Clinical, hormonal and pathomorphological markers of somatotroph pituitary neuroendocrine tumors predicting the treatment outcome in acromegaly.


Journal

Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782

Informations de publication

Date de publication:
2022
Historique:
received: 30 05 2022
accepted: 29 08 2022
entrez: 3 10 2022
pubmed: 4 10 2022
medline: 5 10 2022
Statut: epublish

Résumé

Transsphenoidal adenomectomy (TSS) of somatotroph pituitary neuroendocrine tumor (PitNET) is the first-line treatment of acromegaly. Pharmacological treatment is recommended if surgery is contraindicated or did not lead to disease remission. The choice of treatment best fitting each patient should be based on thorough investigation of patients' characteristics. The current analysis attempts to create a tool for personalized treatment planning. This study aimed to assess whether clinical, biochemical, imaging and pathological characteristics can predict surgical remission and response to first-generation somatostatin receptor ligands (SRLs) and pasireotide-LAR in acromegaly. A retrospective study of 153 acromegaly patients, treated in the Department of Endocrinology in Bielanski Hospital in Warsaw, Poland was performed. Data on demographics, hormonal and imaging results, pathological evaluation, and treatment outcome was extracted from the Polish Acromegaly Registry collecting information from 11 endocrinology centers in Poland and analyzed. Patients with surgical remission had lower GH and IGF-1 concentrations at diagnosis (median GH 5.5 µg/L [IQR: 3.1-16.0] Younger age at diagnosis, male sex, lower GH, IGF-1 and PRL concentrations, smaller tumor size at diagnosis as well as positive α-SU staining, lower Ki-67 index and DG tumors predicted better treatment outcome in acromegaly patients.

Sections du résumé

Background
Transsphenoidal adenomectomy (TSS) of somatotroph pituitary neuroendocrine tumor (PitNET) is the first-line treatment of acromegaly. Pharmacological treatment is recommended if surgery is contraindicated or did not lead to disease remission. The choice of treatment best fitting each patient should be based on thorough investigation of patients' characteristics. The current analysis attempts to create a tool for personalized treatment planning.
Aim
This study aimed to assess whether clinical, biochemical, imaging and pathological characteristics can predict surgical remission and response to first-generation somatostatin receptor ligands (SRLs) and pasireotide-LAR in acromegaly.
Patients and methods
A retrospective study of 153 acromegaly patients, treated in the Department of Endocrinology in Bielanski Hospital in Warsaw, Poland was performed. Data on demographics, hormonal and imaging results, pathological evaluation, and treatment outcome was extracted from the Polish Acromegaly Registry collecting information from 11 endocrinology centers in Poland and analyzed.
Results
Patients with surgical remission had lower GH and IGF-1 concentrations at diagnosis (median GH 5.5 µg/L [IQR: 3.1-16.0]
Conclusions
Younger age at diagnosis, male sex, lower GH, IGF-1 and PRL concentrations, smaller tumor size at diagnosis as well as positive α-SU staining, lower Ki-67 index and DG tumors predicted better treatment outcome in acromegaly patients.

Identifiants

pubmed: 36187106
doi: 10.3389/fendo.2022.957301
pmc: PMC9523725
doi:

Substances chimiques

Ki-67 Antigen 0
Receptors, Somatostatin 0
Insulin-Like Growth Factor I 67763-96-6

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

957301

Informations de copyright

Copyright © 2022 Tomasik, Stelmachowska-Banaś, Maksymowicz, Czajka-Oraniec, Raczkiewicz, Zieliński, Kunicki and Zgliczyński.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Agnieszka Tomasik (A)

Department of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland.

Maria Stelmachowska-Banaś (M)

Department of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland.

Maria Maksymowicz (M)

Department of Cancer Pathomorphology, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Izabella Czajka-Oraniec (I)

Department of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland.

Dorota Raczkiewicz (D)

Department of Medical Statistics, School of Public Health, Centre of Postgraduate Medical Education, Warsaw, Poland.

Grzegorz Zieliński (G)

Department of Neurosurgery, Military Institute of Medicine, Warsaw, Poland.

Jacek Kunicki (J)

Department of Neurosurgery, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Wojciech Zgliczyński (W)

Department of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland.

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Classifications MeSH