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Pituicytoma-An outlook on possible targeted therapies

Authors :
Rolf Buslei
Jakob Matschke
Klaus Christian Mende
Wolfgang Saeger
Manfred Westphal
Michael Buchfelder
Till Burkhardt
Rudolf Fahlbusch
Jörg Flitsch
Source :
CNS Neuroscience & Therapeutics. 23:620-626
Publication Year :
2017
Publisher :
Wiley, 2017.

Abstract

SummaryIntroduction Pituicytoma is a rare neoplasm of the sella region. Tumor resection is the primary treatment option, but remains subtotal due to excessive bleeding in many cases. The search for alternative or additional treatment regimens is necessary. Aims We aimed to determine the receptor expression of pituicytoma to find alternatives or supplements to surgical therapy in the use of targeted therapies. Methods Pituicytoma samples were collected from three institutions between 2006 and 2015 and were stained for vascular endothelial growth factors (VEGF), thyroid transcription factor (TTF1), and somatostatin receptors (SSTR 2/3/5). The stains were classified from 0=no staining to +++=strong staining. A complementary retrospective analysis of the patient charts regarding sex, age, and primary symptoms, pituitary function, and perioperative complications was performed. Results Ten samples were analyzed; mean patient age was 57.8 years SD 16.3 years. Seven samples were acquired from male patients (one relapse) and three from female. All tumors stained strongly positive (+++) for VEGF-R. Six samples stained positive for TTF1. As for somatostatin receptors, three samples were slightly positive for SSTR 2; seven were negative. SSTR 3 was + in one, three were ++, three were +++, and three were 0. SSTR 5 stained +++ in 1, ++ in 5, + in 1, and 0 in three patients. Conclusions Pituicytomas were generally positive for VEGFR and showed regular expression of SSTR 3 and 5 indicating a possible treatment option through targeted therapies in cases where resection remains insufficient. Further research is necessary as to whether tumor growth can be inhibited using these pathways.

Details

ISSN :
17555930
Volume :
23
Database :
OpenAIRE
Journal :
CNS Neuroscience & Therapeutics
Accession number :
edsair.doi.dedup.....c954bbd093b128b372668d663950715d