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ACROMEGALY Prof. Gaetano Lombardi Prof. Gaetano Lombardi Dept. of Clinical and Molecular Endocrinology and Oncology University “Federico II”, Naples,

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Presentation on theme: "ACROMEGALY Prof. Gaetano Lombardi Prof. Gaetano Lombardi Dept. of Clinical and Molecular Endocrinology and Oncology University “Federico II”, Naples,"— Presentation transcript:

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2 ACROMEGALY Prof. Gaetano Lombardi Prof. Gaetano Lombardi Dept. of Clinical and Molecular Endocrinology and Oncology University “Federico II”, Naples, Italy

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4 Sporadic pituitary tumor

5 Syndromic/Familial Pituitary Tumors

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8 MEN1 Pituitary Tumor Primary Hyperparathyroidism Endocrine Pancreatic Tumor Autosomal dominant Gene Men1 11q13

9 McCune-Albright Syndrome Polyostotic fibrous dysplasia Skin pigmentation Hormonal dysfunction - Precocious puberty - Thyrotoxicosis - Gigantism - Cushing’s Syndrome Macroadenoma (50% of cases) Mutation di Gs-alpha

10 Carney Syndrome Autosomal dominant 2p16 Mutation of PRKAR1A Chiazze di iperpigmantazione cutanea Mixoma cardiaco Iperfunzione endocrina sindrome di Cushing acromegalia Hyperplasia or multiple microadenomas

11 RARE DISEASE

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14 Balance of GH influences on cell growth regulation Pathogenesis of cell proliferation/apoptosis in acromegaly

15 COLON CANCER IN ACROMEGALY

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19 TREATMENT GOALS Mortality rate reduction Tumor shrinkage Treatment of comorbidities Relief of symptoms directly caused by GH excess    

20 Medical Therapy SSA, DA, GH-A Radiotherapyconventional stereotactic stereotactic Surgery trans-cranium trans-sphenoidal

21 SURGERY SUCCESS RATE: 72% microadenomas, 50% macroadenomas, 17% giant adenomas Improvement in pituitary function in 60-97% Improvement of visual field defect in 70% Low morbidity and mortality (0-1%) Reduction in tumor size in 90% Tumor residual in 15-50% Complications in 5-18%

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25 MEDICAL THERAPY Dopamine-AgonistsBromocriptineCabergoline Lisuride – Pergolide - Quinagolide Somatostatin Analogues OctreotideLanreotide GH-receptor antagonist GH-receptor antagonist

26 Headache Hypotension Nausea Gastro-intestinal SIDE EFFECTS

27 SOMATOSTATIN ANALOGUES EFFECTIVENESS Clinical Improvement in 70-90% Normalisation of GH levels in 65-70% Normalisation of IGF-I levels in 65-70% Tumor shrinkage >50%   

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32 Baseline 5 month-OCT LAR 10 month-OCT LAR

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35 SIDE EFFECTS Gastro-intestinal Biliary sludge Gallstones Diarrhea

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38 PEGVISOMANT  GH analog (191 amino acids)  9 different amino acids  4 - 5 PEG  molecular weight 42 - 46000 D  half-life >70 hours  subcutaneous administration GH is not a marker of disease Goal of therapy – to reduce IGF-I levels to normal range for age and sex

39 STOP

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44 IC50 nM ◊ sst1 9.3  0.1 ◊ sst21.0  0.1 ◊ sst31.5  0.3 ◊ sst4> 100 ◊ sst50.2  0.1

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46 SOMATOSTATIN AND DOPAMINE RECEPTOR AGONIST

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48 R.S. Auriemma, A. Cozzolino, M. De Leo, M.C. De Martino, C. Di Somma, A. Faggiano, M. Galdiero, L.F.S. Grasso, E. Guerra, F. Milone, R. Pivonello, M.C. Savanelli, P. Vitale, L. Vuolo & A. Colao Dept. of Clinical and Molecular Endocrinology and Oncology

49 QUESTION 1 Induce clinical improvement in 30% Normalize GH levels in 30% Normalize IGF-I levels in 65-70% Induce tumor shrinkage in <20%    SOMATOSTATIN ANALOGUES:

50 QUESTION 2 Normalize IGF-I levels in 30% Normalize IGF-I levels in 50% Normalize IGF-I levels in 70% Normalize IGF-I levels in up to 95%    THE GH-RECEPTOR ANTAGONIST PEGVISOMANT:

51 QUESTION 3 COLONIC NEOPLASM DEVELOPMENT IN ACROMEGALY: Is correlated to GH levels Is correlated to IGF-BP1 levels Is correlated to insulin levels Is correlated to tumor size   


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