A randomized, controlled, multicentre trial comparing pegvisomant alone with combination therapy of pegvisomant and long-acting octreotide in patients with acromegaly

被引:96
作者
Trainer, Peter J. [1 ]
Ezzat, Shereen [4 ]
D'Souza, Gwyn A. [2 ]
Layton, Gary [2 ]
Strasburger, Christian J. [3 ]
机构
[1] Christie Hosp, Dept Endocrinol, Manchester M20 4BX, Lancs, England
[2] Univ Toronto, Dept Med, Toronto, ON, Canada
[3] Charite, Dept Endocrinol, D-13353 Berlin, Germany
[4] Mt Sinai Hosp, Dept Med, Toronto, ON M5G 1X5, Canada
关键词
HORMONE-RECEPTOR ANTAGONIST; GROWTH-HORMONE; GLUCOSE-TOLERANCE; SOMATOSTATIN ANALOGS; INSULIN SENSITIVITY; TERM; QUESTIONNAIRE; COTREATMENT; MORTALITY; EFFICACY;
D O I
10.1111/j.1365-2265.2009.03620.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
P>Objective For patients with acromegaly who are suboptimally controlled on long-acting octreotide (LAR), treatment options are to switch to pegvisomant monotherapy (PM) or add pegvisomant to LAR (P-LAR). Our objective was to evaluate if the safety and efficacy of these regimens differ. Design This was an open-label, multicentre, randomized, 40-week outpatient study. The control arm consisted of patients controlled on LAR (n = 28). Patients A total of 27 patients with suboptimally controlled acromegaly [as indicated by a serum IGF-I level >= 1 center dot 3 x upper limit of normal (ULN) of the age-related reference range] were randomized to PM (10 mg once daily initially, then adjusted in 5-mg increments every 8 weeks based on IGF-I levels) and 29 to P-LAR (LAR dosing remained fixed). Measurements The primary end-point was adverse events (AEs). The secondary end-point was biochemical IGF-I-based efficacy. The RIA for IGF-I was discontinued by the manufacturer during the study and a chemiluminescent assay was subsequently used. Previously obtained IGF-I levels were re-analysed. Results PM and P-LAR were well tolerated and there were no differences in the number of AEs. Patients receiving P-LAR tended to be more likely to have clinically significant increases in hepatic transaminase levels, especially those receiving high-dose LAR. Normalization of IGF-I was similar with both regimens (56% and 62% of patients for PM and P-LAR respectively). The change in IGF-I assay resulted in lower rates of IGF-I normalization than expected. Reductions in fasting glucose levels were greater with PM than with P-LAR (-0 center dot 8 mmol/l; 95% confidence interval -1 center dot 16, -0 center dot 53 mmol/l). Conclusions In patients suboptimally controlled on LAR, PM and P-LAR were equally well tolerated and effective in normalizing IGF-I, and overall clinical improvement was observed with both regimens. Thus, pegvisomant monotherapy and adjunctive therapy are equally viable options for the treatment of LAR-resistant acromegaly.
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收藏
页码:549 / 557
页数:9
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