Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2010-4-19
pubmed:abstractText
Surgical resection is often not curative in patients with acromegaly and long-acting somatostatin analogues (lanreotide or octreotide) are often needed. This study assessed the efficacy and safety of self- or partner-administration of lanreotide in patients with acromegaly. This was a six-month, single-arm, open-label study conducted at 13 endocrinology clinics. Fifty-nine patients received deep subcutaneous lanreotide injections every 28 days. Twelve patients started on 120 mg lanreotide and forty-seven started on 90 mg lanreotide. At week 16, the dose was adjusted to 60, 90 or 120 mg based on insulin-like growth factor-1 (IGF-1) levels at week 12. Fifty-nine patients with acromegaly either switched from long-acting octreotide (switch; n = 33) or were somatostatin analogue treatment-naïve or not currently taking long-acting octreotide ("other"; n = 26). The key endpoints included the percentage of patients/partners able to self- or partner-inject lanreotide and those with normal IGF-1 or growth hormone (GH) levels at week 24/early termination. 100% of patients/partners correctly self- (n = 41) or partner-injected (n = 18) lanreotide by week 4. By week 24/early termination, IGF-1 levels were controlled in 93.7% of switch and 46.2% of "other" patients, while GH levels were controlled in 76.9% and 39.1% of patients, respectively. Both IGF-1 and GH were controlled in 73.1% of switch and 30.4% of "other" patients. Most switch patients (81%) reported they preferred lanreotide over long-acting octreotide for future use (P = 0.0001). Self- or partner-administration of lanreotide is generally well tolerated and associated with IGF-1 and GH control in many lanreotide-naïve patients with acromegaly.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19898989-11788630, http://linkedlifedata.com/resource/pubmed/commentcorrection/19898989-15827109, http://linkedlifedata.com/resource/pubmed/commentcorrection/19898989-16268802, http://linkedlifedata.com/resource/pubmed/commentcorrection/19898989-16322377, http://linkedlifedata.com/resource/pubmed/commentcorrection/19898989-17167139, http://linkedlifedata.com/resource/pubmed/commentcorrection/19898989-17495423, http://linkedlifedata.com/resource/pubmed/commentcorrection/19898989-17892497, http://linkedlifedata.com/resource/pubmed/commentcorrection/19898989-18080837, http://linkedlifedata.com/resource/pubmed/commentcorrection/19898989-18348909, http://linkedlifedata.com/resource/pubmed/commentcorrection/19898989-18492760, http://linkedlifedata.com/resource/pubmed/commentcorrection/19898989-18997495, http://linkedlifedata.com/resource/pubmed/commentcorrection/19898989-19033371, http://linkedlifedata.com/resource/pubmed/commentcorrection/19898989-9745397
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1573-7403
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
115-22
pubmed:dateRevised
2010-9-28
pubmed:meshHeading
pubmed:year
2010
pubmed:articleTitle
Effectiveness of self- or partner-administration of an extended-release aqueous-gel formulation of lanreotide in lanreotide-naïve patients with acromegaly.
pubmed:affiliation
Division of Endocrinology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA. salvator@jhmi.edu
pubmed:publicationType
Journal Article, Clinical Trial, Research Support, Non-U.S. Gov't, Multicenter Study