Department of EndocrinologyOxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, Oxford, UKDepartments of NeuroradiologyNeurosurgeryJohn Radcliffe Hospital, Oxford, UKSchool of Clinical and Experimental MedicineInstitute of Metabolism and Systems Research, University of Birmingham, Wolfson Drive, Edgbaston, Birmingham B15 2TT, UK.
Department of EndocrinologyOxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, Oxford, UKDepartments of NeuroradiologyNeurosurgeryJohn Radcliffe Hospital, Oxford, UKSchool of Clinical and Experimental MedicineInstitute of Metabolism and Systems Research, University of Birmingham, Wolfson Drive, Edgbaston, Birmingham B15 2TT, UK Department of EndocrinologyOxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, Oxford, UKDepartments of NeuroradiologyNeurosurgeryJohn Radcliffe Hospital, Oxford, UKSchool of Clinical and Experimental MedicineInstitute of Metabolism and Systems Research, University of Birmingham, Wolfson Drive, Edgbaston, Birmingham B15 2TT, UK
Eur J Endocrinol. 2016 Feb;174(2):137-45. doi: 10.1530/EJE-15-0967. Epub 2015 Nov 6.
Non-functioning pituitary adenomas (NFAs) have a prevalence of 7-22/100,000 people. A significant number of patients suffer from morbidities related to the tumor, possible recurrence(s), and treatments utilized. Our aim was to assess mortality of patients with macroNFA and predictive factors.
Retrospective cohort study in a tertiary referral center in the UK.
A total of 546 patients operated for a macroNFA between 1963 and 2011 were studied. Mortality data were retrieved through the National Health Service Central Register and hospital records and recorded as standardized mortality ratio (SMR). Mortality was estimated for the total and various subgroups with clinical follow-up data.
Median follow-up was 8 years (range: 1 month-48.5 years). SMR was 3.6 (95% CI, 2.9-4.5), for those operated before 1990, 4.7 (95% CI, 2.7-7.6) and for those after 1990, 3.5 (95% CI, 2.8-4.4). Main causes of death were cardio/cerebrovascular (33.7%), infections (30.1%), and malignancy (28.9%). Cox regression analysis demonstrated that only age at diagnosis remained an independent predictor of mortality (hazard ratio 1.10; 95% CI, 1.07-1.13, P<0.001), whereas sex, presentation with acute apoplexy, extent of tumor removal, radiotherapy, recurrence, untreated GH deficiency, FSH/LH deficiency, ACTH deficiency, TSH deficiency, and treatment with desmopressin had no impact.
Despite the improvement of treatments over the last three decades, the mortality of patients with NFAs in our series remains high. Apart from age, factors related with the management/outcome of the tumor are not independent predictors, and pituitary hormone deficits managed with the currently-used substitution protocols do not adversely affect mortality.
无功能性垂体腺瘤(NFAs)的患病率为 7-22/100,000。相当数量的患者患有与肿瘤相关的疾病、可能的复发和所接受的治疗。我们的目的是评估大腺瘤患者的死亡率和预测因素。
英国一家三级转诊中心的回顾性队列研究。
共研究了 1963 年至 2011 年间因大腺瘤而接受手术的 546 例患者。通过国家卫生服务中心登记处和医院记录检索死亡率数据,并记录为标准化死亡率比(SMR)。对有临床随访数据的所有患者和不同亚组进行死亡率估计。
中位随访时间为 8 年(范围:1 个月至 48.5 年)。SMR 为 3.6(95%CI,2.9-4.5),1990 年前手术的患者为 4.7(95%CI,2.7-7.6),1990 年后手术的患者为 3.5(95%CI,2.8-4.4)。主要死亡原因为心/脑血管疾病(33.7%)、感染(30.1%)和恶性肿瘤(28.9%)。Cox 回归分析表明,只有诊断时的年龄仍然是死亡率的独立预测因素(风险比 1.10;95%CI,1.07-1.13,P<0.001),而性别、急性中风表现、肿瘤切除程度、放疗、复发、未治疗的 GH 缺乏、FSH/LH 缺乏、ACTH 缺乏、TSH 缺乏以及使用去氨加压素治疗无影响。
尽管过去三十年治疗方法有所改善,但本系列中 NFAs 患者的死亡率仍然较高。除年龄外,与肿瘤管理/结果相关的因素不是独立的预测因素,目前使用的替代方案管理的垂体激素缺乏症不会对死亡率产生不利影响。