Suppr超能文献

[伴有鞍外扩展的生长激素腺瘤的治疗策略:内科治疗方法的作用,法国肢端肥大症登记处的一项共识研究]

[Therapeutic strategies in somatotroph adenomas with extrasellar extension: role of the medical approach, a consensus study of the French Acromegaly Registry].

作者信息

Jaquet Ph, Cortet-Rudelli Ch, Sassolas G, Morange-Ramos I, Chanson P, Brue Th, Andrieu J-M, Beckers A, Bertherat J, Borson-Chazot F, Brassier G, Caron Ph, Cogne M, Cottier J-Ph, Delemer B, Dufour H, Enjalbert A, Figarella-Branger D, Gaillard R, Gueydan M, Jan M, Kuhn J-M, Raingeard I, Regis J, Roger P, Rohmer V, Sadoul J-L, Saveanu A, Tabarin A, Travers N, Trouillas J

机构信息

Service d'Endocrinologie, Diabète et Maladies métaboliques, Hôpital de la Timone, 264, rue Saint-Pierre, 13005 Marseille.

出版信息

Ann Endocrinol (Paris). 2003 Dec;64(6):434-41.

Abstract

UNLABELLED

From the first 198 patient files included into the French Acromegaly Registry, we analyzed 68 patients harboring a somatotroph adenoma with extrasellar extension, after exclusion of those treated by stereotactic or conventional radiotherapy. In these patients (including 37 women), aged 21-77 yr. (45.7 +/- 13.3), GH concentrations ranged from 2-260 microg/L (38.6 +/- 44.3), and IGF I from 86-967% of age-matched upper limit of normal (303 +/- 164). Maximal diameter of the adenoma at MRI was 11-36.5 mm (20.4 +/- 6.5), with cavernous sinus involvement in 68% of cases. Three subgroups were defined: 20 patients treated by long-acting somatostatin analogs only (group M), for a mean duration of 3 yr. (extremes 1-7 yr.), 48 patients initially treated by transsphenoidal surgery (group C), of whom 21 were secondarily treated by long-acting somatostatin analogs (group CM) for a mean duration of 1.2 yr. (extremes 0.2-2 yr.). All 3 groups were not statistically different in terms of tumor mass and initial levels of GH and IGF-1. Patients from group M were significantly older than those of the other groups (p<0.05).

RESULTS

46% of patients from group C after surgery vs. 45% of patients from group M had a mean GH below 2.5 microg/L. Biochemical remission (GH<2.5 microg/L and normal IGF1 normal) was obtained in 31% of cases in group C, vs. 25% in group M. In this group, a decrease of the largest tumor diameter was observed in 10 patients (71.5%), ranging from 10-25% in 7 (50%) and exceeded 50% in 3 (21.5%). In group CM, the biochemical remission rate (42%) and final GH or IGF1 values were not significantly different from group M. In conclusion, these data suggest that surgery or long-acting somatostatin analogs have a comparable efficacy in terms of remission rates in somatotroph macroadenomas with extrasellar extensions.

摘要

未标记

从纳入法国肢端肥大症登记处的前198份患者档案中,我们分析了68例患有生长激素腺瘤且有鞍外扩展的患者,排除了接受立体定向或传统放疗的患者。这些患者(包括37名女性)年龄在21 - 77岁(45.7±13.3),生长激素浓度范围为2 - 260μg/L(38.6±44.3),胰岛素样生长因子I为年龄匹配正常上限的86 - 967%(303±164)。磁共振成像(MRI)显示腺瘤最大直径为11 - 36.5mm(20.4±6.5),68%的病例有海绵窦受累。定义了三个亚组:20例仅接受长效生长抑素类似物治疗的患者(M组),平均治疗时间为3年(范围1 - 7年);48例最初接受经蝶窦手术的患者(C组),其中21例随后接受长效生长抑素类似物治疗(CM组),平均治疗时间为1.2年(范围0.2 - 2年)。三组在肿瘤大小以及生长激素和胰岛素样生长因子 - 1的初始水平方面无统计学差异。M组患者明显比其他组患者年龄大(p<0.05)。

结果

C组术后46%的患者与M组45%的患者平均生长激素低于2.5μg/L。C组31%的病例实现了生化缓解(生长激素<2.5μg/L且胰岛素样生长因子1正常),M组为25%。在该组中,10例患者(71.5%)观察到最大肿瘤直径减小,7例(50%)减小幅度为10 - 25%,3例(21.5%)超过50%。CM组的生化缓解率(42%)以及最终生长激素或胰岛素样生长因子1值与M组无显著差异。总之,这些数据表明,在伴有鞍外扩展的生长激素大腺瘤的缓解率方面,手术或长效生长抑素类似物具有相当的疗效。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验