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Erschienen in: Pituitary 4/2016

07.05.2016

Monotherapy with lanreotide depot for acromegaly: long-term clinical experience in a pituitary center

verfasst von: Babak Torabi Sagvand, Shafaq Khairi, Arezoo Haghshenas, Brooke Swearingen, Nicholas A. Tritos, Karen K. Miller, Anne Klibanski, Lisa B. Nachtigall

Erschienen in: Pituitary | Ausgabe 4/2016

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Abstract

Purpose

Long-acting somatostatin analogs are one of the main classes of medical therapy used for acromegaly and most patients require ongoing treatment. Few studies have evaluated the long-term efficacy and safety of lanreotide depot beyond 2 years. The goal of this study was to provide a long-term longitudinal assessment of efficacy and safety of lanreotide depot in lanreotide responders compared to a surgically cured control group.

Methods

In this retrospective longitudinal case-control study, patients with acromegaly receiving lanreotide depot monotherapy continuously for at least 24 months (N = 24) and surgically cured patients (N = 39) were compared. Serum IGF-1, pituitary MRIs, lanreotide dose, co-morbidities and adverse effects were assessed longitudinally.

Results

In the lanreotide group, IGF-1 remained normal and unchanged over 6 years; comparable to the surgery only group. There was no difference in prevalence of normal IGF-1 between the lanreotide and surgery only groups at 6 months (100 vs. 97 %), 6 years (89 vs. 90 %) and at last follow-up (96 vs. 92 %). Tumor size remained stable (79 %) or decreased (21 %) in the lanreotide group. In the surgery only group, tumor size remained unchanged in all patients. Hemoglobin A1C did not differ between lanreotide and surgery only groups (baseline 5.8 vs. 6.1 %; last follow-up 6.0 vs. 5.7 %). Two (8 %) of the lanreotide and none of the surgery only group developed new diabetes mellitus.

Conclusion

Lanreotide depot maintains normalization of IGF-1 in 89 % of responders after 6 years, comparable to surgically cured controls, and controlled tumor size in all without significant adverse effects.
Literatur
2.
Zurück zum Zitat Howlett TA, Willis D, Walker G et al (2013) Control of growth hormone and IGF1 in patients with acromegaly in the UK: responses to medical treatment with somatostatin analogues and dopamine agonists. Clin Endocrinol (Oxf) 79:689–699. doi:10.1111/cen.12207 Howlett TA, Willis D, Walker G et al (2013) Control of growth hormone and IGF1 in patients with acromegaly in the UK: responses to medical treatment with somatostatin analogues and dopamine agonists. Clin Endocrinol (Oxf) 79:689–699. doi:10.​1111/​cen.​12207
5.
Zurück zum Zitat Colao A, Pivonello R, Rosato F et al (2006) First-line octreotide-LAR therapy induces tumour shrinkage and controls hormone excess in patients with acromegaly: results from an open, prospective, multicentre trial. Clin Endocrinol (Oxf) 64:342–351. doi:10.1111/j.1365-2265.2006.02467.x CrossRef Colao A, Pivonello R, Rosato F et al (2006) First-line octreotide-LAR therapy induces tumour shrinkage and controls hormone excess in patients with acromegaly: results from an open, prospective, multicentre trial. Clin Endocrinol (Oxf) 64:342–351. doi:10.​1111/​j.​1365-2265.​2006.​02467.​x CrossRef
6.
Zurück zum Zitat Grottoli S, Celleno R, Gasco V et al (2005) Efficacy and safety of 48 weeks of treatment with octreotide LAR in newly diagnosed acromegalic patients with macroadenomas: an open-label, multicenter, non-comparative study. J Endocrinol Invest 28:978–983CrossRefPubMed Grottoli S, Celleno R, Gasco V et al (2005) Efficacy and safety of 48 weeks of treatment with octreotide LAR in newly diagnosed acromegalic patients with macroadenomas: an open-label, multicenter, non-comparative study. J Endocrinol Invest 28:978–983CrossRefPubMed
7.
Zurück zum Zitat Cozzi R, Montini M, Attanasio R et al (2006) Primary treatment of acromegaly with octreotide LAR: a long-term (up to 9 years) prospective study of its efficacy in the control of disease activity and tumor shrinkage. J Clin Endocrinol Metab 91:1397–1403. doi:10.1210/jc.2005-2347 CrossRefPubMed Cozzi R, Montini M, Attanasio R et al (2006) Primary treatment of acromegaly with octreotide LAR: a long-term (up to 9 years) prospective study of its efficacy in the control of disease activity and tumor shrinkage. J Clin Endocrinol Metab 91:1397–1403. doi:10.​1210/​jc.​2005-2347 CrossRefPubMed
8.
Zurück zum Zitat Ayuk J, Stewart SE, Stewart PM, Sheppard MC (2004) Efficacy of Sandostatin® LAR® (long-acting somatostatin analogue) is similar in patients with untreated acromegaly and in those previously treated with surgery and/or radiotherapy. Clin Endocrinol (Oxf) 60:375–381. doi:10.1111/j.1365-2265.2004.01992.x CrossRef Ayuk J, Stewart SE, Stewart PM, Sheppard MC (2004) Efficacy of Sandostatin® LAR® (long-acting somatostatin analogue) is similar in patients with untreated acromegaly and in those previously treated with surgery and/or radiotherapy. Clin Endocrinol (Oxf) 60:375–381. doi:10.​1111/​j.​1365-2265.​2004.​01992.​x CrossRef
9.
Zurück zum Zitat Cozzi R, Attanasio R, Montini M et al (2003) 4-year treatment with octreotide-long-acting repeatable in 110 acromegalic patients: predictive value of short-term results? J Clin Endocrinol Metab 88:3090–3098. doi:10.1210/jc.2003-030110 CrossRefPubMed Cozzi R, Attanasio R, Montini M et al (2003) 4-year treatment with octreotide-long-acting repeatable in 110 acromegalic patients: predictive value of short-term results? J Clin Endocrinol Metab 88:3090–3098. doi:10.​1210/​jc.​2003-030110 CrossRefPubMed
10.
Zurück zum Zitat Colao A, Ferone D, Marzullo P et al (2001) Long-term effects of depot long-acting somatostatin analog octreotide on hormone levels and tumor mass in acromegaly. J Clin Endocrinol Metab 86:2779–2786. doi:10.1210/jc.86.6.2779 PubMed Colao A, Ferone D, Marzullo P et al (2001) Long-term effects of depot long-acting somatostatin analog octreotide on hormone levels and tumor mass in acromegaly. J Clin Endocrinol Metab 86:2779–2786. doi:10.​1210/​jc.​86.​6.​2779 PubMed
11.
Zurück zum Zitat Lancranjan I, Atkinson AB (1999) Results of a European multicentre study with Sandostatin LAR in acromegalic patients, 1st edn. Sandostatin LAR Group, Pituitary, pp 105–114 Lancranjan I, Atkinson AB (1999) Results of a European multicentre study with Sandostatin LAR in acromegalic patients, 1st edn. Sandostatin LAR Group, Pituitary, pp 105–114
14.
Zurück zum Zitat Alexopoulou O, Abrams P, Verhelst J et al (2004) Efficacy and tolerability of lanreotide Autogel therapy in acromegalic patients previously treated with octreotide LAR. Eur J Endocrinol 151:317–324. doi:10.1530/eje.0.1510317 CrossRefPubMed Alexopoulou O, Abrams P, Verhelst J et al (2004) Efficacy and tolerability of lanreotide Autogel therapy in acromegalic patients previously treated with octreotide LAR. Eur J Endocrinol 151:317–324. doi:10.​1530/​eje.​0.​1510317 CrossRefPubMed
15.
Zurück zum Zitat Van Thiel SW, Romijn JA, Biermasz NR et al (2004) Octreotide long-acting repeatable and lanreotide Autogel are equally effective in controlling growth hormone secretion in acromegalic patients. Eur J Endocrinol 150:489–495. doi:10.1530/eje.0.1500489 CrossRefPubMed Van Thiel SW, Romijn JA, Biermasz NR et al (2004) Octreotide long-acting repeatable and lanreotide Autogel are equally effective in controlling growth hormone secretion in acromegalic patients. Eur J Endocrinol 150:489–495. doi:10.​1530/​eje.​0.​1500489 CrossRefPubMed
16.
Zurück zum Zitat Flogstad AK, Halse J, Bakke S et al (1997) Sandostatin LAR in acromegalic patients: long-term treatment. J Clin Endocrinol Metab 82:23–28CrossRefPubMed Flogstad AK, Halse J, Bakke S et al (1997) Sandostatin LAR in acromegalic patients: long-term treatment. J Clin Endocrinol Metab 82:23–28CrossRefPubMed
17.
Zurück zum Zitat Stewart PM, Kane KF, Stewart SE et al (1995) Depot long-acting somatostatin analog (sandostatin-LAR) is an effective treatment for acromegaly. J Clin Endocrinol Metab 80:3267–3272. doi:10.1210/jc.80.11.3267 PubMed Stewart PM, Kane KF, Stewart SE et al (1995) Depot long-acting somatostatin analog (sandostatin-LAR) is an effective treatment for acromegaly. J Clin Endocrinol Metab 80:3267–3272. doi:10.​1210/​jc.​80.​11.​3267 PubMed
18.
Zurück zum Zitat Ayuk J, Stewart SE, Stewart PM, Sheppard MC (2002) Long-term safety and efficacy of depot long-acting somatostatin analogs for the treatment of acromegaly. J Clin Endocrinol Metab 87:4142–4146. doi:10.1210/jc.2001-011913 CrossRefPubMed Ayuk J, Stewart SE, Stewart PM, Sheppard MC (2002) Long-term safety and efficacy of depot long-acting somatostatin analogs for the treatment of acromegaly. J Clin Endocrinol Metab 87:4142–4146. doi:10.​1210/​jc.​2001-011913 CrossRefPubMed
19.
Zurück zum Zitat Colao A, Auriemma RS, Galdiero M et al (2009) Effects of initial therapy for 5 years with somatostatin analogs for acromegaly on growth hormone and insulin-like growth factor-i levels, tumor shrinkage, and cardiovascular disease: a prospective study. J Clin Endocrinol Metab 94:3746–3756. doi:10.1210/jc.2009-0941 CrossRefPubMed Colao A, Auriemma RS, Galdiero M et al (2009) Effects of initial therapy for 5 years with somatostatin analogs for acromegaly on growth hormone and insulin-like growth factor-i levels, tumor shrinkage, and cardiovascular disease: a prospective study. J Clin Endocrinol Metab 94:3746–3756. doi:10.​1210/​jc.​2009-0941 CrossRefPubMed
21.
Zurück zum Zitat Maiza JC, Vezzosi D, Matta M et al (2007) Long-term (up to 18 years) effects on GH/IGF-1 hypersecretion and tumour size of primary somatostatin analogue (SSTa) therapy in patients with GH-secreting pituitary adenoma responsive to SSTa. Clin Endocrinol (Oxf) 67:282–289. doi:10.1111/j.1365-2265.2007.02878.x CrossRef Maiza JC, Vezzosi D, Matta M et al (2007) Long-term (up to 18 years) effects on GH/IGF-1 hypersecretion and tumour size of primary somatostatin analogue (SSTa) therapy in patients with GH-secreting pituitary adenoma responsive to SSTa. Clin Endocrinol (Oxf) 67:282–289. doi:10.​1111/​j.​1365-2265.​2007.​02878.​x CrossRef
22.
Zurück zum Zitat Gutt B, Bidlingmaier M, Kretschmar K et al (2005) 4-year follow-up of acromegalic patients treated with the new long-acting formulation of lanreotide (lanreotide autogel). Exp Clin Endocrinol Diabetes 113:139–144. doi:10.1055/s-2005-837520 CrossRefPubMed Gutt B, Bidlingmaier M, Kretschmar K et al (2005) 4-year follow-up of acromegalic patients treated with the new long-acting formulation of lanreotide (lanreotide autogel). Exp Clin Endocrinol Diabetes 113:139–144. doi:10.​1055/​s-2005-837520 CrossRefPubMed
23.
Zurück zum Zitat Itoh S, Tanaka K, Kumagae M, Takeda F, Morio K, Kogure M, Hasegawa M, Horiuchi T, Watabe T, Miyabe S et al (1988) Effect of subcutaneous injection of a long-acting analogue of somatostatin (SMS 201-995) on plasma thyroid-stimulating hormone in normal human subjects. Life Sci 42:2691–2699CrossRefPubMed Itoh S, Tanaka K, Kumagae M, Takeda F, Morio K, Kogure M, Hasegawa M, Horiuchi T, Watabe T, Miyabe S et al (1988) Effect of subcutaneous injection of a long-acting analogue of somatostatin (SMS 201-995) on plasma thyroid-stimulating hormone in normal human subjects. Life Sci 42:2691–2699CrossRefPubMed
24.
Zurück zum Zitat Cuttica CM, Fazzuoli L, Cariola G et al (1994) Behavior of the pituitary-thyroid axis in acromegalic subjects during prolonged intermittent and pulsatile treatment with octreotide. Recent Prog Med 85:7–12 Cuttica CM, Fazzuoli L, Cariola G et al (1994) Behavior of the pituitary-thyroid axis in acromegalic subjects during prolonged intermittent and pulsatile treatment with octreotide. Recent Prog Med 85:7–12
25.
Zurück zum Zitat Colao A, Auriemma RS, Pivonello R et al (2015) Interpreting biochemical control response rates with first-generation somatostatin analogues in acromegaly. Pituitary. doi:10.1007/s11102-015-0684-z Colao A, Auriemma RS, Pivonello R et al (2015) Interpreting biochemical control response rates with first-generation somatostatin analogues in acromegaly. Pituitary. doi:10.​1007/​s11102-015-0684-z
26.
27.
Zurück zum Zitat Attanasio R, Barausse M, Cozzi R (2001) GH/IGF-I normalization and tumor shrinkage during long-term treatment of acromegaly by lanreotide. J Endocrinol Invest 24:209–216. doi:10.1007/BF03343849 CrossRefPubMed Attanasio R, Barausse M, Cozzi R (2001) GH/IGF-I normalization and tumor shrinkage during long-term treatment of acromegaly by lanreotide. J Endocrinol Invest 24:209–216. doi:10.​1007/​BF03343849 CrossRefPubMed
29.
Zurück zum Zitat Carmichael JD, Bonert VS, Mirocha JM, Melmed S (2009) The utility of oral glucose tolerance testing for diagnosis and assessment of treatment outcomes in 166 patients with acromegaly. J Clin Endocrinol Metab 94:523–527. doi:10.1210/jc.2008-1371 CrossRefPubMed Carmichael JD, Bonert VS, Mirocha JM, Melmed S (2009) The utility of oral glucose tolerance testing for diagnosis and assessment of treatment outcomes in 166 patients with acromegaly. J Clin Endocrinol Metab 94:523–527. doi:10.​1210/​jc.​2008-1371 CrossRefPubMed
30.
Zurück zum Zitat Zeinalizadeh M, Habibi Z, Fernandez-Miranda JC et al (2015) Discordance between growth hormone and insulin-like growth factor-1 after pituitary surgery for acromegaly: a stepwise approach and management. Pituitary 18:48–59. doi:10.1007/s11102-014-0556-y CrossRefPubMed Zeinalizadeh M, Habibi Z, Fernandez-Miranda JC et al (2015) Discordance between growth hormone and insulin-like growth factor-1 after pituitary surgery for acromegaly: a stepwise approach and management. Pituitary 18:48–59. doi:10.​1007/​s11102-014-0556-y CrossRefPubMed
31.
Zurück zum Zitat Matta M, Bongard V, Grunenwald S et al (2011) Clinical and metabolic characteristics of acromegalic patients with high IGF1/normal GH levels during somatostatin analog treatment. Eur J Endocrinol 164:885–889. doi:10.1530/EJE-11-0098 CrossRefPubMed Matta M, Bongard V, Grunenwald S et al (2011) Clinical and metabolic characteristics of acromegalic patients with high IGF1/normal GH levels during somatostatin analog treatment. Eur J Endocrinol 164:885–889. doi:10.​1530/​EJE-11-0098 CrossRefPubMed
33.
Zurück zum Zitat Wattson DA, Tanguturi SK, Spiegel DY et al (2014) Outcomes of proton therapy for patients with functional pituitary adenomas. Int J Radiat Oncol Biol Phys 90:532–539CrossRefPubMed Wattson DA, Tanguturi SK, Spiegel DY et al (2014) Outcomes of proton therapy for patients with functional pituitary adenomas. Int J Radiat Oncol Biol Phys 90:532–539CrossRefPubMed
35.
Zurück zum Zitat Strasburger CJ, Karavitaki N, Störmann S et al (2016) Patient-reported outcomes of parenteral somatostatin analogue injections in 195 patients with acromegaly. Eur J Endocrinol. doi:10.1530/EJE-15-1042 PubMedCentral Strasburger CJ, Karavitaki N, Störmann S et al (2016) Patient-reported outcomes of parenteral somatostatin analogue injections in 195 patients with acromegaly. Eur J Endocrinol. doi:10.​1530/​EJE-15-1042 PubMedCentral
37.
Zurück zum Zitat Salvatori R, Woodmansee WW, Molitch M et al (2014) Lanreotide extended-release aqueous-gel formulation, injected by patient, partner or healthcare provider in patients with acromegaly in the United States: 1-year data from the SODA registry. Pituitary 17:13–21. doi:10.1007/s11102-012-0460-2 CrossRefPubMed Salvatori R, Woodmansee WW, Molitch M et al (2014) Lanreotide extended-release aqueous-gel formulation, injected by patient, partner or healthcare provider in patients with acromegaly in the United States: 1-year data from the SODA registry. Pituitary 17:13–21. doi:10.​1007/​s11102-012-0460-2 CrossRefPubMed
38.
Zurück zum Zitat Salvatori R, Nachtigall LB, Cook DM et al (2010) Effectiveness of self- or partner-administration of an extended-release aqueous-gel formulation of lanreotide in lanreotide-naïve patients with acromegaly. Pituitary 13:115–122. doi:10.1007/s11102-009-0207-x CrossRefPubMed Salvatori R, Nachtigall LB, Cook DM et al (2010) Effectiveness of self- or partner-administration of an extended-release aqueous-gel formulation of lanreotide in lanreotide-naïve patients with acromegaly. Pituitary 13:115–122. doi:10.​1007/​s11102-009-0207-x CrossRefPubMed
39.
Zurück zum Zitat Mazziotti G, Porcelli T, Bogazzi F et al (2011) Effects of high-dose octreotide lar on glucose metabolism in patients with acromegaly inadequately controlled by conventional somatostatin analog therapy. Eur J Endocrinol 164:341–347. doi:10.1530/EJE-10-0811 CrossRefPubMed Mazziotti G, Porcelli T, Bogazzi F et al (2011) Effects of high-dose octreotide lar on glucose metabolism in patients with acromegaly inadequately controlled by conventional somatostatin analog therapy. Eur J Endocrinol 164:341–347. doi:10.​1530/​EJE-10-0811 CrossRefPubMed
Metadaten
Titel
Monotherapy with lanreotide depot for acromegaly: long-term clinical experience in a pituitary center
verfasst von
Babak Torabi Sagvand
Shafaq Khairi
Arezoo Haghshenas
Brooke Swearingen
Nicholas A. Tritos
Karen K. Miller
Anne Klibanski
Lisa B. Nachtigall
Publikationsdatum
07.05.2016
Verlag
Springer US
Erschienen in
Pituitary / Ausgabe 4/2016
Print ISSN: 1386-341X
Elektronische ISSN: 1573-7403
DOI
https://doi.org/10.1007/s11102-016-0724-3

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