Literature DB >> 15757854

The outcome of surgery in 668 patients with acromegaly using current criteria of biochemical 'cure'.

Panagiotis Nomikos1, Michael Buchfelder, Rudolf Fahlbusch.   

Abstract

BACKGROUND AND AIM: The aim of this study was to illustrate the present role of transsphenoidal surgery as primary therapy in GH-secreting adenomas, and to compare the results concerning control of disease with previous series using older criteria of cure.
METHOD: We report on a consecutive series of 688 acromegalic patients treated over a time period of 19 years. Biochemical cure was defined as normalisation of basal GH level, suppression of GH levels to below 1 ng/ml during an oral glucose load and normalisation of IGF-I levels. Of the 506 patients undergoing primary transsphenoidal surgery, a total of 57.3% postoperatively fulfilled the criteria used.
RESULTS: The rate of biochemical 'cure' correlated with the magnitude of the initial GH levels, the tumour size and invasion. The overall complication rate was below 2%. Mortality in this series was 0.1% (1 of 688). During a follow-up period of 10.7 years only two recurrences (0.4%) occurred. However, in the patients treated by transcranial surgery and by repeat surgery the cure rate was found to be relatively low (5.2 and 21.3% respectively).
CONCLUSIONS: These data suggest that surgery remains with very few exceptions the primary treatment of acromegaly for (i) a high cure rate, (ii) low morbidity, (iii) low recurrence rate and (iv) immediate decline of GH. Based on current criteria of cure, recurrences are uncommon. However, cure by surgery alone is improbable in patients harbouring extended, invasive tumours with high secretory activity, in whom further adjuvant treatment is mandatory.

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Year:  2005        PMID: 15757854     DOI: 10.1530/eje.1.01863

Source DB:  PubMed          Journal:  Eur J Endocrinol        ISSN: 0804-4643            Impact factor:   6.664


  126 in total

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Authors:  Sophie Vallette; Omar Serri
Journal:  Pituitary       Date:  2010-12       Impact factor: 4.107

2.  Pre-surgical treatment with somatostatin analogues in patients with acromegaly: the case against.

Authors:  M Losa; V G Crippa
Journal:  J Endocrinol Invest       Date:  2012-06       Impact factor: 4.256

3.  Immediate and delayed postoperative morbidity in functional and non-functioning pituitary adenomas.

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Journal:  Pituitary       Date:  2012-09       Impact factor: 4.107

Review 4.  Treatment of pituitary tumors: surgery.

Authors:  Michael Buchfelder
Journal:  Endocrine       Date:  2005-10       Impact factor: 3.633

5.  Endoscopic versus microscopic approach for surgical treatment of acromegaly.

Authors:  Hussein Fathalla; Michael D Cusimano; Antonio Di Ieva; John Lee; Omar Alsharif; Jeannette Goguen; Stanley Zhang; Harley Smyth
Journal:  Neurosurg Rev       Date:  2015-02-10       Impact factor: 3.042

6.  Gamma knife radiosurgery for clinically persistent acromegaly.

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Review 7.  First-generation somatostatin receptor ligands and pregnancy: lesson from women with acromegaly.

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Review 8.  Guidelines for the treatment of growth hormone excess and growth hormone deficiency in adults.

Authors:  A Giustina; A Barkan; P Chanson; A Grossman; A Hoffman; E Ghigo; F Casanueva; A Colao; S Lamberts; M Sheppard; S Melmed
Journal:  J Endocrinol Invest       Date:  2008-09       Impact factor: 4.256

9.  Acromegaly with negative pituitary MRI and no evidence of ectopic source: the role of transphenoidal pituitary exploration?

Authors:  Sameera Daud; Amir H Hamrahian; Robert J Weil; Marwan Hamaty; Richard A Prayson; Leann Olansky
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Review 10.  Giant pituitary adenoma: histological types, clinical features and therapeutic approaches.

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