Colao A, Ferone D, Lastoria S, Cerbone G, Di Sarno A, Di Somma C, Lucci R, Lombardi G
Departments of Molecular & Clinical Endocrinology and Oncology, 'Federico II' University of Naples; Nuclear Medicine, National Cancer Institute, 'Fondazione G. Pascale', Naples, Italy.
Clin Endocrinol (Oxf). 2000 Apr;52(4):437-45. doi: 10.1046/j.1365-2265.2000.00951.x.
Dopamine agonists are indicated as primary therapy for PRL-secreting pituitary adenomas, while controversial results have been reported in nonfunctioning adenomas (NFA).
To evaluate whether the in vivo visualization of dopamine D2 receptor expression detected by pituitary scintigraphy using 123I-methoxybenzamide (123I-IBZM) was correlated with the response to chronic treatment with quinagolide or cabergoline.
10 patients affected with NFA (5 men and 5 women, age ranging between 25 and 50 years), and 10 with PRL-secreting naive macroadenomas (3 men and 7 women, age ranging between 22 and 59 years), serving as control.
All patients underwent an acute test with quinagolide: at 3-day intervals and in random order all patients received the drug (0.075 mg at 0800 h), or placebo. Blood samples were taken 15 and 5 minutes before and every 30 minutes for 6 h after drug or placebo administration. The test was considered positive when PRL and/or alpha-subunit levels decreased >/=50% as compared to baseline levels. After 6 months of treatment, 10 patients were randomised to continue the treatment with quinagolide and the remaining 10 received cabergoline for the remaining 6 months. The doses of quinagolide and cabergoline ranged from 0.075 to 0.6 mg/day and from 0.5 to 3 mg/week, respectively. At study entry, a magnetic resonance imaging (MR) study of the pituitary region and 123I-IBZM pituitary scintigraphy were performed. MR was repeated after 12 months of treatment to evaluate tumour shrinkage: reduction of tumour volume = 80% in prolactinomas and = 50% in NFA was considered significant. Basal PRL levels were 9495.0 +/- 1131.6 mU/l in prolactinomas and 602.4 +/- 50.5 mU/l in NFA.
The scintigraphy was negative in 6 out of 10 patients with NFA. Moderate uptake was observed in 3 patients with prolactinoma and 2 patients with NFA whereas intense uptake was observed in the remaining 7 patients with prolactinoma and 2 patients with NFA. Among the 8 patients with NFA and high circulating alpha-subunit levels, the acute test was negative in 5 while it was positive in the remaining 3 patients. The acute test was positive in all 10 patients with prolactinoma. After 12 months of treatment with quinagolide and cabergoline, circulating PRL levels were decreased in all 10 patients with prolactinoma (571.8 +/- 255.9 mU/l), being normalized in 7 patients. Suppression of PRL levels was found in all 10 patients with NFA (89.5 +/- 2.3 mU/l). A significant reduction of alpha-subunit levels was obtained in 9 out of 10 patients with NFA: in 4 out of 8 patients alpha-subunit levels were normalized. Significant adenoma shrinkage was recorded in 4 patients with prolactinoma among the 7 with intense pituitary uptake of 123I-IBZM. Significant adenoma shrinkage was recorded only in the 2 out of 10 patients with NFA with intense pituitary uptake of 123I-IBZM. A significant positive correlation was found between the degree of uptake (considered as score) and the response to quinagolide or cabergoline treatment (considered as percent hormone suppression) either in patients affected with PRL-secreting adenoma (r = 0.856, P < 0.005) or in those affected with NFA (r = 0.787, P < 0.05).
An intense 123I-IBZM uptake in patients with non-functioning adenomas was predictive of a good response to a chronic treatment with quinagolide and cabergoline. This result suggests that a pituitary 123I-IBZM scintigraphy could be considered in selected patients with non-functioning adenomas before starting medical treatment with dopamine agonists.
多巴胺激动剂被用作分泌泌乳素的垂体腺瘤的主要治疗方法,而在无功能腺瘤(NFA)中其治疗效果存在争议。
评估使用123I-甲氧基苄胺(123I-IBZM)进行垂体闪烁扫描检测到的多巴胺D2受体表达的体内可视化是否与喹高利特或卡麦角林的长期治疗反应相关。
10例NFA患者(5男5女,年龄25至50岁),以及10例初发的分泌泌乳素的大腺瘤患者(3男7女,年龄22至59岁)作为对照。
所有患者均接受喹高利特急性试验:所有患者每隔3天随机接受药物(08:00时0.075mg)或安慰剂。在给药或给予安慰剂前15分钟和5分钟以及给药后每30分钟采集血样,共6小时。当泌乳素和/或α亚基水平较基线水平降低≥50%时,试验被认为阳性。治疗6个月后,10例患者随机继续接受喹高利特治疗,其余10例接受卡麦角林治疗6个月。喹高利特和卡麦角林的剂量分别为0.075至0.6mg/天和0.5至3mg/周。研究开始时,对垂体区域进行磁共振成像(MR)研究并进行123I-IBZM垂体闪烁扫描。治疗12个月后重复MR以评估肿瘤缩小情况:泌乳素瘤肿瘤体积缩小≥80%,NFA肿瘤体积缩小≥50%被认为有显著意义。泌乳素瘤患者的基础泌乳素水平为9495.0±1131.6mU/l,NFA患者为602.4±50.5mU/l。
10例NFA患者中有6例闪烁扫描为阴性。3例泌乳素瘤患者和2例NFA患者观察到中度摄取,其余7例泌乳素瘤患者和2例NFA患者观察到强烈摄取。在8例循环α亚基水平高的NFA患者中,急性试验5例为阴性,其余3例为阳性。所有10例泌乳素瘤患者急性试验均为阳性。用喹高利特和卡麦角林治疗12个月后,所有10例泌乳素瘤患者的循环泌乳素水平均降低(571.8±255.9mU/l),7例恢复正常。所有10例NFA患者的泌乳素水平均受到抑制(89.5±2.3mU/l)。10例NFA患者中有9例α亚基水平显著降低:8例患者中有4例α亚基水平恢复正常。在7例垂体对123I-IBZM摄取强烈的泌乳素瘤患者中,4例记录到腺瘤显著缩小。在10例NFA患者中,仅2例垂体对123I-IBZM摄取强烈的患者记录到腺瘤显著缩小。在分泌泌乳素腺瘤患者(r = 0.856,P < 0.005)或NFA患者(r = 0.787,P < 0.05)中,摄取程度(视为评分)与喹高利特或卡麦角林治疗反应(视为激素抑制百分比)之间发现显著正相关。
无功能腺瘤患者123I-IBZM摄取强烈预示着对喹高利特和卡麦角林长期治疗反应良好。这一结果表明,在开始用多巴胺激动剂进行药物治疗前,对于选定的无功能腺瘤患者可考虑进行垂体123I-IBZM闪烁扫描。