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肢端肥大症患者中生长激素(GH)分泌性垂体大腺瘤完全消失:兰瑞肽 Autogel 治疗的效果和停药后果。

Complete disappearance of a GH-secreting pituitary macroadenoma in a patient with acromegaly: effect of treatment with lanreotide Autogel and consequence of treatment withdrawal.

机构信息

Department of Clinical and Molecular Endocrinology and Oncology, Federico II University of Naples, Naples, Italy.

出版信息

Eur J Endocrinol. 2010 May;162(5):993-9. doi: 10.1530/EJE-09-0769. Epub 2010 Feb 15.

Abstract

BACKGROUND

Somatostatin analogs (SA) are the cornerstone in the medical treatment of acromegaly, used as either primary or adjunctive therapy. In particular, SA are effective in inducing the biochemical remission of the disease and tumor shrinkage, although only few cases of complete disappearance of the pituitary tumor in patients treated with SA as long-acting formulations have been reported. SA withdrawal has been demonstrated to keep safe levels of GH and IGF1 at least in a small subset of patients well responsive to SA, although it is generally followed by disease recurrence after several months.

CASE REPORT

A 61-year-old female patient bearing a very large GH-secreting pituitary macroadenoma was treated with 12-month lanreotide Autogel (ATG), at the initial dose of 120 mg/28 days. After 3 months, GH and IGF1 levels were fully normalized, to prolong the administration interval from 28 to 56 days. After 6 months of treatment, a significant tumor shrinkage (90% of baseline size) was observed, whereas GH and IGF1 excess was still well controlled. After 12-month therapy, a complete disappearance of the pituitary tumor was observed, and the hormonal evaluation confirmed the complete biochemical remission of acromegaly. Lanreotide ATG treatment was withdrawn. The clinical, biochemical, and radiological remission of acromegaly was maintained 24 months after lanreotide ATG treatment discontinuation, without evidence of disease recurrence.

CONCLUSIONS

This report represents an exemplary case of the potentiality of treatment with lanreotide ATG in inducing a complete remission of acromegalic disease, persistent after a long period of time from treatment withdrawal.

摘要

背景

生长抑素类似物(SAs)是治疗肢端肥大症的基石,可用作一线或辅助治疗。特别是,SAs在诱导疾病的生化缓解和肿瘤缩小方面非常有效,尽管在用长效制剂治疗的患者中,只有少数报告了垂体肿瘤完全消失的情况。已经证明,在对 SAs 反应良好的小部分患者中,SA 停药可以保持 GH 和 IGF1 的安全水平,尽管在几个月后通常会出现疾病复发。

病例报告

一名 61 岁女性患者患有非常大的 GH 分泌性垂体大腺瘤,接受了 12 个月的兰瑞肽 Autogel(ATG)治疗,初始剂量为 120mg/28 天。治疗 3 个月后,GH 和 IGF1 水平完全正常化,将给药间隔从 28 天延长至 56 天。治疗 6 个月后,观察到肿瘤显著缩小(基线大小的 90%),而 GH 和 IGF1 过多仍得到很好的控制。经过 12 个月的治疗,观察到垂体肿瘤完全消失,激素评估证实肢端肥大症的生化缓解完全。兰瑞肽 ATG 治疗被停止。兰瑞肽 ATG 治疗停止后 24 个月,肢端肥大症的临床、生化和放射学缓解得以维持,没有疾病复发的证据。

结论

本报告代表了使用兰瑞肽 ATG 治疗肢端肥大症的潜在可能性的一个典型病例,在治疗停止后很长一段时间内仍能持续完全缓解肢端肥大症。

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