Combined therapy with somatostatin analogues and weekly pegvisomant in active acromegaly

被引:155
作者
Feenstra, J [1 ]
de Herder, WW [1 ]
ten Have, SMTH [1 ]
van den Beld, AW [1 ]
Feelders, RA [1 ]
Janssen, JAMJL [1 ]
van der Lely, AJ [1 ]
机构
[1] Erasmus MC, Dept Internal Med, NL-3000 CA Rotterdam, Netherlands
关键词
D O I
10.1016/S0140-6736(05)63011-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pegvisomant monotherapy once daily returns concentrations of insulin-like growth factor I (IGF-I) to normal in most patients with acromegaly, but is very costly. In a 42-week dose-finding study, we assessed the efficacy of the combination of long-acting somatostatin analogues once monthly and pegvisomant once weekly in 26 patients with active acromegaly. Dose of pegvisomant was increased until IGF-I concentration became normal or until a weekly dose of 80 mg was reached. IGF-I reached normal concentrations in 18 of 19 (95%) patients who completed 42 weeks of treatment, with a median weekly dose of 60 mg pegvisomant (range 40-80). No signs of pituitary tumour growth were noted, but mild increases in liver enzymes were observed in ten patients (38%). This combined treatment is effective, might increase compliance, and could greatly reduce the costs of medical treatment for acromegaly in some patients.
引用
收藏
页码:1644 / 1646
页数:3
相关论文
共 7 条
  • [1] Insulin sensitivity and glucose tolerance improve in patients with acromegaly converted from depot octreotide to pegvisomant
    Drake, WM
    Rowles, SV
    Roberts, ME
    Fode, FK
    Besser, GM
    Monson, JP
    Trainer, PJ
    [J]. EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2003, 149 (06) : 521 - 527
  • [2] Alternate-day administration of pegvisomant maintains normal serum insulin-like growth factor-I levels in patients with acromegaly
    Jehle, S
    Reyes, CM
    Sundeen, RE
    Freda, PU
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (03) : 1588 - 1593
  • [3] Insulin regulation of human hepatic growth hormone receptors: Divergent effects on biosynthesis and surface translocation
    Leung, KC
    Doyle, N
    Ballesteros, M
    Waters, MJ
    Ho, KKY
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (12) : 4712 - 4720
  • [4] Primary medical therapy for acromegaly
    Sheppard, MC
    [J]. CLINICAL ENDOCRINOLOGY, 2003, 58 (04) : 387 - 399
  • [5] Treatment of acromegaly with the growth hormone-receptor antagonist pegvisomant
    Trainer, PJ
    Drake, WM
    Katznelson, L
    Freda, PU
    Herman-Bonert, V
    van der Lely, AJ
    Dimaraki, EV
    Stewart, PM
    Friend, KE
    Vance, ML
    Besser, GM
    Scarlett, JA
    Thorner, MO
    Parkinson, C
    Klibanski, A
    Powell, JS
    Barkan, AL
    Sheppard, MC
    Maldonado, M
    Rose, DR
    Clemmons, DR
    Johannson, G
    Bengtsson, BÅ
    Stavrou, S
    Kleinberg, DL
    Cook, DM
    Phillips, LS
    Bidlingmaier, M
    Strasburger, CJ
    Hackett, S
    Zib, K
    Bennett, WF
    Davis, RJ
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (16) : 1171 - 1177
  • [6] Control of tumor size and disease activity during cotreatment with octreotide and the growth hormone receptor antagonist pegvisomant in an acromegalic patient
    van der Lely, AJ
    Muller, AF
    Janssen, JA
    Davis, RJ
    Zib, KA
    Scarlett, JA
    Lamberts, SW
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (02) : 478 - 481
  • [7] Long-term treatment of acromegaly with pegvisomant, a growth hormone receptor antagonist
    van der Lely, AJ
    Hutson, RK
    Trainer, PJ
    Besser, GM
    Barkan, AL
    Katznelson, L
    Klibanski, A
    Herman-Bonert, V
    Melmed, S
    Vance, ML
    Freda, PU
    Stewart, PM
    Friend, KE
    Clemmons, DR
    Johannsson, G
    Stavrou, S
    Cook, DM
    Phillips, LS
    Strasburger, CJ
    Hacker, S
    Zib, KA
    Davis, RJ
    Scarlett, JA
    Thorner, M
    [J]. LANCET, 2001, 358 (9295) : 1754 - 1759