Marmara University School of Medicine, Section of Endocrinology and Metabolism, Istanbul, Turkey.
Marmara University School of Medicine, Section of Endocrinology and Metabolism, Istanbul, Turkey.
Growth Horm IGF Res. 2020 Dec;55:101335. doi: 10.1016/j.ghir.2020.101335. Epub 2020 Jul 15.
Gamma knife radiosurgery (GKS) is a treatment option for recurrent or persistent disease in patients with acromegaly.
We aimed to retrospectively evaluate acromegaly patients who had undergone GKS in terms of pituitary hormone status, efficacy of GKS, and prognostic factors.
One-hundred and ten acromegaly patients who underwent GKS, and who were referred to our outpatient endocrinology clinic between 2007 and 2017, were included in the study. Anterior pituitary hormones and radiology imaging during follow-up were recorded. Remission for acromegaly was defined as a normal insulin-like growth factor 1 (IGF-1) level adjusted for age and gender, and a random growth hormone (GH) level < 1 ng/ml. Endocrine control was defined as normal GH and IGF-1 levels under medication.
After a mean follow-up of 6.5 ± 4.7 years; remission, endocrine control, and uncontrolled status was observed in 16.4%, 60%, and 23.6% of patients; respectively. Adenoma volume was decreased after GKS (P < .0001). Remnant adenoma diameter was higher in the uncontrolled group compared to the remission and endocrine control group. The presence of tumor extension was associated with disease status (P = .03) and higher initial GH and IGF-1 levels. The mean time after GKS to remission was 26.5 months. Six (5.4%) patients had new-onset pituitary deficiency after GKS. In the multivariate analysis, pre-GKS IGF-1 levels and patient's age were associated with disease status.
GKS is an effective adjuvant treatment with minimal side effects to control GH and IGF-1 levels, increase remission rates, endocrine control, and reduce tumor diameter in persistent acromegaly patients after surgery.
伽玛刀放射外科(GKS)是治疗肢端肥大症患者复发或持续性疾病的一种选择。
我们旨在回顾性评估接受 GKS 治疗的肢端肥大症患者的垂体激素状态、GKS 的疗效和预后因素。
研究纳入了 2007 年至 2017 年间在我院内分泌门诊就诊的 110 例接受 GKS 的肢端肥大症患者。记录随访期间的垂体前叶激素和影像学检查。肢端肥大症缓解定义为年龄和性别校正后正常的胰岛素样生长因子 1(IGF-1)水平,以及随机生长激素(GH)水平<1ng/ml。内分泌控制定义为药物治疗下正常的 GH 和 IGF-1 水平。
平均随访 6.5±4.7 年后,缓解、内分泌控制和未控制状态分别见于 16.4%、60%和 23.6%的患者。GKS 后肿瘤体积减少(P<0.0001)。未控制组的残余腺瘤直径高于缓解组和内分泌控制组。肿瘤扩展的存在与疾病状态相关(P=0.03),与初始 GH 和 IGF-1 水平较高相关。GKS 后达到缓解的平均时间为 26.5 个月。6 例(5.4%)患者在 GKS 后出现新发垂体功能减退。多因素分析显示,GKS 前 IGF-1 水平和患者年龄与疾病状态相关。
GKS 是一种有效的辅助治疗方法,副作用小,可控制 GH 和 IGF-1 水平,增加缓解率、内分泌控制,并减少手术后持续性肢端肥大症患者的肿瘤直径。