Colao Annamaria, Attanasio Roberto, Pivonello Rosario, Cappabianca Paolo, Cavallo Luigi M, Lasio Giovanni, Lodrini Alessandro, Lombardi Gaetano, Cozzi Renato
Department of Molecular and Clinical Endocrinology and Oncology, Federico II University of Naples, via S. Pansini 5, 80131 Naples, Italy.
J Clin Endocrinol Metab. 2006 Jan;91(1):85-92. doi: 10.1210/jc.2005-1208. Epub 2005 Nov 1.
Surgery is a cornerstone in the treatment of acromegaly, but its efficacy in large, invasive tumors is scant.
The objective of this study was to investigate whether partial surgical removal of GH-secreting pituitary tumors enhances the response rate to somatostatin analogs (SSA; sc octreotide, slow-release octreotide, and lanreotide).
This was a multicenter, open, retrospective study.
The study was performed at university hospitals.
Eighty-six patients (42 women and 44 men; age, 42 +/- 14 yr) with acromegaly were studied.
Patients underwent two courses of octreotide, lanreotide, or slow-release octreotide treatments before and after surgery of at least 6 months.
The main outcome measure was normal IGF-I levels for age.
Presurgical SSA treatment significantly decreased GH and IGF-I levels in all patients. GH levels were less than 2.5 microg/liter in 12 patients (14%); IGF-I levels normalized in nine (10%). After surgery, GH and IGF-I levels further decreased in all patients; tumor removal was greater than 75% in 50 (58%), 50.1-75% in 21 (24%), 25.1-50% in 10 (12%), and less than 25% in five patients (6%). Preoperatively, pituitary function was impaired in 12 patients (14%). Postsurgical SSA treatment lowered GH levels to less than 2.5 microg/liter in 49 (56%) and normalized IGF-I levels in 48 patients (55%). The success rate was significantly increased compared with that before surgery (P < 0.0001). GH (r = -0.48; P < 0.0001) and IGF-I levels (r = -0.38; P = 0.0003) after postsurgery SSA treatment correlated with the amount of tumor surgically removed. After surgery, pituitary function was impaired in 28 patients (32.6%) and was improved in 12 patients (13.9%). The cumulative prevalence of pituitary deficiency did not change during the study (normal function from 40 to 42%; deficiency from 60 to 58%).
Surgical tumor removal (>75%) enhances the response to SSAs without impairing pituitary function. Our data indicate that surgical debulking has a significant place in the treatment algorithm of acromegaly.
手术是肢端肥大症治疗的基石,但对于大型侵袭性肿瘤,其疗效甚微。
本研究旨在探讨部分切除生长激素分泌型垂体瘤是否能提高对生长抑素类似物(SSA;皮下注射奥曲肽、缓释奥曲肽和兰瑞肽)的反应率。
这是一项多中心、开放性回顾性研究。
该研究在大学医院进行。
研究了86例肢端肥大症患者(42例女性和44例男性;年龄42±14岁)。
患者在至少6个月的手术前后接受了两个疗程的奥曲肽、兰瑞肽或缓释奥曲肽治疗。
主要观察指标是年龄标准化的胰岛素样生长因子-I(IGF-I)水平正常。
术前SSA治疗使所有患者的生长激素(GH)和IGF-I水平显著降低。12例患者(14%)的GH水平低于2.5μg/升;9例患者(10%)的IGF-I水平恢复正常。手术后,所有患者的GH和IGF-I水平进一步下降;50例患者(58%)的肿瘤切除率大于75%,21例患者(24%)的切除率为50.1%-75%,10例患者(12%)的切除率为25.1%-50%,5例患者(6%)的切除率小于25%。术前,12例患者(14%)垂体功能受损。术后SSA治疗使49例患者(56%)的GH水平降至低于2.5μg/升,48例患者(55%)的IGF-I水平恢复正常。与手术前相比,成功率显著提高(P<0.0001)。术后SSA治疗后的GH(r=-0.48;P<0.0001)和IGF-I水平(r=-0.38;P=0.0003)与手术切除的肿瘤量相关。手术后,28例患者(32.6%)垂体功能受损,12例患者(13.9%)垂体功能改善。在研究期间垂体功能减退的累积患病率没有变化(正常功能从40%变为42%;功能减退从60%变为58%)。
手术切除肿瘤(>75%)可增强对SSA的反应,且不损害垂体功能。我们的数据表明,手术减瘤在肢端肥大症的治疗方案中具有重要地位。