Cozzi Renato, Montini Marcella, Attanasio Roberto, Albizzi Mascia, Lasio Giovanni, Lodrini Sandro, Doneda Paola, Cortesi Liana, Pagani Giorgio
Division of Endocrinology, Ospedale Niguarda, Viale Ezio 5, I-20149 Milan, Italy.
J Clin Endocrinol Metab. 2006 Apr;91(4):1397-403. doi: 10.1210/jc.2005-2347. Epub 2006 Jan 31.
Neurosurgery is regarded as the first-line treatment of acromegaly. Because of its low cure rate in macro and invasive adenoma, the role of primary medical treatment is debated.
Our objective was to evaluate primary pharmacological treatment in acromegaly.
We conducted an open prospective study at two Italian tertiary level centers.
We studied 67 consecutive patients (36 women; age, 54.9 +/- 14.2 yr; 72% bearing macroadenoma).
Individually tailored octreotide LAR (OCLAR) was administered.
Outcomes included safe GH (<2.5 mug/liter), normal age-matched IGF-I levels, and tumor shrinkage.
After a median follow-up of 48 months (range, 6-108 months), safe GH levels and normal age-matched IGF-I values were obtained by 68.7 and 70.1% of patients, respectively. Hormonal endpoints were achieved regardless of basal levels, and early results were predictive of outcome. Tumor shrank in 82.1% of patients by 62 +/- 31% (range, 0-100%), decreasing from 2101 +/- 2912 to 1010 +/- 2196 mm(3) (P < 0.0001). The higher the basal GH values and the greater the GH/IGF-I changes on treatment, the greater the tumor shrinkage. Tumor disappeared in three patients and was progressively reduced to empty sella in five patients; apparent magnetic resonance imaging cavernous sinus invasion disappeared in three. In males, testosterone increased, restoring eugonadism in 64% of hypogonadal patients.
The efficacy on GH/IGF-I levels in unselected patients and the outstanding volumetric control indicate that treatment with OCLAR may be the first therapeutic approach to all acromegalic patients not amenable to surgical cure. Tumor shrinkage might also encourage the evaluation of primary OCLAR adoption in patients with initial visual field defects.
神经外科手术被视为肢端肥大症的一线治疗方法。由于其在巨大和侵袭性腺瘤中的治愈率较低,因此初级药物治疗的作用存在争议。
我们的目的是评估肢端肥大症的初级药物治疗。
我们在两个意大利三级中心进行了一项开放性前瞻性研究。
我们研究了67例连续患者(36名女性;年龄54.9±14.2岁;72%患有巨大腺瘤)。
给予个体化定制的长效奥曲肽(OCLAR)。
结果包括安全的生长激素(<2.5μg/升)、与年龄匹配的正常胰岛素样生长因子-I水平以及肿瘤缩小。
中位随访48个月(范围6 - 108个月)后,分别有68.7%和70.1%的患者获得了安全的生长激素水平和与年龄匹配的正常胰岛素样生长因子-I值。无论基础水平如何,均达到了激素终点,早期结果可预测结局。82.1%的患者肿瘤缩小了62±31%(范围0 - 100%),体积从2101±2912立方毫米降至1010±2196立方毫米(P < 0.0001)。基础生长激素值越高,治疗期间生长激素/胰岛素样生长因子-I变化越大,肿瘤缩小越明显。3例患者肿瘤消失,5例患者肿瘤逐渐缩小至空蝶鞍;3例患者磁共振成像显示的海绵窦侵袭消失。在男性中,睾酮水平升高,64%性腺功能减退患者恢复了性腺功能正常。
对未选择患者的生长激素/胰岛素样生长因子-I水平的疗效以及出色的体积控制表明,OCLAR治疗可能是所有无法通过手术治愈的肢端肥大症患者的首选治疗方法。肿瘤缩小也可能促使对初始有视野缺损患者采用初级OCLAR治疗进行评估。