首页> 外文期刊>Endocrine journal >Forty Month Follow-Up of Persistent and Difficultly Controlled Acromegalic Patients Treated with Depot Long Acting Somatostatin Analog Octreotide
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Forty Month Follow-Up of Persistent and Difficultly Controlled Acromegalic Patients Treated with Depot Long Acting Somatostatin Analog Octreotide

机译:持久性和难度控制的致癌患者的四十个月随访,治疗仓库长效素苷素类似糖苷蛋白酶

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References(26) Cited-By(9) The objective of the present study was to investigate the effects of octreotide long acting release (S-LAR) preparation on GH and IGF-1 serum concentrations and pituitary tumor size in patients with persistent and difficultly controlled acromegaly even after adjuvant irradiation and/or dopamine agonists. Thirty-three patients with active acromegaly (26 female and 7 male, mean age; 43.94 ± 14.01 SD years) were included in this study. Patients were evaluated at baseline and at 6, 12, 30 and 40 months for GH, IGF-1, and GH response to OGTT and biliary ultrasonography. Sella MRI was performed at initial and at 40 months. All patients received 20 mg S-LAR. Afterwards, the dosage was titrated to improve individual GH response and reduction of IGF-1 into normal ranges. Basal serum IGF-1 levels decreased from median: 530 μg/l [IQR: 420–600] to 340 μg/l [IQR: 230–460] at 6 months (p = 0.01), to 400 μg/l [IQR: 222.4–600] at 12 months (p = 0.48), to 396 μg/l [IQR: 318–468] at 30 months (p = 0.49), to 482 μg/l [308–580] at 40 months (p = 0.47). Nadir GH levels in OGTT fell from 2.70 ng/ml [IQR: 1.35–6.90] to 1.60 ng/ml [IQR: 0.36–4.10] at 6 months (p = 0.03), to 0.31 ng/ml [IQR: 0.18–0.65] at 12 months (p<0.0001), to 1.50 ng/ml [IQR: 0.83–4.00] at 30 months (p = 0.398) and to 0.89 ng/ml [IQR: 0.58–1.35] at 40 months (p<0.0001). Initially, pituitary adenoma volume was median: 1.18 ml [IQR: 0.08–3.50] and it shrank to 0.21 ml [IQR: 0–2.1] at 40 months (p = 0.08). Gallstones were detected in 12 patients and six of them underwent cholecystectomy. S-LAR is an effective treatment regimen in reducing GH and IGF-1 concentrations and as well as in shrinking tumor volume in persistent and difficultly controlled acromegalic patients.
机译:参考文献(26)引用(9)本研究的目的是探讨八月长作用释放(S-LR)制剂对持续性且难以持续的患者GH和IGF-1血清浓度和垂体肿瘤大小的影响甚至在佐剂照射和/或多巴胺激动剂后控制的棘手症。本研究纳入了三十三名活跃的患者(26例女性和7名男性,平均年龄)。患者在基线和6,12,30和40个月内评估GH,IGF-1和GH对OGTT和胆量超声检查的响应。 Sella MRI在初始和40个月内进行。所有患者均接受20毫克S-LAR。然后,滴定剂量以改善单个GH响应并将IGF-1还原成正常范围。基础血清IGF-1水平从中位数降低:530μg/ L [IQR:420-600]在6个月(P = 0.01)至400μg/ L [IQR: 222.4-600]在12个月(p = 0.48),30个月(p = 0.49),在40个月内(p = 0.49)至396μg/ l [IQR:318-468],在40个月内(p = 0.580)(p = 0.47)。 OGTT中的Nadir GH水平从2.70ng / ml [IQR:1.35-6.90]到1.60ng / ml [IQR:0.36-4.10],在6个月内(p = 0.03),至0.31 ng / ml [IQR:0.18-0.65 ]在12个月(P <0.0001),在30个月(P = 0.398)和40.89ng / ml [IQR:0.58-1.35]的1.50ng / ml [IQR:0.83-4.00],40个月(P <0.0001 )。最初,垂体腺瘤体积中位数:1.18毫升[IQR:0.08-3.50],40个月,它在0.21ml [IQR:0-2.1]中(P = 0.08)。在12名患者中检测到胆结石,其中六个是胆囊切除术的6例。 S-LR是减少GH和IGF-1浓度的有效治疗方案,也是持续和难以控制的终身患者的肿瘤体积萎缩。

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