Espinosa de los Monteros Ana Laura, Carrasco Carmen A, Albarrán Alfredo Adolfo Reza, Gadelha Mônica, Abreu Alin, Mercado Moisés
Servicio de Endocrinología, Hospital de Especialidades, Centro Médico Nacional S.XXI, IMSS, Mexico City, Mexico.
Pituitary. 2014 Jan;17 Suppl 1(Suppl 1):S4-10. doi: 10.1007/s11102-013-0530-0.
Primary pharmacological therapy may be the only viable treatment option for many patients with acromegaly, especially those presenting with advanced disease with large inoperable tumors. Long-acting somatostatin analogs are currently the first-line treatment of choice in this setting, where they provide biochemical control and reduce tumor size in a significant proportion of patients. We herein present a brief overview of the role of primary pharmacological therapy in the treatment of acromegaly within the context of Latin America and support this with a representative case study.
A 20 year old male presented with clinical and biochemical evidence of acromegaly. The glucose-suppressed growth hormone (GH) was 5.3 μg/L, his insulin-like growth factor-1(IGF-1) was 3.5 times the ULN and serum prolactin greater than 4,000 μg/L. Pituitary MRI revealed a large and invasive mass, extending superiorly into the optic chiasm and laterally into the left cavernous sinus. He was treated with a combination of octreotide and cabergoline with remarkable clinical improvement, normalization of GH and IGF-1 values and striking shrinkage of the adenoma.
This case illustrates how effective the pharmacological therapy of acromegaly can be and yet at the same time, raises several important issues such as the need for life-long treatment with costly medications such as the somatostatin analogs. Access to these agents may be limited in regions where resources are restricted and clinicians face challenges in order to make the most efficient use of available options.
对于许多肢端肥大症患者而言,初始药物治疗可能是唯一可行的治疗选择,尤其是那些患有晚期疾病且肿瘤无法手术切除的患者。长效生长抑素类似物目前是这种情况下的一线治疗选择,它们能使很大一部分患者实现生化指标的控制并缩小肿瘤大小。我们在此简要概述拉丁美洲背景下初始药物治疗在肢端肥大症治疗中的作用,并通过一个典型病例研究加以佐证。
一名20岁男性出现肢端肥大症的临床和生化证据。葡萄糖抑制生长激素(GH)为5.3μg/L,胰岛素样生长因子-1(IGF-1)是正常上限(ULN)的3.5倍,血清催乳素大于4000μg/L。垂体磁共振成像(MRI)显示一个巨大的侵袭性肿块,向上延伸至视交叉,向外侧延伸至左侧海绵窦。他接受了奥曲肽和卡麦角林联合治疗,临床症状显著改善,GH和IGF-1值恢复正常,腺瘤明显缩小。
该病例说明了肢端肥大症药物治疗的有效性,但同时也引发了几个重要问题,比如需要使用生长抑素类似物等昂贵药物进行终身治疗。在资源有限的地区,获取这些药物可能受到限制,临床医生为了最有效地利用现有选择也面临挑战。