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奥曲肽治疗促甲状腺激素分泌型垂体腺瘤。52例患者的随访

Octreotide therapy for thyroid-stimulating hormone-secreting pituitary adenomas. A follow-up of 52 patients.

作者信息

Chanson P, Weintraub B D, Harris A G

机构信息

Hôpital Lariboisière, Paris, France.

出版信息

Ann Intern Med. 1993 Aug 1;119(3):236-40. doi: 10.7326/0003-4819-119-3-199308010-00010.

Abstract

OBJECTIVE

To evaluate the efficacy of octreotide in the treatment of pituitary thyroid-stimulating hormone (TSH)-secreting adenomas.

DATA SOURCES

Combination of review and original data. Review data included information supplied by Sandoz Pharmaceuticals from patient case report forms and information from abstracts and articles published in the French or English language between 1987 and 1991. Original data included follow-up data on 15 of 37 previously reported cases and data on 15 new cases provided by 11 investigators.

STUDY SELECTION

Fifty-two cases from 24 medical centers in nine countries reported between 1987 and 1991.

DATA EXTRACTION

Chief clinical characteristics of the patients; dose and duration of octreotide treatment; serum TSH, thyroid hormone, and free alpha-subunit levels before and during treatment; serial anatomic evaluation of the pituitary gland by either computed tomographic scanning or magnetic resonance imaging; and side effects.

DATA SYNTHESIS

After the first octreotide dose (50 to 100 micrograms), TSH levels decreased in all but 2 patients (mean decrease for the whole group, 55.8% +/- 27%). Levels of alpha-subunit decreased in 15 of the 19 patients who had alpha-subunit assessments (mean decrease, 37.5% +/- 24%). Reduction of TSH levels after short-term treatment (50 or 100 micrograms two or three times daily) was observed in 30 to 33 patients (mean decrease, 74.1%). Thyroid hormone levels were reduced in all patients and returned to normal in 73%. Despite an initial response to therapy, thyroid hormone levels continued to rise ("true escape") in 2 patients receiving short-term therapy and in 3 patients receiving long-term therapy. Partial shrinkage of the adenoma occurred in 11 patients.

CONCLUSIONS

Octreotide is an effective treatment for TSH-secreting adenomas. Thyroid-stimulating hormone levels almost always decreased, and thyroid hormone levels reverted to normal in about three quarters of patients. Partial tumor shrinkage was observed in one third of patients receiving long-term octreotide treatment.

摘要

目的

评估奥曲肽治疗垂体促甲状腺激素(TSH)分泌腺瘤的疗效。

资料来源

综述与原始数据相结合。综述数据包括山德士制药公司提供的患者病例报告表信息以及1987年至1991年间发表的法语或英语摘要及文章中的信息。原始数据包括之前报告的37例病例中15例的随访数据以及11位研究者提供的15例新病例的数据。

研究选择

1987年至1991年间9个国家24个医疗中心报告的52例病例。

资料提取

患者的主要临床特征;奥曲肽治疗的剂量和疗程;治疗前及治疗期间的血清TSH、甲状腺激素和游离α亚基水平;通过计算机断层扫描或磁共振成像对垂体进行的系列解剖学评估;以及副作用。

资料综合

首次给予奥曲肽剂量(50至100微克)后,除2例患者外,所有患者的TSH水平均下降(全组平均下降55.8%±27%)。19例进行α亚基评估的患者中有15例α亚基水平下降(平均下降37.5%±24%)。30至33例患者在短期治疗(每日2或3次,每次50或100微克)后TSH水平降低(平均下降74.1%)。所有患者的甲状腺激素水平均降低,73%的患者恢复正常。尽管对治疗有初始反应,但2例接受短期治疗的患者和3例接受长期治疗的患者甲状腺激素水平持续升高(“真正逃逸”)。11例患者的腺瘤出现部分缩小。

结论

奥曲肽是治疗TSH分泌腺瘤的有效药物。促甲状腺激素水平几乎总是下降,约四分之三的患者甲状腺激素水平恢复正常。接受长期奥曲肽治疗的患者中有三分之一观察到肿瘤部分缩小。

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