Krassas G E, Kaltsas T, Dumas A, Pontikides N, Tolis G
Endocrine Clinic Panagia Hospital, Thessaloniki, Greece.
Eur J Endocrinol. 1997 Apr;136(4):416-22. doi: 10.1530/eje.0.1360416.
Octreotide, a potent synthetic somatostatin (SM) analogue, was recently evaluated and found to have a beneficial effect in thyroid eye disease (TED), mostly in those patients with a positive Octreoscan-111. Lanreotide (LRT; Somatuline-Ipsen), a new SM long-acting analogue, is more active than natural SM and shows a much longer duration of action. The aim of the present preliminary study was to evaluate the therapeutic effect of LRT in the treatment of TED. Five patients, three males and two females, mean age 50.6 +/- 7.6 S.D. (45-64) years, all with severe symptoms of TED were studied. A similar number of patients, matched for age, sex and severity of ophthalmopathy served as controls. All the patients and controls were investigated with orbital scintigraphy using 111 In DTPA-D-Phe1-octreotide (Octreoscan-111) and selected on the basis of positive octreoscan. The NOSPECS system, as adapted by Donaldson et al. (Journal of Clinical Endocrinology and Metabolism 1973 37 276-285) and a disease activity score, as proposed recently by an International Workshop, have been followed in this study in order to evaluate the response to treatment. The five patients who comprised the treatment group received 0.04 g LRT i.m. once every 2 weeks over a period of 3 months, after which the Octreoscan-111 was repeated. The control patients were given an injection of water i.m., also once every 2 weeks for 3 months, after which they were evaluated clinically. No Octreoscan-111 was performed in the controls. All patients and controls were evaluated by the same physician, who was unaware of the type of treatment used. A decrease in the NOSPECS score and the clinical activity score was regarded as a positive response, while no change or an increase in the NOSPECS score along with no clinical improvement was regarded as a negative response. After 3 months of treatment with LRT, four patients showed a statistically significant improvement in ophthalmopathy in both eyes and one in one eye. Three of the control patients with TED did not show any change, one showed a minor improvement in one eye and no change in the other and one showed deterioration in both eyes. An interesting finding was that orbital Octreoscan-111 activity was absent in all the patients after LRT treatment. In conclusion, these preliminary results show that LRT has a beneficial effect on patients with TED, and that since it has to be given only once every 2 weeks, it is probably superior to any other form of SM treatment. However, as the number of patients was small, further studies are needed to confirm our results.
奥曲肽是一种强效的合成生长抑素(SM)类似物,最近经过评估发现其对甲状腺眼病(TED)有有益作用,主要对奥曲肽扫描-111呈阳性的患者有效。兰瑞肽(LRT;索马杜林-益普生)是一种新型长效SM类似物,比天然SM活性更强,作用持续时间长得多。本初步研究的目的是评估LRT治疗TED的疗效。研究了5例患者,3例男性和2例女性,平均年龄50.6±7.6标准差(45 - 64)岁,均有严重的TED症状。选取了数量相近、年龄、性别和眼病严重程度相匹配的患者作为对照。所有患者和对照均使用111铟-二乙三胺五乙酸- D -苯丙氨酸1 -奥曲肽(奥曲肽扫描-111)进行眼眶闪烁显像,并根据奥曲肽扫描阳性进行选择。本研究遵循了Donaldson等人改编的NOSPECS系统(《临床内分泌与代谢杂志》1973年第37卷,第276 - 285页)以及国际研讨会最近提出的疾病活动评分,以评估治疗反应。治疗组的5例患者每2周肌肉注射0.04 g LRT,持续3个月,之后重复进行奥曲肽扫描-111检查。对照患者肌肉注射水,同样每2周1次,持续3个月,之后进行临床评估。对照患者未进行奥曲肽扫描-111检查。所有患者和对照均由同一位医生评估,该医生不知道所采用的治疗类型。NOSPECS评分和临床活动评分降低被视为阳性反应,而NOSPECS评分无变化或升高且临床无改善被视为阴性反应。用LRT治疗3个月后,4例患者双眼的眼病有统计学显著改善,1例患者单眼改善。3例患有TED的对照患者无任何变化,1例患者单眼有轻微改善,另一只眼无变化,1例患者双眼病情恶化。一个有趣的发现是,LRT治疗后所有患者眼眶奥曲肽扫描-111活性均消失。总之,这些初步结果表明LRT对TED患者有有益作用,而且由于只需每2周给药1次,它可能优于任何其他形式的SM治疗。然而,由于患者数量较少,需要进一步研究来证实我们的结果。