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T2-weighted MRI signal intensity of pituitary adenomas in acromegaly correlates with the response to primary medical therapy with somatostatin analogues

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Academic year: 2021

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T2-weighted MRI signal intensity of pituitary adenomas in acromegaly correlates with the response to primary medical therapy with somatostatin analogues

Authors: Iulia Potorac1, Patrick Petrossians1, Adrian F Daly1, Mona Sahnoun-Fathallah2, Frederic Castinetti2, Thierry Brue2, Orsalia Alexopoulou3, Dominique Maiter3, Franck Schillo4, France Devuyst5, Bernard Corvilain5, Ammar Muhammad6, Sebastian J.C.M.M. Neggers6, Fahrettin Kelestimur7, Christof Schofl8, Flavius Zoicas8, Michael Buchfelder8, Elena Nazzari9, Laura Roffredo9, Diego Ferone9, Florina Luca10, Bernard Goichot10, Gerald Raverot11, Veronique Lapras11, Sophie Kalfon11, Emmanuel Jouanneau11, Susan M. Webb12, Analia Emilce Ramos13, Frederic Illouz14, Vincent Rohmer14, Patrice Rodien14, Isabelle Simoneau15, Jean-Michel Petit15, Alpha M Diallo16, Brigitte Delemer16, Marie-Lise Jaffrain-Rea17, Rogelio Garcia Centeno18, Marie-Laure Nunes19, Antoine Tabarin19, Vaclav Hana20, Véronique Pascal-Vigneron21, Farida Nasybullina22, Gulnar Vagapova22, Luaba Tshibanda1, Jean-François Bonneville1 and Albert Beckers1

Affiliations: 1CHU de Liège-University of Liège, Liège, Belgium, 2CHU Marseille, Marseille, France,

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Université Catholique de Louvain, Brussels, Belgium, 4CHU Besancon, Besancon, France, 5Université Libre de Bruxelles, Bruxelles, Belgium, 6Erasmus University Medical Center Rotterdam, Rotterdam, Netherlands, 7Faculty of Medicine, Erciyes University, Kayseri, Turkey, 8Universitätsklinikum Erlangen, Erlangen, Germany, 9University of Genova, Genova, Italy, 10CHU Strasbourg, Strasbourg, France,

11CHU Lyon, Lyon, France, 12Hospital Sant Pau, Centro de Investigación Biomédica en Red de

Enfermedades Raras (CIBER-ER, Unidad 747), ISCIII and Universitat Autònoma de Barcelona (UAB), Barcelona, Spain, 13Universitat Autonoma de Barcelona, Barcelona, Spain, 14CHU Angers, Angers, France, 15CHU Bocage, Dijon, France, 16CHU Reims, Reims, France, 17University of L’Aquila, Italy,

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Hospital Univesitario Gregorio Maranon, Madrid, Spain, 19CHU Bordeaux, Bordeaux, France,

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Charles University, Prague, Czech Republic, 21CHU Nancy, Nancy, France, 22Kazan State Medical Academy, Kazan, Russia

Introduction: GH-secreting pituitary adenomas can be hypo-, iso- or hyperintense on T2-weighted MRI sequences. We observed that GH-secreting adenomas differ in their presentation and response to somatostatin analogues (SSA) depending on their T2-intensities. We conducted the current multicenter study to validate these results in a large population of patients with acromegaly that received SSA as primary monotherapy.

Method: Acromegaly patients primarily treated with SSA for at least 3 months were included in the study. Hormonal, clinical and general MRI assessments were performed and the data were

centralized. In addition, ROI measurement of the adenoma, normal pituitary tissue and temporal grey matter was performed. A ratio between the adenoma ROI and that of the reference tissues was calculated in order to correct for inter-exam variations.

Results: 106 acromegalic patients were included. Of these, 76 were T2-hypointense, 14 iso- and 16 hyperintense at diagnosis. SSA treatment duration was similar in the 3 groups. T2-hypointense adenomas had a better response to SSA treatment. The response correlated with the calculated ratio

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of T2-intensity. The lower the T2-weighted intensity, the greater the decrease of random GH (p<0.0001, r2=0.49), IGF1%ULN (p=0.0003, r2=0.113) and adenoma volume (p<0.0001, r2=0.378). Conclusion: T2-weighted signal intensity of GH-secreting adenomas correlates with the response to SSA primary treatment in acromegaly. This information could help in initial management decisions, as the information is available at the baseline diagnosis. Routine use of pituitary adenoma T2-weighted signal intensity on MRI could be useful in acromegaly assessment and management. Further studies are underway to explain the molecular mechanisms underlying the behavior of adenomas with different T2-weighted signal intensities.

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