Literature DB >> 17555503

Does partial surgical tumour removal influence the response to octreotide-LAR in acromegalic patients previously resistant to the somatostatin analogue?

Raquel S Jallad1, Nina R Musolino, Sergio Kodaira, Valter A Cescato, Marcello D Bronstein.   

Abstract

OBJECTIVE: To compare the intrapatient response to the same dose of slow-release octreotide (OCT-LAR) before and after noncurative surgery in acromegalic patients who did not attain disease control after primary treatment with OCT-LAR.
DESIGN: Prospective clinical study. PATIENTS: Eleven acromegalic patients (eight men, aged 42.45 +/- 11.15 years, 10 macroadenomas) received OCT-LAR (20 mg, n = 1; 30 mg, n = 10) every 28 days as the primary treatment (1stOCT-LAR) for 11.3 +/- 4.2 months, without IGF-I normalization. They were subsequently submitted to surgery without cure and were then treated with the same dose of OCT-LAR for 8.0 +/- 6.5 months (2ndOCT-LAR). MEASUREMENTS: GH and IGF-I serum concentrations were obtained under basal conditions as well as during treatment. Pituitary tumour volume was assessed by magnetic resonance imaging (MRI) of the sella. IGF-I was also expressed as a percentage of the upper limit of the normal age- and sex-matched range (%ULNR IGF-I).
RESULTS: After 1stOCT-LAR, there was a decrease in GH levels (P = 0.003) and %ULNR IGF-I (P = 0.009) compared to baseline (B), but no IGF-I normalization. Tumour shrinkage was observed in eight of 10 patients with macroadenomas (median 63.7%, range 24.5-75.5%). After surgery, mean levels of GH and %ULNR IGF-I were lower than those at baseline (P = 0.0004 and P = 0.003, respectively), but not when compared to values during 1stOCT-LAR (P = 1.000 and P = 0.957, respectively). MRI confirmed surgical tumour removal (median 64%, range 4.9-96.6%) in eight of the 10 patients. Comparing the 2ndOCT-LAR results with postsurgical results, there were no significant decrease in %ULNR IGF-I (P = 0.061) and GH levels (P = 0.414). Nine patients (82%) achieved IGF-I normalization. The degree of surgical tumour reduction did not correlate with IGF-I normalization (P = 0.794). When comparing the results between 1stOCT-LAR and 2ndOCT-LAR, there was a decrease, albeit not statistically significant, in serum GH levels (P = 0.059) and a significant decrease in %ULNR IGF-I (P = 0.011).
CONCLUSIONS: Using strict criteria (same patient, same drug, same dose) our results strongly suggest that the surgical reduction of tumour mass can improve the outcome of OCT-LAR treatment in acromegalic patients resistant to primary therapy with SA.

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Year:  2007        PMID: 17555503     DOI: 10.1111/j.1365-2265.2007.02885.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


  18 in total

Review 1.  Acromegaly.

Authors:  Anat Ben-Shlomo; Shlomo Melmed
Journal:  Endocrinol Metab Clin North Am       Date:  2008-03       Impact factor: 4.741

Review 2.  Pharmacological treatment of acromegaly: its place in the overall therapeutic approach.

Authors:  Evgenia Korytnaya; Ariel Barkan
Journal:  J Neurooncol       Date:  2014-01-18       Impact factor: 4.130

3.  Surgical debulking of pituitary adenomas improves responsiveness to octreotide lar in the treatment of acromegaly.

Authors:  Rudolf Fahlbusch; David Kleinberg; Beverly Biller; Vivien Bonert; Michael Buchfelder; Paolo Cappabianca; John Carmichael; William Chandler; Annamaria Colao; Ajax George; Anne Klibanski; Edmond Knopp; Juergen Kreutzer; Neehar Kundurti; Martin Lesser; Adam Mamelak; Rosario Pivonello; Kalmon Post; Brooke Swearingen; Mary Lee Vance; Ariel Barkan
Journal:  Pituitary       Date:  2017-12       Impact factor: 4.107

Review 4.  Octreotide long-acting release (LAR): a review of its use in the management of acromegaly.

Authors:  Lily P H Yang; Gillian M Keating
Journal:  Drugs       Date:  2010-09-10       Impact factor: 9.546

5.  Octreotide LAR treatment of acromegaly in "real life": long-term outcome at a tertiary care center.

Authors:  Ana Laura Espinosa-de-los-Monteros; Baldomero Gonzalez; Guadalupe Vargas; Ernesto Sosa; Moises Mercado
Journal:  Pituitary       Date:  2015-06       Impact factor: 4.107

Review 6.  The surgical treatment of acromegaly.

Authors:  Michael Buchfelder; Sven-Martin Schlaffer
Journal:  Pituitary       Date:  2017-02       Impact factor: 4.107

Review 7.  Acromegaly pathogenesis and treatment.

Authors:  Shlomo Melmed
Journal:  J Clin Invest       Date:  2009-11-02       Impact factor: 14.808

Review 8.  Medical therapy of acromegaly: efficacy and safety of somatostatin analogues.

Authors:  Richard A Feelders; Leo J Hofland; Maarten O van Aken; Sebastian J Neggers; Steven W J Lamberts; Wouter W de Herder; Aart-Jan van der Lely
Journal:  Drugs       Date:  2009-11-12       Impact factor: 9.546

9.  Combined treatment with octreotide LAR and pegvisomant in patients with pituitary gigantism: clinical evaluation and genetic screening.

Authors:  Ruth Mangupli; Liliya Rostomyan; Emilie Castermans; Jean-Hubert Caberg; Paul Camperos; Jaime Krivoy; Elvia Cuauro; Vincent Bours; Adrian F Daly; Albert Beckers
Journal:  Pituitary       Date:  2016-10       Impact factor: 4.107

Review 10.  Management of acromegaly in Latin America: expert panel recommendations.

Authors:  Ariel Barkan; Marcello D Bronstein; Oscar D Bruno; Alejandro Cob; Ana Laura Espinosa-de-los-Monteros; Monica R Gadelha; Gloria Garavito; Mirtha Guitelman; Ruth Mangupli; Moisés Mercado; Lesly Portocarrero; Michael Sheppard
Journal:  Pituitary       Date:  2010-06       Impact factor: 4.107

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