[Survival predictors in patients with ectopic acth syndrome].

Q4 Medicine
O O Golounina, Zh/ E Belaya, L Ya Rozhinskaya, M Yu Pikunov, A A Markovich, L K Dzeranova, E I Marova, N S Kuznetsov, V V Fadeev, G A Melnichenko, I I Dedov
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引用次数: 0

Abstract

Aim: To determine significant factors affecting the survival of patients with ectopic ACTH syndrome (EAS).

Materials and methods: A multi-center, observational study with a retrospective analysis of patients with EAS. The end point of the study was the fatal outcome of patients from various causes. In order to identify predictors of survival or mortality, univariate and multifactorial Cox regression analyses were carried out. ROC-analysis was used to determine the prognostic threshold values of individual predictors. The survival analysis was carried out using the Kaplan-Mayer method. Statistical data processing was carried out by using IBM SPSS Statistics 23.

Results: The age of patients at the time of diagnosis ranged from 12 to 76 years (Me 40 years [28;54]). The age of the studied population was 55 years [38; 64] for women and 42 years [32; 54] for men. The median period of observation was 50 months [13;91], with a maximum follow-up of 382 months. 92 patients (60,9%) had bronchopulmonary NET, 17 (11,3%) - thymic carcinoid, 8 - pancreatic NET, 5 -pheochromocytoma, 1- cecum NET, 1- appendix carcinoid tumor, 1 - medullary thyroid cancer and 26 (17,2%) patients had an occult NET. The primary tumor was removed in 101 patients (66,9%). Bilateral adrenalectomy was performed in 42 (27,8%) cases. Metastases were revealed in 23,2% (n=35) of patients. Relapse of the disease was observed in 24,4%, long-term remission was preserved in 64 patients (74,4%). Death occurred in 42 patients (28%). The average age of survivors was 47,0±15,2 versus 53,5±15,6 years for the deceased (p=0,022). The average survival time from diagnosis for the deceased was 32 months, Me 16,5 months [7;54]. Multivariate analysis revealed that the following factors have a direct impact on survival: age of diagnosis ≥51 years (OR 4,493; 95% CI 2,056-9,818, p<0,001), bronchopulmonary neuroendocrine tumor (NET) (OR 0,281; 95% CI 0,119-0,665, p=0,004), the presence of distant metastases (OR 2,489; 95% CI 1,141-5,427, p=0,022), late-night salivary cortisol (LNSC) ≥122,2 nmol/L (OR 2,493; 95% CI 1,014-6,128, p=0,047).

Conclusion: The prognosis of patients with EAS is influenced by the age of diagnosis, NET localization, distant metastases and level of LNSC. The most common cause of ectopic ACTH syndrome was bronchopulmonary NET which was associated with the best survival rate.

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[异位acth综合征患者的生存预测]。
目的:确定影响异位促肾上腺皮质激素综合征(EAS)患者生存的重要因素:对EAS患者进行回顾性分析的多中心观察研究。研究的终点是患者因各种原因导致的死亡结果。为了确定存活率或死亡率的预测因素,进行了单因素和多因素 Cox 回归分析。ROC分析用于确定单个预测因子的预后阈值。生存分析采用 Kaplan-Mayer 法进行。统计数据处理采用 IBM SPSS Statistics 23:患者确诊时的年龄从 12 岁到 76 岁不等(平均 40 岁 [28;54])。研究对象的年龄为女性 55 岁 [38; 64],男性 42 岁 [32; 54]。观察期的中位数为 50 个月 [13;91],最长随访时间为 382 个月。92名患者(60.9%)患有支气管肺癌,17名患者(11.3%)患有胸腺类癌,8名患者患有胰腺NET,5名患者患有嗜铬细胞瘤,1名患者患有盲肠NET,1名患者患有阑尾类癌,1名患者患有甲状腺髓样癌,26名患者(17.2%)患有隐匿性NET。101名患者(66.9%)的原发肿瘤被切除。42例(27.8%)患者进行了双侧肾上腺切除术。23.2%的患者(35例)发现了转移灶。24.4%的患者病情复发,64名患者(74.4%)病情长期缓解。42名患者(28%)死亡。幸存者的平均年龄为(47.0±15.2)岁,而死亡者的平均年龄为(53.5±15.6)岁(P=0.022)。从确诊到死亡的平均存活时间为 32 个月,我为 16.5 个月 [7;54]。多变量分析显示,以下因素对存活率有直接影响:诊断年龄≥51岁(OR 4,493; 95% CI 2,056-9,818, p<0,001)、支气管肺神经内分泌肿瘤(NET)(OR 0,281;95%CI为0,119-0,665,P=0,004)、存在远处转移(OR为2,489;95%CI为1,141-5,427,P=0,022)、深夜唾液皮质醇(LNSC)≥122,2 nmol/L(OR为2,493;95%CI为1,014-6,128,P=0,047)。结论EAS患者的预后受诊断年龄、NET定位、远处转移和LNSC水平的影响。异位ACTH综合征最常见的病因是支气管肺NET,其存活率最高。
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来源期刊
Problemy endokrinologii
Problemy endokrinologii Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
1.40
自引率
0.00%
发文量
59
期刊介绍: Since 1955 the “Problems of Endocrinology” (or “Problemy Endocrinologii”) Journal publishes timely articles, balancing both clinical and experimental research, case reports, reviews and lectures on pressing problems of endocrinology. The Journal is aimed to the most topical issues of endocrinology: to chemical structure, biosynthesis and metabolism of hormones, the mechanism of their action at cellular and molecular level; pathogenesis and to clinic of the endocrine diseases, new methods of their diagnostics and treatment. The Journal: features original national and foreign research articles, reflecting world endocrinology development; issues thematic editions on specific areas; publishes chronicle of major international congress sessions and workshops on endocrinology, as well as state-of-the-art guidelines; is intended for scientists, endocrinologists diabetologists and specialists of allied trade, general practitioners, family physicians and pediatrics.
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