Searchable abstracts of presentations at key conferences in endocrinology

ea0073aep537 | Pituitary and Neuroendocrinology | ECE2021

The perspective of patients with pituitary disease on work according to the expanded ICF model: A qualitative study

Merel Van der Meulen , Lobatto Daniel J. , Wouter R. van Furth , Huisman Sasja D. , Heerkens Yvonne F. , Thea P.M. Vliet Vlieland , Biermasz Nienke R. , Andela Cornelie D.

PurposeAs the majority of patients with pituitary disease are of working age, their health situation may negatively impact their functioning at work. However, work participation can also be influenced by contextual (environmental and personal) factors. The aim of this qualitative study was to investigate the perspective of patients with pituitary disease on their functioning at work and on contextual factors contributing to work-related problems, using t...

ea0081oc4.3 | Oral Communications 4: Pituitary and Neuroendocrinology 1 | ECE2022

Long-term efficacy and safety data for oral octreotide capsules in acromegaly: mpowered trial open-label extension phase

Fleseriu Maria , Molitch Mark E , Dreval Alexander , Pokramovich Yulia G , Bondar Irina , Poteshkin Yury E , Macut Djuro P , Obermayer-Pietsch Barbara , Gilgun-Sherki Yossi , Haviv Asi , Biermasz Nienke , Melmed Shlomo , Strasburger Christian J

Background: Oral octreotide capsules (OOC) are a treatment option for patients with acromegaly in the United States. The MPOWERED trial (NCT02685709) showed that OOC were noninferior to injectable somatostatin receptor ligands (iSRLs; octreotide or lanreotide) in maintenance of biochemical control in patients previously responding to both treatments, as well as demonstrated improvements in patient-reported outcomes among patients receiving OOC.Objective:...

ea0081p170 | Pituitary and Neuroendocrinology | ECE2022

Safety comparison of 40- vs 60- mg/day doses of oral octreotide capsules for treatment of acromegaly in the chiasma optimal trial

L. Samson Susan , Nachtigall Lisa B. , Fleseriu Maria , Molitch Mark E. , Giustina Andrea , Haviv Asi , Biermasz Nienke , Kennedy Laurence , Jensterle Mojca , Manning Patrick , Elenkova Atanaska , Melmed Shlomo , Strasburger Christian J.

Background: Oral octreotide capsules (OOC) are a treatment option for patients with acromegaly in the United States who have previously responded to injectable somatostatin receptor ligands (iSRLs, octreotide or lanreotide). In previous phase 3 studies, the safety of OOC was shown to be consistent with iSRLs, without dose-dependent adverse reactions. In the double-blind, placebo-controlled period (DPC) of the CHIASMA OPTIMAL trial (NCT03252353), patients were randomized to twi...

ea0037gp.21.03 | Pituitary – Diagnosis of Cushing's disease | ECE2015

Altered neural processing during emotional faces in remitted Cushing's disease

Andela Cornelie , Hoogendam Janna Marie , Van der Werff Steven , Pannekoek Nienke , Van Steenbergen Henk , Meijer Onno , Van Buchem Mark , Rombouts Serge , Van der Mast Roos , Biermasz Nienke , Van der Wee Nic , Pereira Alberto

Background: Patients with long-term remission of Cushing’s disease (CD) demonstrate residual psychological complaints. At present, it is not known how previous exposure to hypercortisolism affects psychological functioning in the long-term. In foregoing Magnetic Resonance Imaging (MRI) studies, abnormalities of brain structure and resting-state connectivity were demonstrated in patients with long-term remission of CD. However, no data are available on functional alteratio...

ea0070aep44 | Adrenal and Cardiovascular Endocrinology | ECE2020

Etiology and extent of impaired quality of life, fatigue and affective, cognitive, and emotional dysfunction in patients with cushing’s syndrome – The IQFACE-CS study

de Vries Friso , Papakokkinou Eleni , Santos Alicia , van Haalen Femke , Valassi Elena , Biermasz Nienke , Johansson Birgitta , Gómez-Ansón Beatriz , Bauduin Stéphanie , Resmini Eugenia , van der Wee Nic , Pereira Alberto M , Webb Susan , Ragnarsson Oskar

Background: Patients with Cushing’s Syndrome (CS) suffer from a variety of neuropsychiatric and cognitive problems. Following remission, some, but not all of these symptoms resolve. Recent cross-sectional studies in patients with CS show persistent structural and functional brain abnormalities. However, longitudinal studies using magnetic resonance imaging, and a detailed neurocognitive assessment, performed before and after treatment, are not available.<p class="abs...

ea0070aep576 | Pituitary and Neuroendocrinology | ECE2020

Sustained response to treatment with oral octreotide capsules: Results from the phase 3, randomized, double blind, placebo-controlled optimal study

Samson Susan , Nachtigall Lisa , Fleseriu Maria , Baldys Waligorska Agata , Jensterle Mojca , Ur Ehud , Molitch Mark E , Ludlam William , Patou Gary , Haviv Asi , Biermasz Nienke , Kennedy Laurence , Melmed Shlomo , Strasburger Christian J

Background: Patients with acromegaly responding to injectable somatostatin receptor ligands (SRL) are often treated for decades without deterioration of biochemical response (except for routine fluctuations in IGF-I control), unless there are changing clinical circumstances such as persistent or recurrent tumor growth. Oral octreotide capsules (OOC) have been formulated as a potential therapy for acromegaly and the safety and efficacy was evaluated in the CHIASMA OPTIMAL pivot...

ea0070aep612 | Pituitary and Neuroendocrinology | ECE2020

IGF-I variability and its association with demographic and clinical characteristics in patients with acromegaly treated with injectable somatostatin receptor ligands (SRLs); results from OPTIMAL, an international prospective phase 3 study

Samson Susan , Nachtigall Lisa , Fleseriu Maria , Ur Ehud , E Molitch Mark , Ludlam William , Patou Gary , Haviv Asi , Gilgun-Sherki Yossi , Biermasz Nienke , Strasburger Christian J , Kennedy Laurence , Melmed Shlomo

Background: Most patients responding to injectable somatostatin receptor ligands exhibit IGF-I variability around the upper limit of normal (ULN) during long-term follow up. These fluctuations are thought to result from assay variability, nutrition, comorbid conditions, concomitant medications and other unknown factors. The magnitude and factors affecting this variability arenot well understood in patients with acromegaly treated with injectable SRLs.Met...

ea0070aep613 | Pituitary and Neuroendocrinology | ECE2020

Analysis of adverse events in adult patients with acromegaly receiving oral octreotide capsules: Results from the phase 3, randomized, double-blind, placebo-controlled optimal study

Labadzhyan Artak , Samson Susan , Nachtigall Lisa , Fleseriu Maria , Molitch Mark E , Ludlam William , Patou Gary , Haviv Asi , Baldys Waligorska Agata , Biermasz Nienke , Trainer Peter , Kennedy Laurence , Melmed Shlomo , Strasburger Christian J

Background: Distinguishing non-specific signs/symptoms of acromegaly from treatment-emergent adverse events (TEAEs) in patients treated with somatostatin receptor ligands has proven difficult given limited data from placebo-controlled studies. The CHIASMA OPTIMALstudy provides a novel data set to evaluate the incidence of adverse events (AEs) in patients randomized to oral octreotide capsules (OOC) or placebo.Methods: A multinational, randomized, placebo...

ea0070aep668 | Pituitary and Neuroendocrinology | ECE2020

Withdrawal from long-acting somatostatin receptor ligand injections in adult patients with acromegaly: Results from the phase 3, randomized, double-blind, placebo-controlled optimal study

Nachtigall Lisa , Samson Susan , Fleseriu Maria , Bolanowski Marek , E Molitch Mark , Ludlam William , Patou Gary , Haviv Asi , Manning Patrick , Biermasz Nienke , Giustina Andrea , Strasburger Christian J , Melmed Shlomo , Kennedy Laurence

Background: Data on the impact of withdrawal from long-acting somatostatin receptor ligand (SRL) injections on disease activity in patients with acromegaly are limited. The CHIASMA OPTIMAL study assessed the efficacy and safety of oral octreotide capsules (OOC) in adult patients with acromegaly responding to SRL injections. The placebo arm of this study allowed for assessment of acromegaly activity in patients after withdrawal from SRL treatment.Methods:...

ea0070aep669 | Pituitary and Neuroendocrinology | ECE2020

Impact of imputation method on efficacy results from the phase 3 optimal study of oral octreotide capsules in adult patients with acromegaly

Samson Susan , Nachtigall Lisa , Fleseriu Maria , Gordon Murray , Jensterle Mojca , Elenkova Atanaska , Molitch Mark E , Ludlam William , Patou Gary , Haviv Asi , Biermasz Nienke , Trainer Peter , Strasburger Christian J , Kennedy Laurence , Melmed Shlomo

Objective: The phase 3 CHIASMA OPTIMAL study assessed efficacy and safety of oral octreotide capsules (OOC) in patients with acromegaly controlled on injectable somatostatin receptor ligands (SRLs). Sensitivity analyses were conducted for efficacy endpoints using two methods of imputation (i.e., the process of replacing clinical data with substitution values) to address missing data points due to some subjects reverting back to their prior injectable SRL treatment.<p class...