Evidence map›Paper›PMID 28556544›Full record

ArticleCNS neuroscience & therapeutics2017

Pituicytoma-An outlook on possible targeted therapies.

Klaus Christian Mende, Jakob Matschke, Till Burkhardt, Wolfgang Saeger, Rolf Buslei, Michael Buchfelder, Rudolf Fahlbusch, Manfred Westphal, Jörg Flitsch

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Primary tumors of the posterior pituitary: A systematic review.Reviews in endocrine & metabolic disorders · 2019
    Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Clinical features, diagnosis and therapy of pituicytoma: an update.Journal of endocrinological investigation · 2019
    Review
  9. Article
  10. Pituicytoma-An outlook on possible targeted therapies.CNS neuroscience & therapeutics · 2017
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Klaus Christian MendeDepartment of Neurosurgery, Hamburg University Medical Center, Hamburg, Germany.ORCID http://orcid.org/0000-0003-4317-1718
Jakob MatschkeInstitute of Neuropathology, Hamburg University Medical Center, Hamburg, Germany.
Till BurkhardtDepartment of Neurosurgery, Hamburg University Medical Center, Hamburg, Germany.
Wolfgang SaegerInstitute of Neuropathology, Hamburg University Medical Center, Hamburg, Germany.
Rolf BusleiDepartment of Neuropathology, University of Erlangen, Erlangen, Germany.
Michael BuchfelderDepartment of Neurosurgery, University of Erlangen, Erlangen, Germany.
Rudolf FahlbuschInternational Neuroscience Institute Hannover GmbH, Hannover, Germany.
Manfred WestphalDepartment of Neurosurgery, Hamburg University Medical Center, Hamburg, Germany.
Jörg FlitschDepartment of Neurosurgery, Hamburg University Medical Center, Hamburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPituicytoma 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.

aimsWe aimed to determine the receptor expression of pituicytoma to find alternatives or supplements to surgical therapy in the use of targeted therapies.

methodsPituicytoma 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.

resultsTen 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.

conclusionsPituicytomas 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.

Indexed as

AdultAgedDNA-Binding ProteinsFemaleHumansIntraoperative ComplicationsMaleMiddle AgedNeoplasm Recurrence, LocalPituitary NeoplasmsPostoperative ComplicationsReceptors, SomatostatinRetrospective StudiesTranscription FactorsVascular Endothelial Growth Factor AYoung AdultDNA-Binding ProteinsReceptors, SomatostatinTranscription FactorsTTF1 protein, humanVascular Endothelial Growth Factor AVEGFA protein, humanpituicytomaSSTRtargeted therapyVEGF

Identifiers

PMID28556544
PMCPMC6492650

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.