Searchable abstracts of presentations at key conferences in endocrinology

ea0063s4.2 | Immunology and endocrinology (Endorsed by Endocrine Connections) | ECE2019

Clinical: Immunotherapy and endocrine disease

Stelmachowska-Banaś Maria

Immunotherapy with immune checkpoint inhibitors has become an effective treatment of many malignancies resistant to conventional chemotherapies. Immune checkpoints are molecules on the surface of immune cells involved in the regulation of the immune response and immune checkpoint inhibitors are monoclonal antibodies directed against certain immune checkpoints, such as cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) and programmed death 1 (PD-1) and its ligand (PD-L1), res...

ea0073aep492 | Pituitary and Neuroendocrinology | ECE2021

GH and IGF-1 discrepancies in acromegaly patients after pituitary surgery – an observational single-center study

Tomasik Agnieszka , Maria Stelmachowska-Banaś , Wojciech Zgliczynski

IntroductionTreatment of choice in acromegaly is transsphenoidal resection of GH-secreting pituitary adenoma. Its efficacy ranges from 28% to 83% depending on tumor size and location. Random GH < 1 µg/l or nadir GH in OGTT < 0.4 µg/l and normal IGF-1 are found to be the evidence of effective surgery. However, some patients diagnosed with acromegaly remission after surgery present discordant GH and IGF-1 results.Ai...

ea0070ep293 | Pituitary and Neuroendocrinology | ECE2020

Pasireotide LAR in acromegaly resistant to first generation somatostatin analogs – single-center prospective interventional study

Majos Agnieszka , Stelmachowska-Banaś Maria , Czajka-Oraniec Izabella , Zgliczyński Wojciech

Introduction: The treatment of choice in persistent acromegaly after transsphenoidal adenomectomy is pharmacological treatment with first generation somatostatin analogs. They are effective in 25% to 45% of patients. Second generation somatostatin analog – pasireotide seems to be more effective.Aim: The aim of the study was to assess the efficacy and safety of pasireotide LAR in acromegaly patients resistant to first generation somatostatin analogs...

ea0090p428 | Pituitary and Neuroendocrinology | ECE2023

Effects of acromegaly treatment on left ventricular systolic function assessed by speckle tracking echocardiography: results from a prospective single-center study

Popielarz-Grygalewicz Agata , Stelmachowska-Banaś Maria , Raczkiewicz Dorota , Kochman Wacław , Zgliczyński Wojciech

Background: Despite the preserved left ventricular(LV) ejection fraction, patients with acromegaly are characterized by subclinical systolic dysfunction, i.e. abnormal global longitudinal strain(GLS) assessed by speckle-tracking echocardiography(STE). The effect of acromegaly treatment on LV systolic function assesed by STE has not been evaluated so far.Patients and methods: Thirty two naïve acromegaly patients with no detectable heart disease were ...

ea0090p467 | Reproductive and Developmental Endocrinology | ECE2023

A rare co-occurence of Turner syndrome and acromegaly complicated by the presence of a solid pseudopapillary neoplasm of pancreas-a case report

Cylke-Falkowska Karolina , Stelmachowska-Banaś Maria , Cichocki Andrzej , Zieliński Grzegorz , Zgliczyński Wojciech

Background: Turner syndrome (TS) is the most common chromosome deficiency in women, with an incidence of 1 in 2 000 female newborns. Acromegaly is a rare disease, which occurs with a frequency of 1:140 000–250 000 of the population. To our knowledge only several cases of TS and acromegaly coexistance have been reported up to date.Case presentation: A 43-year-old woman with TS was referred to our Department with an accidentally discovered pituitary m...

ea0090ep699 | Pituitary and Neuroendocrinology | ECE2023

Pathologic characteristics of somatotroph pituitary tumors – an observational single-center study

Tomasik Agnieszka , Stelmachowska-Banaś Maria , Maksymowicz Maria , Czajka-Oraniec Izabella , Dorota Raczkiewicz , Zgliczyński Wojciech

Background: The first-line treatment in acromegaly is transsphenoidal adenomectomy of GH-secreting pituitary tumor. Pathologic evaluation of postoperative tissue is an essential part of patient’s assessment.Aim: The aim of this study was to analyse pathologic characteristics of pituitary tumors in patients with acromegaly.Patients and methods: One hundred twenty patients with acromegaly after at least one pituitary surgery tre...

ea0063gp51 | Acromegaly and GH | ECE2019

Prognostic value of short-acting pasireotide test for response prediction to pasireotide LAR in patients with acromegaly resistant to first-generation analogs. Can a short-acting pasireotide test predict the response of long-acting pasireotide treatment in patients with acromegaly resistant to first generation somatostatin analogs?

Majos Agnieszka , Stelmachowska-Banaś Maria , Czajka-Oraniec Izabella , Gęsior Jakub , Zgliczyński Wojciech

Introduction: The treatment of choice in acromegaly is a transsphenoidal surgery of a growth hormone (GH) - producing pituitary adenoma. In patients with persistent acromegaly after surgery medical treatment is recommended. First generation somatostatin analogs: lanreotide autogel and octreotide LAR are effective in 25% to 45% of patients depending on population and study protocol. Second-generation somatostatin analog – pasireotide LAR seems to be more effective. The pos...

ea0081ep657 | Pituitary and Neuroendocrinology | ECE2022

Pathomorphological markers of somatotroph neuroendocrine tumors predicting the treatment outcome in acromegaly

Tomasik Agnieszka , Stelmachowska-Banaś Maria , Maksymowicz Maria , Czajka-Oraniec Izabella , Raczkiewicz Dorota , Zieliński Grzegorz , Kunicki Jacek , Zgliczyński Wojciech

Background: Transsphenoidal adenomectomy of GH-secreting pituitary tumour is a first-line treatment of acromegaly. Pharmacological treatment is recommended if surgery did not lead to disease remission. Pathological assessment of postoperative tissue provides clinicians with valuable information on the disease course.Aim: The aim of this study was to assess whether clinical, imaging, and pathological characteristics can predict surgical remission and resp...

ea0086p106 | Neuroendocrinology and Pituitary | SFEBES2022

Identifying and characterising variants in patients with pachydermoperiostosis

Angurala Ishita , Barry Sayka , Rice Tom , Magid Kesson , Rai Ashutosh , Benjamin Loughrey Paul , Dutta Pinaki , Stelmachowska Banaś Maria , Korbonits Marta

Introduction: Pachydermoperiostosis (primary hypertrophic osteoarthropathy, PHOA) is a rare genetic condition characterised by digital clubbing, pachydermia, hyperhidrosis, cutis verticis gyrata and periostosis. The SLCO2A1 transporter and HPGD enzyme genes play an important role in prostaglandin metabolism, hence loss of function mutations in them causes PHOA. To date, according to the VarSome database 101 and 41 variants have been identified in the SLCO...

ea0063p724 | Pituitary and Neuroendocrinology 2 | ECE2019

The influence of acromegaly treatment on subclinical left ventricular dysfunction assessed by two-dimensional speckle tracking echocardiography (2D-STE)-preliminary results

Popielarz-Grygalewicz Agata , Stelmachowska-Banaś Maria , Gęsior Jakub , Czubalska Magdalena , Zgliczyński Wojciech , Kochman Wacław

Introduction: Cardiac disease called acromegalic cardiomyopathy may be present in patients with acromegaly at diagnosis, however most echocardiographic studies showed that systolic function, measured by ejection fraction (EF), in these patients is normal. Speckle tracking echocardiography (STE) is a novel method that allows for the study of global longitudinal strain (GLS), a marker of early and subclinical left ventricular (LV) systolic dysfunction. Some studies show subclini...