follow-up was 8.0 years (range, 0.5-15). Overall survival at 1, 5, and 10 years after SRS was 94%, 71%, and 71%, respectively. Tumor progression (local solid progression, n = 4; local solid progression + distant, n = 1; distant, n = 2; cyst development/progression, n = 4) was noted in 11 patients (61%). Progression-free survival at 1, 5, and 10 years was 65%, 41%, and 17%, respectively. Prior EBRT was associated with inferior overall survival (5-year risk, 100% vs. 50%, p = 0.03) and progression-free survival (5-year risk, 71% vs. 20%, p = 0.008). Nine of 11 patients with tumor-related symptoms improved after SRS. Symptomatic edema after SRS occurred in 8 patients (44%), which resolved with short-term corticosteroid therapy in the majority of those without early disease progression.
SRS has low permanent radiation-related morbidity and durable local tumor control, making it a meaningful treatment option for patients with recurrent or unresectable PA in whom surgery and/or EBRT has failed.
报告在接受伽玛刀立体定向放射外科(SRS)治疗的复发性或不可切除毛细胞星形细胞瘤(PA)患者中的结果。
对 1992 年至 2005 年在我们机构接受 SRS 治疗的 18 例(20 个病灶)活检证实为 PA 的患者进行回顾性研究。
SRS 时患者的中位年龄为 23 岁(范围,4-56)。13 例(72%)患者曾接受过一次或多次手术切除,10 例(56%)曾接受过外照射放疗(EBRT)。SRS 治疗体积的中位值为 9.1cm³(范围,0.7-26.7)。肿瘤边缘剂量的中位数为 15Gy(范围,12-20)。中位随访时间为 8.0 年(范围,0.5-15)。SRS 后 1、5 和 10 年的总生存率分别为 94%、71%和 71%。11 例(61%)患者出现肿瘤进展(局部实体进展,n=4;局部实体进展+远处,n=1;远处,n=2;囊肿发展/进展,n=4)。1、5 和 10 年的无进展生存率分别为 65%、41%和 17%。先前的 EBRT 与总生存率降低相关(5 年风险,100%比 50%,p=0.03)和无进展生存率降低相关(5 年风险,71%比 20%,p=0.008)。11 例有肿瘤相关症状的患者中有 9 例在 SRS 后得到改善。SRS 后发生 8 例(44%)患者出现症状性水肿,其中大多数无早期疾病进展的患者经短期皮质激素治疗后得到缓解。
SRS 具有较低的永久性放射相关发病率和持久的局部肿瘤控制,因此对于手术和/或 EBRT 失败的复发性或不可切除的 PA 患者,SRS 是一种有意义的治疗选择。