Kondziolka D, Flickinger J C, Perez B
Department of Neurological Surgery, University of Pittsburgh, Pennsylvania, USA.
Neurosurgery. 1998 Sep;43(3):405-13; discussion 413-4. doi: 10.1097/00006123-199809000-00001.
Parasagittal meningiomas, especially when associated with the middle or posterior third of the superior sagittal sinus, pose difficult management challenges. Initial surgical excision is associated with high morbidity and frequent tumor recurrence after subtotal resection. Neurological deficits are cumulative when multiple resections are required. No consistent management approach exists for patients with such tumors. In addition to observation, management options include resection, stereotactic radiosurgery, or fractionated radiation therapy used alone or in combination.
Sixteen centers where resection, gamma knife radiosurgery, and/or radiation therapy were available provided management data on 203 patients with histologically benign meningiomas from the time of initial diagnosis through follow-up after radiosurgery. The timing of resections, parameters of radiosurgery, rates of tumor control, morbidity, and functional patient outcomes were studied. The median follow-up duration in this study was 3.5 years (maximum, 33 yr after presentation and 6 yr after radiosurgery).
The tumors were located in the anterior superior sagittal sinus in 52 patients, at the middle of the sinus in 91, and at the posterior portion of the sinus in 60. The mean tumor volume at the time of radiosurgery was 10 cc. In patients who underwent radiosurgery as the primary therapy (n = 66), the 5-year actuarial tumor control rate was 93 +/- 4%. No clinical failure (need for additional therapy or worsened neurological function) occurred in patients who had smaller tumors (<7.5 cc) and who had never undergone resection (n = 41). The 5-year control rate for patients with previous surgery was only 60 +/- 10%; the control rate for the radiosurgery-treated volume was 85%. Most failures resulted from remote tumor growth. Multivariate analyses identified significantly decreased tumor control with increasing tumor volume (P = 0.002) and previous neurological deficits (P = 0.002). The rate of transient, symptomatic edema after radiosurgery was 16%, was more common with larger tumors, and occurred within 2 years. Of 33 patients who were employed at the time of radiosurgery for whom a minimum of 1 year of follow-up data were available, 30 remained employed (91%). A decrease in functional status after radiosurgery was noted in only 3 of 33 (9%) employed and 7 of 77 (9%) unemployed patients.
In patients with smaller tumors (<3 cm in diameter) and patent sagittal sinuses, we advocate radiosurgery alone as the first surgical procedure. Patients with larger tumors and those with progressive neurological deficits resulting from brain compression should first undergo resection. Planned second-stage radiosurgery should be performed soon afterward for any residual tumor nodule or neoplastic dural remnant. Multimodality management may enhance long-term tumor control, reduce the need for multiple resections, and maintain the functional status of the patient.
矢状窦旁脑膜瘤,尤其是与上矢状窦中后三分之一相关的脑膜瘤,带来了棘手的治疗挑战。初次手术切除与高发病率以及次全切除后肿瘤频繁复发相关。当需要多次切除时,神经功能缺损会累积。对于这类肿瘤患者,不存在一致的治疗方法。除了观察,治疗选择包括单独或联合使用的切除、立体定向放射外科手术或分次放射治疗。
16个可进行切除、伽玛刀放射外科手术和/或放射治疗的中心提供了203例组织学上为良性脑膜瘤患者从初次诊断到放射外科手术后随访的治疗数据。研究了切除时间、放射外科手术参数、肿瘤控制率、发病率和患者功能结局。本研究的中位随访时间为3.5年(最长,就诊后33年和放射外科手术后6年)。
52例患者的肿瘤位于上矢状窦前部,91例位于窦中部,60例位于窦后部。放射外科手术时的平均肿瘤体积为10立方厘米。作为主要治疗方法接受放射外科手术的患者(n = 66),5年精算肿瘤控制率为93±4%。肿瘤较小(<7.5立方厘米)且从未接受过切除的患者(n = 41)未出现临床失败(需要额外治疗或神经功能恶化)。既往接受过手术的患者5年控制率仅为60±10%;放射外科手术治疗体积的控制率为85%。大多数失败是由于远处肿瘤生长。多变量分析确定,随着肿瘤体积增大(P = 0.002)和既往存在神经功能缺损(P = 0.002),肿瘤控制显著降低。放射外科手术后短暂性症状性水肿的发生率为16%,在较大肿瘤中更常见,且发生在2年内。在放射外科手术时就业且有至少1年随访数据的33例患者中,30例仍在工作(91%)。在33例就业患者中,只有3例(9%)和77例失业患者中的7例(9%)在放射外科手术后功能状态下降。
对于肿瘤较小(直径<3厘米)且矢状窦通畅的患者,我们主张单独将放射外科手术作为首选手术方法。肿瘤较大以及因脑受压导致进行性神经功能缺损的患者应首先接受切除。对于任何残留肿瘤结节或肿瘤性硬脑膜残余,应随后尽快进行计划性二期放射外科手术。多模式治疗可能会增强长期肿瘤控制,减少多次切除的必要性,并维持患者的功能状态。