Bevan J S, Atkin S L, Atkinson A B, Bouloux P-M, Hanna F, Harris P E, James R A, McConnell M, Roberts G A, Scanlon M F, Stewart P M, Teasdale E, Turner H E, Wass J A H, Wardlaw J M
Department of Endocrinology, Aberdeen Royal Infirmary, Aberdeen, United Kingdom AB25 2ZN.
J Clin Endocrinol Metab. 2002 Oct;87(10):4554-63. doi: 10.1210/jc.2001-012012.
Conventional surgery and radiotherapy for acromegaly have limitations. There are few data on the use of the somatostatin analog octreotide (Oct) as primary medical therapy. An open prospective study of 27 patients with newly diagnosed acromegaly was conducted in nine endocrine centers in the United Kingdom. Twenty patients had macroadenomas, and 7 had microadenomas. For the first 24 wk (phase 1), patients received sc Oct in an initial dose of 100 microg, 3 times daily, increased to 200 micro g three times daily after 4 wk in the 13 patients whose mean serum GH remained greater than 5 mU/liter (2 microg/liter). Five-point GH profiles were performed at 0, 4, 12, and 24 wk, and high resolution pituitary imaging using a standard protocol was performed at 0, 12, and 24 wk (magnetic resonance imaging in 25 patients and computed tomography in 2). Tumor dimensions and volumes were calculated by a central, reporting neuroradiologist, and the results were audited by a second, independent neuroradiologist. After 24 wk, 15 patients proceeded to phase 2 of the study with a direct switch to monthly injections of the depot formulation of Oct, Sandostatin long-acting release (Oct-LAR). Further GH profiles were performed at 36 and 48 wk, and pituitary imaging was performed at 48 wk. The median pretreatment serum GH concentration was 30.7 mU/liter (range, 6.7-141.4). During sc Oct, serum GH fell to less than 5 mU/liter in 9 patients (38%), and IGF-I fell to normal in 8 patients (33%). All 27 tumors shrank during sc Oct; for microadenomas the median tumor volume reduction was 49% (range, 12-73), and for macroadenomas it was 43% (range, 6-92). After 24 wk of Oct-LAR (end of phase 2), the GH level was less than 5 mU/liter in 11 of 14 patients (79%), and IGF-I was normal in 8 of 15 patients (53%). In the 15 patients given Oct-LAR (10 macroadenomas), wk 48 scans showed a further overall median tumor volume reduction of 24%. At the end of the study 79% of patients had mean serum GH levels below 5 mU/liter, 53% had normal IGF-I levels, and 73% showed greater than 30% tumor shrinkage. Twenty-nine percent of patients achieved all 3 targets, but no patient with pretreatment GH levels above 50 mU/liter did so at any stage of the study. Primary medical therapy with Oct offers the prospect of normalization of GH/IGF-I levels together with substantial tumor shrinkage in a significant subset of acromegalic patients. This is most likely to occur in patients with pretreatment GH levels less than 50 mU/liter (20 microg/liter).
肢端肥大症的传统手术和放射治疗存在局限性。关于使用生长抑素类似物奥曲肽(Oct)作为主要药物治疗的数据较少。在英国的9个内分泌中心对27例新诊断的肢端肥大症患者进行了一项开放性前瞻性研究。20例患者患有大腺瘤,7例患有微腺瘤。在最初的24周(第1阶段),患者接受皮下注射奥曲肽,初始剂量为100μg,每日3次,4周后,13例平均血清生长激素(GH)仍大于5mU/L(2μg/L)的患者剂量增加至每日3次,每次200μg。在0、4、12和24周进行五点GH谱测定,并在0、12和24周使用标准方案进行高分辨率垂体成像(25例患者进行磁共振成像,2例患者进行计算机断层扫描)。肿瘤大小和体积由一名中心放射神经科医生计算并报告,结果由另一名独立的放射神经科医生审核。24周后,15例患者进入研究的第2阶段,直接改用每月注射一次奥曲肽长效释放制剂(Oct-LAR)。在36和48周进行进一步的GH谱测定,并在48周进行垂体成像。治疗前血清GH浓度中位数为30.7mU/L(范围为6.7 - 141.4)。在皮下注射奥曲肽期间,9例患者(38%)的血清GH降至低于5mU/L,8例患者(33%)的胰岛素样生长因子-I(IGF-I)降至正常。所有27个肿瘤在皮下注射奥曲肽期间均缩小;微腺瘤的肿瘤体积中位数减少49%(范围为12 - 73),大腺瘤为43%(范围为6 - 92)。在奥曲肽长效释放制剂治疗24周(第2阶段结束)后,14例患者中的11例(79%)的GH水平低于5mU/L,15例患者中的8例(53%)的IGF-I正常。在接受奥曲肽长效释放制剂治疗的15例患者(10例大腺瘤)中,48周扫描显示肿瘤总体积中位数进一步减少24%。研究结束时,79%的患者平均血清GH水平低于5mU/L,53%的患者IGF-I水平正常,73%的患者肿瘤缩小超过30%。29%的患者实现了所有3个目标,但治疗前GH水平高于50mU/L的患者在研究的任何阶段均未实现。奥曲肽作为主要药物治疗为一部分肢端肥大症患者提供了使GH/IGF-I水平正常化以及肿瘤显著缩小的前景。这最有可能发生在治疗前GH水平低于50mU/L(20μg/L)的患者中。