Tsagarakis S, Tsiganou E, Tzavara I, Nikolou H, Thalassinos N
Department of Endocrinology, Evangelismos Hospital, Athens, Greece.
Clin Endocrinol (Oxf). 1995 Jun;42(6):593-9. doi: 10.1111/j.1365-2265.1995.tb02685.x.
With the development of new long-acting depot preparations of bromocriptine (bromocriptine LAR), we investigated the effectiveness of intramuscular injections of long-acting bromocriptine in patients with prolactin and GH secreting macroadenomas.
Fourteen patients with PRL secreting (8 patients) and GH secreting (6 patients) macroadenomas were treated with monthly intramuscular injections of a long-acting and repeatable form of bromocriptine for 3-6 months. A 50-mg monthly dose was administered in the majority of patients with PRL secreting macroadenomas. A 100-mg monthly dose was administered in all patients with GH secreting macroadenomas.
Plasma PRL and/or GH levels were measured 6 and 12 hours after the first injection and then on days 1, 2, 14 and 28 after each injection, up to a maximum period of 6 months. Patients were hospitalized for 48 hours after each injection and were specifically questioned with respect to side-effects. Pituitary imaging with MRI or CT scans was performed in all patients before commencing treatment and was subsequently repeated in 5/8 patients with macroprolactinomas and 5/6 patients with GH secreting macroadenomas after the completion of a 6-month course of treatment.
In all patients with macroprolactinomas, serum PRL levels decreased significantly after their first 50-mg injection with nadir levels obtained by 24-48 hours post injection (12815 +/- 8704 vs 1480 +/- 1859 mU/l; mean +/- SD, P < 0.01). At their latest follow-up, on a 50-mg monthly dose, 4 patients developed normoprolactinaemia (PRL levels < 360 mU/l) while two patients demonstrated a significant reduction in serum PRL levels (70 and 87% or pretreatment values). In two patients, although a substantial decrement of serum PRL levels was achieved 12-24 hours post injection, serum PRL levels increased to pretreatment values by day 14 post injection. Both patients received a higher (100 mg) monthly dose which was partially effective in one patient. In two patients with GH secreting macroadenomas, a sustained decrease of elevated GH levels was observed; in two patients, while a substantial reduction of the elevated serum GH levels was achieved 12-24 hours after the first and subsequent injections, serum GH levels increased to pretreatment values by day 14 post injection; in two patients there was no effect on the elevated serum GH levels. Significant tumour shrinkage (24-50%) was observed in 5/5 patients with PRL secreting macroadenomas assessed at completion of a 6-month course of treatment. Significant tumour shrinkage was also documented in 2/5 acromegalics tested (29 and 46% respectively).
It is concluded that bromocriptine LAR is an effective treatment in the majority of patients with macroprolactinomas; it is also partially effective in some patients with GH secreting macroadenomas.
随着溴隐亭长效注射制剂(溴隐亭LAR)的研发,我们研究了肌肉注射长效溴隐亭对催乳素瘤和生长激素分泌型大腺瘤患者的疗效。
14例催乳素分泌型(8例)和生长激素分泌型(6例)大腺瘤患者接受每月一次的长效且可重复使用的溴隐亭肌肉注射,疗程为3 - 6个月。大多数催乳素分泌型大腺瘤患者每月注射剂量为50毫克。所有生长激素分泌型大腺瘤患者每月注射剂量为100毫克。
首次注射后6小时和12小时测量血浆催乳素和/或生长激素水平,之后在每次注射后的第1、2、14和28天测量,最长测量6个月。每次注射后患者住院48小时,并专门询问副作用情况。所有患者在开始治疗前进行垂体MRI或CT扫描成像,在6个月疗程结束后,8例催乳素大腺瘤患者中的5例和6例生长激素分泌型大腺瘤患者中的5例再次进行成像检查。
所有催乳素大腺瘤患者在首次注射50毫克后血清催乳素水平显著下降,注射后24 - 48小时达到最低点(12815±8704对1480±1859 mU/l;均值±标准差,P<0.01)。在最近一次随访时,每月50毫克剂量组中,4例患者催乳素水平恢复正常(催乳素水平<360 mU/l),2例患者血清催乳素水平显著降低(分别为治疗前值的70%和87%)。2例患者虽然在注射后12 - 24小时血清催乳素水平大幅下降,但在注射后第14天血清催乳素水平又回升至治疗前值。这2例患者均接受了更高剂量(100毫克)的每月注射,其中1例患者部分有效。2例生长激素分泌型大腺瘤患者观察到生长激素水平持续下降;2例患者在首次及后续注射后12 - 24小时血清生长激素水平大幅降低,但在注射后第14天血清生长激素水平又回升至治疗前值;2例患者血清生长激素水平升高无变化。在6个月疗程结束时评估,5/5例催乳素分泌型大腺瘤患者观察到肿瘤显著缩小(24 - 50%)。在2/5例接受检测的肢端肥大症患者中也记录到肿瘤显著缩小(分别为29%和46%)。
得出结论,溴隐亭LAR对大多数催乳素大腺瘤患者是一种有效的治疗方法;对一些生长激素分泌型大腺瘤患者也有部分疗效。