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立体定向放射外科治疗肢端肥大症:临床结局的国际系统评价和荟萃分析。

Stereotactic radiosurgery for acromegaly: an international systematic review and meta-analysis of clinical outcomes.

机构信息

Department of Radiation Oncology, Virginia Commonwealth University Health System, Richmond, VA, USA.

Rady School of Management, University of California at San Diego, San Diego, CA, USA.

出版信息

J Neurooncol. 2020 Jul;148(3):401-418. doi: 10.1007/s11060-020-03552-2. Epub 2020 Jun 6.

Abstract

INTRODUCTION

We performed a systematic review and meta-analysis of clinical outcomes for patients with acromegaly treated with stereotactic radiosurgery (SRS).

METHODS

Primary outcomes were 5- and 10-year endocrine remission (ER) and endocrine control (EC). Secondary outcomes were 10-year radiographic local control (LC), visual toxicity, and hypopituitarism rates. Weighted random effects meta-analyses using the DerSimonian and Laird methods were conducted to characterize and compare effect sizes. Mixed effects regression models were used to examine correlations between potential prognostic factors and primary and secondary outcomes.

RESULTS

In total, 1533 patients across 20 published studies with acromegaly treated with SRS were included. At 5-years, estimated ER and EC rates were 43.2% (95% CI 31.7-54.6%) and 55.0% (95% CI 27.6-82.4%), respectively. At 10-years, estimated ER and EC rates were 56.9% (95% CI 47.5-66.4%) and 69.7% (95% CI 47.7-91.8%), respectively. The estimated 10-year LC rate was 92.8% (95% CI 83.0-100%). Visual toxicity and hypopituitarism following SRS were estimated to be 2.7% (95% CI 1.3-4.2%) and 26.8% (95% CI 16.9-36.7%), respectively. Every 1 Gy increase in margin prescription dose beyond 17 Gy was estimated to result in a 0.41% increased risk of visual toxicity (p = 0.03). No prognostic factors were associated with EC, ER, LC, or hypopituitarism.

CONCLUSIONS

SRS was well-tolerated in the management of pituitary acromegaly resulting in gradually improving ER and EC rates over time that approached 60% and 70%. SRS-related visual loss is an uncommon treatment-related side effect, and patient-specific clinical decision making remains critical.

摘要

简介

我们对接受立体定向放射外科(SRS)治疗的肢端肥大症患者的临床结局进行了系统评价和荟萃分析。

方法

主要结局是 5 年和 10 年内分泌缓解(ER)和内分泌控制(EC)。次要结局是 10 年的放射学局部控制(LC)、视觉毒性和垂体功能减退发生率。使用 DerSimonian 和 Laird 方法进行加权随机效应荟萃分析,以描述和比较效应大小。混合效应回归模型用于检查潜在预后因素与主要和次要结局之间的相关性。

结果

共纳入 20 项发表的肢端肥大症 SRS 治疗研究中的 1533 例患者。5 年时,估计 ER 和 EC 率分别为 43.2%(95%CI 31.7-54.6%)和 55.0%(95%CI 27.6-82.4%)。10 年时,估计 ER 和 EC 率分别为 56.9%(95%CI 47.5-66.4%)和 69.7%(95%CI 47.7-91.8%)。估计 10 年 LC 率为 92.8%(95%CI 83.0-100%)。SRS 后估计视觉毒性和垂体功能减退发生率分别为 2.7%(95%CI 1.3-4.2%)和 26.8%(95%CI 16.9-36.7%)。超过 17 Gy 的边缘处方剂量每增加 1 Gy,估计视觉毒性的风险增加 0.41%(p=0.03)。没有预后因素与 EC、ER、LC 或垂体功能减退相关。

结论

SRS 在管理垂体肢端肥大症中耐受性良好,导致 ER 和 EC 率逐渐提高,在 5 年和 10 年时分别接近 60%和 70%。SRS 相关的视力丧失是一种罕见的治疗相关副作用,患者特定的临床决策仍然至关重要。

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