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Partial surgical removal of growth hormone-secreting pituitary tumors enhances the response to somatostatin analogs in acromegaly
- Publication Year :
- 2006
-
Abstract
- Context: Surgery is a cornerstone in the treatment of acromegaly, but its efficacy in large, invasive tumors is scant. Objective: The objective of this study was to investigate whether partial surgical removal of GH-secreting pituitary tumors enhances the response rate to somatostatin analogs (SSA; sc octreotide, slow-release octreotide, and lanreotide). Design: This was a multicenter, open, retrospective study. Setting: The study was performed at university hospitals. Subjects and Methods: Eighty-six patients (42 women and 44 men; age, 42 ± 14 yr) with acromegaly were studied. Interventions: Patients underwent two courses of octreotide, lanreotide, or slow-release octreotide treatments before and after surgery of at least 6 months. Main Outcome Measure: The main outcome measure was normal IGF-I levels for age. Results: Presurgical SSA treatment significantly decreased GH and IGF-I levels in all patients. GH levels were less than 2.5 μg/liter in 12 patients (14%); IGF-I levels normalized in nine (10%). After surgery, GH and IGF-I levels further decreased in all patients; tumor removal was greater than 75% in 50 (58%), 50.1–75% in 21 (24%), 25.1–50% in 10 (12%), and less than 25% in five patients (6%). Preoperatively, pituitary function was impaired in 12 patients (14%). Postsurgical SSA treatment lowered GH levels to less than 2.5 μg/liter in 49 (56%) and normalized IGF-I levels in 48 patients (55%). The success rate was significantly increased compared with that before surgery (P < 0.0001). GH (r = −0.48; P < 0.0001) and IGF-I levels (r = −0.38; P = 0.0003) after postsurgery SSA treatment correlated with the amount of tumor surgically removed. After surgery, pituitary function was impaired in 28 patients (32.6%) and was improved in 12 patients (13.9%). The cumulative prevalence of pituitary deficiency did not change during the study (normal function from 40 to 42%; deficiency from 60 to 58%). Conclusions: Surgical tumor removal (>75%) enhances the response to SSAs without impairing pituitary function. Our data indicate that surgical debulking has a significant place in the treatment algorithm of acromegaly.
- Subjects :
- Adenoma
Adult
Male
medicine.medical_specialty
Antineoplastic Agents, Hormonal
Endocrinology, Diabetes and Metabolism
Clinical Biochemistry
Octreotide
Hypopituitarism
Pituitary neoplasm
Lanreotide
Peptides, Cyclic
Biochemistry
Cohort Studies
chemistry.chemical_compound
Endocrinology
Internal medicine
Acromegaly
medicine
Humans
Pituitary Neoplasms
Insulin-Like Growth Factor I
Hypophysectomy
Retrospective Studies
somatostatin analogues
Human Growth Hormone
business.industry
Biochemistry (medical)
Pituitary tumors
Middle Aged
medicine.disease
Debulking
Combined Modality Therapy
Magnetic Resonance Imaging
GH
IGF-I
Treatment Outcome
Somatostatin
chemistry
acromegaly
Female
business
medicine.drug
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....3b6efec4754879c98901cacca6f4fa25