Department of Neurosurgery, Boston Medical Center, Boston, MA, USA.
Faculdade de Medicina de São José do Rio Preto (FAMERP), São José do Rio Preto, SP, Brazil.
Acta Neurochir (Wien). 2024 Oct 2;166(1):392. doi: 10.1007/s00701-024-06296-4.
Nonfunctioning pituitary adenomas (NFPAs) are a significant subtype of pituitary tumors, accounting for 30% of all pituitary tumors and 10-20% of intracranial tumors. The primary treatment for NFPAs is resection, but complete resection is often challenging due to the tumor's proximity to critical structures, leading to frequent recurrences. Stereotactic radiosurgery (SRS) has emerged as a viable treatment option for recurrent or residual NFPAs, but its long-term efficacy and safety profile require further investigation.
This systematic review followed PRISMA guidelines and included studies published up to February 2024. We searched MEDLINE, Embase, and Cochrane databases for studies evaluating SRS for recurrent/residual NFPAs. Inclusion criteria focused on studies reporting outcomes and complications of SRS, while exclusion criteria omitted case reports, case series, and non-English studies. Data extracted included demographic details, dosimetry parameters, and follow-up durations. The risk of bias was assessed using the ROBINS-I tool, and statistical analyses were performed using single-arm meta-analyses.
A total of 24 studies involving 3,781 patients were included. The mean follow-up duration was 60 months. Tumor control was achieved in approximately 92.3% of patients. The risk of developing hypopituitarism post-SRS was 13.62%, while the risk for panhypopituitarism was 2.55%. New visual field deficits occurred in 3.94% of patients. Cranial nerve deficits were rare, with event rates below 1% for CN III, CN V, and CN VI.
SRS is effective in managing recurrent or residual NFPAs, achieving high tumor control rates. However, the risk of hypopituitarism remains a significant concern, necessitating regular endocrinological monitoring. While generally safe, the potential for new visual field deficits and other cranial nerve deficits must be considered. SRS remains a valuable treatment option, but clinicians should be aware of its potential complications.
无功能垂体腺瘤(NFPAs)是垂体肿瘤的一个重要亚型,占所有垂体肿瘤的 30%,占颅内肿瘤的 10-20%。NFPAs 的主要治疗方法是切除,但由于肿瘤与关键结构的接近,常难以完全切除,导致频繁复发。立体定向放射外科(SRS)已成为治疗复发性或残留 NFPAs 的可行选择,但需要进一步研究其长期疗效和安全性。
本系统评价遵循 PRISMA 指南,纳入截至 2024 年 2 月发表的研究。我们检索了 MEDLINE、Embase 和 Cochrane 数据库,以评估 SRS 治疗复发性/残留 NFPAs 的研究。纳入标准侧重于报告 SRS 结果和并发症的研究,排除标准包括病例报告、病例系列和非英语研究。提取的数据包括人口统计学细节、剂量学参数和随访时间。使用 ROBINS-I 工具评估偏倚风险,并使用单臂荟萃分析进行统计分析。
共纳入 24 项研究,涉及 3781 例患者。平均随访时间为 60 个月。约 92.3%的患者实现了肿瘤控制。SRS 后发生垂体功能减退的风险为 13.62%,全垂体功能减退的风险为 2.55%。新出现的视野缺损发生率为 3.94%。颅神经缺损罕见,III、V 和 VI 颅神经的发生率均低于 1%。
SRS 治疗复发性或残留 NFPAs 有效,肿瘤控制率高。然而,垂体功能减退的风险仍然是一个重要的关注点,需要定期进行内分泌监测。虽然总体安全,但仍需考虑新的视野缺损和其他颅神经缺损的潜在风险。SRS 仍然是一种有价值的治疗选择,但临床医生应了解其潜在并发症。