Department of Neurosurgery, University of Virginia, Charlottesville, VA, USA.
Department of Neurological Surgery, University of Virginia, Charlottesville, VA, 22908, USA.
J Neurooncol. 2017 Oct;135(1):67-74. doi: 10.1007/s11060-017-2520-y. Epub 2017 Sep 14.
Silent corticotroph staining pituitary adenoma (SCA) represents an uncommon subset of Non-Functioning adenomas (NFAs), hypothesized to be more locally aggressive. In this retrospective multicenter study, we investigate the safety and effectiveness of Stereotactic Radiosurgery (SRS) in patients with SCA compared with other non-SCA NFA's. Eight centers participating in the International Gamma-Knife Research Foundation (IGKRF) contributed to this study. Outcomes of 50 patients with confirmed SCAs and 307 patients with confirmed non-SCA NFA's treated with SRS were evaluated. Groups were matched. SCA was characterized by a lack of clinical evidence of Cushing disease, yet with positive immunostaining for corticotroph. Median age was 55.2 years (13.7-87). All patients underwent at least one trans-sphenoidal tumor resection prior to SRS. SRS parameters were comparable as well. Median follow-up 40 months (6-163). Overall tumor control rate (TCR) 91.2% (n = 280). In the SCA group, TCR were 82% (n = 41) versus 94.1% (n = 289) for the control-NFA (p = 0.0065). The SCA group showed a significantly higher incidence of new post-SRS visual deficit (p < 0.0001) assigned to tumor progression and growth, and post-SRS weakness and fatigue (p < 0.0001). In univariate and multivariate analysis, only the status of silent corticotroph staining (p = 0.005, p = 0.009 respectively) and margin dose (p < 0.0005, p = 0.0037 respectively) significantly influenced progression rate. A margin dose of ≥17 Gy was noted to influence the adenoma progression rate in the entire cohort (p = 0.003). Silent corticotroph staining represents an independent factor for adenoma progression and hypopituitarism after SRS. A higher margin dose may convey a greater chance of TCR.
无功能垂体腺瘤中的静默促皮质激素染色型(SCA)是一个罕见的亚型,被认为具有更高的局部侵袭性。在这项回顾性多中心研究中,我们调查了 SCA 患者接受立体定向放射外科(SRS)治疗的安全性和有效性,并与其他非 SCA 无功能腺瘤(NFA)进行了比较。有 8 个参与国际伽玛刀研究基金会(IGKRF)的中心为本研究做出了贡献。评估了 50 例确诊的 SCA 患者和 307 例接受 SRS 治疗的确诊非 SCA NFA 患者的治疗结果。对两组患者进行了匹配。SCA 的特点是缺乏库欣病的临床证据,但促皮质激素免疫染色阳性。中位年龄为 55.2 岁(13.7-87 岁)。所有患者在 SRS 治疗前至少接受过一次经蝶窦肿瘤切除术。SRS 参数也相似。中位随访时间为 40 个月(6-163 个月)。总体肿瘤控制率(TCR)为 91.2%(n=280)。在 SCA 组中,TCR 为 82%(n=41),而对照组非 SCA NFA 组为 94.1%(n=289)(p=0.0065)。SCA 组在 SRS 后出现新的视觉缺损(与肿瘤进展和生长有关)、SRS 后无力和疲劳的发生率明显更高(p<0.0001)。单因素和多因素分析均表明,仅静默促皮质激素染色状态(p=0.005,p=0.009)和边缘剂量(p<0.0005,p=0.0037)显著影响进展率。在整个队列中,边缘剂量≥17 Gy 与腺瘤进展率有关(p=0.003)。静默促皮质激素染色是 SRS 后腺瘤进展和垂体功能减退的独立因素。较高的边缘剂量可能会增加 TCR 的机会。