Literature DB >> 24443791

Impact of long-acting octreotide in patients with early-stage MEN1-related duodeno-pancreatic neuroendocrine tumours.

V Ramundo1, M Del Prete, V Marotta, F Marciello, L Camera, V Napolitano, L De Luca, L Circelli, V Colantuoni, A Di Sarno, A C Carratù, C de Luca di Roseto, A Colao, A Faggiano.   

Abstract

BACKGROUND: Somatostatin analogues (SSA) represent one of the main therapeutic option in patients affected with functioning well-differentiated neuroendocrine tumours (NETs). There are no studies specifically focusing on NETs associated with Multiple Endocrine Neoplasia type 1 (MEN1). AIM: To evaluate the efficacy of the long-acting SSA octreotide in MEN1 patients with early-stage duodeno-pancreatic NETs. PATIENTS AND METHODS: Forty patients with MEN1 were retrospectively evaluated. Twenty patients with evidence of one or more MEN1-related duodeno-pancreatic NETs < 20 mm in size (age range 26-61 years) were treated with octreotide long-acting octreotide (LAR) as first-line therapy. Treatment duration ranged 12-75 months. At the baseline radiological evaluation, multiple duodeno-pancreatic NETs (range 1-8, size 3-18 mm) were detected.
RESULTS: An objective tumour response was observed in 10%, stable disease in 80% and progression of disease in 10% of cases. In six patients with abnormally increased CgA, gastrin and/or insulin serum concentrations, a significant clinical and hormonal response occurred in 100% of cases and was stable along the time.
CONCLUSIONS: Therapy with SSA is highly safe and effective in patients with early-stage MEN1 duodeno-pancreatic NETs, resulting in long-time suppression of tumour and hormonal activity and 10% objective response. This suggests to early start therapy with SSA in patients with MEN1-related NETs.
© 2014 John Wiley & Sons Ltd.

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Year:  2014        PMID: 24443791     DOI: 10.1111/cen.12411

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


  11 in total

1.  Systemic therapy in incurable gastroenteropancreatic neuroendocrine tumours: a clinical practice guideline.

Authors:  S Singh; D Sivajohanathan; T Asmis; C Cho; N Hammad; C Law; R Wong; K Zbuk
Journal:  Curr Oncol       Date:  2017-08-31       Impact factor: 3.677

2.  The LARO-MEN1 study: a longitudinal clinical experience with octreotide Long-Acting Release in patients with Multiple Endocrine Neoplasia type 1 Syndrome.

Authors:  Federica Cioppi; Luisella Cianferotti; Laura Masi; Francesca Giusti; Maria Luisa Brandi
Journal:  Clin Cases Miner Bone Metab       Date:  2017-10-25

Review 3.  Everolimus-based combination for the treatment of advanced gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs): biological rationale and critical review of published data.

Authors:  Omar Abdel-Rahman; Mona Fouad
Journal:  Tumour Biol       Date:  2015-01-18

4.  Cinacalcet therapy in patients affected by primary hyperparathyroidism associated to Multiple Endocrine Neoplasia Syndrome type 1 (MEN1).

Authors:  Francesca Giusti; Luisella Cianferotti; Giorgio Gronchi; Federica Cioppi; Laura Masi; Antongiulio Faggiano; Annamaria Colao; Piero Ferolla; Maria Luisa Brandi
Journal:  Endocrine       Date:  2015-07-30       Impact factor: 3.633

5.  Prognostic role of the CDNK1B V109G polymorphism in multiple endocrine neoplasia type 1.

Authors:  Luisa Circelli; Valeria Ramundo; Vincenzo Marotta; Concetta Sciammarella; Francesca Marciello; Michela Del Prete; Lina Sabatino; Daniela Pasquali; Francesco Izzo; Stefania Scala; Annamaria Colao; Antongiulio Faggiano; Vittorio Colantuoni
Journal:  J Cell Mol Med       Date:  2015-03-30       Impact factor: 5.310

6.  Predictive factors of antiproliferative activity of octreotide LAR as first-line therapy for advanced neuroendocrine tumours.

Authors:  Faidon-Marios Laskaratos; Martin Walker; Keval Naik; Emmanouil Maragkoudakis; Nikolaos Oikonomopoulos; Lee Grant; Tim Meyer; Martyn Caplin; Christos Toumpanakis
Journal:  Br J Cancer       Date:  2016-11-03       Impact factor: 7.640

7.  Octreotide Use in a Patient with MEN-1 Syndrome and Multifocal Pancreatic Neuroendocrine Tumors: A Case Report and Review of the Literature.

Authors:  Matthew H Kemm; Cory D Manly; Thanh D Hoang; Vinh Q Mai; Mohamed K M Shakir
Journal:  Case Rep Gastrointest Med       Date:  2019-04-30

Review 8.  Current and emerging therapies for PNETs in patients with or without MEN1.

Authors:  Morten Frost; Kate E Lines; Rajesh V Thakker
Journal:  Nat Rev Endocrinol       Date:  2018-02-16       Impact factor: 43.330

Review 9.  Multiple Endocrine Neoplasia Type 1: Latest Insights.

Authors:  Maria Luisa Brandi; Sunita K Agarwal; Nancy D Perrier; Kate E Lines; Gerlof D Valk; Rajesh V Thakker
Journal:  Endocr Rev       Date:  2021-03-15       Impact factor: 19.871

10.  A Direct Comparison of Patients With Hereditary and Sporadic Pancreatic Neuroendocrine Tumors: Evaluation of Clinical Course, Prognostic Factors and Genotype-Phenotype Correlations.

Authors:  Przemysław Soczomski; Beata Jurecka-Lubieniecka; Aleksandra Krzywon; Alexander Jorge Cortez; Stanisław Zgliczynski; Natalia Rogozik; Małgorzata Oczko-Wojciechowska; Agnieszka Pawlaczek; Tomasz Bednarczuk; Barbara Jarzab
Journal:  Front Endocrinol (Lausanne)       Date:  2021-05-28       Impact factor: 5.555

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