无功能垂体偶发瘤的真实世界纵向研究:PRECES 微腺瘤子分析。

IF 2.9 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Mihai Costachescu, Claudiu Nistor, Ana Valea, Oana-Claudia Sima, Adrian Ciuche, Mihaela Stanciu, Mara Carsote, Mihai-Lucian Ciobica
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引用次数: 0

摘要

背景。由于影像学评估的普及,意外瘤在全世界的发病率越来越高,内分泌意外瘤也不例外,其中包括垂体意外瘤(PIs)。目的。我们的目的是分析成年患者在初步确诊为 PI(无功能微腺瘤)后进行第二次计算机断层扫描(CT)时的动态变化。研究方法这是一项多中心、纵向、回顾性研究,研究对象为成年人(年龄在 20 岁至 70 岁之间),研究过程中收集了真实世界的数据。我们排除了基线垂体激素过多或缺乏的患者,也排除了肿瘤大于 1 厘米的患者。结果。共纳入 117 名成年人(94.02% 为女性),平均年龄(43.86 ± 11.99)岁,随访 6-156 个月,中位数(M)为 40 个月(Q1 Q3:13.50, 72.00)。确诊 PI 时,横向平均直径为 0.53 ± 0.16 厘米,纵向平均直径为 0.41 ± 0.13 厘米,最大直径为 0.55 ± 0.16 厘米。在随访期间,没有一个 PI 出现功能障碍,既未伴有垂体功能减退,直径也未增大超过 1 厘米。共有 46/117 例(39.32%)患者在随访期间直径增大(增大组 = IG),而非增大组(非 IG;N = 71,60.68%)包括直径静止或缩小的受试者。IG 与非 IG 相比,初始横向、纵向和最大直径均较低:分别为 0.45 ± 0.12 对 0.57 ± 0.17(p < 0.0001)、0.36 ± 0.11 对 0.43 ± 0.13(p = 0.004)、0.46 ± 0.12 对 0.6 ± 0.16(p < 0.0001)。IG 与非 IG 相比,监测时间更长:M(Q1,Q3)为 48(24,84)个月对 32.5(12,72)个月(p = 0.045),基线时的年龄、垂体激素谱和肿瘤侧位相似,中位直径变化为 +0.14 厘米对 -0.03 厘米(p < 0.0001)。总之,在较长的随访期内,有相当高比例的患者(包括初始肿瘤较小的患者)的PI直径可能会增大,而诊断时的年龄并不能预测肿瘤的生长。这可能有助于医生制定进一步的长期监测方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Real-World Longitudinal Study in Non-Functioning Pituitary Incidentalomas: A PRECES Micro-Adenomas Sub-Analysis.

Background. Incidentalomas have an increasing incidence all over the world due to a larger access to imaging assessments, and endocrine incidentalomas make no exception in this matter, including pituitary incidentalomas (PIs). Objective. Our objective was to analyse the dynamic changes amid a second computed tomography (CT) scan after adult patients were initially confirmed with a PI (non-functioning micro-adenoma). Methods. This was a multi-centric, longitudinal, retrospective study in adults (aged between 20 and 70 y) amid real-world data collection. We excluded patients who experienced baseline pituitary hormonal excess or deficiency or those with tumours larger than 1 cm. Results. A total of 117 adults were included (94.02% females) with a mean age of 43.86 ± 11.99 years, followed between 6 and 156 months with a median (M) of 40 months (Q1 Q3: 13.50, 72.00). At the time of PI diagnosis, the transverse diameter had a mean value of 0.53 ± 0.16 cm, the longitudinal mean diameter was 0.41 ± 0.13 cm, and the largest diameter was 0.55 ± 0.16 cm. No PI became functioning during follow-up, neither associated hypopituitarism nor increased >1 cm diameter. A total of 46/117 (39.32%) patients had a larger diameter during follow-up (increase group = IG) versus a non-increase group (non-IG; N = 71, 60.68%) that included the subjects with stationary or decreased diameters. IG had lower initial transverse, longitudinal, and largest diameter versus non-IG: 0.45 ± 0.12 versus 0.57 ± 0.17 (p < 0.0001), 0.36 ± 0.11 versus 0.43 ± 0.13 (p = 0.004), respectively, 0.46 ± 0.12 versus 0.6 ± 0.16 (p < 0.0001). IG versus non-IG had a larger period of surveillance: M (Q1, Q3) of 48 (24, 84) versus 32.5 (12, 72) months (p = 0.045) and showed similar age, pituitary hormone profile, and tumour lateralisation at baseline and displayed a median diameter change of +0.14 cm versus -0.03 cm (p < 0.0001). To conclude, a rather high percent of patients might experience PI diameter increase during a longer period of follow-up, including those with a smaller initial size, while the age at diagnosis does not predict the tumour growth. This might help practitioners with further long-term surveillance protocols.

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