The Rose Ella Burkhardt Brain Tumor and Neuro-Oncology Center,.
Departments of 2 Neurosurgery and.
J Neurosurg. 2017 Mar;126(3):735-743. doi: 10.3171/2016.3.JNS153014. Epub 2016 May 27.
OBJECTIVE The impact of the stereotactic radiosurgery (SRS) prescription dose (PD) on local progression and radiation necrosis for small (≤ 2 cm) brain metastases was evaluated. METHODS An institutional review board-approved retrospective review was performed on 896 patients with brain metastases ≤ 2 cm (3034 tumors) who were treated with 1229 SRS procedures between 2000 and 2012. Local progression and/or radiation necrosis were the primary end points. Each tumor was followed from the date of radiosurgery until one of the end points was reached or the last MRI follow-up. Various criteria were used to differentiate tumor progression and radiation necrosis, including the evaluation of serial MRIs, cerebral blood volume on perfusion MR, FDG-PET scans, and, in some cases, surgical pathology. The median radiographic follow-up per lesion was 6.2 months. RESULTS The median patient age was 56 years, and 56% of the patients were female. The most common primary pathology was non-small cell lung cancer (44%), followed by breast cancer (19%), renal cell carcinoma (14%), melanoma (11%), and small cell lung cancer (5%). The median tumor volume and median largest diameter were 0.16 cm and 0.8 cm, respectively. In total, 1018 lesions (34%) were larger than 1 cm in maximum diameter. The PD for 2410 tumors (80%) was 24 Gy, for 408 tumors (13%) it was 19 to 23 Gy, and for 216 tumors (7%) it was 15 to 18 Gy. In total, 87 patients (10%) had local progression of 104 tumors (3%), and 148 patients (17%) had at least radiographic evidence of radiation necrosis involving 199 tumors (7%; 4% were symptomatic). Univariate and multivariate analyses were performed for local progression and radiation necrosis. For local progression, tumors less than 1 cm (subhazard ratio [SHR] 2.32; p < 0.001), PD of 24 Gy (SHR 1.84; p = 0.01), and additional whole-brain radiation therapy (SHR 2.53; p = 0.001) were independently associated with better outcome. For the development of radiographic radiation necrosis, independent prognostic factors included size greater than 1 cm (SHR 2.13; p < 0.001), location in the corpus callosum (SHR 5.72; p < 0.001), and uncommon pathologies (SHR 1.65; p = 0.05). Size (SHR 4.78; p < 0.001) and location (SHR 7.62; p < 0.001)-but not uncommon pathologies-were independent prognostic factors for the subgroup with symptomatic radiation necrosis. CONCLUSIONS A PD of 24 Gy results in significantly better local control of metastases measuring < 2 cm than lower doses. In addition, tumor size is an independent prognostic factor for both local progression and radiation necrosis. Some tumor pathologies and locations may also contribute to an increased risk of radiation necrosis.
评估立体定向放射外科 (SRS) 处方剂量 (PD) 对直径≤2cm 的小(≤2cm)脑转移瘤局部进展和放射性坏死的影响。
对 2000 年至 2012 年间接受 1229 次 SRS 治疗的 896 例脑转移瘤患者(3034 个肿瘤)进行了机构审查委员会批准的回顾性研究。局部进展和/或放射性坏死是主要终点。从放射外科治疗日期到达到终点或最后一次 MRI 随访为止,对每个肿瘤进行随访。使用各种标准来区分肿瘤进展和放射性坏死,包括连续 MRI 评估、灌注 MRI 的脑血容量、FDG-PET 扫描,以及在某些情况下进行手术病理检查。每个病变的中位影像学随访时间为 6.2 个月。
患者中位年龄为 56 岁,56%为女性。最常见的原发病理学是非小细胞肺癌(44%),其次是乳腺癌(19%)、肾细胞癌(14%)、黑色素瘤(11%)和小细胞肺癌(5%)。肿瘤体积中位数和最大直径中位数分别为 0.16cm 和 0.8cm。共有 1018 个病变(34%)最大直径大于 1cm。2410 个肿瘤(80%)的 PD 为 24Gy,408 个肿瘤(13%)为 19 至 23Gy,216 个肿瘤(7%)为 15 至 18Gy。共有 87 例患者(10%)的 104 个肿瘤(3%)出现局部进展,148 例患者(17%)至少有影像学证据的放射性坏死涉及 199 个肿瘤(7%;4%为症状性)。对局部进展和放射性坏死进行了单因素和多因素分析。对于局部进展,小于 1cm 的肿瘤(风险比[SHR]2.32;p<0.001)、24Gy 的 PD(SHR 1.84;p=0.01)和额外的全脑放疗(SHR 2.53;p=0.001)与更好的结果独立相关。对于放射性坏死的发展,独立的预后因素包括肿瘤大小大于 1cm(SHR 2.13;p<0.001)、位于胼胝体(SHR 5.72;p<0.001)和不常见的病理学(SHR 1.65;p=0.05)。大小(SHR 4.78;p<0.001)和位置(SHR 7.62;p<0.001)——而不是不常见的病理学——是症状性放射性坏死亚组的独立预后因素。
24Gy 的 PD 可显著提高直径<2cm 的转移瘤的局部控制率,低于低剂量。此外,肿瘤大小是局部进展和放射性坏死的独立预后因素。一些肿瘤病理学和位置也可能增加放射性坏死的风险。