Department of Medicine, Endocrinology section, Pituitary Center Rotterdam, Erasmus University Medical Center, Rotterdam, the Netherlands.
Endocrinologie Centre Hospitalier Universitaire de Liège, Domaine Universitaire du Sart-Tilman, Liège, Belgium.
J Clin Endocrinol Metab. 2020 Sep 1;105(9). doi: 10.1210/clinem/dgaa387.
First-generation somatostatin receptor ligands (fg-SRLs) represent the mainstay of medical therapy for acromegaly, but they provide biochemical control of disease in only a subset of patients. Various pretreatment biomarkers might affect biochemical response to fg-SRLs.
To identify clinical predictors of the biochemical response to fg-SRLs monotherapy defined as biochemical response (insulin-like growth factor (IGF)-1 ≤ 1.3 × ULN (upper limit of normal)), partial response (>20% relative IGF-1 reduction without normalization), and nonresponse (≤20% relative IGF-1 reduction), and IGF-1 reduction.
Retrospective multicenter study.
Eight participating European centers.
We performed a meta-analysis of participant data from 2 cohorts (Rotterdam and Liège acromegaly survey, 622 out of 3520 patients). Multivariable regression models were used to identify predictors of biochemical response to fg-SRL monotherapy.
Lower IGF-1 concentration at baseline (odds ratio (OR) = 0.82, 95% confidence interval (CI) 0.72-0.95 IGF-1 ULN, P = .0073) and lower bodyweight (OR = 0.99, 95% CI 0.98-0.99 kg, P = .038) were associated with biochemical response. Higher IGF-1 concentration at baseline (OR = 1.40, (1.19-1.65) IGF-1 ULN, P ≤ .0001), the presence of type 2 diabetes (oral medication OR = 2.48, (1.43-4.29), P = .0013; insulin therapy OR = 2.65, (1.02-6.70), P = .045), and higher bodyweight (OR = 1.02, (1.01-1.04) kg, P = .0023) were associated with achieving partial response. Younger patients at diagnosis are more likely to achieve nonresponse (OR = 0.96, (0.94-0.99) year, P = .0070). Baseline IGF-1 and growth hormone concentration at diagnosis were associated with absolute IGF-1 reduction (β = 0.90, standard error (SE) = 0.02, P ≤ .0001 and β = 0.002, SE = 0.001, P = .014, respectively).
Baseline IGF-1 concentration was the best predictor of biochemical response to fg-SRL, followed by bodyweight, while younger patients were more likely to achieve nonresponse.
第一代生长抑素受体配体(fg-SRL)是肢端肥大症的主要药物治疗方法,但它们仅在一部分患者中提供疾病的生化控制。各种预处理生物标志物可能会影响 fg-SRL 对生化反应的影响。
确定 fg-SRL 单药治疗生化反应的临床预测因素,定义为生化反应(胰岛素样生长因子 1(IGF-1)≤1.3×正常值上限(ULN))、部分反应(IGF-1 降低>20%但未正常化)和无反应(IGF-1 降低≤20%)和 IGF-1 降低。
回顾性多中心研究。
欧洲 8 个参与中心。
我们对来自 2 个队列(鹿特丹和列日肢端肥大症调查,3520 名患者中的 622 名)的数据进行了荟萃分析。使用多变量回归模型确定 fg-SRL 单药治疗的生化反应预测因素。
基线时 IGF-1 浓度较低(优势比(OR)=0.82,95%置信区间(CI)0.72-0.95 IGF-1 ULN,P=0.0073)和较低的体重(OR=0.99,95%CI 0.98-0.99 kg,P=0.038)与生化反应相关。基线时 IGF-1 浓度较高(OR=1.40,(1.19-1.65)IGF-1 ULN,P≤.0001)、存在 2 型糖尿病(口服药物治疗 OR=2.48,(1.43-4.29),P=0.0013;胰岛素治疗 OR=2.65,(1.02-6.70),P=0.045)和较高的体重(OR=1.02,(1.01-1.04)kg,P=0.0023)与实现部分反应相关。诊断时较年轻的患者更有可能出现无反应(OR=0.96,(0.94-0.99)年,P=0.0070)。诊断时 IGF-1 和生长激素的基线浓度与 IGF-1 的绝对降低相关(β=0.90,标准误差(SE)=0.02,P≤.0001 和 β=0.002,SE=0.001,P=0.014)。
基线 IGF-1 浓度是 fg-SRL 生化反应的最佳预测因素,其次是体重,而年轻患者更有可能出现无反应。