Wei Nathan, Gunawan Kevin, Tsai Chiao-Ling, Yang Shih-Hung, Hsu Feng-Ming, Lai Dar-Ming, Xiao Furen
Department of Neurosurgery, National Taiwan University Hospital, Taipei , Taiwan.
Department of Neurosurgery, Cipto Mangunkusumo National General Hospital, Faculty of Medicine Universitas Indonesia, Jakarta , Indonesia.
Neurosurgery. 2025 Apr 1;96(4):892-900. doi: 10.1227/neu.0000000000003174. Epub 2024 Sep 12.
Stereotactic radiosurgery (SRS) has been widely adopted as an important adjunctive treatment modality for managing nonfunctioning pituitary adenomas (NFPAs). However, current studies on the long-term effects of SRS on pituitary adenomas have been largely limited by small sample sizes and short follow-up periods. The aim of this study was to evaluate the long-term outcomes of SRS for NFPAs.
We conducted a retrospective review of 178 patients with NFPAs who received CyberKnife radiosurgery at a single institution between February 2008 and July 2021. Long-term outcomes of tumor control, new-onset hypopituitarism, and new visual disorders were assessed.
During a median radiological follow-up of 49.7 months (range, 2.5-158.1 months), only 11 (7.0%) patients experienced tumor progression. The progression-free survival at 3, 5, and 10 years was 97.47%, 95.57%, and 93.04%, respectively. New-onset hypopituitarism was diagnosed in 27 (16.9%) patients with a median clinical follow-up duration of 71.2 months (range, 11.5-175.4 months). The median time from SRS to new-onset hypopituitarism was 28.3 months (range, 2.8-101.7 months). The cumulative incidence of new-onset hypopituitarism at 3, 5, and 10 years was 8.47%, 12.43%, and 15.25%, respectively. Biological effective dose >140 Gy and single fraction equivalent dose >16.0 Gy were significant risk factors for new-onset hypopituitarism ( P = .046). Other adverse events were experienced by 15 (8.4%) patients, 9 (5.1%) of whom presented with new visual disorders. Development of new visual disorders was associated with a pretreatment tumor volume of >2.5 mL ( P = .044).
SRS is an effective and relatively safe means of managing both primary and residual/recurrent NFPAs.
立体定向放射外科(SRS)已被广泛用作治疗无功能垂体腺瘤(NFPAs)的重要辅助治疗方式。然而,目前关于SRS对垂体腺瘤长期影响的研究在很大程度上受到样本量小和随访期短的限制。本研究的目的是评估SRS治疗NFPAs的长期疗效。
我们对2008年2月至2021年7月期间在单一机构接受射波刀放射外科治疗的178例NFPAs患者进行了回顾性研究。评估了肿瘤控制、新发垂体功能减退和新发视觉障碍的长期疗效。
在中位放射学随访49.7个月(范围2.5 - 158.1个月)期间,只有11例(7.0%)患者出现肿瘤进展。3年、5年和10年的无进展生存率分别为97.47%、95.57%和93.04%。在中位临床随访71.2个月(范围11.5 - 175.4个月)时,27例(16.9%)患者被诊断为新发垂体功能减退。从SRS到新发垂体功能减退的中位时间为28.3个月(范围2.8 - 101.7个月)。3年、5年和10年新发垂体功能减退的累积发生率分别为8.47%、12.43%和15.25%。生物有效剂量>140 Gy和单次分割等效剂量>16.0 Gy是新发垂体功能减退的显著危险因素(P = 0.046)。15例(8.4%)患者出现其他不良事件,其中9例(5.1%)出现新发视觉障碍。新发视觉障碍的发生与治疗前肿瘤体积>2.5 mL有关(P = 0.044)。
SRS是治疗原发性和残留/复发性NFPAs的一种有效且相对安全的方法。