Department of Neurological Surgery, University of Virginia, Charlottesville, Virginia 22908, USA.
J Neurosurg. 2012 Jul;117(1):129-35. doi: 10.3171/2012.4.JNS112250. Epub 2012 May 11.
Nonfunctioning pituitary macroadenomas often recur after microsurgery and thereby require further treatment. Gamma Knife surgery (GKS) has been used to treat recurrent adenomas. In this study, the authors evaluated outcomes following GKS of nonfunctioning pituitary macroadenomas and assessed predictors of tumor control, neurological deficits, and delayed hypopituitarism.
Between June 1989 and March 2010, 140 consecutive patients with nonfunctioning pituitary macroadenomas were treated using GKS at the University of Virginia. The median patient age was 51 years (range 21-82 years), and 56% of patients were male. Mean tumor volume was 5.6 cm3 (range 0.6-35 cm3). Thirteen patients were treated with GKS as primary therapy, and 127 had undergone at least 1 open resection prior to GKS. Ninety-three patients had a history of hormone therapy prior to GKS. The mean maximal dose of GKS was 38.6 Gy (range 10-70 Gy), the mean marginal dose was 18 Gy (range 5-25 Gy), and the mean number of isocenters was 9.8 (range 1-26). Follow-up evaluations were performed in all 140 patients, ranging from 0.5 to 17 years (mean 5 years, median 4.2 years).
Tumor volume remained stable or decreased in 113 (90%) of 125 patients with available follow-up imaging. Kaplan-Meier analysis demonstrated radiographic progression free survival at 2, 5, 8, and 10 years to be 98%, 97%, 91%, and 87%, respectively. In multivariate analysis, a tumor volume greater than 5 cm3 (hazard ratio=5.0, 95% CI 1.5-17.2; p=0.023) was the only factor predictive of tumor growth. The median time to tumor progression was 14.5 years. Delayed hypopituitarism occurred in 30.3% of patients. No factor was predictive of post-GKS hypopituitarism. A new or worsening cranial nerve deficit occurred in 16 (13.7%) of 117 patients. Visual decline was the most common neurological deficit (12.8%), and all patients experiencing visual decline had evidence of tumor progression. In multivariate analysis, a tumor volume greater than 5 cm3 (OR=3.7, 95% CI 1.2-11.7; p=0.025) and pre-GKS hypopituitarism (OR=7.5, 95% CI 1.1-60.8; p=0.05) were predictive of a new or worsened neurological deficit.
In patients with nonfunctioning pituitary macroadenomas, GKS confers a high rate of tumor control and a low rate of neurological deficits. The most common complication following GKS is delayed hypopituitarism, and this occurs in a minority of patients.
垂体无功能大腺瘤经显微手术后常复发,因此需要进一步治疗。伽玛刀治疗(GKS)已用于治疗复发性腺瘤。在这项研究中,作者评估了 GKS 治疗无功能垂体大腺瘤的结果,并评估了肿瘤控制、神经功能缺损和延迟性垂体功能减退的预测因素。
1989 年 6 月至 2010 年 3 月,弗吉尼亚大学对 140 例无功能垂体大腺瘤患者进行了 GKS 治疗。患者中位年龄为 51 岁(21-82 岁),56%为男性。平均肿瘤体积为 5.6cm3(0.6-35cm3)。13 例患者为 GKS 作为一线治疗,127 例患者在 GKS 治疗前至少进行过一次开放手术。93 例患者在 GKS 治疗前接受过激素治疗。GKS 的最大剂量平均为 38.6Gy(10-70Gy),边缘剂量平均为 18Gy(5-25Gy),等中心点平均为 9.8(1-26)。140 例患者均进行了随访评估,随访时间为 0.5-17 年(平均 5 年,中位数 4.2 年)。
125 例有随访影像学资料的患者中,113 例(90%)肿瘤体积稳定或缩小。Kaplan-Meier 分析显示,2、5、8 和 10 年的无进展生存放射性为 98%、97%、91%和 87%。多因素分析显示,肿瘤体积大于 5cm3(风险比=5.0,95%可信区间 1.5-17.2;p=0.023)是肿瘤生长的唯一预测因素。肿瘤进展的中位时间为 14.5 年。30.3%的患者发生延迟性垂体功能减退。无任何因素可预测 GKS 后垂体功能减退。117 例患者中有 16 例(13.7%)出现新发或加重的颅神经功能障碍。视力下降是最常见的神经功能缺损(12.8%),所有出现视力下降的患者均有肿瘤进展的证据。多因素分析显示,肿瘤体积大于 5cm3(比值比=3.7,95%可信区间 1.2-11.7;p=0.025)和 GKS 前垂体功能减退(比值比=7.5,95%可信区间 1.1-60.8;p=0.05)是新发或加重神经功能障碍的预测因素。
对于无功能垂体大腺瘤患者,GKS 具有较高的肿瘤控制率和较低的神经功能缺损率。GKS 后最常见的并发症是延迟性垂体功能减退,少数患者会发生这种情况。