Turner H E, Vadivale A, Keenan J, Wass J A
Department of Endocrinology, Radcliffe Infirmary, Oxford, UK.
Clin Endocrinol (Oxf). 1999 Sep;51(3):275-80. doi: 10.1046/j.1365-2265.1999.00853.x.
Two long-acting depot somatostatin analogues have recently been licensed for the treatment of acromegaly. We wished to assess the effectiveness of both these drugs in suppressing mean GH to a target of < 5 mU/l in patients with acromegaly unselected for responsiveness to octreotide, and also to compare the effects of both drugs
We prospectively studied 10 unselected patients with acromegaly who were treated first with lanreotide (LAN) and then octreotide LAR (LAR) following a washout period. The target for therapy was to achieve mean GH less than 5 mU/l.
Five (50%) patients achieved mean GH < 5 mU/l on lanreotide 30 mg every 10 days, and 7 out of 9 (77.8%) achieved this level when the dose frequency was increased to every 7 days. On 20 mg octreotide LAR, 6 (60%) patients achieved the target mean GH and a further 2 (80%) when the dose was increased to 30 mg. Normalization of IGF-1 occurred in 5/9 (55.6%) patients who received lanreotide and 7/10 (70%) of those who received octreotide LAR. There was a significant difference in mean GH attained on the 2 drugs. The patients' mean GH was significantly lower when treated with octreotide LAR 20 mg every 4 weeks compared with lanreotide 30 mg every 10 days (P = 0.037). Maximal suppression of mean GH with 30 mg octreotide LAR or 7 day dosing of lanreotide was significantly greater on octreotide LAR (P < 0.02).
At current dose recommendations, lanreotide and octreotide LAR are both effective in lowering mean GH to 'safe' (< 5 mU/l) levels in 80% patients but octreotide LAR treatment leads to significantly lower mean GH.
两种长效缓释生长抑素类似物最近已获许可用于治疗肢端肥大症。我们希望评估这两种药物在将未根据对奥曲肽的反应性进行选择的肢端肥大症患者的平均生长激素水平抑制至<5 mU/l目标值方面的有效性,同时比较这两种药物的效果。
我们前瞻性地研究了10例未经过选择的肢端肥大症患者,在经过洗脱期后,先给予兰瑞肽(LAN)治疗,然后给予奥曲肽长效释放制剂(LAR)治疗。治疗目标是使平均生长激素水平低于5 mU/l。
每10天给予30 mg兰瑞肽时,5例(50%)患者的平均生长激素水平<5 mU/l;当给药频率增加至每7天时,9例患者中的7例(77.8%)达到了该水平。给予20 mg奥曲肽LAR时,6例(60%)患者达到了目标平均生长激素水平,剂量增加至30 mg时,又有2例(80%)患者达到该水平。接受兰瑞肽治疗的9例患者中有5例(55.6%)的胰岛素样生长因子-1恢复正常,接受奥曲肽LAR治疗的10例患者中有7例(70%)恢复正常。两种药物达到的平均生长激素水平存在显著差异。与每10天给予30 mg兰瑞肽相比,每4周给予20 mg奥曲肽LAR治疗时患者的平均生长激素水平显著更低(P = 0.037)。30 mg奥曲肽LAR或每7天给药一次的兰瑞肽对平均生长激素的最大抑制作用在奥曲肽LAR组显著更大(P < 0.02)。
按照当前的剂量推荐,兰瑞肽和奥曲肽LAR在将80%患者的平均生长激素水平降低至“安全”(<5 mU/l)水平方面均有效,但奥曲肽LAR治疗导致的平均生长激素水平显著更低。