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肢端肥大症控制不佳患者的立体定向放射治疗结果

Outcome of stereotactic radiotherapy for patients with uncontrolled acromegaly.

作者信息

Imran Syed Ali, Fleetwood Ian G, O'Connell Colleen M, Ransom Thomas P, Mulroy Liam A, Ur Ehud, Clarke David B

机构信息

Halifax Neuropituitary Program, Department of Medicine Endocrinology, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

Can J Neurol Sci. 2009 Jul;36(4):468-74. doi: 10.1017/s0317167100007800.

Abstract

OBJECTIVE

Linear accelerator based stereotactic radiation therapy (SRT) has been used for the treatment of pituitary tumours; however, little is known concerning the use of this modality for the treatment of patients with acromegaly. We have prospectively studied the short-term outcome of SRT in 12 acromegaly patients who failed to achieve biochemical remission despite surgery and/or pharmacologic therapy.

METHODS

We identified all patients who had biochemically uncontrolled acromegaly and were treated with SRT between April 2003 and December 2006. All patients were followed prospectively based on a pre-defined protocol that included Goldman visual field examination, MRI of the sella, and pituitary hormone testing at 3, 6, 12 months, and then yearly.

RESULTS

A total of 12 patients with acromegaly were treated with SRT. There were 9 females and the median age of the group was 50 years. The median follow-up was 28.5 months during which time the mean tumor volume decreased by 40%, the median GH fell from 4.1 microg/L to 1.3 microg/L (p = 0.003) and the median IGF-1 dropped more than half from 545.5 microg/L to 260.5 microg/L (p = 0.002). Four patients achieved normal, while an additional 2 achieved near-normal, IGF-1 levels. One patient was able to discontinue and two were able to reduce their acromegaly medications while maintaining a normal IGF-1. A new pituitary hormonal deficit was found at 24 months in one patient who developed hypoadrenalism requiring corticosteroid replacement.

CONCLUSION

Based on our early experience, we believe that SRT should be considered in treating patients with uncontrolled acromegaly.

摘要

目的

基于直线加速器的立体定向放射治疗(SRT)已用于垂体肿瘤的治疗;然而,关于这种治疗方式用于肢端肥大症患者的治疗情况,人们了解甚少。我们前瞻性地研究了12例肢端肥大症患者接受SRT的短期疗效,这些患者尽管接受了手术和/或药物治疗,但仍未实现生化缓解。

方法

我们确定了所有生化指标未得到控制且在2003年4月至2006年12月期间接受SRT治疗的肢端肥大症患者。所有患者均按照预先定义的方案进行前瞻性随访,该方案包括戈德曼视野检查、蝶鞍磁共振成像(MRI)以及在3、6、12个月时进行垂体激素检测,之后每年检测一次。

结果

共有12例肢端肥大症患者接受了SRT治疗。其中女性9例,该组患者的中位年龄为50岁。中位随访时间为28.5个月,在此期间,平均肿瘤体积减少了40%,中位生长激素(GH)从4.1μg/L降至1.3μg/L(p = 0.003),中位胰岛素样生长因子-1(IGF-1)从545.5μg/L降至260.5μg/L,降幅超过一半(p = 0.002)。4例患者的IGF-1水平恢复正常,另有2例患者的IGF-1水平接近正常。1例患者能够停用,2例患者能够减少肢端肥大症药物用量,同时维持IGF-1水平正常。1例患者在24个月时出现新的垂体激素缺乏,发生肾上腺功能减退,需要进行皮质类固醇替代治疗。

结论

基于我们的早期经验,我们认为对于生化指标未得到控制的肢端肥大症患者,应考虑采用SRT进行治疗。

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