CHARACTERIZATION OF ACROMEGALY ACCORDING TO TUMOR SIZE AT DIAGNOSIS

Leticia Marinho Del Corso, Vicente Florentino Castaldo Andrade, Solena Ziemer Kusma Fidalski, Cesar Luiz Boguszewski
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Abstract

Purpose: To evaluate the clinical, laboratory, radiological, therapeutic, and prognostic characteristics of patients with acromegaly according to the size of the growth hormone (GH)-secreting pituitary adenoma at diagnosis. Patients and Methods: Observational, retrospective, single-center study of patients with acromegaly followed at a tertiary center. Data from medical records were evaluated regarding age, symptoms, presence of arterial hypertension, type 2 diabetes mellitus, hypopituitarism, size of the initial lesion, invasiveness (cavernous sinus invasion), T2-weighted magnetic resonance imaging signal intensity, GH and insulin-like growth factor type 1 (IGF-1) levels, treatment performed [surgery, use of somatostatin receptor ligands (SRL), pegvisomant, cabergoline and bromocriptine and radiotherapy] and response to surgical or adjuvant treatment (normal levels of GH and/or IGF-1 after each treatment instituted).Patients were divided into groups according to the size of the adenoma at diagnosis (group I = smaller than 10 mm, II = 10-19 mm, III = 20-29 mm, IV = 30-39 mm and V = greater than 40 mm), and comparisons were made between the 5 groups and two-by-two comparisons. Results: 117 patients were studied (59 women, age at diagnosis 43 SD 13 years). Group I consisted of 11 patients (9%), group II of 54 (46%), group III of 34 (29%), group IV of 10 (9%) and group V of 8 patients (7%). The prevalence of hypertension, diabetes mellitus and hypopituitarism were 49%, 25% and 28%, respectively. Hypopituitarism, invasiveness, and the use of SRL had their prevalence increased according to the size of the adenoma, as well as GH levels. Age, on the other hand, showed a negative correlation with tumor size, and group I was older when compared to the group with macroadenoma. The ROC curves showed that in relation to the size of the adenoma at diagnosis, most of the outcomes evaluated (hypopituitarism, invasiveness, radiotherapy, use of SRL, use of medications other than SRL, disease control after surgery) occurred with a tumor diameter of around 20 mm. Conclusion: Our study demonstrated that microadenomas and macroadenomas smaller than 20 mm are associated with lower morbidity and better therapeutic response in acromegaly. From a tumor diameter of 20 mm, there was no significant difference in the clinical, therapeutic and prognostic behavior of GH-secreting pituitary adenomas.
根据诊断时的肿瘤大小确定肢端肥大症的特征
目的:根据确诊时分泌生长激素(GH)的垂体腺瘤的大小,评估肢端肥大症患者的临床、实验室、放射学、治疗和预后特征。患者和方法:观察性、回顾性、单中心研究,对象是在一家三级中心接受随访的肢端肥大症患者。对病历中有关年龄、症状、动脉高血压、2 型糖尿病、垂体功能减退、初始病变大小、侵袭性(海绵窦侵袭)、T2 加权磁共振成像信号强度的数据进行了评估、GH和1型胰岛素样生长因子(IGF-1)水平、所接受的治疗[手术、体生长抑素受体配体(SRL)、培维索曼、卡麦角林和溴隐亭以及放射治疗]以及对手术或辅助治疗的反应(每次治疗后GH和/或IGF-1水平正常)。根据确诊时腺瘤的大小将患者分为几组(I组=小于10毫米,II组=10-19毫米,III组=20-29毫米,IV组=30-39毫米,V组=大于40毫米),并进行5组之间的比较和两两比较。研究结果共研究了 117 名患者(59 名女性,诊断时年龄 43 SD 13 岁)。第一组有 11 名患者(9%),第二组有 54 名患者(46%),第三组有 34 名患者(29%),第四组有 10 名患者(9%),第五组有 8 名患者(7%)。高血压、糖尿病和垂体功能减退症的发病率分别为 49%、25% 和 28%。垂体功能减退症、侵袭性和使用 SRL 的发病率随腺瘤的大小和 GH 水平而增加。另一方面,年龄与肿瘤大小呈负相关,与大腺瘤组相比,I组年龄更大。ROC 曲线显示,就诊断时腺瘤的大小而言,大多数评估结果(垂体功能减退、侵袭性、放疗、SRL 的使用、SRL 以外药物的使用、术后疾病控制)都发生在肿瘤直径约为 20 毫米时。结论我们的研究表明,小于20毫米的微腺瘤和大腺瘤与肢端肥大症较低的发病率和较好的治疗反应有关。肿瘤直径在20毫米以上的分泌GH垂体腺瘤在临床、治疗和预后方面没有明显差异。
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