Katsoulakis Evangelia, Laufer Ilya, Bilsky Mark, Agaram Narasimhan P, Lovelock Michael, Yamada Yoshiya
Departments of1Radiation Oncology.
4Neurosurgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Neurosurg Focus. 2017 Jan;42(1):E7. doi: 10.3171/2016.10.FOCUS16368.
OBJECTIVE Spine radiosurgery is increasingly being used to treat spinal metastases. As patients are living longer because of the increasing efficacy of systemic agents, appropriate follow-up and posttreatment management for these patients is critical. Tumor progression after spine radiosurgery is rare; however, vertebral compression fractures are recognized as a more common posttreatment effect. The use of radiographic imaging alone posttreatment may makeit difficult to distinguish tumor progression from postradiation changes such as fibrosis. This is the largest series from a prospective database in which the authors examine histopathology of samples obtained from patients who underwent surgical intervention for presumed tumor progression or mechanical pain secondary to compression fracture. The majority of patients had tumor ablation and resulting fibrosis rather than tumor progression. The aim of this study was to evaluate tumor histopathology and characteristics of patients who underwent pathological sampling because of radiographic tumor progression, fibrosis, or collapsed vertebrae after receiving high-dose single-fraction stereotactic radiosurgery. METHODS Between January 2005 and January 2014, a total of 582 patients were treated with linear accelerator-based single-fraction (18-24 Gy) stereotactic radiosurgery. The authors retrospectively identified 30 patients (5.1%) who underwent surgical intervention for 32 lesions with vertebral cement augmentation for either mechanical pain or instability secondary to vertebral compression fracture (n = 17) or instrumentation (n = 15) for radiographic tumor progression. Radiation and surgical treatment, histopathology, and long-term outcomes were reviewed. Survival and time to recurrence were calculated using the Kaplan-Meier method. RESULTS The mean age at the time of radiosurgery was 59 years (range 36-80 years). The initial pathological diagnoses were obtained for all patients and primarily included radioresistant tumor types, including renal cell carcinoma in 7 (22%), melanoma in 6 (19%), lung carcinoma in 4 (12%), and sarcoma in 3 (9%). The median time to surgical intervention was 24.7 months (range 1.6-50.8 months). The median follow-up and overall survival for all patients were 42.5 months and 41 months (overall survival range 7-86 months), respectively. The majority of assessed lesions showed no evidence of tumor on pathological review (25 of 32, 78%), while a minority of lesions revealed residual tumor (7 of 32, 22%). The median survival for patients after tumor recurrence was 5 months (range 2-70 months). CONCLUSIONS High-dose single-fraction radiosurgery is tumor ablative in the majority of instances. In a minority of cases, tumor persists and salvage treatments should be considered.
目的 脊柱放射外科越来越多地用于治疗脊柱转移瘤。由于全身治疗药物疗效提高,患者生存期延长,因此对这些患者进行适当的随访和治疗后管理至关重要。脊柱放射外科术后肿瘤进展罕见;然而,椎体压缩骨折被认为是更常见的治疗后效应。仅采用影像学检查进行治疗后评估可能难以区分肿瘤进展与放疗后改变,如纤维化。这是来自前瞻性数据库的最大系列研究,作者检查了因假定的肿瘤进展或继发于压缩骨折的机械性疼痛而接受手术干预的患者所取样本的组织病理学。大多数患者存在肿瘤消融及由此导致的纤维化,而非肿瘤进展。本研究的目的是评估因高剂量单次分割立体定向放射外科治疗后影像学上肿瘤进展、纤维化或椎体塌陷而接受病理采样的患者的肿瘤组织病理学及特征。方法 2005年1月至2014年1月,共有582例患者接受了基于直线加速器的单次分割(18 - 24 Gy)立体定向放射外科治疗。作者回顾性确定了30例患者(5.1%),这些患者因继发于椎体压缩骨折的机械性疼痛或不稳定(n = 17)或影像学上肿瘤进展而接受了32处病变的椎体强化手术(n = 15)。对放疗和手术治疗、组织病理学及长期结局进行了回顾。采用Kaplan - Meier方法计算生存率和复发时间。结果 放射外科治疗时的平均年龄为59岁(范围36 - 80岁)。所有患者均获得了初始病理诊断,主要包括放疗抵抗性肿瘤类型,其中肾细胞癌7例(22%)、黑色素瘤6例(19%)、肺癌4例(12%)、肉瘤3例(9%)。手术干预的中位时间为24.7个月(范围1.6 - 50.8个月)。所有患者的中位随访时间和总生存期分别为42.5个月和41个月(总生存期范围7 - 86个月)。大多数评估病变在病理检查中未显示肿瘤证据(32处病变中的25处,78%),而少数病变显示有残留肿瘤(32处病变中的7处,22%)。肿瘤复发后患者的中位生存期为5个月(范围2 -